Pedigree disequilibrium tests for multilocus haplotypes.
paper
Cited
Public
Unavailable
- Authors
- Dudbridge, Frank
- Year
- 2003
- Journal
- Genetic epidemiology
- PMID
- 12916020
- DOI
- 10.1002/gepi.10252
Association tests of multilocus haplotypes are of interest both in linkage disequilibrium mapping and in candidate gene studies. For case-parent trios, I discuss the extension of existing multilocus methods to include ambiguous haplotypes in tests of models which distinguish between the cis and trans phase. A likelihood-ratio test is proposed, using the expectation-maximization (E-M) algorithm to account for haplotype ambiguities. Assumptions about the population structure are required, but realistic situations, including population stratification, which violate the assumptions lead to conservative tests. I describe a permutation procedure for the null hypothesis of interest, which controls for violation of the assumptions. For general pedigrees, I describe extensions of the pedigree disequilibrium test to include uncertain haplotypes. The summary statistics are replaced by their expected values over prior distributions of haplotype frequencies. If prior distributions are not available, a valid test is possible by using the E-M algorithm to estimate the null distribution of haplotype frequencies. Similar methods are available for quantitative traits. Exact permutation tests are difficult to construct in small samples, but an approximate procedure is appropriate in large samples, and can be used to account for dependencies between tests of multiple haplotypes and loci.
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| Prolactin as a biomarker for treatment response and tardive dyskinesia in schizophrenia subjects: old thoughts revisited from a genetic perspective. | Souza RP et al. | β | 2011 | β |
| Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability. | Bhowmik AD et al. | β | 2011 | β |
| Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands. | Das M et al. | β | 2011 | β |
| Serotonin 1A receptor gene, schizophrenia and bipolar disorder: an association study and meta-analysis. | Kishi T et al. | β | 2011 | β |
| Serotonin 6 receptor gene is associated with methamphetamine-induced psychosis in a Japanese population. | Kishi T et al. | β | 2011 | β |
| SIRT1 gene, schizophrenia and bipolar disorder in the Japanese population: an association study. | Kishi T et al. | β | 2011 | β |
| Smoking and two human leukocyte antigen genes interact to increase the risk for multiple sclerosis. | HedstrΓΆm AK et al. | β | 2011 | β |
| SP-A1, SP-A2 and SP-D gene polymorphisms in severe acute respiratory syncytial infection in Chilean infants. | Ampuero S et al. | β | 2011 | β |
| The association of schizophrenia risk D-amino acid oxidase polymorphisms with sensorimotor gating, working memory and personality in healthy males. | Roussos P et al. | β | 2011 | β |
| The CACNA1C and ANK3 risk alleles impact on affective personality traits and startle reactivity but not on cognition or gating in healthy males. | Roussos P et al. | β | 2011 | β |
| The CLOCK gene and mood disorders: a case-control study and meta-analysis. | Kishi T et al. | β | 2011 | β |
| The influence of schizophrenia-related neuregulin-1 polymorphisms on sensorimotor gating in healthy males. | Roussos P et al. | β | 2011 | β |
| The Ξ±7 nicotinic acetylcholine receptor and the acute stress response: maternal genotype determines offspring phenotype. | Sinkus ML et al. | β | 2011 | β |
| Weak association of the platelet-derived growth factor beta (PDGFB) and PDGF receptor beta (PDGFRB) genes with schizophrenia and schizoaffective disorder. | Zai G et al. | β | 2011 | β |
| X chromosome and suicide. | Fiori LM et al. | β | 2011 | β |
| A common polymorphism in the cannabinoid receptor 1 (CNR1) gene is associated with antipsychotic-induced weight gain in Schizophrenia. | Tiwari AK et al. | β | 2010 | β |
| A functional haplotype in the 3'untranslated region of TNFRSF1B is associated with tuberculosis in two African populations. | MΓΆller M et al. | β | 2010 | β |
| Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1. | Palmieri L et al. | β | 2010 | β |
| A megalin polymorphism associated with promoter activity and Alzheimer's disease risk. | Vargas T et al. | β | 2010 | β |
| Analysis of eight genes modulating interferon gamma and human genetic susceptibility to tuberculosis: a case-control association study. | MΓΆller M et al. | β | 2010 | β |
| A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry. | Strohmaier J et al. | β | 2010 | β |
| A RecQ Protein-like 5 Haplotype is Associated With Colon Cancer. | Ochs-Balcom HM et al. | β | 2010 | β |
| Association analyses between brain-expressed fatty-acid binding protein (FABP) genes and schizophrenia and bipolar disorder. | Iwayama Y et al. | β | 2010 | β |
| Association analysis of DAOA and DAO in bipolar disorder: results from two independent case-control studies. | Gaysina D et al. | β | 2010 | β |
| Association analysis of GRM2 and HTR2A with methamphetamine-induced psychosis and schizophrenia in the Japanese population. | Tsunoka T et al. | β | 2010 | β |
| Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder. | Walker RM et al. | β | 2010 | β |
| Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS). | Thiselton DL et al. | β | 2010 | β |
| Association between TGFB3 and nonsyndromic cleft lip with or without cleft palate in a Chilean population. | Suazo J et al. | β | 2010 | β |
| Association of DISC1 and TSNAX genes and affective disorders in the depression case-control (DeCC) and bipolar affective case-control (BACCS) studies. | Schosser A et al. | β | 2010 | β |
| Association of functional variants in the dopamine D2-like receptors with risk for gambling behaviour in healthy Caucasian subjects. | Lobo DS et al. | β | 2010 | β |
| Association of HPA axis genes with suicidal behaviour in schizophrenia. | De Luca V et al. | β | 2010 | β |
| Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide. | Fiori LM et al. | β | 2010 | β |
| Association of polymorphisms in the BDNF, DRD1 and DRD3 genes with tobacco smoking in schizophrenia. | Novak G et al. | β | 2010 | β |
| Association of single nucleotide gene polymorphism at interleukin-1beta +3954, -511, and -31 in chronic periodontitis and aggressive periodontitis in Dravidian ethnicity. | Shete AR et al. | β | 2010 | β |
| Association of the GABRD gene and childhood-onset mood disorders. | Feng Y et al. | β | 2010 | β |
| Association of the orphan nuclear receptor NR4A1 with tardive dyskinesia. | Novak G et al. | β | 2010 | β |
| Associations between common arginine vasopressin 1b receptor and glucocorticoid receptor gene variants and HPA axis responses to psychosocial stress in a child psychiatric population. | van West D et al. | β | 2010 | β |
| Association study between a polymorphism at the 3'-untranslated region of CLOCK gene and attention deficit hyperactivity disorder. | Xu X et al. | β | 2010 | β |
| Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women. | Costas J et al. | β | 2010 | β |
| Association study of SNAP25 and schizophrenia in Irish family and case-control samples. | Fanous AH et al. | β | 2010 | β |
| Association study of the GSK-3B gene with tardive dyskinesia in European Caucasians. | Souza RP et al. | β | 2010 | β |
| Association study of the serotoninergic system in migraine in the Spanish population. | Corominas R et al. | β | 2010 | β |
| Association study of ubiquitin-specific peptidase 46 (USP46) with bipolar disorder and schizophrenia in a Japanese population. | Kushima I et al. | β | 2010 | β |
| Brain cannabinoid CB2 receptor in schizophrenia. | Ishiguro H et al. | β | 2010 | β |
| Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy. | Hershberger RE et al. | β | 2010 | β |
| Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci. | International Multiple Sclerosis Genetics Consortium (IMSGC) | β | 2010 | β |
| Depletion of potential A2M risk haplotype for Alzheimer's disease in long-lived individuals. | Flachsbart F et al. | β | 2010 | β |
| Differential allelic distribution of V-ets erythroblastosis virus E26 oncogene homolog2 (ETS2) functional polymorphisms in different group of patients. | Chatterjee A et al. | β | 2010 | β |
| DTNBP1 gene is associated with some symptom factors of schizophrenia in Chinese Han nationality. | Sun YH et al. | β | 2010 | β |
| Effect of dopamine D3 receptor gene polymorphisms and clozapine treatment response: exploratory analysis of nine polymorphisms and meta-analysis of the Ser9Gly variant. | Hwang R et al. | β | 2010 | β |
| Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD. | Park J et al. | β | 2010 | β |
| Failure to confirm genetic association of the FXYD6 gene with schizophrenia: the Japanese population and meta-analysis. | Iwata Y et al. | β | 2010 | β |
| Family-based studies indicate association of Engrailed 2 gene with autism in an Indian population. | Sen B et al. | β | 2010 | β |
| Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort. | Amundsen SS et al. | β | 2010 | β |
| GABRR1 and GABRR2, encoding the GABA-A receptor subunits rho1 and rho2, are associated with alcohol dependence. | Xuei X et al. | β | 2010 | β |
| Genetic association of the interaction between the BDNF and GSK3B genes and major depressive disorder in a Chinese population. | Zhang K et al. | β | 2010 | β |
| Genetic associations in Italian primary sclerosing cholangitis: heterogeneity across Europe defines a critical role for HLA-C. | Hov JR et al. | β | 2010 | β |
| Genetic polymorphisms and human sensitivity to opioid analgesics. | Nishizawa D et al. | β | 2010 | β |
| Genetic polymorphisms in the SCN8A gene are associated with suicidal behavior in psychiatric disorders in the Chinese population. | Wang Y et al. | β | 2010 | β |
| Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia. | Nishizawa H et al. | β | 2010 | β |
| Genome-wide association study of alcohol dependence implicates a region on chromosome 11. | Edenberg HJ et al. | β | 2010 | β |
| Haplotype association analyses in resources of mixed structure using Monte Carlo testing. | Abo R et al. | β | 2010 | β |
| HLA-class I markers and multiple sclerosis susceptibility in the Italian population. | Bergamaschi L et al. | β | 2010 | β |
| HTR2A is associated with SSRI response in major depressive disorder in a Japanese cohort. | Kishi T et al. | β | 2010 | β |
| Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study. | Burdon KP et al. | β | 2010 | β |
| Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population. | So HC et al. | β | 2010 | β |
| Impact of the AHI1 gene on the vulnerability to schizophrenia: a case-control association study. | Rivero O et al. | β | 2010 | β |
| Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease. | Prescott NJ et al. | β | 2010 | β |
| Inferring haplotype/disease association by joint use of case-parents trios and case-parent pairs. | Hu YQ et al. | β | 2010 | β |
| Interethnic diversity of NAT2 polymorphisms in Brazilian admixed populations. | Talbot J et al. | β | 2010 | β |
| Lack of association between MAGEL2 and schizophrenia and mood disorders in the Japanese population. | Fukuo Y et al. | β | 2010 | β |
| Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. | International Multiple Sclerosis Genetics Consortium (IMSGC) et al. | β | 2010 | β |
| Low CD38 expression in lymphoblastoid cells and haplotypes are both associated with autism in a family-based study. | Lerer E et al. | β | 2010 | β |
| MicroRNAs and target site screening reveals a pre-microRNA-30e variant associated with schizophrenia. | Xu Y et al. | β | 2010 | β |
| No association between AKT1 polymorphism and schizophrenia: a case-control study in a Korean population and a meta-analysis. | Lee KY et al. | β | 2010 | β |
| No association between oxytocin or prolactin gene variants and childhood-onset mood disorders. | Strauss JS et al. | β | 2010 | β |
| No association of dysbindin with symptom factors of schizophrenia in an Irish case-control sample. | Bergen SE et al. | β | 2010 | β |
| No evidence of an association between two genes, EDN1 and ACE, and childhood-onset mood disorders. | Dempster EL et al. | β | 2010 | β |
| NRG1 gene in recurrent major depression: no association in a large-scale case-control association study. | Schosser A et al. | β | 2010 | β |
| ParallABEL: an R library for generalized parallelization of genome-wide association studies. | Sangket U et al. | β | 2010 | β |
| Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis. | Chao MJ et al. | β | 2010 | β |
| Pharmacogenetic study of serotonin 6 receptor gene with antidepressant response in major depressive disorder in the Japanese population. | Kishi T et al. | β | 2010 | β |
| Polymorphisms of the HTR2C gene and antipsychotic-induced weight gain: an update and meta-analysis. | Sicard MN et al. | β | 2010 | β |
| Polymorphisms of XRCC4 are involved in reduced colorectal cancer risk in Chinese schizophrenia patients. | Wang Y et al. | β | 2010 | β |
| Population-genetic nature of copy number variations in the human genome. | Kato M et al. | β | 2010 | β |
| Replicated association of the NR4A3 gene with smoking behaviour in schizophrenia and in bipolar disorder. | Novak G et al. | β | 2010 | β |
| Schizophrenia: an association study targets phospholipase A2 genes as potential sites of susceptible genes. | Meng X et al. | β | 2010 | β |
| Schizophrenia severity and clozapine treatment outcome association with oxytocinergic genes. | Souza RP et al. | β | 2010 | β |
| Serotonin 1A receptor gene is associated with Japanese methamphetamine-induced psychosis patients. | Kishi T et al. | β | 2010 | β |
| Serotonin 6 receptor gene and mood disorders: case-control study and meta-analysis. | Fukuo Y et al. | β | 2010 | β |
| Single nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish cohort. | FernΓ‘ndez-Rozadilla C et al. | β | 2010 | β |
| SIRT1 gene is associated with major depressive disorder in the Japanese population. | Kishi T et al. | β | 2010 | β |
| Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India. | Bhaduri N et al. | β | 2010 | β |
| The catechol-O-methyl-transferase gene in tardive dyskinesia. | Zai CC et al. | β | 2010 | β |
| The combined effects of the BDNF and GSK3B genes modulate the relationship between negative life events and major depressive disorder. | Yang C et al. | β | 2010 | β |
| The PTPN22 locus and rheumatoid arthritis: no evidence for an effect on risk independent of Arg620Trp. | Wan Taib WR et al. | β | 2010 | β |
| The tryptophan hydroxylase 1 (TPH1) gene, schizophrenia susceptibility, and suicidal behavior: a multi-centre case-control study and meta-analysis. | Saetre P et al. | β | 2010 | β |
| Translin-associated factor X gene (TSNAX) may be associated with female major depressive disorder in the Japanese population. | Okuda A et al. | β | 2010 | β |
| TSLP polymorphisms are associated with asthma in a sex-specific fashion. | Hunninghake GM et al. | β | 2010 | β |
| VEGF polymorphisms are associated with endocardial cushion defects: a family-based case-control study. | Smedts HP et al. | β | 2010 | β |
| A case-control association study and family-based expression analysis of the bipolar disorder candidate gene PI4K2B. | Houlihan LM et al. | β | 2009 | β |
| A case-control association study between the CYP3A4 and CYP3A5 genes and schizophrenia in the Chinese Han population. | Du J et al. | β | 2009 | β |
| A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia. | Costas J et al. | β | 2009 | β |
| Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene. | Fritsche LG et al. | β | 2009 | β |
| Alternative-splicing in the exon-10 region of GABA(A) receptor beta(2) subunit gene: relationships between novel isoforms and psychotic disorders. | Zhao C et al. | β | 2009 | β |
| Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta. | Kauwe JS et al. | β | 2009 | β |
| A method to correct for population structure using a segregation model. | Feng Q et al. | β | 2009 | β |
| Analyses of associations with asthma in four asthma population samples from Canada and Australia. | Daley D et al. | β | 2009 | β |
| Analyses of multiple single-nucleotide polymorphisms in the SUMO4/IDDM5 region in affected sib-pair families with type I diabetes. | Podolsky R et al. | β | 2009 | β |
| Analysis of FTO gene variants with measures of obesity and glucose homeostasis in the IRAS Family Study. | Wing MR et al. | β | 2009 | β |
| Analysis of genotype and haplotype effects of ABCB1 (MDR1) polymorphisms in the risk of medically refractory epilepsy in an Indian population. | Vahab SA et al. | β | 2009 | β |
| An association study of the serotonin transporter and receptor genes with the suicidal ideation of major depression in a Chinese Han population. | Wang S et al. | β | 2009 | β |
| An association study of the SLC26A4 gene in children with mental retardation. | Li J et al. | β | 2009 | β |
| An examination of MUTED as a schizophrenia susceptibility gene. | Gerrish A et al. | β | 2009 | β |
| Apolipoprotein E genotype as a risk factor for susceptibility to and dementia in Parkinson's disease. | Williams-Gray CH et al. | β | 2009 | β |
| Apoptotic engulfment pathway and schizophrenia. | Chen X et al. | β | 2009 | β |
| A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). | Djurovic S et al. | β | 2009 | β |
| A psycho-genetic study of associations between the symptoms of binge eating disorder and those of attention deficit (hyperactivity) disorder. | Davis C et al. | β | 2009 | β |
| A risk PRODH haplotype affects sensorimotor gating, memory, schizotypy, and anxiety in healthy male subjects. | Roussos P et al. | β | 2009 | β |
| Association analysis of group II metabotropic glutamate receptor genes (GRM2 and GRM3) with mood disorders and fluvoxamine response in a Japanese population. | Tsunoka T et al. | β | 2009 | β |
| Association and expression study of synapsin III and schizophrenia. | Chen Q et al. | β | 2009 | β |
| Association between arginine vasopressin 1a receptor (AVPR1a) promoter region polymorphisms and prepulse inhibition. | Levin R et al. | β | 2009 | β |
| Association between harmful alcohol consumption behavior and dopamine transporter (DAT1) gene polymorphisms in a male Finnish population. | Lind PA et al. | β | 2009 | β |
| Association between sodium- and potassium-activated adenosine triphosphatase alpha isoforms and bipolar disorders. | Goldstein I et al. | β | 2009 | β |
| Association between the PDE4D gene and ischaemic stroke in the Chinese Han population. | Sun Y et al. | β | 2009 | β |
| Association of a polymorphism in the ABCB1 gene with Parkinson's disease. | Westerlund M et al. | β | 2009 | β |
| Association of a polymorphism in the NRXN3 gene with the degree of smoking in schizophrenia: a preliminary study. | Novak G et al. | β | 2009 | β |
| Association of a specific ERAP1/ARTS1 haplotype with disease susceptibility in ankylosing spondylitis. | Maksymowych WP et al. | β | 2009 | β |
| Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. | Couto JM et al. | β | 2009 | β |
| Association of polymorphisms in cyclooxygenase (COX)-2 with coronary and carotid calcium in the Diabetes Heart Study. | Rudock ME et al. | β | 2009 | β |
| Association of SLITRK1 to Gilles de la Tourette Syndrome. | Miranda DM et al. | β | 2009 | β |
| Association of the 5'-upstream regulatory region of the alpha7 nicotinic acetylcholine receptor subunit gene (CHRNA7) with schizophrenia. | Stephens SH et al. | β | 2009 | β |
| Association of the dystrobrevin binding protein 1 gene (DTNBP1) in a bipolar case-control study (BACCS). | Gaysina D et al. | β | 2009 | β |
| Associations between polymorphisms in dopamine neurotransmitter pathway genes and pain response in healthy humans. | Treister R et al. | β | 2009 | β |
| Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder. | Anitha A et al. | β | 2009 | β |
| Association studies on ghrelin and ghrelin receptor gene polymorphisms with obesity. | Gueorguiev M et al. | β | 2009 | β |
| Association study of clock gene (CLOCK) and schizophrenia and mood disorders in the Japanese population. | Kishi T et al. | β | 2009 | β |
| Association study of N-methyl-D-aspartate glutamate receptor subunit genes and childhood-onset mood disorders. | Dorval KM et al. | β | 2009 | β |
| Association study of promoter polymorphisms at the dopamine transporter gene in Attention Deficit Hyperactivity Disorder. | Xu X et al. | β | 2009 | β |
| Association study of tardive dyskinesia and five DRD4 polymorphisms in schizophrenia patients. | Zai CC et al. | β | 2009 | β |
| Association study on the mitochondrial gene NDUFV2 and bipolar disorder in the Chinese Han population. | Zhang J et al. | β | 2009 | β |
| Association study on the NAPG gene and bipolar disorder in the Chinese Han population. | Li X et al. | β | 2009 | β |
| A thymic stromal lymphopoietin gene variant is associated with asthma and airway hyperresponsiveness. | He JQ et al. | β | 2009 | β |
| A TLR2 polymorphism is associated with type 1 diabetes and allergic asthma. | BjΓΈrnvold M et al. | β | 2009 | β |
| BDNF is not associated with schizophrenia: data from a Japanese population study and meta-analysis. | Kawashima K et al. | β | 2009 | β |
| Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorder. | RibasΓ©s M et al. | β | 2009 | β |
| Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1. | HΓΌffmeier U et al. | β | 2009 | β |
| Choline transporter gene variation is associated with attention-deficit hyperactivity disorder. | English BA et al. | β | 2009 | β |
| Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region. | Laurin N et al. | β | 2009 | β |
| CLOCK may predict the response to fluvoxamine treatment in Japanese major depressive disorder patients. | Kishi T et al. | β | 2009 | β |
| Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23. | Orozco G et al. | β | 2009 | β |
| Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro. | Wilson SG et al. | β | 2009 | β |
| Conditional analyses on the T1DGC MHC dataset: novel associations with type 1 diabetes around HLA-G and confirmation of HLA-B. | Eike MC et al. | β | 2009 | β |
| Correlation between cystathionine beta synthase gene polymorphisms, plasma homocysteine and idiopathic mental retardation in Indian individuals from Kolkata. | Dutta S et al. | β | 2009 | β |
| CTLA4 and generalized vitiligo: two genetic association studies and a meta-analysis of published data. | Birlea SA et al. | β | 2009 | β |
| Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder. | Cohen-Woods S et al. | β | 2009 | β |
| Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex. | Chao MJ et al. | β | 2009 | β |
| Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: a two-stage Spanish case-control study. | Vega A et al. | β | 2009 | β |
| Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate. | Kremeyer B et al. | β | 2009 | β |
| Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence. | Agrawal A et al. | β | 2009 | β |
| Evidence for association with hepatocellular carcinoma at the PAPSS1 locus on chromosome 4q25 in a family-based study. | Shih WL et al. | β | 2009 | β |
| Evidence of association of serotonin transporter gene polymorphisms with schizophrenia in a South Indian population. | Vijayan NN et al. | β | 2009 | β |
| Evidence of epistasis between the catechol-O-methyltransferase and aldehyde dehydrogenase 3B1 genes in paranoid schizophrenia. | Wang Y et al. | β | 2009 | β |
| Evidence that variation in the oligodendrocyte lineage transcription factor 2 (OLIG2) gene is associated with psychosis in Alzheimer's disease. | Sims R et al. | β | 2009 | β |
| Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB. | RibasΓ©s M et al. | β | 2009 | β |
| Failure to confirm genetic association of the CHI3L1 gene with schizophrenia in Japanese and Chinese populations. | Yamada K et al. | β | 2009 | β |
| Family-based analysis of tumor necrosis factor and lymphotoxin-alpha tag polymorphisms with type 1 diabetes in the population of South Croatia. | Boraska V et al. | β | 2009 | β |
| Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32. | Conroy J et al. | β | 2009 | β |
| Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease. | Sharma M et al. | β | 2009 | β |
| Further evidence for DYX1C1 as a susceptibility factor for dyslexia. | Dahdouh F et al. | β | 2009 | β |
| Further genetic evidence implicates the vasopressin system in childhood-onset mood disorders. | Dempster EL et al. | β | 2009 | β |
| G72/G30 (DAOA) and juvenile-onset mood disorders. | Gomez L et al. | β | 2009 | β |
| Genetic analysis of MDR1 and inflammatory bowel disease reveals protective effect of heterozygous variants for ulcerative colitis. | Huebner C et al. | β | 2009 | β |
| Genetic association analysis of NRG1 with methamphetamine-induced psychosis in a Japanese population. | Okochi T et al. | β | 2009 | β |
| Genetic association analysis of serotonin 2A receptor gene (HTR2A) with bipolar disorder and major depressive disorder in the Japanese population. | Kishi T et al. | β | 2009 | β |
| Genetic association and post-mortem brain mRNA analysis of DISC1 and related genes in schizophrenia. | Rastogi A et al. | β | 2009 | β |
| Genetic study of BDNF, DRD3, and their interaction in tardive dyskinesia. | Zai CC et al. | β | 2009 | β |
| Genetic variants of the HLA-A, HLA-B and AIF1 loci show independent associations with type 1 diabetes in Norwegian families. | Eike MC et al. | β | 2009 | β |
| Genetic variation in the CHRNA5 gene affects mRNA levels and is associated with risk for alcohol dependence. | Wang JC et al. | β | 2009 | β |
| Genetic variation in the nuclear factor kappaB pathway in relation to susceptibility to rheumatoid arthritis. | Dieguez-Gonzalez R et al. | β | 2009 | β |
| Genetic variation in the serotonin 2A receptor and suicidal ideation in a sample of 270 Irish high-density schizophrenia families. | Fanous AH et al. | β | 2009 | β |
| Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population: clinical investigation. | Boraska V et al. | β | 2009 | β |
| High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions. | Barcellos LF et al. | β | 2009 | β |
| Hypertension genes and retinal vascular calibre: the Cardiovascular Health Study. | Sun C et al. | β | 2009 | β |
| Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE). | Hellquist A et al. | β | 2009 | β |
| Interacting genes in lithium prophylaxis: preliminary results of an exploratory analysis on the role of DGKH and NR1D1 gene polymorphisms in 199 Sardinian bipolar patients. | Manchia M et al. | β | 2009 | β |
| Interacting haplotypes at the NPAS3 locus alter risk of schizophrenia and bipolar disorder. | Pickard BS et al. | β | 2009 | β |
| Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer. | MΓΆckelmann N et al. | β | 2009 | β |
| Investigation of the colorectal cancer susceptibility region on chromosome 8q24.21 in a large German case-control sample. | Schafmayer C et al. | β | 2009 | β |
| Investigation of the serotonin 2C receptor gene in attention deficit hyperactivity disorder in UK samples. | Xu X et al. | β | 2009 | β |
| Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression. | Lintas C et al. | β | 2009 | β |
| Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis. | Lorentzen AR et al. | β | 2009 | β |
| KIR2DL4 (CD158d) polymorphisms and susceptibility to multiple sclerosis. | Goris A et al. | β | 2009 | β |
| Marked differences in CRP genotype frequencies between the Fulani and sympatric ethnic groups in Africa. | Israelsson E et al. | β | 2009 | β |
| MDR1 gene in tardive dyskinesia scale scores: comparison of strategies for quantitative trait haplotype analysis. | De Luca V et al. | β | 2009 | β |
| MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels. | Xiong L et al. | β | 2009 | β |
| Meta-analysis of association between genetic variants in COMT and schizophrenia: an update. | Okochi T et al. | β | 2009 | β |
| Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD). | Mill J et al. | β | 2009 | β |
| New genetic evidence for involvement of the dopamine system in migraine with aura. | Todt U et al. | β | 2009 | β |
| No association between polymorphisms of neuronal oxide synthase 1 gene (NOS1) and schizophrenia in a Japanese population. | Okumura T et al. | β | 2009 | β |
| No association of the IRS1 and PAX4 genes with type I diabetes. | Bergholdt R et al. | β | 2009 | β |
| No evidence for association between an MAOA functional polymorphism and susceptibility to Parkinson's disease. | Williams-Gray C et al. | β | 2009 | β |
| No evidence for genetic association of interferon regulatory factor 3 in systemic lupus erythematosus. | SΓ‘nchez E et al. | β | 2009 | β |
| P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? | Green EK et al. | β | 2009 | β |
| Path: a tool to facilitate pathway-based genetic association analysis. | Zamar D et al. | β | 2009 | β |
| Polymorphisms in serotonin-related genes in anorexia nervosa. The first study in Czech population and metaanalyses with previously performed studies. | MartΓ‘skovΓ‘ D et al. | β | 2009 | β |
| Polymorphisms in SLC6A4, PAH, GABRB3, and MAOB and modification of psychotic disorder features. | Bergen SE et al. | β | 2009 | β |
| Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients. | Heck A et al. | β | 2009 | β |
| Polymorphisms in the neural nicotinic acetylcholine receptor Ξ±4 subunit (CHRNA4) are associated with ADHD in a genetic isolate. | Wallis D et al. | β | 2009 | β |
| Positive association of neuroligin-4 gene with nonspecific mental retardation in the Qinba Mountains Region of China. | Qi H et al. | β | 2009 | β |
| Possible association of prokineticin 2 receptor gene (PROKR2) with mood disorders in the Japanese population. | Kishi T et al. | β | 2009 | β |
| Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility. | Mitchell AL et al. | β | 2009 | β |
| Remapping the type I diabetes association of the CTLA4 locus. | Qu HQ et al. | β | 2009 | β |
| Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. | Ban M et al. | β | 2009 | β |
| Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder. | Doyle C et al. | β | 2009 | β |
| Reproducible association with type 1 diabetes in the extended class I region of the major histocompatibility complex. | Viken MK et al. | β | 2009 | β |
| Serotonin 1A receptor gene and major depressive disorder: an association study and meta-analysis. | Kishi T et al. | β | 2009 | β |
| Serotonin genes and gene-gene interactions in borderline personality disorder in a matched case-control study. | Ni X et al. | β | 2009 | β |
| Study of the association between polymorphisms of the COL1A1 gene and HBV-related liver cirrhosis in Chinese patients. | Zhao YP et al. | β | 2009 | β |
| Tagging SNP association study of the IL-1beta gene (IL1B) and childhood-onset mood disorders. | Misener VL et al. | β | 2009 | β |
| The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals. | Kovacs D et al. | β | 2009 | β |
| The effect of the MHC locus on autoantibodies in type 1 diabetes. | Qu HQ et al. | β | 2009 | β |
| The largest prospective warfarin-treated cohort supports genetic forecasting. | Wadelius M et al. | β | 2009 | β |
| The norepinephrine transporter gene modulates the relationship between urban/rural residency and major depressive disorder in a Chinese population. | Xu Y et al. | β | 2009 | β |
| The oxytocin receptor (OXTR) contributes to prosocial fund allocations in the dictator game and the social value orientations task. | Israel S et al. | β | 2009 | β |
| The retinoic acid receptor alpha (RARA) gene is not associated with myopia, hypermetropia, and ocular biometric measures. | Veerappan S et al. | β | 2009 | β |
| The TGM2 gene is associated with schizophrenia in a British population. | Bradford M et al. | β | 2009 | β |
| The trace amine associated receptor (TAAR6) gene is not associated with schizophrenia in the Irish Case-Control Study of Schizophrenia (ICCSS) sample. | Vladimirov VI et al. | β | 2009 | β |
| The type I diabetes association of the IL2RA locus. | Qu HQ et al. | β | 2009 | β |
| TNFSF15 polymorphisms are associated with susceptibility to inflammatory bowel disease in a new European cohort. | ThiΓ©baut R et al. | β | 2009 | β |
| Transcription factor SP4 is a susceptibility gene for bipolar disorder. | Zhou X et al. | β | 2009 | β |
| Two-stage case-control association study of dopamine-related genes and migraine. | Corominas R et al. | β | 2009 | β |
| Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for systemic lupus erythematosus within the MHC. | Ramos PS et al. | β | 2009 | β |
| Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia. | Zoledziewska M et al. | β | 2009 | β |
| Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. | Liu Y et al. | β | 2009 | β |
| 5-HT2C receptor and MAO-A interaction analysis: no association with suicidal behaviour in bipolar patients. | De Luca V et al. | β | 2008 | β |
| A case-control association study of the PDLIM5 gene and bipolar disorder in a Sardinian sample. | Squassina A et al. | β | 2008 | β |
| A family- and population-based study of the UFD1L gene for schizophrenia. | Xie L et al. | β | 2008 | β |
| A family-based association study of the myelin-associated glycoprotein and 2',3'-cyclic nucleotide 3'-phosphodiesterase genes with schizophrenia. | Voineskos AN et al. | β | 2008 | β |
| A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population. | Ito Y et al. | β | 2008 | β |
| A genetic study of the NOS3 gene for ischemic stroke in a Chinese population. | Du D et al. | β | 2008 | β |
| A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. | Baum AE et al. | β | 2008 | β |
| Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA. | Fritsche LG et al. | β | 2008 | β |
| A haplotype of the DRD1 gene is associated with alcohol dependence. | Batel P et al. | β | 2008 | β |
| AKT1 is associated with schizophrenia across multiple symptom dimensions in the Irish study of high density schizophrenia families. | Thiselton DL et al. | β | 2008 | β |
| Alpha-CaMKII deficiency causes immature dentate gyrus, a novel candidate endophenotype of psychiatric disorders. | Yamasaki N et al. | β | 2008 | β |
| AMBIENCE: a novel approach and efficient algorithm for identifying informative genetic and environmental associations with complex phenotypes. | Chanda P et al. | β | 2008 | β |
| Analysis of BDNF Val66Met allele-specific mRNA levels in bipolar disorder. | De Luca V et al. | β | 2008 | β |
| Analysis of single nucleotide polymorphisms and haplotypes in the neuropeptide Y gene: no evidence for association with alcoholism in a German population sample. | Zill P et al. | β | 2008 | β |
| An association analysis of murine anxiety genes in humans implicates novel candidate genes for anxiety disorders. | Donner J et al. | β | 2008 | β |
| An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia. | Jungerius BJ et al. | β | 2008 | β |
| An association study of ADSS gene polymorphisms with schizophrenia. | Zhang F et al. | β | 2008 | β |
| An association study of RGS4 polymorphisms with clinical phenotypes of schizophrenia in a Chinese population. | So HC et al. | β | 2008 | β |
| A network of dopaminergic gene variations implicated as risk factors for schizophrenia. | Talkowski ME et al. | β | 2008 | β |
| Application of the Linux cluster for exhaustive window haplotype analysis using the FBAT and Unphased programs. | Mishima H et al. | β | 2008 | β |
| A regulatory variation in OPRK1, the gene encoding the kappa-opioid receptor, is associated with alcohol dependence. | Edenberg HJ et al. | β | 2008 | β |
| A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy. | D'Alfonso S et al. | β | 2008 | β |
| A SNP in the ACT gene associated with astrocytosis and rapid cognitive decline in AD. | Belbin O et al. | β | 2008 | β |
| Association analyses of the interaction between the ADSS and ATM genes with schizophrenia in a Chinese population. | Zhang F et al. | β | 2008 | β |
| Association analysis of genes encoding the nociceptin receptor (OPRL1) and its endogenous ligand (PNOC) with alcohol or illicit drug dependence. | Xuei X et al. | β | 2008 | β |
| Association analysis of nuclear receptor Rev-erb alpha gene (NR1D1) with mood disorders in the Japanese population. | Kishi T et al. | β | 2008 | β |
| Association analysis of schizophrenia on 18 genes involved in neuronal migration: MDGA1 as a new susceptibility gene. | KΓ€hler AK et al. | β | 2008 | β |
| Association analysis of the pituitary adenylate cyclase-activating polypeptide (PACAP/ADCYAP1) gene in bipolar disorder. | Lohoff FW et al. | β | 2008 | β |
| Association between ADORA2A and DRD2 polymorphisms and caffeine-induced anxiety. | Childs E et al. | β | 2008 | β |
| Association between the catechol-O-methyltransferase Val158Met polymorphism and cocaine dependence. | Lohoff FW et al. | β | 2008 | β |
| Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition. | Lerer E et al. | β | 2008 | β |
| Association between tryptophan hydroxylase 2, performance on a continuance performance test and response to methylphenidate in ADHD participants. | Manor I et al. | β | 2008 | β |
| Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region. | Wigg KG et al. | β | 2008 | β |
| Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity. | Brookes KJ et al. | β | 2008 | β |
| Association of common ATM variants with familial breast cancer in a South American population. | GonzΓ‘lez-HormazΓ‘bal P et al. | β | 2008 | β |
| Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden. | Valdmanis PN et al. | β | 2008 | β |
| Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction. | Vilella E et al. | β | 2008 | β |
| Association of the neurotrophic tyrosine kinase receptor 3 (NTRK3) gene and childhood-onset mood disorders. | Feng Y et al. | β | 2008 | β |
| Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder. | Brookes KJ et al. | β | 2008 | β |
| Association of vitamin D receptor gene 3'-variants with Hashimoto's thyroiditis in the Croatian population. | StefaniΔ M et al. | β | 2008 | β |
| Association of vitamin D receptor gene variants, adiposity and colon cancer. | Ochs-Balcom HM et al. | β | 2008 | β |
| Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorder. | Amano K et al. | β | 2008 | β |
| Association study between the serotonin 1A receptor (HTR1A) gene and neuroticism, major depression, and anxiety disorders. | Hettema JM et al. | β | 2008 | β |
| Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder. | Laurin N et al. | β | 2008 | β |
| Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder. | RibasΓ©s M et al. | β | 2008 | β |
| Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression. | Wray NR et al. | β | 2008 | β |
| Association study of candidate variants of COMT with neuroticism, anxiety and depression. | Wray NR et al. | β | 2008 | β |
| Association study of CSF2RB with schizophrenia in Irish family and case - control samples. | Chen Q et al. | β | 2008 | β |
| Association study of GSK3 gene polymorphisms with schizophrenia and clozapine response. | Souza RP et al. | β | 2008 | β |
| Association study of the estrogen receptor alpha gene (ESR1) and childhood-onset mood disorders. | Mill J et al. | β | 2008 | β |
| Association study of tryptophan hydroxylase 1 and arylalkylamine N-acetyltransferase polymorphisms with adolescent idiopathic scoliosis in Han Chinese. | Wang H et al. | β | 2008 | β |
| Association study on glutathione S-transferase omega 1 and 2 and familial ALS. | van de Giessen E et al. | β | 2008 | β |
| ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands. | Weersma RK et al. | β | 2008 | β |
| Bone structural effects of variation in the TNFRSF1B gene encoding the tumor necrosis factor receptor 2. | Mullin BH et al. | β | 2008 | β |
| Cannabinoid receptor 1 gene association with nicotine dependence. | Chen X et al. | β | 2008 | β |
| Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes. | Hettema JM et al. | β | 2008 | β |
| Cerebellar alpha-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material. | Westerlund M et al. | β | 2008 | β |
| Chitinase-3-like 1 (CHI3L1) gene and schizophrenia: genetic association and a potential functional mechanism. | Yang MS et al. | β | 2008 | β |
| Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm. | Shi J et al. | β | 2008 | β |
| Common variation in the ABO glycosyltransferase is associated with susceptibility to severe Plasmodium falciparum malaria. | Fry AE et al. | β | 2008 | β |
| Comprehensive analysis of polymorphisms throughout GAD1 gene: a family-based association study in schizophrenia. | Du J et al. | β | 2008 | β |
| Comprehensive association study of genetic variants in the IL-1 gene family in systemic juvenile idiopathic arthritis. | Stock CJ et al. | β | 2008 | β |
| Comprehensive evaluation of positional candidates in the IL-18 pathway reveals suggestive associations with schizophrenia and herpes virus seropositivity. | Shirts BH et al. | β | 2008 | β |
| Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection. | de Kovel CG et al. | β | 2008 | β |
| Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth. | Brookes KJ et al. | β | 2008 | β |
| Dysbindin (DTNBP1) and the biogenesis of lysosome-related organelles complex 1 (BLOC-1): main and epistatic gene effects are potential contributors to schizophrenia susceptibility. | Morris DW et al. | β | 2008 | β |
| EDA2R is associated with androgenetic alopecia. | Prodi DA et al. | β | 2008 | β |
| Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the alcohol challenge twin study. | Lind PA et al. | β | 2008 | β |
| Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations. | Benzinou M et al. | β | 2008 | β |
| Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder. | Liu L et al. | β | 2008 | β |
| Examining the statistical properties of fine-scale mapping in large-scale association studies. | Wiltshire S et al. | β | 2008 | β |
| Failure to replicate the association between NRG1 and schizophrenia using Japanese large sample. | Ikeda M et al. | β | 2008 | β |
| Family-based analysis of vitamin D receptor gene polymorphisms and type 1 diabetes in the population of South Croatia. | Boraska V et al. | β | 2008 | β |
| Family-based association analysis of functional VNTR polymorphisms in the dopamine transporter gene in migraine with and without aura. | Karwautz A et al. | β | 2008 | β |
| Family-based association studies of CAPON and schizophrenia in the Chinese Han population. | Fang C et al. | β | 2008 | β |
| Family-based methods for linkage and association analysis. | Laird NM et al. | β | 2008 | β |
| FBXL21 association with schizophrenia in Irish family and case-control samples. | Chen X et al. | β | 2008 | β |
| Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32. | Adamovic S et al. | β | 2008 | β |
| Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus. | Kozyrev SV et al. | β | 2008 | β |
| Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21. | Schumacher J et al. | β | 2008 | β |
| Further evidence of association between two NET single-nucleotide polymorphisms with ADHD. | Kim JW et al. | β | 2008 | β |
| Gene and expression analyses reveal enhanced expression of pericentrin 2 (PCNT2) in bipolar disorder. | Anitha A et al. | β | 2008 | β |
| Genes causing clefting syndromes as candidates for non-syndromic cleft lip with or without cleft palate: a family-based association study. | Scapoli L et al. | β | 2008 | β |
| Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population. | Dutta S et al. | β | 2008 | β |
| Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder. | Yoshimi A et al. | β | 2008 | β |
| Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians. | Xiong L et al. | β | 2008 | β |
| Genetic examination of the PLXNA2 gene in Japanese and Chinese people with schizophrenia. | Takeshita M et al. | β | 2008 | β |
| Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high-risk non BRCA1/2 French Canadian breast and ovarian cancer families. | Desjardins S et al. | β | 2008 | β |
| Genetic variants in the cocaine- and amphetamine-regulated transcript gene (CARTPT) and cocaine dependence. | Lohoff FW et al. | β | 2008 | β |
| Genetic variation in immune signaling genes differentially expressed in asthmatic lung tissues. | Tremblay K et al. | β | 2008 | β |
| Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis. | Barcellos LF et al. | β | 2008 | β |
| Haplotype-association analysis. | Liu N et al. | β | 2008 | β |
| HHEX gene polymorphisms are associated with type 2 diabetes in the Dutch Breda cohort. | van Vliet-Ostaptchouk JV et al. | β | 2008 | β |
| HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility. | Chao MJ et al. | β | 2008 | β |
| HLA-DRB1 and multiple sclerosis in Malta. | Dean G et al. | β | 2008 | β |
| Identification of a role for the ARHGEF3 gene in postmenopausal osteoporosis. | Mullin BH et al. | β | 2008 | β |
| Identification of YWHAE, a gene encoding 14-3-3epsilon, as a possible susceptibility gene for schizophrenia. | Ikeda M et al. | β | 2008 | β |
| IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. | Weber F et al. | β | 2008 | β |
| Individual differences in allocation of funds in the dictator game associated with length of the arginine vasopressin 1a receptor RS3 promoter region and correlation between RS3 length and hippocampal mRNA. | Knafo A et al. | β | 2008 | β |
| Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing. | Kumar RA et al. | β | 2008 | β |
| Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder. | Sonuga-Barke EJ et al. | β | 2008 | β |
| Interaction between CRHR1 gene and stressful life events predicts adolescent heavy alcohol use. | Blomeyer D et al. | β | 2008 | β |
| Investigation of MYH14 as a candidate gene in cleft lip with or without cleft palate. | Martinelli M et al. | β | 2008 | β |
| Investigation of the G protein subunit Galphaolf gene (GNAL) in attention deficit/hyperactivity disorder. | Laurin N et al. | β | 2008 | β |
| Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility. | Ban M et al. | β | 2008 | β |
| Is the histidine triad nucleotide-binding protein 1 (HINT1) gene a candidate for schizophrenia? | Chen Q et al. | β | 2008 | β |
| Is there protective haplotype of dysbindin gene (DTNBP1) 3 polymorphisms for major depressive disorder. | Kim JJ et al. | β | 2008 | β |
| Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes. | BjΓΈrnvold M et al. | β | 2008 | β |
| Lack of association between down syndrome and polymorphisms in dopamine receptor D4 and serotonin transporter genes. | Das Bhowmik A et al. | β | 2008 | β |
| Lack of association between the amiloride-sensitive cation channel 2 (ACCN2) gene and anxiety spectrum disorders. | Hettema JM et al. | β | 2008 | β |
| Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data. | Dudbridge F | β | 2008 | β |
| MDR1 gene polymorphism: therapeutic response to paroxetine among patients with major depression. | Mihaljevic Peles A et al. | β | 2008 | β |
| MEGF10 association with schizophrenia. | Chen X et al. | β | 2008 | β |
| Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism. | Loat CS et al. | β | 2008 | β |
| Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene. | Buxbaum JD et al. | β | 2008 | β |
| Multilocus analyses reveal involvement of the ESR1, ESR2, and FSHR genes in migraine. | Oterino A et al. | β | 2008 | β |
| Neural networks for genetic epidemiology: past, present, and future. | Motsinger-Reif AA et al. | β | 2008 | β |
| Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence. | Wetherill L et al. | β | 2008 | β |
| New evidence for the association of the serotonin transporter gene (SLC6A4) haplotypes, threatening life events, and depressive phenotype. | Lazary J et al. | β | 2008 | β |
| No association between tagging SNPs of SNARE complex genes (STX1A, VAMP2 and SNAP25) and schizophrenia in a Japanese population. | Kawashima K et al. | β | 2008 | β |
| No association between the oligodendrocyte-related gene PLP1 and schizophrenia in the Japanese population. | Aleksic B et al. | β | 2008 | β |
| No association between the protein tyrosine phosphatase, receptor-type, Z Polypeptide 1 (PTPRZ1) gene and schizophrenia in the Japanese population. | Ito Y et al. | β | 2008 | β |
| No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder. | Xu X et al. | β | 2008 | β |
| No evidence for genetic association between DARPP-32 (PP1R1B) polymorphisms and attention deficit hyperactivity disorder. | Laurin N et al. | β | 2008 | β |
| No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level. | Wermter AK et al. | β | 2008 | β |
| No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans. | Bolduc V et al. | β | 2008 | β |
| NOS-I and -III gene variants are differentially associated with facets of suicidal behavior and aggression-related traits. | Rujescu D et al. | β | 2008 | β |
| No significant association between the genetic polymorphisms in the GSK-3 beta gene and schizophrenia in the Chinese population. | Meng J et al. | β | 2008 | β |
| No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics. | Sanders AR et al. | β | 2008 | β |
| Nucleotide sequence variation within the PI3K p85 alpha gene associates with alcohol risk drinking behaviour in adolescents. | DesriviΓ¨res S et al. | β | 2008 | β |
| ORMDL3 gene is associated with asthma in three ethnically diverse populations. | Galanter J et al. | β | 2008 | β |
| PDLIM5 and susceptibility to bipolar disorder: a family-based association study and meta-analysis. | Shi J et al. | β | 2008 | β |
| Polymorphism in postinsulin receptor signaling pathway is not associated with polycystic ovary syndrome. | Jones MR et al. | β | 2008 | β |
| Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder. | Unschuld PG et al. | β | 2008 | β |
| Positional pathway screen of wnt signaling genes in schizophrenia: association with DKK4. | Proitsi P et al. | β | 2008 | β |
| Positive association between PDLIM5 and schizophrenia in the Chinese Han population. | Li C et al. | β | 2008 | β |
| Positive association of the FTSJ1 gene polymorphisms with nonsyndromic X-linked mental retardation in young Chinese male subjects. | Dai L et al. | β | 2008 | β |
| Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans. | Wermter AK et al. | β | 2008 | β |
| PRODH gene is associated with executive function in schizophrenic families. | Li T et al. | β | 2008 | β |
| Rapid evolving RNA gene HAR1A and schizophrenia. | Tolosa A et al. | β | 2008 | β |
| Recessive genetic mode of an ADH4 variant in substance dependence in African-Americans: A model of utility of the HWD test. | Luo X et al. | β | 2008 | β |
| Refining genetic associations in multiple sclerosis. | International Multiple Sclerosis Genetics Consortium (IMSGC) | β | 2008 | β |
| Replication of the tumor necrosis factor receptor-associated factor 1/complement component 5 region as a susceptibility locus for rheumatoid arthritis in a European family-based study. | Kurreeman FA et al. | β | 2008 | β |
| Replication study of the insulin receptor gene in migraine with aura. | Netzer C et al. | β | 2008 | β |
| Sequence variants in host cell factor C1 are associated with MΓ©niΓ¨re's disease. | Vrabec JT et al. | β | 2008 | β |
| Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study. | Biederman J et al. | β | 2008 | β |
| Single nucleotide polymorphisms in human Paneth cell defensin A5 may confer susceptibility to inflammatory bowel disease in a New Zealand Caucasian population. | Ferguson LR et al. | β | 2008 | β |
| Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13. | Kemlink D et al. | β | 2008 | β |
| Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia. | Georgieva L et al. | β | 2008 | β |
| The association between the IFIH1 locus and type 1 diabetes. | Qu HQ et al. | β | 2008 | β |
| The association between type 1 diabetes and the ITPR3 gene polymorphism due to linkage disequilibrium with HLA class II. | Qu HQ et al. | β | 2008 | β |
| The combined effect of norepinephrine transporter gene and negative life events in major depression of Chinese Han population. | Sun N et al. | β | 2008 | β |
| The effects of beta2 adrenergic receptor gene polymorphism in lipid profiles. | Kao WT et al. | β | 2008 | β |
| The estrogen hypothesis of schizophrenia implicates glucose metabolism: association study in three independent samples. | Olsen L et al. | β | 2008 | β |
| The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of autoimmune diseases. | Eike MC et al. | β | 2008 | β |
| The MTHFD1 gene is not involved in cleft lip with or without palate onset among the Italian population. | Palmieri A et al. | β | 2008 | β |
| The PDLIM5 gene and lithium prophylaxis: an association and gene expression analysis in Sardinian patients with bipolar disorder. | Squassina A et al. | β | 2008 | β |
| The 'Pokemon' (ZBTB7) Gene: No Evidence of Association with Sporadic Breast Cancer. | Salas A et al. | β | 2008 | β |
| The PPARD gene may be associated with schizophrenia in a Chinese population. | Sun SL et al. | β | 2008 | β |
| The role of aldehyde dehydrogenase-1 (ALDH1A1) polymorphisms in harmful alcohol consumption in a Finnish population. | Lind PA et al. | β | 2008 | β |
| The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample. | Lind PA et al. | β | 2008 | β |
| The SH2D2A gene and susceptibility to multiple sclerosis. | Lorentzen AR et al. | β | 2008 | β |
| The tachykinin receptor 3 is associated with alcohol and cocaine dependence. | Foroud T et al. | β | 2008 | β |
| TIRAP (MAL) S180L polymorphism is a common protective factor against developing tuberculosis and systemic lupus erythematosus. | Castiblanco J et al. | β | 2008 | β |
| TNF-alpha polymorphisms are associated with obsessive-compulsive disorder. | Hounie AG et al. | β | 2008 | β |
| Toll-like receptor heterodimer variants protect from childhood asthma. | Kormann MS et al. | β | 2008 | β |
| UGT1A1 and UGT1A9 functional variants, meat intake, and colon cancer, among Caucasians and African-Americans. | Girard H et al. | β | 2008 | β |
| Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis. | Caillier SJ et al. | β | 2008 | β |
| Variants of ST8SIA1 are associated with risk of developing multiple sclerosis. | Husain S et al. | β | 2008 | β |
| Variation in the ICAM1 gene is not associated with severe malaria phenotypes. | Fry AE et al. | β | 2008 | β |
| Variation in the purinergic P2RX(7) receptor gene and schizophrenia. | Hansen T et al. | β | 2008 | β |
| A dopamine D4 receptor exon 3 VNTR allele protecting against migraine without aura. | de Sousa SC et al. | β | 2007 | β |
| A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. | Buch S et al. | β | 2007 | β |
| A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. | Hampe J et al. | β | 2007 | β |
| Allelic variation in BTNL2 and susceptibility to tuberculosis in a South African population. | MΓΆller M et al. | β | 2007 | β |
| Analyses of single marker and pairwise effects of candidate loci for rheumatoid arthritis using logistic regression and random forests. | Glaser B et al. | β | 2007 | β |
| Analysis of cystathionine beta-synthase 31 bp variable number tandem repeats in mentally retarded patients. | Dutta S et al. | β | 2007 | β |
| Analysis of monoamine oxidase A promoter polymorphism in mentally retarded individuals. | Das Bhowmik A et al. | β | 2007 | β |
| Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents. | HΓΆlter K et al. | β | 2007 | β |
| An evaluation of power and type I error of single-nucleotide polymorphism transmission/disequilibrium-based statistical methods under different family structures, missing parental data, and population stratification. | Nicodemus KK et al. | β | 2007 | β |
| Anorexia nervosa, perfectionism, and dopamine D4 receptor (DRD4). | Bachner-Melman R et al. | β | 2007 | β |
| A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription. | Ohnishi T et al. | β | 2007 | β |
| A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families. | Vladimirov V et al. | β | 2007 | β |
| A second major histocompatibility complex susceptibility locus for multiple sclerosis. | Yeo TW et al. | β | 2007 | β |
| Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasm. | Clarimon J et al. | β | 2007 | β |
| Association analyses of the DAOA/G30 and D-amino-acid oxidase genes in schizophrenia: further evidence for a role in schizophrenia. | Shinkai T et al. | β | 2007 | β |
| Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease. | Lie BA et al. | β | 2007 | β |
| Association analysis of AKT1 and schizophrenia in a UK case control sample. | Norton N et al. | β | 2007 | β |
| Association analysis of the chromosome 4p15-p16 candidate region for bipolar disorder and schizophrenia. | Christoforou A et al. | β | 2007 | β |
| Association and synergistic interaction between promoter variants of the DRD4 gene in Japanese schizophrenics. | Nakajima M et al. | β | 2007 | β |
| Association between obesity and insulin resistance with UCP2-UCP3 gene variants in Spanish children and adolescents. | Ochoa MC et al. | β | 2007 | β |
| Association between the 5q31.1 gene neurogenin1 and schizophrenia. | Fanous AH et al. | β | 2007 | β |
| Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings. | Zinkstok JR et al. | β | 2007 | β |
| Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD). | Zhou XL et al. | β | 2007 | β |
| Association of alcohol craving with alpha-synuclein (SNCA). | Foroud T et al. | β | 2007 | β |
| Association of alpha2-Heremans-Schmid glycoprotein polymorphisms with subclinical atherosclerosis. | Lehtinen AB et al. | β | 2007 | β |
| Association of CHRM2 with IQ: converging evidence for a gene influencing intelligence. | Dick DM et al. | β | 2007 | β |
| Association of DLG5 variants with inflammatory bowel disease in the New Zealand Caucasian population and meta-analysis of the DLG5 R30Q variant. | Browning BL et al. | β | 2007 | β |
| Association of dopamine receptor polymorphisms with schizophrenia and antipsychotic response in a South Indian population. | Vijayan NN et al. | β | 2007 | β |
| Association of GRIK4 with outcome of antidepressant treatment in the STAR*D cohort. | Paddock S et al. | β | 2007 | β |
| Association of HLA genes with ankylosing spondylitis in Han population of eastern China. | Fang M et al. | β | 2007 | β |
| Association of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish population. | Thomson PA et al. | β | 2007 | β |
| Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis. | Nicholas B et al. | β | 2007 | β |
| Association of synapsin 2 with schizophrenia in families of Northern European ancestry. | Saviouk V et al. | β | 2007 | β |
| Association of the dopamine receptor D4 (DRD4) gene 7-repeat allele with children with attention-deficit/hyperactivity disorder (ADHD): an update. | Gornick MC et al. | β | 2007 | β |
| Association of the estrogen receptor-alpha gene with the metabolic syndrome and its component traits in African-American families: the Insulin Resistance Atherosclerosis Family Study. | Gallagher CJ et al. | β | 2007 | β |
| Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder. | Dorval KM et al. | β | 2007 | β |
| Association of variants of transcription factor 7-like 2 (TCF7L2) with susceptibility to type 2 diabetes in the Dutch Breda cohort. | van Vliet-Ostaptchouk JV et al. | β | 2007 | β |
| Association of warfarin dose with genes involved in its action and metabolism. | Wadelius M et al. | β | 2007 | β |
| Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP). | Nowotny P et al. | β | 2007 | β |
| Association study between the monoamine oxidase A gene and attention deficit hyperactivity disorder in Taiwanese samples. | Xu X et al. | β | 2007 | β |
| Association study of four dopamine D1 receptor gene polymorphisms and clozapine treatment response. | Hwang R et al. | β | 2007 | β |
| Association study of tardive dyskinesia and twelve DRD2 polymorphisms in schizophrenia patients. | Zai CC et al. | β | 2007 | β |
| Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease. | Belin AC et al. | β | 2007 | β |
| A study of the PEMT gene in schizophrenia. | Liu Y et al. | β | 2007 | β |
| Brain expressed microRNAs implicated in schizophrenia etiology. | Hansen T et al. | β | 2007 | β |
| Case-control association study of Disrupted-in-Schizophrenia-1 (DISC1) gene and schizophrenia in the Chinese population. | Chen QY et al. | β | 2007 | β |
| Chromosome 7p linkage and GPR154 gene association in Italian families with allergic asthma. | Malerba G et al. | β | 2007 | β |
| Cleft lip with or without cleft palate: implication of the heavy chain of non-muscle myosin IIA. | Martinelli M et al. | β | 2007 | β |
| Clinical involvement of catechol-O-methyltransferase polymorphisms in schizophrenia spectrum disorders: influence on the severity of psychotic symptoms and on the response to neuroleptic treatment. | Molero P et al. | β | 2007 | β |
| Common genetic variation in the gene encoding interleukin-1-receptor antagonist (IL-1RA) is associated with altered circulating IL-1RA levels. | Rafiq S et al. | β | 2007 | β |
| Common variants of the novel type 2 diabetes genes CDKAL1 and HHEX/IDE are associated with decreased pancreatic beta-cell function. | Pascoe L et al. | β | 2007 | β |
| Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects. | Owen KR et al. | β | 2007 | β |
| Comparison of artificial neural network analysis with other multimarker methods for detecting genetic association. | Curtis D | β | 2007 | β |
| Connexin 50 gene on human chromosome 1q21 is associated with schizophrenia in matched case control and family-based studies. | Ni X et al. | β | 2007 | β |
| CTLA4 gene polymorphisms and multiple sclerosis in Northern Ireland. | Heggarty S et al. | β | 2007 | β |
| Dealing with missing data in family-based association studies: a multiple imputation approach. | Croiseau P et al. | β | 2007 | β |
| Differences in CYP3A41G genotype distribution and haplotypes of CYP3A4, CYP3A5 and CYP3A7 in 3 Chinese populations. | Du J et al. | β | 2007 | β |
| Dopamine genes and pathological gambling in discordant sib-pairs. | da Silva Lobo DS et al. | β | 2007 | β |
| Dysbindin associated with selective serotonin reuptake inhibitor antidepressant efficacy. | Pae CU et al. | β | 2007 | β |
| Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotype. | Watanabe A et al. | β | 2007 | β |
| Family-based analysis of serotonin transporter gene polymorphisms in migraine with and without aura. | Karwautz AF et al. | β | 2007 | β |
| Family-based association study of neuregulin-1 gene and psychosis in a Spanish sample. | Rosa A et al. | β | 2007 | β |
| Family-based association study of the restless legs syndrome loci 2 and 3 in a European population. | Kemlink D et al. | β | 2007 | β |
| FAT and bipolar affective disorder. | Light KJ et al. | β | 2007 | β |
| Functional variants in the promoter region of Chitinase 3-like 1 (CHI3L1) and susceptibility to schizophrenia. | Zhao X et al. | β | 2007 | β |
| Further evidence for association of GRK3 to bipolar disorder suggests a second disease mutation. | Barrett TB et al. | β | 2007 | β |
| Further evidence of MAO-A gene variants associated with bipolar disorder. | MΓΌller DJ et al. | β | 2007 | β |
| Further evidence that the chromogranin B gene confers predisposition to schizophrenia: a family-based association study in Chinese. | Wu S et al. | β | 2007 | β |
| GABRB2 association with schizophrenia: commonalities and differences between ethnic groups and clinical subtypes. | Lo WS et al. | β | 2007 | β |
| Gap junction coding genes and schizophrenia: a genetic association study. | Aleksic B et al. | β | 2007 | β |
| Genetic analysis of the calcineurin pathway identifies members of the EGR gene family, specifically EGR3, as potential susceptibility candidates in schizophrenia. | Yamada K et al. | β | 2007 | β |
| Genetic investigation of DNA-repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancer. | Schafmayer C et al. | β | 2007 | β |
| Genetic markers of suicidal ideation emerging during citalopram treatment of major depression. | Laje G et al. | β | 2007 | β |
| Genetic polymorphisms associated with inflammatory bowel disease do not confer risk for primary sclerosing cholangitis. | Karlsen TH et al. | β | 2007 | β |
| Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis. | Steer S et al. | β | 2007 | β |
| Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use. | Zammit S et al. | β | 2007 | β |
| Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder. | Dutta S et al. | β | 2007 | β |
| GPR50 is not associated with childhood-onset mood disorders in a large sample of Hungarian families. | Feng Y et al. | β | 2007 | β |
| Haplotype association study between DRD1 gene and bipolar type I affective disorder in two samples from Canada and Sardinia. | Del Zompo M et al. | β | 2007 | β |
| Has toll-like receptor 4 been prematurely dismissed as an inflammatory bowel disease gene? Association study combined with meta-analysis shows strong evidence for association. | Browning BL et al. | β | 2007 | β |
| HO-1 promoter polymorphism associated with rheumatoid arthritis. | Rueda B et al. | β | 2007 | β |
| HTR2C and HTR1A gene variants in German and Italian suicide attempters and completers. | Serretti A et al. | β | 2007 | β |
| HTR2C haplotypes and antipsychotics-induced weight gain: X-linked multimarker analysis. | De Luca V et al. | β | 2007 | β |
| Identification of two risk haplotypes for schizophrenia and bipolar disorder in the synaptic vesicle monoamine transporter gene (SVMT). | GutiΓ©rrez B et al. | β | 2007 | β |
| IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease. | Tremelling M et al. | β | 2007 | β |
| Information-theoretic metrics for visualizing gene-environment interactions. | Chanda P et al. | β | 2007 | β |
| Interleukin 3 and schizophrenia: the impact of sex and family history. | Chen X et al. | β | 2007 | β |
| Investigation of parent-of-origin effects in ADHD candidate genes. | Kim JW et al. | β | 2007 | β |
| Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease. | Goris A et al. | β | 2007 | β |
| Investigation of the Lith6 candidate genes APOBEC1 and PPARG in human gallstone disease. | Schafmayer C et al. | β | 2007 | β |
| IRAK-M is involved in the pathogenesis of early-onset persistent asthma. | Balaci L et al. | β | 2007 | β |
| Lack of association of alcohol dependence and habitual smoking with catechol-O-methyltransferase. | Foroud T et al. | β | 2007 | β |
| Lack of association of HOXA1 and HOXB1 variants with autism in the Indian population. | Sen B et al. | β | 2007 | β |
| Linkage disequilibrium and association analysis of alpha-synuclein and alcohol and drug dependence in two American Indian populations. | Clarimon J et al. | β | 2007 | β |
| Low-density lipoprotein receptor-related protein 5 (LRP5) gene polymorphisms are associated with bone mass in both Chinese and whites. | Xiong DH et al. | β | 2007 | β |
| LRRK2 is not a significant cause of Parkinson's disease in French-Canadians. | DuprΓ© N et al. | β | 2007 | β |
| MICA marks additional risk factors for Type 1 diabetes on extended HLA haplotypes: an association and meta-analysis. | Alizadeh BZ et al. | β | 2007 | β |
| Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families. | Xiong L et al. | β | 2007 | β |
| Monoamine oxidase a gene is associated with borderline personality disorder. | Ni X et al. | β | 2007 | β |
| Mutation screen of the GAD2 gene and association study of alcoholism in three populations. | Lappalainen J et al. | β | 2007 | β |
| Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories. | Addington AM et al. | β | 2007 | β |
| No association between the glutamate decarboxylase 67 gene (GAD1) and schizophrenia in the Japanese population. | Ikeda M et al. | β | 2007 | β |
| No association of trace amine receptor genes with bipolar disorder. | Liu C et al. | β | 2007 | β |
| No associations between OPG gene polymorphisms or serum levels and measures of osteoporosis in elderly Australian women. | Ueland T et al. | β | 2007 | β |
| No evidence for genetic association of interferon regulatory factor 1 in juvenile idiopathic arthritis. | Fife MS et al. | β | 2007 | β |
| No evidence of association between a functional polymorphism in the MTHFR gene and childhood-onset mood disorders. | Dempster EL et al. | β | 2007 | β |
| No evidence of association of the PDCD1 gene with Type 1 diabetes. | Asad S et al. | β | 2007 | β |
| Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis. | Cronin S et al. | β | 2007 | β |
| Particular genetic variants of ligands for natural killer cell receptors may contribute to the HLA associated risk of primary sclerosing cholangitis. | Karlsen TH et al. | β | 2007 | β |
| Pattern-recognition techniques with haplotype analysis in pharmacogenomics. | Lin E et al. | β | 2007 | β |
| Pharmacogenetics of the 5-lipoxygenase biosynthetic pathway and variable clinical response to montelukast. | Klotsman M et al. | β | 2007 | β |
| Polymorphism in the epidermal growth factor gene is associated with birthweight in Sinhalese and white Western Europeans. | Dissanayake VH et al. | β | 2007 | β |
| Polymorphism of the follistatin gene in polycystic ovary syndrome. | Jones MR et al. | β | 2007 | β |
| Polymorphisms in ALOX12, but not ALOX15, are significantly associated with BMD in postmenopausal women. | Mullin BH et al. | β | 2007 | β |
| Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis. | Viken MK et al. | β | 2007 | β |
| Polymorphisms in the neuromyelitis optica auto-antigen AQP4 and susceptibility to multiple sclerosis. | Ban M et al. | β | 2007 | β |
| Polymorphisms in the neuronal isoform of tryptophan hydroxylase 2 are associated with bipolar disorder in French Canadian pedigrees. | Harvey M et al. | β | 2007 | β |
| Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder. | Unschuld PG et al. | β | 2007 | β |
| Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample. | Georgi A et al. | β | 2007 | β |
| Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population. | Yang MS et al. | β | 2007 | β |
| Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism. | Dutta S et al. | β | 2007 | β |
| RhoA, encoding a Rho GTPase, is associated with smoking initiation. | Chen X et al. | β | 2007 | β |
| Risk alleles for multiple sclerosis identified by a genomewide study. | International Multiple Sclerosis Genetics Consortium et al. | β | 2007 | β |
| Risk factors for hypospadias in the estrogen receptor 2 gene. | Beleza-Meireles A et al. | β | 2007 | β |
| Screening for SNPs and haplotypes in the CYP3A7 gene in Chinese populations. | Du J et al. | β | 2007 | β |
| Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis. | Capon F et al. | β | 2007 | β |
| Sequence variation in DOCK9 and heterogeneity in bipolar disorder. | Detera-Wadleigh SD et al. | β | 2007 | β |
| Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy. | Manna I et al. | β | 2007 | β |
| Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects. | Siddiq A et al. | β | 2007 | β |
| SNP- and haplotype analysis of the tryptophan hydroxylase 2 gene in alcohol-dependent patients and alcohol-related suicide. | Zill P et al. | β | 2007 | β |
| Studies in 3,523 Norwegians and meta-analysis in 11,571 subjects indicate that variants in the hepatocyte nuclear factor 4 alpha (HNF4A) P2 region are associated with type 2 diabetes in Scandinavians. | Johansson S et al. | β | 2007 | β |
| Systematic association mapping identifies NELL1 as a novel IBD disease gene. | Franke A et al. | β | 2007 | β |
| Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's disease. | Goris A et al. | β | 2007 | β |
| The discoidin domain receptor 1 as a novel susceptibility gene for schizophrenia. | Roig B et al. | β | 2007 | β |
| The MHC2TA-168A/G and +1614G/C polymorphisms and risk for multiple sclerosis or chronic inflammatory arthropathies. | O'Doherty C et al. | β | 2007 | β |
| The MYO9B gene is a strong risk factor for developing refractory celiac disease. | Wolters VM et al. | β | 2007 | β |
| The neuropeptide genes TAC1, TAC3, TAC4, VIP and PACAP(ADCYAP1), and susceptibility to multiple sclerosis. | Cunningham S et al. | β | 2007 | β |
| The opioid system in alcohol and drug dependence: family-based association study. | Xuei X et al. | β | 2007 | β |
| The PDE4B gene confers sex-specific protection against schizophrenia. | Pickard BS et al. | β | 2007 | β |
| The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophrenia. | Bakker SC et al. | β | 2007 | β |
| The polymorphisms of Eotaxin 1 and CCR3 genes influence on serum IgE, Eotaxin levels and mild asthmatic children in Taiwan. | Wang TN et al. | β | 2007 | β |
| The SERPINE2 gene is associated with chronic obstructive pulmonary disease in two large populations. | Zhu G et al. | β | 2007 | β |
| The uncoupling protein 1 gene, UCP1, is expressed in mammalian islet cells and associated with acute insulin response to glucose in African American families from the IRAS Family Study. | Sale MM et al. | β | 2007 | β |
| TNFa microsatellite polymorphism modulates the risk of type 1 diabetes in the Belgian population, independent of HLA-DQ. | Aminkeng F et al. | β | 2007 | β |
| Tumor necrosis factor alpha -308 polymorphism is associated with rheumatoid arthritis in Han population of Eastern China. | Chen R et al. | β | 2007 | β |
| UCP2 A55V variant is associated with obesity and related phenotypes in an aboriginal community in Taiwan. | Wang TN et al. | β | 2007 | β |
| Variants in EMX2 and PTEN do not contribute to risk of endometriosis. | Treloar SA et al. | β | 2007 | β |
| WHAP: haplotype-based association analysis. | Purcell S et al. | β | 2007 | β |
| A cholinergic receptor gene (CHRM2) affects event-related oscillations. | Jones KA et al. | β | 2006 | β |
| A combined effect of the KPNA3 and KPNB3 genes on susceptibility to schizophrenia. | Zhang H et al. | β | 2006 | β |
| A common haplotype of the glucokinase gene alters fasting glucose and birth weight: association in six studies and population-genetics analyses. | Weedon MN et al. | β | 2006 | β |
| ADAM33 haplotypes are associated with asthma in a large Australian population. | Kedda MA et al. | β | 2006 | β |
| A family-based and case-control association study of SOX10 in schizophrenia. | Iwamoto K et al. | β | 2006 | β |
| A functional variant in the CARD4 gene and risk of premature coronary heart disease. | El Mokhtari NE et al. | β | 2006 | β |
| A further study of a possible locus for schizophrenia on the X chromosome. | Wei J et al. | β | 2006 | β |
| Altered transmission of maternal angiotensin II receptor haplotypes in fetal growth restriction. | Tower C et al. | β | 2006 | β |
| Analysis of common PTPN1 gene variants in type 2 diabetes, obesity and associated phenotypes in the French population. | Cheyssac C et al. | β | 2006 | β |
| Analysis of GABRB2 association with schizophrenia in German population with DNA sequencing and one-label extension method for SNP genotyping. | Yu Z et al. | β | 2006 | β |
| Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. | Glaser B et al. | β | 2006 | β |
| Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder. | Barden N et al. | β | 2006 | β |
| An association analysis of candidate genes on chromosome 15 q11-13 and autism spectrum disorder. | Curran S et al. | β | 2006 | β |
| A review and re-evaluation of an association between the NOTCH4 locus and schizophrenia. | Wang Z et al. | β | 2006 | β |
| A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease. | Harold D et al. | β | 2006 | β |
| Association analysis of 6,736 U.K. subjects provides replication and confirms TCF7L2 as a type 2 diabetes susceptibility gene with a substantial effect on individual risk. | Groves CJ et al. | β | 2006 | β |
| Association analysis of MYO9B gene polymorphisms and inflammatory bowel disease in a Norwegian cohort. | Amundsen SS et al. | β | 2006 | β |
| Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort. | Amundsen SS et al. | β | 2006 | β |
| Association analysis of SOD2 variants with methamphetamine psychosis in Japanese and Taiwanese populations. | Nakamura K et al. | β | 2006 | β |
| Association analysis of the chromosome 4p-located G protein-coupled receptor 78 (GPR78) gene in bipolar affective disorder and schizophrenia. | Underwood SL et al. | β | 2006 | β |
| Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors. | Sakurai T et al. | β | 2006 | β |
| Association between GABRA1 and drinking behaviors in the collaborative study on the genetics of alcoholism sample. | Dick DM et al. | β | 2006 | β |
| Association between glutamic acid decarboxylase genes and anxiety disorders, major depression, and neuroticism. | Hettema JM et al. | β | 2006 | β |
| Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skills. | Yirmiya N et al. | β | 2006 | β |
| Association of fatty acid desaturase genes with attention-deficit/hyperactivity disorder. | Brookes KJ et al. | β | 2006 | β |
| Association of GABRA2 with drug dependence in the collaborative study of the genetics of alcoholism sample. | Agrawal A et al. | β | 2006 | β |
| Association of interferon-gamma and interferon regulatory factor 1 polymorphisms with asthma in a family-based association study in Taiwan. | Wang TN et al. | β | 2006 | β |
| Association of Reelin gene polymorphisms with autism. | Serajee FJ et al. | β | 2006 | β |
| Association of the kappa-opioid system with alcohol dependence. | Xuei X et al. | β | 2006 | β |
| Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15. | Traherne JA et al. | β | 2006 | β |
| Association of the Val158Met catechol O-methyltransferase genetic polymorphism with panic disorder. | Rothe C et al. | β | 2006 | β |
| Association study of genetic variants of pro-inflammatory chemokine and cytokine genes in systemic lupus erythematosus. | SΓ‘nchez E et al. | β | 2006 | β |
| Association study of IL10, IL1beta, and IL1RN and schizophrenia using tag SNPs from a comprehensive database: suggestive association with rs16944 at IL1beta. | Shirts BH et al. | β | 2006 | β |
| Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples. | Holliday EG et al. | β | 2006 | β |
| Autism spectrum disorders associated with X chromosome markers in French-Canadian males. | Gauthier J et al. | β | 2006 | β |
| Brain-derived neurotrophic factor (BDNF) gene and rapid-cycling bipolar disorder: family-based association study. | MΓΌller DJ et al. | β | 2006 | β |
| Breakthroughs in the search for dyslexia candidate genes. | McGrath LM et al. | β | 2006 | β |
| CACNA1C polymorphisms are associated with the efficacy of calcium channel blockers in the treatment of hypertension. | Bremer T et al. | β | 2006 | β |
| Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity. | Lorenz S et al. | β | 2006 | β |
| Case-parent triads: estimating single- and double-dose effects of fetal and maternal disease gene haplotypes. | Gjessing HK et al. | β | 2006 | β |
| Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration. | Schmidt S et al. | β | 2006 | β |
| Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases. | Di Duca M et al. | β | 2006 | β |
| Confirmation of association of the GABRA2 gene with alcohol dependence by subtype-specific analysis. | Fehr C et al. | β | 2006 | β |
| Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. | Clarimon J et al. | β | 2006 | β |
| Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. | Georgieva L et al. | β | 2006 | β |
| Cytogenetic and genetic evidence supports a role for the kainate-type glutamate receptor gene, GRIK4, in schizophrenia and bipolar disorder. | Pickard BS et al. | β | 2006 | β |
| Definition of novel GP6 polymorphisms and major difference in haplotype frequencies between populations by a combination of in-depth exon resequencing and genotyping with tag single nucleotide polymorphisms. | Watkins NA et al. | β | 2006 | β |
| Distinguishable haplotype blocks in the HTR3A and HTR3B region in the Japanese reveal evidence of association of HTR3B with female major depression. | Yamada K et al. | β | 2006 | β |
| Dopamine D2 receptor gene variants and quantitative measures of positive and negative symptom response following clozapine treatment. | Hwang R et al. | β | 2006 | β |
| Effects of differential genotyping error rate on the type I error probability of case-control studies. | Moskvina V et al. | β | 2006 | β |
| Elevated expression and genetic association links the SOCS3 gene to atopic dermatitis. | Ekelund E et al. | β | 2006 | β |
| Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment. | Carayol J et al. | β | 2006 | β |
| Evidence for linkage to and association with type 1 diabetes at the 3q21 region in the Finnish population. | Laine AP et al. | β | 2006 | β |
| Failure to find association between TRAR4 and schizophrenia in the Chinese Han population. | Duan S et al. | β | 2006 | β |
| Failure to support a genetic contribution of AKT1 polymorphisms and altered AKT signaling in schizophrenia. | Ide M et al. | β | 2006 | β |
| Family-based association studies of the TCP1 gene and schizophrenia in the Chinese Han population. | Tang W et al. | β | 2006 | β |
| Family-based association study of Epsin 4 and Schizophrenia. | Tang RQ et al. | β | 2006 | β |
| Family-based association study of TPH1 and TPH2 polymorphisms in autism. | Ramoz N et al. | β | 2006 | β |
| Family-based designs in the age of large-scale gene-association studies. | Laird NM et al. | β | 2006 | β |
| Fine mapping of genetic susceptibility to polycystic ovary syndrome on chromosome 19p13.2 and tests for regulatory activity. | Stewart DR et al. | β | 2006 | β |
| Functional polymorphism of the NFKB1 gene promoter is not relevant in predisposition to celiac disease. | Rueda B et al. | β | 2006 | β |
| Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. | Harold D et al. | β | 2006 | β |
| Gene-gene interaction between MAOA and COMT in suicidal behavior: analysis in schizophrenia. | De Luca V et al. | β | 2006 | β |
| Genetic and expression analyses of the STOP (MAP6) gene in schizophrenia. | Shimizu H et al. | β | 2006 | β |
| Genetic association of the human corticotropin releasing hormone receptor 1 (CRHR1) with binge drinking and alcohol intake patterns in two independent samples. | Treutlein J et al. | β | 2006 | β |
| Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study. | Sutton BS et al. | β | 2006 | β |
| Genetic variants of RANTES are associated with serum RANTES level and protection for type 1 diabetes. | Zhernakova A et al. | β | 2006 | β |
| Genome-wide expression analysis detects eight genes with robust alterations specific to bipolar I disorder: relevance to neuronal network perturbation. | Nakatani N et al. | β | 2006 | β |
| Genome-wide linkage of plasma adiponectin reveals a major locus on chromosome 3q distinct from the adiponectin structural gene: the IRAS family study. | Guo X et al. | β | 2006 | β |
| GENOMIZER: an integrated analysis system for genome-wide association data. | Franke A et al. | β | 2006 | β |
| Haplotypes spanning SPEC2, PDZ-GEF2 and ACSL6 genes are associated with schizophrenia. | Chen X et al. | β | 2006 | β |
| Heterogeneity at the JME 6p11-12 locus: absence of mutations in the EFHC1 gene in linked Dutch families. | Pinto D et al. | β | 2006 | β |
| HLA class II haplotype DRB1*04-DQB1*0301 contributes to risk of familial generalized vitiligo and early disease onset. | Fain PR et al. | β | 2006 | β |
| Human leukocyte antigen non-class II determinants for type 1 diabetes in the Finnish population. | Gombos Z et al. | β | 2006 | β |
| Human QKI, a new candidate gene for schizophrenia involved in myelination. | Aberg K et al. | β | 2006 | β |
| Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia. | Mah S et al. | β | 2006 | β |
| Individual SNP allele reconstruction from informative markers selected by a non-linear Gauss-type algorithm. | Moskvina V et al. | β | 2006 | β |
| Inducible and endothelial nitric oxide synthase genes polymorphism in inflammatory bowel disease. | Oliver J et al. | β | 2006 | β |
| Interleukin-1 gene cluster polymorphism in chagas disease in a Colombian case-control study. | FlΓ³rez O et al. | β | 2006 | β |
| Investigation of the Lith1 candidate genes ABCB11 and LXRA in human gallstone disease. | Schafmayer C et al. | β | 2006 | β |
| KRAS variation and risk of endometriosis. | Zhao ZZ et al. | β | 2006 | β |
| Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism. | Ramoz N et al. | β | 2006 | β |
| Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort. | Wilson SG et al. | β | 2006 | β |
| Low mRNA levels of RGS4 splice variants in Alzheimer's disease: association between a rare haplotype and decreased mRNA expression. | Emilsson L et al. | β | 2006 | β |
| Lymphoid tyrosine phosphatase (LYP/PTPN22) Arg620Trp variant regulates insulin autoimmunity and progression to type 1 diabetes. | Hermann R et al. | β | 2006 | β |
| MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children. | Das M et al. | β | 2006 | β |
| MICA is associated with type 1 diabetes in the Belgian population, independent of HLA-DQ. | Van Autreve JE et al. | β | 2006 | β |
| No association between the functional CARD4 insertion/deletion polymorphism and inflammatory bowel diseases in the German population. | Franke A et al. | β | 2006 | β |
| No association of complexin1 and complexin2 genes with schizophrenia in a Japanese population. | Kishi T et al. | β | 2006 | β |
| No association of serotonin transporter gene (SLC6A4) with schizophrenia and bipolar disorder in Japanese patients: association analysis based on linkage disequilibrium. | Ikeda M et al. | β | 2006 | β |
| No evidence for association between NOTCH4 and schizophrenia in a large family-based and case-control association analysis. | Ivo R et al. | β | 2006 | β |
| No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening. | Goris A et al. | β | 2006 | β |
| No evidence of association of ENPP1 variants with type 2 diabetes or obesity in a study of 8,089 U.K. Caucasians. | Weedon MN et al. | β | 2006 | β |
| Novel IL10 gene family associations with systemic juvenile idiopathic arthritis. | Fife MS et al. | β | 2006 | β |
| Perils and pitfalls of permutation tests for distinguishing the effects of neighbouring polymorphisms. | Biernacka JM et al. | β | 2006 | β |
| Polymorphism in HSD17B6 is associated with key features of polycystic ovary syndrome. | Jones MR et al. | β | 2006 | β |
| Polymorphisms in four candidate genes in young patients with essential hypertension. | Marcun Varda N et al. | β | 2006 | β |
| Polymorphisms in the dopamine D4 receptor gene (DRD4) contribute to individual differences in human sexual behavior: desire, arousal and sexual function. | Ben Zion IZ et al. | β | 2006 | β |
| Positive association of the serotonin 5-HT7 receptor gene with schizophrenia in a Japanese population. | Ikeda M et al. | β | 2006 | β |
| Protection from type 1 diabetes by vitamin D receptor haplotypes. | Ramos-Lopez E et al. | β | 2006 | β |
| RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity. | Liebetanz KM et al. | β | 2006 | β |
| Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia. | Seal JL et al. | β | 2006 | β |
| Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31. | Onnie C et al. | β | 2006 | β |
| Serotonin 2A receptor gene is associated with personality traits, but not to disorder, in patients with borderline personality disorder. | Ni X et al. | β | 2006 | β |
| Significant linkage of BMI to chromosome 10p in the U.K. population and evaluation of GAD2 as a positional candidate. | Groves CJ et al. | β | 2006 | β |
| SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. | Blasi F et al. | β | 2006 | β |
| SNP-SNP interactions in breast cancer susceptibility. | Onay VU et al. | β | 2006 | β |
| Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. | Schumacher J et al. | β | 2006 | β |
| Study of the role of functional variants of SLC22A4, RUNX1 and SUMO4 in systemic lupus erythematosus. | Orozco G et al. | β | 2006 | β |
| Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder. | Nievergelt CM et al. | β | 2006 | β |
| Systematic screening for polymorphisms in the CYP3A4 gene in the Chinese population. | Du J et al. | β | 2006 | β |
| The APL test: extension to general nuclear families and haplotypes and examination of its robustness. | Chung RH et al. | β | 2006 | β |
| The molecular genetic architecture of human personality: beyond self-report questionnaires. | Ebstein RP | β | 2006 | β |
| The mu-opioid receptor gene and smoking initiation and nicotine dependence. | Zhang L et al. | β | 2006 | β |
| The PLA2G4A gene and negative symptoms in a Chinese population. | Tao R et al. | β | 2006 | β |
| The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations. | Sharma M et al. | β | 2006 | β |
| Transmission disequilibrium test provides evidence of association between promoter polymorphisms in 22q11 gene DGCR14 and schizophrenia. | Wang H et al. | β | 2006 | β |
| Transmission distortion of BDNF variants to bipolar disorder type I patients from a South American population isolate. | Kremeyer B et al. | β | 2006 | β |
| Two isoforms of GABA(A) receptor beta2 subunit with different electrophysiological properties: Differential expression and genotypical correlations in schizophrenia. | Zhao C et al. | β | 2006 | β |
| Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. | Smemo S et al. | β | 2006 | β |
| Use of phenotypic covariates in association analysis by sequential addition of cases. | Macgregor S et al. | β | 2006 | β |
| Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura. | Todt U et al. | β | 2006 | β |
| Variations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar i disorder. | Lohoff FW et al. | β | 2006 | β |
| ADH4 gene variation is associated with alcohol and drug dependence: results from family controlled and population-structured association studies. | Luo X et al. | β | 2005 | β |
| A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia. | Aoki-Suzuki M et al. | β | 2005 | β |
| A family-based association study of schizophrenia with polymorphisms at three candidate genes. | Duan S et al. | β | 2005 | β |
| Age-associated skewing of X-inactivation ratios of blood cells in normal females: a candidate-gene analysis approach. | Chagnon P et al. | β | 2005 | β |
| A high-density screen for linkage in multiple sclerosis. | Sawcer S et al. | β | 2005 | β |
| A locus on chromosome 9p predisposes to a specific disease manifestation, acute anterior uveitis, in ankylosing spondylitis, a genetically complex, multisystem, inflammatory disease. | Martin TM et al. | β | 2005 | β |
| Analysis of a functional BTNL2 polymorphism in type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosus. | Orozco G et al. | β | 2005 | β |
| Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population. | GuΓ©rardel A et al. | β | 2005 | β |
| Analysis of vascular endothelial growth factor (VEGF) functional variants in rheumatoid arthritis. | Rueda B et al. | β | 2005 | β |
| A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy. | Gu W et al. | β | 2005 | β |
| An exact maternal-fetal genotype incompatibility (MFG) test. | Minassian SL et al. | β | 2005 | β |
| A novel tissue inhibitor of metalloproteinase-1 (TIMP-1) polymorphism associated with asthma in Australian women. | Lose F et al. | β | 2005 | β |
| A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis. | Lincoln MR et al. | β | 2005 | β |
| Assessing the power of tag SNPs in the mapping of quantitative trait loci (QTL) with extremal and random samples. | Zhang K et al. | β | 2005 | β |
| Association analysis of chromosome 5 GABAA receptor cluster in Japanese schizophrenia patients. | Ikeda M et al. | β | 2005 | β |
| Association analysis of malic enzyme 2 gene polymorphisms with idiopathic generalized epilepsy. | Lenzen KP et al. | β | 2005 | β |
| Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children. | Domschke K et al. | β | 2005 | β |
| Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia. | Zhang F et al. | β | 2005 | β |
| Association between alcoholism and gamma-amino butyric acid alpha2 receptor subtype in a Russian population. | Lappalainen J et al. | β | 2005 | β |
| Association between BDNF val66 met genotype and episodic memory. | Dempster E et al. | β | 2005 | β |
| Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population. | Thomson PA et al. | β | 2005 | β |
| Association of a haplotype block spanning SDAD1 gene and CXC chemokine genes with allergic rhinitis. | Zhang J et al. | β | 2005 | β |
| Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations. | RibasΓ©s M et al. | β | 2005 | β |
| Association of proopiomelanocortin gene polymorphisms with obesity in the IRAS family study. | Sutton BS et al. | β | 2005 | β |
| Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder. | Laurin N et al. | β | 2005 | β |
| Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. | Kent L et al. | β | 2005 | β |
| Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. | Nowotny P et al. | β | 2005 | β |
| Association study of 12 polymorphisms spanning the dopamine D(2) receptor gene and clozapine treatment response in two treatment refractory/intolerant populations. | Hwang R et al. | β | 2005 | β |
| Association study of a novel functional polymorphism of the serotonin transporter gene in bipolar disorder and suicidal behaviour. | De Luca V et al. | β | 2005 | β |
| AVPR1a and SLC6A4 gene polymorphisms are associated with creative dance performance. | Bachner-Melman R et al. | β | 2005 | β |
| Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). | Raybould R et al. | β | 2005 | β |
| Bone mass effects of a BMP4 gene polymorphism in postmenopausal women. | Ramesh Babu L et al. | β | 2005 | β |
| C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition. | Rueda B et al. | β | 2005 | β |
| Chromosome 11-q24 region in Tourette syndrome: association and linkage disequilibrium study in the French Canadian population. | DΓaz-AnzaldΓΊa A et al. | β | 2005 | β |
| Common VKORC1 and GGCX polymorphisms associated with warfarin dose. | Wadelius M et al. | β | 2005 | β |
| Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31. | Segurado R et al. | β | 2005 | β |
| CTLA4/CT60 polymorphism is not relevant in susceptibility to autoimmune inflammatory intestinal disorders. | Rueda B et al. | β | 2005 | β |
| CTLA4 is differentially associated with autoimmune diseases in the Dutch population. | Zhernakova A et al. | β | 2005 | β |
| DAT1, DRD4, and DRD5 polymorphisms are not associated with ADHD in Dutch families. | Bakker SC et al. | β | 2005 | β |
| DNA pooling analysis of ADHD and genes regulating vesicle release of neurotransmitters. | Brookes KJ et al. | β | 2005 | β |
| Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS). | Gornick MC et al. | β | 2005 | β |
| Estrogen receptor beta (ESR2) polymorphisms in familial and sporadic breast cancer. | Maguire P et al. | β | 2005 | β |
| Functional variants in SUMO4, TAB2, and NFkappaB and the risk of type 1 diabetes. | Kosoy R et al. | β | 2005 | β |
| GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss. | Addington AM et al. | β | 2005 | β |
| Gene-gene interaction between MAOA and COMT in suicidal behavior. | De Luca V et al. | β | 2005 | β |
| Genetic analysis of adiponectin and obesity in Hispanic families: the IRAS Family Study. | Sutton BS et al. | β | 2005 | β |
| Genetic analysis of the maximum drinks phenotype. | Saccone SF et al. | β | 2005 | β |
| Genetic association studies. | Cordell HJ et al. | β | 2005 | β |
| Genetic association studies in complex disease: disentangling additional predisposing loci from associated neutral loci using a constrained - permutation approach. | Spijker GT et al. | β | 2005 | β |
| Genetics of autoimmune myasthenia gravis: the multifaceted contribution of the HLA complex. | Vandiedonck C et al. | β | 2005 | β |
| Genetic variation in the brain derived neurotrophic factor gene in Alzheimer's disease. | Bodner SM et al. | β | 2005 | β |
| Genetic variation in the MTHFR gene influences thiopurine methyltransferase activity. | Arenas M et al. | β | 2005 | β |
| Haplotype analysis of a 100 kb region spanning TNF-LTA identifies a polymorphism in the LTA promoter region that is associated with atopic asthma susceptibility in Japan. | Migita O et al. | β | 2005 | β |
| Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism. | Philippi A et al. | β | 2005 | β |
| Human p53 tumor suppressor gene (TP53) and schizophrenia: case-control and family studies. | Ni X et al. | β | 2005 | β |
| Identification of a potential bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4. | Glaser B et al. | β | 2005 | β |
| Identification of multiple serine racemase (SRR) mRNA isoforms and genetic analyses of SRR and DAO in schizophrenia and D-serine levels. | Yamada K et al. | β | 2005 | β |
| Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations. | Li T et al. | β | 2005 | β |
| Interleukin 12 (IL12B) and interleukin 12 receptor (IL12RB1) gene polymorphisms in rheumatoid arthritis. | Orozco G et al. | β | 2005 | β |
| Interleukin-18-promoter polymorphisms are not relevant in rheumatoid arthritis. | Rueda B et al. | β | 2005 | β |
| Investigation of the DAOA/G30 locus in panic disorder. | Schumacher J et al. | β | 2005 | β |
| Klotho gene polymorphisms are associated with osteocalcin levels but not bone density of aged postmenopausal women. | Mullin BH et al. | β | 2005 | β |
| Lack of association between variations in the brain-derived neurotrophic factor (BDNF) gene and temporal lobe epilepsy. | Lohoff FW et al. | β | 2005 | β |
| Lack of support for the association between GAD2 polymorphisms and severe human obesity. | Swarbrick MM et al. | β | 2005 | β |
| LRP5 gene polymorphisms predict bone mass and incident fractures in elderly Australian women. | Bollerslev J et al. | β | 2005 | β |
| Multiple testing in the context of haplotype analysis revisited: application to case-control data. | Becker T et al. | β | 2005 | β |
| No association between common variations in the human alpha 2 subunit gene (ATP1A2) of the sodium-potassium-transporting ATPase and idiopathic generalized epilepsy. | Lohoff FW et al. | β | 2005 | β |
| No association between common variations in the neuronal nicotinic acetylcholine receptor alpha2 subunit gene (CHRNA2) and bipolar I disorder. | Lohoff FW et al. | β | 2005 | β |
| No association between schizophrenia and polymorphisms in COMT in two large samples. | Williams HJ et al. | β | 2005 | β |
| Poly (ADP-ribose) polymerase-1 haplotypes are associated with coeliac disease. | Rueda B et al. | β | 2005 | β |
| Polymorphisms in the 5-lipoxygenase activating protein (ALOX5AP) gene are not associated with asthma in an Australian population. | Kedda MA et al. | β | 2005 | β |
| Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. | TΓΆrΓΆk HP et al. | β | 2005 | β |
| Polymorphisms in the NMDA subunit 2B are not associated with alcohol dependence and alcohol withdrawal-induced seizures and delirium tremens. | Tadic A et al. | β | 2005 | β |
| Positive association of the human GABA-A-receptor beta 2 subunit gene haplotype with schizophrenia in the Chinese Han population. | Liu J et al. | β | 2005 | β |
| Promoter polymorphism of second tryptophan hydroxylase isoform (TPH2) in schizophrenia and suicidality. | De Luca V et al. | β | 2005 | β |
| P-selectin gene haplotype associations with albuminuria in the Diabetes Heart Study. | Liu Y et al. | β | 2005 | β |
| Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia. | Handoko HY et al. | β | 2005 | β |
| Sequence analysis of the serotonin transporter and associations with antidepressant response. | Kraft JB et al. | β | 2005 | β |
| Serotonin gene polymorphisms and bipolar I disorder: focus on the serotonin transporter. | Mansour HA et al. | β | 2005 | β |
| Serotonin receptor 2C (HTR2C) and schizophrenia: examination of possible medication and genetic influences on expression levels. | Castensson A et al. | β | 2005 | β |
| Sex-specific association between bipolar affective disorder in women and GPR50, an X-linked orphan G protein-coupled receptor. | Thomson PA et al. | β | 2005 | β |
| Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population. | Scapoli L et al. | β | 2005 | β |
| Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. | Cope N et al. | β | 2005 | β |
| Support for association between ADHD and two candidate genes: NET1 and DRD1. | Bobb AJ et al. | β | 2005 | β |
| Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus. | Benayed R et al. | β | 2005 | β |
| The influence of the -401G/T and -402G/A polymorphisms of the coagulation FVII promoter on plasma levels of FVII. | Lindman AS et al. | β | 2005 | β |
| The power of sample size and homogenous sampling: association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder. | Hoefgen B et al. | β | 2005 | β |
| Variants in the vitamin D receptor gene and asthma. | Wjst M | β | 2005 | β |
| A functional variant of IFNgamma gene is associated with coeliac disease. | Rueda B et al. | β | 2004 | β |
| Association of AKT1 with schizophrenia confirmed in a Japanese population. | Ikeda M et al. | β | 2004 | β |
| Association of polymorphisms and haplotypes in the elastin gene in Dutch patients with sporadic aneurysmal subarachnoid hemorrhage. | Ruigrok YM et al. | β | 2004 | β |
| A survey of current software for haplotype phase inference. | Weale ME | β | 2004 | β |
| Body mass index, leptin and leptin receptor polymorphisms, and non-hodgkin lymphoma. | Skibola CF et al. | β | 2004 | β |
| Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. | Chen WY et al. | β | 2004 | β |
| Convergent evidence for impaired AKT1-GSK3beta signaling in schizophrenia. | Emamian ES et al. | β | 2004 | β |
| Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies. | Dudbridge F et al. | β | 2004 | β |
| Failure to confirm association between AKT1 haplotype and schizophrenia in a Japanese case-control population. | Ohtsuki T et al. | β | 2004 | β |
| Genetic and expression analyses of FZD3 in schizophrenia. | Ide M et al. | β | 2004 | β |
| Genetic studies in familial ankylosing spondylitis susceptibility. | Zhang G et al. | β | 2004 | β |
| Interaction and association analysis of a type 1 diabetes susceptibility locus on chromosome 5q11-q13 and the 7q32 chromosomal region in Scandinavian families. | Holm P et al. | β | 2004 | β |
| Meta-analysis of genome-wide studies of psoriasis susceptibility reveals linkage to chromosomes 6p21 and 4q28-q31 in Caucasian and Chinese Hans population. | Sagoo GS et al. | β | 2004 | β |
| Neuregulin 1: genetic support for schizophrenia subtypes. | Bakker SC et al. | β | 2004 | β |
| No association between interferon-gamma receptor-1 gene polymorphism and pulmonary tuberculosis in a Gambian population sample. | Awomoyi AA et al. | β | 2004 | β |
| Novel haplotypes in 17q21 are associated with progressive supranuclear palsy. | Pastor P et al. | β | 2004 | β |
| Pleiotropic effects of the 8.1 HLA haplotype in patients with autoimmune myasthenia gravis and thymus hyperplasia. | Vandiedonck C et al. | β | 2004 | β |
| Polymorphism in NOD2, Crohn's disease, and susceptibility to pulmonary tuberculosis. | Stockton JC et al. | β | 2004 | β |
| Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified. | Addington AM et al. | β | 2004 | β |
| Polymorphisms in the amino acid transporter solute carrier family 6 (neurotransmitter transporter) member 14 gene contribute to polygenic obesity in French Caucasians. | Durand E et al. | β | 2004 | β |
| Single nucleotide polymorphism and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene in suicide victims. | Zill P et al. | β | 2004 | β |
| SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depression. | Zill P et al. | β | 2004 | β |
| Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria. | Kirov G et al. | β | 2004 | β |
| Support for the involvement of TPH2 gene in affective disorders. | Harvey M et al. | β | 2004 | β |
| The contribution of three strong candidate schizophrenia susceptibility genes in demographically distinct populations. | Hall D et al. | β | 2004 | β |
| Depression, the bΓͺte noire of cardiology? | Lambert G | β | 2002 | β |