GOLD--graphical overview of linkage disequilibrium.
paper
Cited
Public
Unavailable
- Authors
- Abecasis, G R; Cookson, W O
- Year
- 2000
- Journal
- Bioinformatics (Oxford, England)
- PMID
- 10842743
- DOI
- 10.1093/bioinformatics/16.2.182
SUMMARY: We describe a software package that provides a graphical summary of linkage disequilibrium in human genetic data. It allows for the analysis of family data and is well suited to the analysis of dense genetic maps. AVAILABILITY: http://www.well.ox.ac.uk/asthma/GOLD CONTACT: goncalo@well.ox.ac.uk
No figures extracted from this document.
No chunks — full text not yet ingested.
No entities extracted from this document yet.
No uploaded files.
Not in any collection.
No citations found.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Interleukin-1 Beta rs16944 and rs1143634 and Interleukin-6 Receptor rs12083537 Single Nucleotide Polymorphisms as Potential Predictors of COVID-19 Severity. | Ahmed IA et al. | — | 2024 | → |
| Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer. | Brugger M et al. | — | 2024 | → |
| Associations between Omega-3 Index, Dopaminergic Genetic Variants and Aggressive and Metacognitive Traits: A Study in Adult Male Prisoners. | Fernandez F et al. | — | 2022 | → |
| Cluster of Differentiation 24 Polymorphism Has No Significant Association with Chronic Hepatitis B Virus Infection in the Chinese Han Population: A Family-Based Association Study. | Xia S et al. | — | 2022 | → |
| <i>ARID5B</i> rs10821936 and rs10994982 gene polymorphism and susceptibility to juvenile systemic lupus erythematosus and lupus nephritis. | Mosaad YM et al. | — | 2021 | → |
| Notes on Three Decades of Methodology Workshops. | Maes HH | — | 2021 | → |
| The identification of a major sex QTL in the white-leg shrimp, Litopenaeus vannamei | Jones DB et al. | — | 2021 | — |
| LDscaff: LD-based scaffolding of de novo genome assemblies. | Zhao Z et al. | — | 2020 | → |
| Genomic data provide new insights on the demographic history and the extent of recent material transfers in Norway spruce. | Chen J et al. | — | 2019 | → |
| Update on the genetics of primary open-angle glaucoma. | Youngblood H et al. | — | 2019 | → |
| A comparative integrated gene-based linkage and locus ordering by linkage disequilibrium map for the Pacific white shrimp, Litopenaeus vannamei. | Jones DB et al. | — | 2017 | → |
| CYP2A6 Polymorphisms Associate with Outcomes of S-1 Plus Oxaliplatin Chemotherapy in Chinese Gastric Cancer Patients. | Yang L et al. | — | 2017 | → |
| Estimating Disequilibrium Coefficients. | Vens M et al. | — | 2017 | → |
| Selection against recombinant hybrids maintains reproductive isolation in hybridizing Populus species despite F1 fertility and recurrent gene flow. | Christe C et al. | — | 2016 | → |
| UGT1A1*6, UGT1A7*3 and UGT1A9*1b polymorphisms are predictive markers for severe toxicity in patients with metastatic gastrointestinal cancer treated with irinotecan-based regimens. | Cui C et al. | — | 2016 | → |
| Effective Population Size and Signatures of Selection Using Bovine 50K SNP Chips in Korean Native Cattle (Hanwoo). | Li Y et al. | — | 2015 | → |
| Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study. | Li J et al. | — | 2015 | → |
| Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease. | Moteki Y et al. | — | 2015 | → |
| The Impact of Genetic Relationship and Linkage Disequilibrium on Genomic Selection. | Liu H et al. | — | 2015 | → |
| Genetic mapping of a new race specific resistance allele effective to Puccinia hordei at the Rph9/Rph12 locus on chromosome 5HL in barley. | Dracatos PM et al. | — | 2014 | → |
| Population-specific differences in gene conversion patterns between human SUZ12 and SUZ12P are indicative of the dynamic nature of interparalog gene conversion. | Mussotter T et al. | — | 2014 | → |
| Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay. | Weber ML et al. | — | 2014 | → |
| Accuracy of predicting genomic breeding values for residual feed intake in Angus and Charolais beef cattle. | Chen L et al. | — | 2013 | → |
| A high-density SNP genetic linkage map for the silver-lipped pearl oyster, Pinctada maxima: a valuable resource for gene localisation and marker-assisted selection. | Jones DB et al. | — | 2013 | → |
| Assessing footprints of selection in commercial Atlantic salmon populations using microsatellite data. | Martinez V et al. | — | 2013 | → |
| Association between PARK16 and Parkinson's disease in the Han Chinese population: a meta-analysis. | Chang KH et al. | — | 2013 | → |
| Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2. | Hawthorne F et al. | — | 2013 | → |
| Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis. | Connelly JJ et al. | — | 2013 | → |
| Fine-mapping of 5q12.1-13.3 unveils new genetic contributors to caries. | Shimizu T et al. | — | 2013 | → |
| Folate metabolism genes, dietary folate and response to antidepressant medications in late-life depression. | Jamerson BD et al. | — | 2013 | → |
| Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease. | Chen YC et al. | — | 2013 | → |
| Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype. | Soldano KL et al. | — | 2013 | → |
| Genetic variants ofLRRK2 in Taiwanese Parkinson's disease. | Wu YR et al. | — | 2013 | → |
| Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis. | Hofmann S et al. | — | 2013 | → |
| Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci. | Flaquer A et al. | — | 2013 | → |
| Genomic dissection of variation in clutch size and egg mass in a wild great tit (Parus major) population. | Santure AW et al. | — | 2013 | → |
| Identification of single nucleotide polymorphisms in genes involved in digestive and metabolic processes associated with feed efficiency and performance traits in beef cattle. | Abo-Ismail MK et al. | — | 2013 | → |
| Interpreting joint SNP analysis results: when are two distinct signals really two distinct signals? | Schwantes-An TH et al. | — | 2013 | → |
| Killer cell immunoglobulin-like receptor (KIR) genes and their HLA-C ligands in a Ugandan population. | Nakimuli A et al. | — | 2013 | → |
| Novel genomic approaches unravel genetic architecture of complex traits in apple. | Kumar S et al. | — | 2013 | → |
| Role of TRAV locus in low caries experience. | Briseño-Ruiz J et al. | — | 2013 | → |
| Analytical methods for immunogenetic population data. | Mack SJ et al. | — | 2012 | → |
| Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease. | Belin AC et al. | — | 2012 | → |
| A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis. | Cagliani R et al. | — | 2012 | → |
| Changes in uric acid levels following bariatric surgery are not associated with SLC2A9 variants in the Swedish Obese Subjects Study. | Sarzynski MA et al. | — | 2012 | → |
| Enamel formation genes influence enamel microhardness before and after cariogenic challenge. | Shimizu T et al. | — | 2012 | → |
| Estimating disequilibrium coefficients. | Vens M et al. | — | 2012 | → |
| Genetic variations in genes involved in heparan sulphate biosynthesis are associated with Plasmodium falciparum parasitaemia: a familial study in Burkina Faso. | Atkinson A et al. | — | 2012 | → |
| Genomic selection for fruit quality traits in apple (Malus×domestica Borkh.). | Kumar S et al. | — | 2012 | → |
| Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate. | Letra A et al. | — | 2012 | → |
| MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. | Velez Edwards DR et al. | — | 2012 | → |
| Mitochondrial haplotype does not influence sperm motility in a UK population of men. | Mossman JA et al. | — | 2012 | → |
| Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis. | Bogaert E et al. | — | 2012 | → |
| Refining the genetic portrait of Portuguese Roma through X-chromosomal markers. | Pereira V et al. | — | 2012 | → |
| Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot. | Lu W et al. | — | 2012 | → |
| Adaptive evolution of a key gene affecting queen and worker traits in the honey bee, Apis mellifera. | Kent CF et al. | — | 2011 | → |
| Analysis of CYP3A4 genetic polymorphisms in Han Chinese. | Zhou Q et al. | — | 2011 | → |
| An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal. | Dutta S et al. | — | 2011 | → |
| Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men. | Shi YC et al. | — | 2011 | → |
| Associations of markers in 11 obesity candidate genes with maximal weight loss and weight regain in the SOS bariatric surgery cases. | Sarzynski MA et al. | — | 2011 | → |
| CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate. | Letra A et al. | — | 2011 | → |
| Effect of heme oxygenase-1 polymorphisms on lung function and gene expression. | Tanaka G et al. | — | 2011 | → |
| Endothelial nitric oxide synthase gene haplotype association with systemic lupus erythematosus. | Alfadhli S et al. | — | 2011 | → |
| Folate pathway and nonsyndromic cleft lip and palate. | Blanton SH et al. | — | 2011 | → |
| Genetic studies of the protein kinase AKT1 in Parkinson's disease. | Ran C et al. | — | 2011 | → |
| Genetic variants in the KIF6 region and coronary event reduction from statin therapy. | Li Y et al. | — | 2011 | → |
| Genetic variants of NPAT-ATM and AURKA are associated with an early adverse reaction in the gastrointestinal tract of patients with cervical cancer treated with pelvic radiation therapy. | Ishikawa A et al. | — | 2011 | → |
| Genome-wide association studies for feedlot and growth traits in cattle. | Bolormaa S et al. | — | 2011 | → |
| Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and Argentina. | Morris GA et al. | — | 2011 | → |
| Lifestyle and socioeconomic-status modify the effects of ADRB2 and NOS3 on adiposity in European-American and African-American adolescents. | Lagou V et al. | — | 2011 | → |
| Nonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connection. | Chiquet BT et al. | — | 2011 | → |
| Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease. | Minear MA et al. | — | 2011 | → |
| Smoking, the xenobiotic pathway, and clubfoot. | Sommer A et al. | — | 2011 | → |
| SNP-by-fitness and SNP-by-BMI interactions from seven candidate genes and incident hypertension after 20 years of follow-up: the CARDIA Fitness Study. | Sarzynski MA et al. | — | 2011 | → |
| The impact of natural selection on an ABCC11 SNP determining earwax type. | Ohashi J et al. | — | 2011 | → |
| Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot. | Weymouth KS et al. | — | 2011 | → |
| X chromosome and suicide. | Fiori LM et al. | — | 2011 | → |
| A 3' UTR transition within DEFB1 is associated with chronic and aggressive periodontitis. | Schaefer AS et al. | — | 2010 | → |
| A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis. | Schaefer AS et al. | — | 2010 | → |
| Allele-specific CDH1 downregulation and hereditary diffuse gastric cancer. | Pinheiro H et al. | — | 2010 | → |
| AQP1 and SLC4A10 as candidate genes for primary open-angle glaucoma. | Liu W et al. | — | 2010 | → |
| A quantitative trait locus for faecal worm egg and blood eosinophil counts on chromosome 23 in Australian goats. | Bolormaa S et al. | — | 2010 | → |
| Assignment of chromosomal locations for unassigned SNPs/scaffolds based on pair-wise linkage disequilibrium estimates. | Khatkar MS et al. | — | 2010 | → |
| Association analyses of vitamin D-binding protein gene with compression strength index variation in Caucasian nuclear families. | Xu XH et al. | — | 2010 | → |
| Association between TGFB3 and nonsyndromic cleft lip with or without cleft palate in a Chilean population. | Suazo J et al. | — | 2010 | → |
| Association of single-nucleotide polymorphisms from 17 candidate genes with baseline symptom-limited exercise test duration and decrease in duration over 20 years: the Coronary Artery Risk Development in Young Adults (CARDIA) fitness study. | Sarzynski MA et al. | — | 2010 | → |
| A unified framework for detecting genetic association with multiple SNPs in a candidate gene or region: contrasting genotype scores and LD patterns between cases and controls. | Pan W | — | 2010 | → |
| A validated genome-wide association study in 2 dairy cattle breeds for milk production and fertility traits using variable length haplotypes. | Pryce JE et al. | — | 2010 | → |
| Caspase-8 polymorphisms and risk of gallbladder cancer in a northern Indian population. | Srivastava K et al. | — | 2010 | → |
| CYP1A2 is more variable than previously thought: a genomic biography of the gene behind the human drug-metabolizing enzyme. | Browning SL et al. | — | 2010 | → |
| Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability. | Emison ES et al. | — | 2010 | → |
| Differential regulation of alpha7 nicotinic receptor gene (CHRNA7) expression in schizophrenic smokers. | Mexal S et al. | — | 2010 | → |
| Ethnic heterogeneity of IRF6 AP-2a binding site promoter SNP association with nonsyndromic cleft lip and palate. | Blanton SH et al. | — | 2010 | → |
| FAM5C contributes to aggressive periodontitis. | Carvalho FM et al. | — | 2010 | → |
| Family-based study shows heterogeneity of a susceptibility locus on chromosome 8q24 for nonsyndromic cleft lip and palate. | Blanton SH et al. | — | 2010 | → |
| Fine mapping of calcineurin (PPP3CA) gene reveals novel alternative splicing patterns, association of 5'UTR trinucleotide repeat with addiction vulnerability, and differential isoform expression in Alzheimer's disease. | Chiocco MJ et al. | — | 2010 | → |
| Genetic and functional analysis of the DLG4 gene encoding the post-synaptic density protein 95 in schizophrenia. | Cheng MC et al. | — | 2010 | → |
| Genetic polymorphisms and human sensitivity to opioid analgesics. | Nishizawa D et al. | — | 2010 | → |
| Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families. | Markunas CA et al. | — | 2010 | → |
| Genomic hotspots for adaptation: the population genetics of Müllerian mimicry in Heliconius erato. | Counterman BA et al. | — | 2010 | → |
| Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure. | Chen Y et al. | — | 2010 | → |
| Linkage disequilibrium organization of the human KIR superlocus: implications for KIR data analyses. | Gourraud PA et al. | — | 2010 | → |
| Population-genetic nature of copy number variations in the human genome. | Kato M et al. | — | 2010 | → |
| Power of a genome scan to detect and locate quantitative trait loci in cattle using dense single nucleotide polymorphisms. | MacLeod IM et al. | — | 2010 | → |
| Pronounced inter- and intrachromosomal variation in linkage disequilibrium across the zebra finch genome. | Stapley J et al. | — | 2010 | → |
| Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea. | Kim HJ et al. | — | 2010 | → |
| Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependence. | Chen AC et al. | — | 2010 | → |
| SNPTransformer: a lightweight toolkit for genome-wide association studies. | Dong C | — | 2010 | → |
| Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer. | Mrkonjic M et al. | — | 2010 | → |
| The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD). | Pointon JJ et al. | — | 2010 | → |
| The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach. | Gawlik M et al. | — | 2010 | → |
| The genetic basis of recessive self-colour pattern in a wild sheep population. | Gratten J et al. | — | 2010 | → |
| Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans. | Velez DR et al. | — | 2010 | → |
| Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot. | Ester AR et al. | — | 2009 | → |
| Association between angiopoietin-like 6 (ANGPTL6) gene polymorphisms and metabolic syndrome-related phenotypes in the French MONICA Study. | Legry V et al. | — | 2009 | → |
| Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locus. | Fernandez F et al. | — | 2009 | → |
| Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependence. | Chen AC et al. | — | 2009 | → |
| Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and Caucasians. | Velez DR et al. | — | 2009 | → |
| Association of the 3' region of COMT with schizophrenia in Taiwan. | Chien YL et al. | — | 2009 | → |
| 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. | — | 2009 | → |
| Association studies on ghrelin and ghrelin receptor gene polymorphisms with obesity. | Gueorguiev M et al. | — | 2009 | → |
| Association study and mutation analysis of adiponectin shows association of variants in APM1 with complex obesity in women. | Beckers S et al. | — | 2009 | → |
| Association study of polymorphisms in the group III metabotropic glutamate receptor genes, GRM4 and GRM7, with schizophrenia. | Shibata H et al. | — | 2009 | → |
| Autonomic function in hypertension; role of genetic variation at the catecholamine storage vesicle protein chromogranin B. | Zhang K et al. | — | 2009 | → |
| AXIN2 and CDH1 polymorphisms, tooth agenesis, and oral clefts. | Letra A et al. | — | 2009 | → |
| Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis. | Callahan N et al. | — | 2009 | → |
| C957T polymorphism of dopamine D2 receptor gene affects striatal DRD2 in vivo availability by changing the receptor affinity. | Hirvonen MM et al. | — | 2009 | → |
| C957T polymorphism of the human dopamine D2 receptor gene predicts extrastriatal dopamine receptor availability in vivo. | Hirvonen MM et al. | — | 2009 | → |
| Candidate genes involved in neural plasticity and the risk for attention-deficit hyperactivity disorder: a meta-analysis of 8 common variants. | Forero DA et al. | — | 2009 | → |
| Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1. | Hüffmeier U et al. | — | 2009 | → |
| Characterization of pharmacogenetically relevant CYP2D6 and ABCB1 gene polymorphisms in a Portuguese population sample. | Correia C et al. | — | 2009 | → |
| COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. | Metlapally R et al. | — | 2009 | → |
| COL4A1 is associated with arterial stiffness by genome-wide association scan. | Tarasov KV et al. | — | 2009 | → |
| 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. | — | 2009 | → |
| Confirmation and fine-mapping of a major QTL for resistance to infectious pancreatic necrosis in Atlantic salmon (Salmo salar): population-level associations between markers and trait. | Moen T et al. | — | 2009 | → |
| Contribution of functional variation in the IL13 gene to allergy, hay fever and asthma in the NSHD longitudinal 1946 birth cohort. | Black S et al. | — | 2009 | → |
| Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter. | Treutlein J et al. | — | 2009 | → |
| Genetic variants associated with deep vein thrombosis: the F11 locus. | Li Y et al. | — | 2009 | → |
| 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. | — | 2009 | → |
| Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study. | Tanaka T et al. | — | 2009 | → |
| Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate. | Chiquet BT et al. | — | 2009 | → |
| Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis. | Schaefer AS et al. | — | 2009 | → |
| Impact of interacting functional variants in COMT on regional gray matter volume in human brain. | Honea R et al. | — | 2009 | → |
| Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. | Birnbaum S et al. | — | 2009 | → |
| KIF5B gene sequence variation and response of cardiac stroke volume to regular exercise. | Argyropoulos G et al. | — | 2009 | → |
| Linkage disequilibrium patterns and genetic structure of Amerindian and non-Amerindian Brazilian populations revealed by long-range X-STR markers. | Leite FP et al. | — | 2009 | → |
| Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFbeta gene variants. | Barreto M et al. | — | 2009 | → |
| Molecular population genetics of human CYP3A locus: signatures of positive selection and implications for evolutionary environmental medicine. | Chen X et al. | — | 2009 | → |
| Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes. | Saccone NL et al. | — | 2009 | → |
| Multiple variants in toll-like receptor 4 gene modulate risk of liver fibrosis in Caucasians with chronic hepatitis C infection. | Li Y et al. | — | 2009 | → |
| Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs. | Rana BK et al. | — | 2009 | → |
| Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis. | Shah SH et al. | — | 2009 | → |
| Population-specific functional variant of the TPH2 gene 2755C>A polymorphism contributes risk association to major depression and anxiety in Chinese peripartum women. | Lin YM et al. | — | 2009 | → |
| Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation. | Cheung CL et al. | — | 2009 | → |
| SSRI response in depression may be influenced by SNPs in HTR1B and HTR1A. | Villafuerte SM et al. | — | 2009 | → |
| Studies of palatine rugae and interferon regulatory factor 6 variations in a group of families with sporadic hypodontia. | Murdoch AM et al. | — | 2009 | → |
| Three microsatellites from the T1DGC MHC data set show highly significant association with type 1 diabetes, independent of the HLA-DRB1, -DQA1 and -DQB1 genes. | Eike MC et al. | — | 2009 | → |
| Transforming growth factor-alfa gene (TGFA), human tooth agenesis, and evidence of segmental uniparental isodisomy. | Callahan N et al. | — | 2009 | → |
| Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele. | Hodge JC et al. | — | 2009 | → |
| Adiponectin gene ADIPOQ SNP associations with serum adiponectin in two female populations and effects of SNPs on promoter activity. | Kyriakou T et al. | — | 2008 | → |
| A functional intronic variant in the tyrosine hydroxylase (TH) gene confers risk of essential hypertension in the Northern Chinese Han population. | Wang L et al. | — | 2008 | → |
| A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2. | Chang M et al. | — | 2008 | → |
| A linkage map of the Atlantic salmon (Salmo salar) based on EST-derived SNP markers. | Moen T et al. | — | 2008 | → |
| A major haplotype block at the rho-associated kinase 2 locus is associated with a lower risk of hypertension in a recessive manner: the HYPGENE study. | Rankinen T et al. | — | 2008 | → |
| Application of association mapping to understanding the genetic diversity of plant germplasm resources. | Abdurakhmonov IY et al. | — | 2008 | → |
| Association between liver X receptor alpha gene polymorphisms and risk of metabolic syndrome in French populations. | Legry V et al. | — | 2008 | → |
| Association of low-density lipoprotein receptor-related protein 5 (LRP5) promoter SNP with peak bone mineral density in Chinese women. | Cheung CL et al. | — | 2008 | → |
| Association of polymorphisms in the melanocortin receptor type 2 (MC2R, ACTH receptor) gene with heroin addiction. | Proudnikov D et al. | — | 2008 | → |
| Association of the dopamine transporter gene and ADHD symptoms in a Canadian population-based sample of same-age twins. | Ouellet-Morin I et al. | — | 2008 | → |
| Association of the gene encoding neurogranin with schizophrenia in males. | Ruano D et al. | — | 2008 | → |
| Association of USP26 haplotypes in men in Taiwan, China with severe spermatogenic defect. | Lee IW et al. | — | 2008 | → |
| Association study of polymorphisms in the neutral amino acid transporter genes SLC1A4, SLC1A5 and the glycine transporter genes SLC6A5, SLC6A9 with schizophrenia. | Deng X et al. | — | 2008 | → |
| Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women. | Oosterhuis BE et al. | — | 2008 | → |
| Chromogranin A polymorphisms are associated with hypertensive renal disease. | Salem RM et al. | — | 2008 | → |
| Common ATP-binding cassette B1 variants are associated with increased digoxin serum concentration. | Aarnoudse AJ et al. | — | 2008 | → |
| Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets. | Sutton BS et al. | — | 2008 | → |
| Detailed genetic characterization of the interleukin-23 receptor in psoriasis. | Garcia VE et al. | — | 2008 | → |
| Dopaminergic mutations: within-family association and linkage in multiplex alcohol dependence families. | Hill SY et al. | — | 2008 | → |
| Evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and isolate tooth agenesis, in a Turkish population. | Vieira AR et al. | — | 2008 | → |
| Expression levels of FAS are regulated through an evolutionary conserved element in intron 2, which modulates cystic fibrosis disease severity. | Kumar V et al. | — | 2008 | → |
| Extent of genome-wide linkage disequilibrium in Australian Holstein-Friesian cattle based on a high-density SNP panel. | Khatkar MS et al. | — | 2008 | → |
| Family-based association of a low producing lymphotoxin-alpha allele with reduced Plasmodium falciparum parasitemia. | Barbier M et al. | — | 2008 | → |
| Gene-gene interaction between FGF20 and MAOB in Parkinson disease. | Gao X et al. | — | 2008 | → |
| Genetic and functional association of FAM5C with myocardial infarction. | Connelly JJ et al. | — | 2008 | → |
| Genetic evaluation of the serotonergic system in chronic fatigue syndrome. | Smith AK et al. | — | 2008 | → |
| Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD. | Zhou K et al. | — | 2008 | → |
| Genetic variation in AKT1 is linked to dopamine-associated prefrontal cortical structure and function in humans. | Tan HY et al. | — | 2008 | → |
| Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2. | Franke A et al. | — | 2008 | → |
| Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. | Uda M et al. | — | 2008 | → |
| Genomic regulation of CTLA4 and multiple sclerosis. | Palacios R et al. | — | 2008 | → |
| High density linkage disequilibrium maps of chromosome 14 in Holstein and Angus cattle. | Marques E et al. | — | 2008 | → |
| HSPA5 promoter polymorphisms and risk of Parkinson's disease in Taiwan. | Chen CM et al. | — | 2008 | → |
| Identification of a role for the ARHGEF3 gene in postmenopausal osteoporosis. | Mullin BH et al. | — | 2008 | → |
| IL12B polymorphisms are linked but not associated with Plasmodium falciparum parasitemia: a familial study in Burkina Faso. | Barbier M et al. | — | 2008 | → |
| In search of causal variants: refining disease association signals using cross-population contrasts. | Saccone NL et al. | — | 2008 | → |
| Intriguing balancing selection on the intron 5 region of LMBR1 in human population. | He F et al. | — | 2008 | → |
| Latitudinal and cold-tolerance variation associate with DNA repeat-number variation in the hsr-omega RNA gene of Drosophila melanogaster. | Collinge JE et al. | — | 2008 | → |
| Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3. | Züchner S et al. | — | 2008 | → |
| Linkage disequilibrium analysis in the genetically isolated Norfolk Island population. | Bellis C et al. | — | 2008 | → |
| Linkage disequilibrium and persistence of phase in Holstein-Friesian, Jersey and Angus cattle. | de Roos AP et al. | — | 2008 | → |
| Linkage disequilibrium and signatures of selection on chromosomes 19 and 29 in beef and dairy cattle. | Prasad A et al. | — | 2008 | → |
| Linkage disequilibrium between STRPs and SNPs across the human genome. | Payseur BA et al. | — | 2008 | → |
| Linkage disequilibrium--understanding the evolutionary past and mapping the medical future. | Slatkin M | — | 2008 | → |
| Naturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion. | Chen Y et al. | — | 2008 | → |
| Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function. | Arnaud-Lopez L et al. | — | 2008 | → |
| Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease. | Wang L et al. | — | 2008 | → |
| Promoter polymorphisms modulating HSPA5 expression may increase susceptibility to Taiwanese Alzheimer's disease. | Hsu WC et al. | — | 2008 | → |
| Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families. | Wedenoja J et al. | — | 2008 | → |
| SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families. | Kollins SH et al. | — | 2008 | → |
| The MTHFD1 gene is not involved in cleft lip with or without palate onset among the Italian population. | Palmieri A et al. | — | 2008 | → |
| The 'Pokemon' (ZBTB7) Gene: No Evidence of Association with Sporadic Breast Cancer. | Salas A et al. | — | 2008 | → |
| TPH2 and TPH1: association of variants and interactions with heroin addiction. | Nielsen DA et al. | — | 2008 | → |
| Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein. | Wang G et al. | — | 2008 | → |
| Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate. | Chiquet BT et al. | — | 2008 | → |
| Variation of the gene encoding the nuclear bile salt receptor FXR and gallstone susceptibility in mice and humans. | Kovacs P et al. | — | 2008 | → |
| X-LRT: a likelihood approach to estimate genetic risks and test association with X-linked markers using a case-parents design. | Zhang L et al. | — | 2008 | → |
| ABCB1 and GST polymorphisms associated with TP53 status in breast cancer. | Nordgard SH et al. | — | 2007 | → |
| Admixture and patterns of linkage disequilibrium in a free-living vertebrate population. | Slate J et al. | — | 2007 | → |
| Admixture in European Populus hybrid zones makes feasible the mapping of loci that contribute to reproductive isolation and trait differences. | Lexer C et al. | — | 2007 | → |
| A functional CD86 polymorphism associated with asthma and related allergic disorders. | Corydon TJ et al. | — | 2007 | → |
| A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes. | Cargill M et al. | — | 2007 | → |
| Allelic association and recombination hotspots in the mucin gene (MUC) complex on chromosome 11p15.5. | Rousseau K et al. | — | 2007 | → |
| Allelic variation in GAD1 (GAD67) is associated with schizophrenia and influences cortical function and gene expression. | Straub RE et al. | — | 2007 | → |
| Alpha7 nicotinic acetylcholine receptor mRNA expression and binding in postmortem human brain are associated with genetic variation in neuregulin 1. | Mathew SV et al. | — | 2007 | → |
| Angiotensin-converting enzyme gene polymorphism predicts the time-course of blood pressure response to angiotensin converting enzyme inhibition in the AASK trial. | Bhatnagar V et al. | — | 2007 | → |
| Apoptotic gene analysis in idiopathic talipes equinovarus (clubfoot). | Ester AR et al. | — | 2007 | → |
| Arrayed primer extension in the "array of arrays" format: a rational approach for microarray-based SNP genotyping. | Klitø NG et al. | — | 2007 | → |
| Association analyses of NCR3 polymorphisms with P. falciparum mild malaria. | Delahaye NF et al. | — | 2007 | → |
| Association analysis of AKT1 and schizophrenia in a UK case control sample. | Norton N et al. | — | 2007 | → |
| Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer disease. | Liang X et al. | — | 2007 | → |
| Association between SNP and haplotypes in PPARGC1 and adiponectin genes and bone mineral density in Chinese nuclear families. | Zhang ZL et al. | — | 2007 | → |
| Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families. | Liu CM et al. | — | 2007 | → |
| Association of lipin 1 gene polymorphisms with measures of energy and glucose metabolism. | Loos RJ et al. | — | 2007 | → |
| Association of the neuronal nicotinic receptor beta2 subunit gene (CHRNB2) with subjective responses to alcohol and nicotine. | Ehringer MA et al. | — | 2007 | → |
| Association study between the TNXB locus and schizophrenia in a Japanese population. | Tochigi M et al. | — | 2007 | → |
| Association study of polymorphisms in the glutamate transporter genes SLC1A1, SLC1A3, and SLC1A6 with schizophrenia. | Deng X et al. | — | 2007 | → |
| Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease. | Belin AC et al. | — | 2007 | → |
| A TNF region haplotype offers protection from typhoid fever in Vietnamese patients. | Dunstan SJ et al. | — | 2007 | → |
| A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration. | Kanda A et al. | — | 2007 | → |
| Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia. | Ellis JA et al. | — | 2007 | → |
| Campora: a young genetic isolate in South Italy. | Colonna V et al. | — | 2007 | → |
| CETP genotypes and HDL-cholesterol phenotypes in the HERITAGE Family Study. | Spielmann N et al. | — | 2007 | → |
| CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. | Gao X et al. | — | 2007 | → |
| Cleft lip with or without cleft palate: implication of the heavy chain of non-muscle myosin IIA. | Martinelli M et al. | — | 2007 | → |
| Combining linkage data sets for meta-analysis and mega-analysis: the GAW15 rheumatoid arthritis data set. | Segurado R et al. | — | 2007 | → |
| Comparison of GIST and LAMP on the GAW15 simulated data. | Lou X et al. | — | 2007 | → |
| C-reactive protein, an 'intermediate phenotype' for inflammation: human twin studies reveal heritability, association with blood pressure and the metabolic syndrome, and the influence of common polymorphism at catecholaminergic/beta-adrenergic pathway loci. | Wessel J et al. | — | 2007 | → |
| CRISPLD2: a novel NSCLP candidate gene. | Chiquet BT et al. | — | 2007 | → |
| Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'. | Gaunt TR et al. | — | 2007 | → |
| Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk. | Zhang L et al. | — | 2007 | → |
| Effectiveness of in silico tagSNP selection methods: virtual analysis of the genotypes of pharmacogenetic genes. | Nam MH et al. | — | 2007 | → |
| Effects of genetic variation in the human retinol binding protein-4 gene (RBP4) on insulin resistance and fat depot-specific mRNA expression. | Kovacs P et al. | — | 2007 | → |
| Examining the candidacy of ghrelin as a gene responsible for variation in adult stature in a United Kingdom population with type 2 diabetes. | Gueorguiev M et al. | — | 2007 | → |
| Extent of linkage disequilibrium in chicken. | Aerts J et al. | — | 2007 | → |
| Family-based and case-control studies reveal no association of lipocalin-type prostaglandin D2 synthase with schizophrenia. | Ruano D et al. | — | 2007 | → |
| 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. | — | 2007 | → |
| Genetic association between the PRKCH gene encoding protein kinase Ceta isozyme and rheumatoid arthritis in the Japanese population. | Takata Y et al. | — | 2007 | → |
| Genetic evidence implicating DARPP-32 in human frontostriatal structure, function, and cognition. | Meyer-Lindenberg A et al. | — | 2007 | → |
| Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach. | Kanková K et al. | — | 2007 | → |
| Genetic variability at the leptin receptor (LEPR) locus is a determinant of plasma fibrinogen and C-reactive protein levels. | Zhang YY et al. | — | 2007 | → |
| Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. | Moffatt MF et al. | — | 2007 | → |
| Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. | Scuteri A et al. | — | 2007 | → |
| Glucocorticoid receptor polymorphisms and haplotypes associated with chronic fatigue syndrome. | Rajeevan MS et al. | — | 2007 | → |
| Haplotype-based analysis of genes associated with risk of adverse skin reactions after radiotherapy in breast cancer patients. | Suga T et al. | — | 2007 | → |
| Haplotypic structure across the I kappa B alpha gene (NFKBIA) and association with multiple myeloma. | Spink CF et al. | — | 2007 | → |
| Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locus. | Heijmans BT et al. | — | 2007 | → |
| Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies. | Hayes MG et al. | — | 2007 | → |
| Increased gallstone risk in humans conferred by common variant of hepatic ATP-binding cassette transporter for cholesterol. | Grünhage F et al. | — | 2007 | → |
| Influence of IL-10RA and IL-22 polymorphisms on outcome of hepatitis C virus infection. | Hennig BJ et al. | — | 2007 | → |
| Interaction of soy and 17beta-HSD1 gene polymorphisms in the risk of endometrial cancer. | Dai Q et al. | — | 2007 | → |
| Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis. | Vieira AR et al. | — | 2007 | → |
| Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis. | Gregory SG et al. | — | 2007 | → |
| Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk. | Ashley-Koch AE et al. | — | 2007 | → |
| KIR haplotype content at the allele level in 77 Northern Irish families. | Middleton D et al. | — | 2007 | → |
| Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables. | Mei H et al. | — | 2007 | → |
| NAT2 variation and idiopathic talipes equinovarus (clubfoot). | Hecht JT et al. | — | 2007 | → |
| No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families. | Liu CM et al. | — | 2007 | → |
| No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases. | Bell CG et al. | — | 2007 | → |
| Non-B27 MHC associations of ankylosing spondylitis. | Sims AM et al. | — | 2007 | → |
| Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease. | Wang L et al. | — | 2007 | → |
| Peroxisome proliferator-activated receptor-delta polymorphisms are associated with physical performance and plasma lipids: the HERITAGE Family Study. | Hautala AJ et al. | — | 2007 | → |
| Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with peak bone mass in non-sedentary men: results from the Odense androgen study. | Brixen K et al. | — | 2007 | → |
| Population-based case-control association studies. | Hancock DB et al. | — | 2007 | → |
| Positive replication and linkage disequilibrium mapping of the chromosome 21q22.1 malaria susceptibility locus. | Khor CC et al. | — | 2007 | → |
| Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes. | Willer CJ et al. | — | 2007 | → |
| Sequence variation within the major histocompatibility complex subregion centromeric of HLA class II in type 1 diabetes. | van der Slik AR et al. | — | 2007 | → |
| SHP-2 and PI3-kinase genes PTPN11 and PIK3R1 may influence serum apoB and LDL cholesterol levels in normal women. | Jamshidi Y et al. | — | 2007 | → |
| Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations. | Gu S et al. | — | 2007 | → |
| Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in recurrent major depressive disorder. | Van Den Eede F et al. | — | 2007 | → |
| Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects. | Siddiq A et al. | — | 2007 | → |
| Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations. | Brown AM et al. | — | 2007 | → |
| The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts. | Li S et al. | — | 2007 | → |
| The null distribution of stochastic search gene suggestion: a Bayesian approach to gene mapping. | Swartz MD et al. | — | 2007 | → |
| The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophrenia. | Bakker SC et al. | — | 2007 | → |
| Tumor necrosis factor-alpha promoter polymorphism is associated with the risk of Parkinson's disease. | Wu YR et al. | — | 2007 | → |
| Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo. | Rao F et al. | — | 2007 | → |
| Variants of C1GALT1 gene are associated with the genetic susceptibility to IgA nephropathy. | Li GS et al. | — | 2007 | → |
| Whole genome linkage disequilibrium maps in cattle. | McKay SD et al. | — | 2007 | → |
| A cholinergic receptor gene (CHRM2) affects event-related oscillations. | Jones KA et al. | — | 2006 | → |
| A detailed Hapmap of the Sitosterolemia locus spanning 69 kb; differences between Caucasians and African-Americans. | Pandit B et al. | — | 2006 | → |
| A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q. | Mathias RA et al. | — | 2006 | → |
| AMP-kinase alpha2 subunit gene PRKAA2 variants are associated with total cholesterol, low-density lipoprotein-cholesterol and high-density lipoprotein-cholesterol in normal women. | Spencer-Jones NJ et al. | — | 2006 | → |
| An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder. | Ashley-Koch AE et al. | — | 2006 | → |
| A quantitative trait locus for body fat on chromosome 1q43 in French Canadians: linkage and association studies. | Aissani B et al. | — | 2006 | → |
| Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes. | Levenstien MA et al. | — | 2006 | → |
| Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach. | Gloyn AL et al. | — | 2006 | → |
| Association analyses of CYP19 gene polymorphisms with height variation in a large sample of Caucasian nuclear families. | Yang TL et al. | — | 2006 | → |
| Association analysis of polymorphisms in serotonin 1B receptor (HTR1B) gene with heroin addiction: a comparison of molecular and statistically estimated haplotypes. | Proudnikov D et al. | — | 2006 | → |
| Association analysis of SOD2 variants with methamphetamine psychosis in Japanese and Taiwanese populations. | Nakamura K et al. | — | 2006 | → |
| Association between a 19 bp deletion polymorphism at the dopamine beta-hydroxylase (DBH) locus and migraine with aura. | Fernandez F et al. | — | 2006 | → |
| Association between GABRA1 and drinking behaviors in the collaborative study on the genetics of alcoholism sample. | Dick DM et al. | — | 2006 | → |
| Association between non-Hodgkin lymphoma and haplotypes in the TNF region. | Spink CF et al. | — | 2006 | → |
| Association between the transforming growth factor alpha gene and nonsyndromic oral clefts: a HuGE review. | Vieira AR | — | 2006 | → |
| Association of alpha1A adrenergic receptor gene variants on chromosome 8p21 with human stage 2 hypertension. | Gu D et al. | — | 2006 | → |
| Association of DAZL haplotypes with spermatogenic failure in infertile men. | Teng YN et al. | — | 2006 | → |
| Association of interferon-gamma gene haplotype in the Chinese population with hepatitis B virus infection. | Liu M et al. | — | 2006 | → |
| Association of Reelin gene polymorphisms with autism. | Serajee FJ et al. | — | 2006 | → |
| Association of the progesterone receptor gene with breast cancer risk: a single-nucleotide polymorphism tagging approach. | Pooley KA et al. | — | 2006 | → |
| Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sample. | Scott LJ et al. | — | 2006 | → |
| Association of tumor necrosis factor alpha polymorphism, but not the shared epitope, with increased radiographic progression in a seropositive rheumatoid arthritis inception cohort. | Khanna D et al. | — | 2006 | → |
| Associations of allelic variants of the multidrug resistance gene (ABCB1 or MDR1) and inflammatory bowel disease and their effects on disease behavior: a case-control and meta-analysis study. | Onnie CM et al. | — | 2006 | → |
| Association studies of cholesterol metabolism genes (CH25H, ABCA1 and CH24H) in Alzheimer's disease. | Shibata N et al. | — | 2006 | → |
| Association study of genetic polymorphisms of SLC2A10 gene and type 2 diabetes in the Taiwanese population. | Lin WH et al. | — | 2006 | → |
| Association study of polymorphisms in the GluR7, KA1 and KA2 kainate receptor genes (GRIK3, GRIK4, GRIK5) with schizophrenia. | Shibata H et al. | — | 2006 | → |
| Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples. | Holliday EG et al. | — | 2006 | → |
| Association study with 33 single-nucleotide polymorphisms in 11 candidate genes for hypertension in Chinese. | Gu D et al. | — | 2006 | → |
| A tutorial on statistical methods for population association studies. | Balding DJ | — | 2006 | → |
| Bardet-Biedl syndrome gene variants are associated with both childhood and adult common obesity in French Caucasians. | Benzinou M et al. | — | 2006 | → |
| Cannabis receptor haplotype associated with fewer cannabis dependence symptoms in adolescents. | Hopfer CJ et al. | — | 2006 | → |
| CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration. | Li M et al. | — | 2006 | → |
| Class II cytokine receptor gene cluster is a major locus for hepatitis B persistence. | Frodsham AJ et al. | — | 2006 | → |
| Clustering of haplotypes based on phylogeny: how good a strategy for association testing? | Bardel C et al. | — | 2006 | → |
| Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21. | Giardina E et al. | — | 2006 | → |
| Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in Finns. | Bonnycastle LL et al. | — | 2006 | → |
| Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene. | Hobbs CA et al. | — | 2006 | → |
| Contrasting linkage-disequilibrium patterns between cases and controls as a novel association-mapping method. | Zaykin DV et al. | — | 2006 | → |
| Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism. | Suviolahti E et al. | — | 2006 | → |
| Data-mining methods as useful tools for predicting individual drug response: application to CYP2D6 data. | Sabbagh A et al. | — | 2006 | → |
| Diplotype trend regression analysis of the ADH gene cluster and the ALDH2 gene: multiple significant associations with alcohol dependence. | Luo X et al. | — | 2006 | → |
| Endophenotypes successfully lead to gene identification: results from the collaborative study on the genetics of alcoholism. | Dick DM et al. | — | 2006 | → |
| Endothelin-1 gene variants and levels associate with adaptation to hypobaric hypoxia in high-altitude natives. | Rajput C et al. | — | 2006 | → |
| Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study. | Ogata T et al. | — | 2006 | → |
| Examination of PPP1R3B as a candidate gene for the type 2 diabetes and MODY loci on chromosome 8p23. | Dunn JS et al. | — | 2006 | → |
| Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease. | Lin PI et al. | — | 2006 | → |
| Family based association analysis of the IL2 and IL15 genes in allergic disorders. | Christensen U et al. | — | 2006 | → |
| Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease. | Kang SJ et al. | — | 2006 | → |
| Functional polymorphism in ALOX15 results in increased allele-specific transcription in macrophages through binding of the transcription factor SPI1. | Wittwer J et al. | — | 2006 | → |
| GATA2 is associated with familial early-onset coronary artery disease. | Connelly JJ et al. | — | 2006 | → |
| Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history. | Traherne JA et al. | — | 2006 | → |
| Genetic variation in the visfatin gene (PBEF1) and its relation to glucose metabolism and fat-depot-specific messenger ribonucleic acid expression in humans. | Böttcher Y et al. | — | 2006 | → |
| Genomewide association analysis of human narcolepsy and a new resistance gene. | Kawashima M et al. | — | 2006 | → |
| Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles. | Lantieri F et al. | — | 2006 | → |
| Haplotype structure of five SNPs within the ACE gene in the Tunisian population. | Rebaï M et al. | — | 2006 | → |
| Haplotypic variation in MRE11, RAD50 and NBS1 and risk of non-Hodgkin's lymphoma. | Rollinson S et al. | — | 2006 | → |
| Heart rate recovery after maximal exercise is associated with acetylcholine receptor M2 (CHRM2) gene polymorphism. | Hautala AJ et al. | — | 2006 | → |
| Human ALOX12, but not ALOX15, is associated with BMD in white men and women. | Ichikawa S et al. | — | 2006 | → |
| ICAM gene cluster SNPs and prostate cancer risk in African Americans. | Chen H et al. | — | 2006 | → |
| Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples. | Greenwood TA et al. | — | 2006 | → |
| IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancer. | Al-Zahrani A et al. | — | 2006 | → |
| Impact of complex genetic variation in COMT on human brain function. | Meyer-Lindenberg A et al. | — | 2006 | → |
| Investigation of autism and GABA receptor subunit genes in multiple ethnic groups. | Collins AL et al. | — | 2006 | → |
| JLIN: a java based linkage disequilibrium plotter. | Carter KW et al. | — | 2006 | → |
| KCNQ4: a gene for age-related hearing impairment? | Van Eyken E et al. | — | 2006 | → |
| Lack of association between UBQLN1 and Alzheimer disease. | Slifer MA et al. | — | 2006 | → |
| Linkage disequilibrium, haplotype and association studies of a chromosome 4 GABA receptor gene cluster: candidate gene variants for addictions. | Drgon T et al. | — | 2006 | → |
| Linkage disequilibrium on chromosome 6 in Australian Holstein-Friesian cattle. | Khatkar MS et al. | — | 2006 | → |
| Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. | Service S et al. | — | 2006 | → |
| MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers. | Gaunt TR et al. | — | 2006 | → |
| MUC7 haplotype analysis: results from a longitudinal birth cohort support protective effect of the MUC7*5 allele on respiratory function. | Rousseau K et al. | — | 2006 | → |
| Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes. | Pezzolesi MG et al. | — | 2006 | → |
| Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions. | Boyles AL et al. | — | 2006 | → |
| Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the disease. | Law AJ et al. | — | 2006 | → |
| No association of G72 and D-amino acid oxidase genes with schizophrenia. | Liu YL et al. | — | 2006 | → |
| NOS2A and the modulating effect of cigarette smoking in Parkinson's disease. | Hancock DB et al. | — | 2006 | → |
| Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis. | Lin PI et al. | — | 2006 | → |
| Phosphatidylinositol 3-kinase p85alpha regulatory subunit gene PIK3R1 haplotype is associated with body fat and serum leptin in a female twin population. | Jamshidi Y et al. | — | 2006 | → |
| Plasminogen activator inhibitor-1 gene: selection of tagging single nucleotide polymorphisms and association with coronary heart disease. | Su S et al. | — | 2006 | → |
| Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women. | Ichikawa S et al. | — | 2006 | → |
| Polymorphisms in the leptin and leptin receptor genes in relation to resting metabolic rate and respiratory quotient in the Québec Family Study. | Loos RJ et al. | — | 2006 | → |
| Polymorphism within the interferon-gamma/receptor complex is associated with pulmonary tuberculosis. | Cooke GS et al. | — | 2006 | → |
| Power-based, phase-informed selection of single nucleotide polymorphisms for disease association screens. | Saccone SF et al. | — | 2006 | → |
| Predominance of interaction among wild-type alleles of CYP11B2 in Himalayan natives associates with high-altitude adaptation. | Rajput C et al. | — | 2006 | → |
| Regulatory polymorphisms in extracellular matrix protease genes and susceptibility to rheumatoid arthritis: a case-control study. | Rodriguez-Lopez J et al. | — | 2006 | → |
| Selection of SNP subsets for association studies in candidate genes: comparison of the power of different strategies to detect single disease susceptibility locus effects. | Cousin E et al. | — | 2006 | → |
| SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. | Blasi F et al. | — | 2006 | → |
| Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium. | Paisán-Ruíz C et al. | — | 2006 | → |
| UGT1A polymorphisms in a Swedish cohort and a human diversity panel, and the relation to bilirubin plasma levels in males and females. | Mercke Odeberg J et al. | — | 2006 | → |
| Variants in the SP110 gene are associated with genetic susceptibility to tuberculosis in West Africa. | Tosh K et al. | — | 2006 | → |
| Variation in MICA and MICB genes and enhanced susceptibility to paucibacillary leprosy in South India. | Tosh K et al. | — | 2006 | → |
| VizStruct for visualization of genome-wide SNP analyses. | Bhasi K et al. | — | 2006 | → |
| ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease. | Macé S et al. | — | 2005 | → |
| ACDC/adiponectin and PPAR-gamma gene polymorphisms: implications for features of obesity. | Tankó LB et al. | — | 2005 | → |
| Age-associated skewing of X-inactivation ratios of blood cells in normal females: a candidate-gene analysis approach. | Chagnon P et al. | — | 2005 | → |
| A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms. | Miretti MM et al. | — | 2005 | → |
| A large-scale association analysis of common variation of the HNF1alpha gene with type 2 diabetes in the U.K. Caucasian population. | Weedon MN et al. | — | 2005 | → |
| Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2. | Deak KL et al. | — | 2005 | → |
| Analysis of CARD15/NOD2 haplotypes fails to identify common variants associated with rheumatoid arthritis susceptibility. | Addo A et al. | — | 2005 | → |
| Analysis of the RELN gene as a genetic risk factor for autism. | Skaar DA et al. | — | 2005 | → |
| Association analysis of transcripts from the bipolar susceptibility locus on chromosome 4q35, exclusion of a pathogenic role for eight positional candidate genes. | Blair IP et al. | — | 2005 | → |
| Association and linkage of alpha-2A adrenergic receptor gene polymorphisms with childhood ADHD. | Park L et al. | — | 2005 | → |
| Association between a complex insertion/deletion polymorphism in NOD1 (CARD4) and susceptibility to inflammatory bowel disease. | McGovern DP et al. | — | 2005 | → |
| Association between single-nucleotide polymorphisms in the SEC8L1 gene, which encodes a subunit of the exocyst complex, and rheumatoid arthritis in a Japanese population. | Hamada D et al. | — | 2005 | → |
| Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease. | Noureddine MA et al. | — | 2005 | → |
| Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity. | Bell CG et al. | — | 2005 | → |
| Association of sporadic chondrocalcinosis with a -4-basepair G-to-A transition in the 5'-untranslated region of ANKH that promotes enhanced expression of ANKH protein and excess generation of extracellular inorganic pyrophosphate. | Zhang Y et al. | — | 2005 | → |
| Association of the TSHR gene with Graves' disease: the first disease specific locus. | Dechairo BM et al. | — | 2005 | → |
| Association study of CREB1 and childhood-onset mood disorders. | Burcescu I et al. | — | 2005 | → |
| A synonymous coding polymorphism in the alpha2-Heremans-schmid glycoprotein gene is associated with type 2 diabetes in French Caucasians. | Siddiq A et al. | — | 2005 | → |
| A variant in the CD209 promoter is associated with severity of dengue disease. | Sakuntabhai A et al. | — | 2005 | → |
| Beta(2)-adrenergic receptor polymorphisms and response to salbutamol among Indian asthmatics*. | Kukreti R et al. | — | 2005 | → |
| Bias of allele-sharing linkage statistics in the presence of intermarker linkage disequilibrium. | Goode EL et al. | — | 2005 | → |
| Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT. | Barnby G et al. | — | 2005 | → |
| CHRM2 gene predisposes to alcohol dependence, drug dependence and affective disorders: results from an extended case-control structured association study. | Luo X et al. | — | 2005 | → |
| Chromosome 11-q24 region in Tourette syndrome: association and linkage disequilibrium study in the French Canadian population. | Díaz-Anzaldúa A et al. | — | 2005 | → |
| Common polymorphisms in the USF1 gene are not associated with type 2 diabetes in French Caucasians. | Gibson F et al. | — | 2005 | → |
| Comparison of genotype- and haplotype-based approaches for fine-mapping of alcohol dependence using COGA data. | Pinnaduwage D et al. | — | 2005 | → |
| Contribution of the LRP5 gene to normal variation in peak BMD in women. | Koller DL et al. | — | 2005 | → |
| DCDC2 is associated with reading disability and modulates neuronal development in the brain. | Meng H et al. | — | 2005 | → |
| Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene. | Ertekin-Taner N et al. | — | 2005 | → |
| Evaluation of linkage disequilibrium and its effect on non-parametric multipoint linkage analysis using two high density single-nucleotide polymorphism mapping panels. | Murray SS | — | 2005 | → |
| Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population. | Swanson DA et al. | — | 2005 | → |
| Family-based association analysis implicates IL-4 in susceptibility to Kawasaki disease. | Burns JC et al. | — | 2005 | → |
| 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. | — | 2005 | → |
| Genetic analysis of HNF4A polymorphisms in Caucasian-American type 2 diabetes. | Bagwell AM et al. | — | 2005 | → |
| Genetic analysis of the maximum drinks phenotype. | Saccone SF et al. | — | 2005 | → |
| Genetic and genomic studies of PADI4 in rheumatoid arthritis. | Harney SM et al. | — | 2005 | → |
| Genetic modifiers of lung disease in cystic fibrosis. | Drumm ML et al. | — | 2005 | → |
| Genetic study of ICAM1 in clinical malaria in Senegal. | Ndiaye R et al. | — | 2005 | → |
| Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population. | Iwasaki N et al. | — | 2005 | → |
| Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia. | Hillmer AM et al. | — | 2005 | → |
| Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers. | Abecasis GR et al. | — | 2005 | → |
| Haplotypes and haplotype-tagging single-nucleotide polymorphism: presentation Group 8 of Genetic Analysis Workshop 14. | Beckmann L et al. | — | 2005 | → |
| Haplotypes in the tumour necrosis factor region and myeloma. | Morgan GJ et al. | — | 2005 | → |
| Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study. | Newhouse SJ et al. | — | 2005 | → |
| Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia. | Sanders AR et al. | — | 2005 | → |
| HLA antigens in Greek children with allergic bronchial asthma. | Parapanissiou E et al. | — | 2005 | → |
| Identification of a potential bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4. | Glaser B et al. | — | 2005 | → |
| Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease. | Oliveira SA et al. | — | 2005 | → |
| Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism. | Ma DQ et al. | — | 2005 | → |
| Identifying nineteenth century genealogical links from genotypes. | Stankovich J et al. | — | 2005 | → |
| Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study design. | Vitart V et al. | — | 2005 | → |
| Inferring haplotypes at the NAT2 locus: the computational approach. | Sabbagh A et al. | — | 2005 | → |
| Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population. | Ghassibé M et al. | — | 2005 | → |
| Introduction to statistical analysis of population data in immunogenetics. | Gourraud PA et al. | — | 2005 | → |
| Linkage and association analyses of microsatellites and single-nucleotide polymorphisms in nuclear families. | Lin J et al. | — | 2005 | → |
| Linkage disequilibrium analysis identifies an FGFR1 haplotype-tag SNP associated with normal variation in craniofacial shape. | Coussens AK et al. | — | 2005 | → |
| Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356. | Glaser B et al. | — | 2005 | → |
| Linkage of ischemic stroke to the PDE4D region on 5q in a Swedish population. | Nilsson-Ardnor S et al. | — | 2005 | → |
| Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR. | Helms C et al. | — | 2005 | → |
| Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy. | Greenberg DA et al. | — | 2005 | → |
| Molecular evolution of the sheep prion protein gene. | Slate J | — | 2005 | → |
| Mutation screen and association study of EZH2 as a susceptibility gene for aggressive prostate cancer. | Bachmann N et al. | — | 2005 | → |
| No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample. | Dick DM et al. | — | 2005 | → |
| NOD1 variation, immunoglobulin E and asthma. | Hysi P et al. | — | 2005 | → |
| No evidence for association between polymorphisms in GRM3 and schizophrenia. | Norton N et al. | — | 2005 | → |
| Novel IL-6 haplotypes and disease association. | Fife MS et al. | — | 2005 | → |
| On the use of haplotype phylogeny to detect disease susceptibility loci. | Bardel C et al. | — | 2005 | → |
| Patterns of linkage disequilibrium in the type 2 diabetes gene calpain-10. | Hayes MG et al. | — | 2005 | → |
| Platelet glycoprotein I(b)alpha and integrin alpha2 beta1 polymorphisms: gene frequencies and linkage disequilibrium in a population diversity panel. | Di Paola J et al. | — | 2005 | → |
| Polymorphisms in GLTSCR1 and ERCC2 are associated with the development of oligodendrogliomas. | Yang P et al. | — | 2005 | → |
| Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women. | Ichikawa S et al. | — | 2005 | → |
| Positional identification of an asthma susceptibility gene on human chromosome 5q33. | Noguchi E et al. | — | 2005 | → |
| Power and sample size calculations for genetic case/control studies using gene-centric SNP maps: application to human chromosomes 6, 21, and 22 in three populations. | De La Vega FM et al. | — | 2005 | → |
| Protein tyrosine phosphatase-1B gene PTPN1: selection of tagging single nucleotide polymorphisms and association with body fat, insulin sensitivity, and the metabolic syndrome in a normal female population. | Spencer-Jones NJ et al. | — | 2005 | → |
| PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis. | Carlton VE et al. | — | 2005 | → |
| Single- and multilocus allelic variants within the GABA(B) receptor subunit 2 (GABAB2) gene are significantly associated with nicotine dependence. | Beuten J et al. | — | 2005 | → |
| Single-point haplotype scores telomeric to human leukocyte antigen-C give a high susceptibility major histocompatibility complex haplotype for psoriasis in a Caucasian population. | Lench N et al. | — | 2005 | → |
| SLC18A2 promoter haplotypes and identification of a novel protective factor against alcoholism. | Lin Z et al. | — | 2005 | → |
| SNPAnalyzer: a web-based integrated workbench for single-nucleotide polymorphism analysis. | Yoo J et al. | — | 2005 | → |
| SNP selection for association studies: maximizing power across SNP choice and study size. | Pardi F et al. | — | 2005 | → |
| SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. | Deak KL et al. | — | 2005 | → |
| 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. | — | 2005 | → |
| Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus. | Benayed R et al. | — | 2005 | → |
| Systematic linkage disequilibrium analysis of SLC12A8 at PSORS5 confirms a role in susceptibility to psoriasis vulgaris. | Hüffmeier U et al. | — | 2005 | → |
| TaqMan assays for genotyping of single nucleotide polymorphisms present at a disease susceptibility locus on chromosome 6. | Koch W et al. | — | 2005 | → |
| The heritage of pathogen pressures and ancient demography in the human innate-immunity CD209/CD209L region. | Barreiro LB et al. | — | 2005 | → |
| The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population. | Ng MC et al. | — | 2005 | → |
| The presence of tandem endothelial nitric oxide synthase gene polymorphisms identifying brain aneurysms more prone to rupture. | Khurana VG et al. | — | 2005 | → |
| TNF as a malaria candidate gene: polymorphism-screening and family-based association analysis of mild malaria attack and parasitemia in Burkina Faso. | Flori L et al. | — | 2005 | → |
| Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population. | Orloff MS et al. | — | 2005 | → |
| Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia. | Callicott JH et al. | — | 2005 | → |
| Variation in IRF6 contributes to nonsyndromic cleft lip and palate. | Blanton SH et al. | — | 2005 | → |
| WNK1 kinase polymorphism and blood pressure response to a thiazide diuretic. | Turner ST et al. | — | 2005 | → |
| Worldwide haplotype diversity and coding sequence variation at human bitter taste receptor loci. | Kim U et al. | — | 2005 | → |
| X-chromosome as a marker for population history: linkage disequilibrium and haplotype study in Eurasian populations. | Laan M et al. | — | 2005 | → |
| A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. | Francks C et al. | — | 2004 | → |
| A highly informative SNP linkage panel for human genetic studies. | Murray SS et al. | — | 2004 | → |
| A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism. | McCauley JL et al. | — | 2004 | → |
| Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes. | Rabionet R et al. | — | 2004 | → |
| Analysis of the contribution to type 2 diabetes susceptibility of sequence variation in the gene encoding stearoyl-CoA desaturase, a key regulator of lipid and carbohydrate metabolism. | Liew CF et al. | — | 2004 | → |
| An association study of asthma and total serum immunoglobin E levels for Toll-like receptor polymorphisms in a Japanese population. | Noguchi E et al. | — | 2004 | → |
| Angiotensinogen promoter B-haplotype associated with cerebral small vessel disease enhances basal transcriptional activity. | Schmidt H et al. | — | 2004 | → |
| A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. | Nyholt DR | — | 2004 | → |
| Association analysis of FEZ1 variants with schizophrenia in Japanese cohorts. | Yamada K et al. | — | 2004 | → |
| Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer's disease. | Riemenschneider M et al. | — | 2004 | → |
| Association between a polymorphism in cysteinyl leukotriene receptor 2 on chromosome 13q14 and atopic asthma. | Fukai H et al. | — | 2004 | → |
| Association between evolutionary history of angiotensinogen haplotypes and plasma levels. | Fejerman L et al. | — | 2004 | → |
| Association of estrogen receptor alpha polymorphisms with susceptibility to chronic hepatitis B virus infection. | Deng G et al. | — | 2004 | → |
| Association of GABRG3 with alcohol dependence. | Dick DM et al. | — | 2004 | → |
| Association of interleukin-15 protein and interleukin-15 receptor genetic variation with resistance exercise training responses. | Riechman SE et al. | — | 2004 | → |
| Association of neural cell adhesion molecule 1 gene polymorphisms with bipolar affective disorder in Japanese individuals. | Arai M et al. | — | 2004 | → |
| Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes. | Bento JL et al. | — | 2004 | → |
| Association of T-786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease. | Sharan K et al. | — | 2004 | → |
| Association of tryptophan 2,3 dioxygenase gene polymorphism with autism. | Nabi R et al. | — | 2004 | → |
| Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology. | Wen G et al. | — | 2004 | → |
| Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. population. | Weedon MN et al. | — | 2004 | → |
| Common variants within the interleukin 4 receptor alpha gene (IL4R) are associated with susceptibility to osteoarthritis. | Forster T et al. | — | 2004 | → |
| Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene. | Nejentsev S et al. | — | 2004 | → |
| Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease. | Nicodemus KK et al. | — | 2004 | → |
| Confirmation and fine mapping of the chromosome 1 alcohol dependence risk locus. | Lappalainen J et al. | — | 2004 | → |
| Defining haplotype blocks and tag single-nucleotide polymorphisms in the human genome. | Schulze TG et al. | — | 2004 | → |
| Distribution of genome-wide linkage disequilibrium based on microsatellite loci in the Samoan population. | Tsai HJ et al. | — | 2004 | → |
| Effect of sex and haplotype on plasma tryptase levels in healthy adults. | Min HK et al. | — | 2004 | → |
| Endogenous opioid receptor genes and alcohol dependence among Taiwanese Han. | Loh el W et al. | — | 2004 | → |
| Ethnic differences in the linkage disequilibrium and distribution of single-nucleotide polymorphisms in 35 candidate genes for cardiovascular diseases. | Ng MC et al. | — | 2004 | → |
| Evidence for a cluster of genes on chromosome 17q11-q21 controlling susceptibility to tuberculosis and leprosy in Brazilians. | Jamieson SE et al. | — | 2004 | → |
| Evidence for a novel rheumatoid arthritis susceptibility locus on chromosome 6p. | Brintnell W et al. | — | 2004 | → |
| Evidence for CTLA4 as a susceptibility gene for systemic lupus erythematosus. | Barreto M et al. | — | 2004 | → |
| Evidence for genetic linkage between a polymorphism in the adenosine 2A receptor and panic disorder. | Hamilton SP et al. | — | 2004 | → |
| Examination of candidate genes in language disorder: a model of genetic association for treatment studies. | Haines J et al. | — | 2004 | → |
| Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes. | Hutcheson HB et al. | — | 2004 | → |
| Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis. | Rubio JP et al. | — | 2004 | → |
| Extended linkage disequilibrium surrounding the hemoglobin E variant due to malarial selection. | Ohashi J et al. | — | 2004 | → |
| Failure to confirm association between AKT1 haplotype and schizophrenia in a Japanese case-control population. | Ohtsuki T et al. | — | 2004 | → |
| Family-based association study of schizophrenia with 444 markers and analysis of a new susceptibility locus mapped to 11q13.3. | Yamada K et al. | — | 2004 | → |
| Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease. | van der Walt JM et al. | — | 2004 | → |
| Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33. | Chen YS et al. | — | 2004 | → |
| Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region. | Latini V et al. | — | 2004 | → |
| Genetics and visceral leishmaniasis in the Sudan: seeking a link. | Blackwell JM et al. | — | 2004 | → |
| Genetics of the APM1 locus and its contribution to type 2 diabetes susceptibility in French Caucasians. | Gibson F et al. | — | 2004 | → |
| Genetic variants in a haplotype block spanning IDE are significantly associated with plasma Abeta42 levels and risk for Alzheimer disease. | Ertekin-Taner N et al. | — | 2004 | → |
| Genetic variation in COL17A1 and the development of bullous pemphigoid. | Winsey S et al. | — | 2004 | → |
| Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes. | Silander K et al. | — | 2004 | → |
| Genomic profiling of interpopulation diversity guides prioritization of candidate-genes for autoimmunity. | Grossman I et al. | — | 2004 | → |
| Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies. | Zhang K et al. | — | 2004 | → |
| Haplotype block structures show significant variation among populations. | Liu N et al. | — | 2004 | → |
| Haplotype mapping of the bronchiolitis susceptibility locus near IL8. | Hull J et al. | — | 2004 | → |
| Influence of LRP5 polymorphisms on normal variation in BMD. | Koay MA et al. | — | 2004 | → |
| 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. | — | 2004 | → |
| Interaction between RANKL and HLA-DRB1 genotypes may contribute to younger age at onset of seropositive rheumatoid arthritis in an inception cohort. | Wu H et al. | — | 2004 | → |
| Interleukin-1 gene cluster polymorphisms and susceptibility to clinical malaria in a Gambian case-control study. | Walley AJ et al. | — | 2004 | → |
| Investigation of polymorphisms in the CREM gene in panic disorder. | Hamilton SP et al. | — | 2004 | → |
| Investigation of serotonin-related genes in antidepressant response. | Peters EJ et al. | — | 2004 | → |
| Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene. | Orlacchio A et al. | — | 2004 | → |
| Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism. | McCauley JL et al. | — | 2004 | → |
| Linkage disequilibrium and association of MAPT H1 in Parkinson disease. | Skipper L et al. | — | 2004 | → |
| Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype. | Oliveira SA et al. | — | 2004 | → |
| Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. | Brzustowicz LM et al. | — | 2004 | → |
| Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens. | Taillon-Miller P et al. | — | 2004 | → |
| Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia. | Bah J et al. | — | 2004 | → |
| Mutation history of the roma/gypsies. | Morar B et al. | — | 2004 | → |
| Neither single-marker nor haplotype analyses support an association between genetic variation near NOTCH4 and bipolar disorder. | Prathikanti S et al. | — | 2004 | → |
| No association between the APOE gene and autism. | Raiford KL et al. | — | 2004 | → |
| No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF). | Thiselton DL et al. | — | 2004 | → |
| Polymorphic variation in the CBLB gene in human type 1 diabetes. | Kosoy R et al. | — | 2004 | → |
| Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified. | Addington AM et al. | — | 2004 | → |
| Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia. | Duan J et al. | — | 2004 | → |
| Polymorphisms in xenobiotic metabolism genes and autism. | Serajee FJ et al. | — | 2004 | → |
| Positional identification of hypertension susceptibility genes on chromosome 2. | Barkley RA et al. | — | 2004 | → |
| Promoter haplotypes of the interleukin-10 gene influence proliferation of peripheral blood cells in response to helminth antigen. | Timmann C et al. | — | 2004 | → |
| Redefinition of the human kappa opioid receptor gene (OPRK1) structure and association of haplotypes with opiate addiction. | Yuferov V et al. | — | 2004 | → |
| Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses. | Deffenbacher KE et al. | — | 2004 | → |
| Single nucleotide polymorphism screening and association analysis--exclusion of integrin beta 7 and vitamin D receptor (chromosome 12q) as candidate genes for asthma. | Vollmert C et al. | — | 2004 | → |
| Susceptibility to leprosy is associated with PARK2 and PACRG. | Mira MT et al. | — | 2004 | → |
| TCR beta polymorphisms and multiple sclerosis. | Dyment DA et al. | — | 2004 | → |
| The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus. | Wang E et al. | — | 2004 | → |
| The G/G genotype of a resistin single-nucleotide polymorphism at -420 increases type 2 diabetes mellitus susceptibility by inducing promoter activity through specific binding of Sp1/3. | Osawa H et al. | — | 2004 | → |
| The impact of SNP density on fine-scale patterns of linkage disequilibrium. | Ke X et al. | — | 2004 | → |
| The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis. | Timms AE et al. | — | 2004 | → |
| Transcription of the IL10 gene reveals allele-specific regulation at the mRNA level. | Kurreeman FA et al. | — | 2004 | → |
| Variation in GRM3 affects cognition, prefrontal glutamate, and risk for schizophrenia. | Egan MF et al. | — | 2004 | → |
| Variations in GABRA2, encoding the alpha 2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations. | Edenberg HJ et al. | — | 2004 | → |
| A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. | Bray NJ et al. | — | 2003 | → |
| Analysis of reelin as a candidate gene for autism. | Bonora E et al. | — | 2003 | → |
| Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease. | Negoro K et al. | — | 2003 | → |
| Association of erosive hand osteoarthritis with a single nucleotide polymorphism on the gene encoding interleukin-1 beta. | Stern AG et al. | — | 2003 | → |
| Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism. | Serajee FJ et al. | — | 2003 | → |
| Association of specific language impairment (SLI) to the region of 7q31. | O'Brien EK et al. | — | 2003 | → |
| CD36 polymorphism is associated with protection from cerebral malaria. | Omi K et al. | — | 2003 | → |
| Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. | Jezewski PA et al. | — | 2003 | → |
| Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism. | Nurmi EL et al. | — | 2003 | → |
| Endothelial nitric oxide synthase polymorphisms are associated with type 2 diabetes and the insulin resistance syndrome. | Monti LD et al. | — | 2003 | → |
| Estimation of linkage disequilibrium in a sample of the United Kingdom dairy cattle population using unphased genotypes. | Tenesa A et al. | — | 2003 | → |
| Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. | Ertekin-Taner N et al. | — | 2003 | → |
| Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2. | Shi M et al. | — | 2003 | → |
| Haplotype information and linkage disequilibrium mapping for single nucleotide polymorphisms. | Lu X et al. | — | 2003 | → |
| Insulin degrading enzyme (IDE) genetic variants and risk of Alzheimer's disease: evidence of effect modification by apolipoprotein E (APOE). | Edland SD et al. | — | 2003 | → |
| Interferon-alpha receptor-1 (IFNAR1) variants are associated with protection against cerebral malaria in the Gambia. | Aucan C et al. | — | 2003 | → |
| LD mapping of maternally and non-maternally derived alleles and atopy in FcepsilonRI-beta. | Traherne JA et al. | — | 2003 | → |
| Linkage and association between serotonin 2A receptor gene polymorphisms and bipolar I disorder. | Ranade SS et al. | — | 2003 | → |
| Linkage disequilibrium analysis of the human adenosine deaminase (ada) gene provides evidence for a lack of correlation between hot spots of equal and unequal homologous recombination. | Cruciani F et al. | — | 2003 | → |
| No evidence of type 1 diabetes susceptibility genes in the region centromeric of the HLA complex. | Johansson S et al. | — | 2003 | → |
| Novel association suggests multiple independent QTLs within chromosome 5q21-33 region control variation in total humans IgE levels. | Ahmadi KR et al. | — | 2003 | → |
| Patterns of linkage disequilibrium in mitochondrial DNA of 16 ruminant populations. | Slate J et al. | — | 2003 | → |
| Phenotypic heterogeneity and associations of two aldose reductase gene polymorphisms with nephropathy and retinopathy in type 2 diabetes. | Wang Y et al. | — | 2003 | → |
| Polymorphisms in the 5'-untranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression. | Duan J et al. | — | 2003 | → |
| Positional cloning of a novel gene influencing asthma from chromosome 2q14. | Allen M et al. | — | 2003 | → |
| Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma. | Zhang Y et al. | — | 2003 | → |
| Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene. | Bacchelli E et al. | — | 2003 | → |
| The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism. | Serajee FJ et al. | — | 2003 | → |
| Titin is a candidate gene for stroke volume response to endurance training: the HERITAGE Family Study. | Rankinen T et al. | — | 2003 | → |
| Variants of the CD40 ligand gene are not associated with increased susceptibility to tuberculosis in West Africa. | Campbell SJ et al. | — | 2003 | → |
| Variation in the protocadherin gamma A gene cluster. | Kirov G et al. | — | 2003 | → |
| A first-generation linkage disequilibrium map of human chromosome 22. | Dawson E et al. | — | 2002 | → |
| A linkage disequilibrium study of bipolar disorder and microsatellite markers on 22q13. | Liang SG et al. | — | 2002 | → |
| Association between TNFA polymorphism and the development of asthma in the Japanese population. | Noguchi E et al. | — | 2002 | → |
| Association of angiotensin-converting enzyme polymorphisms with systemic lupus erythematosus and nephritis: analysis of 644 SLE families. | Parsa A et al. | — | 2002 | → |
| Association of low-density lipoprotein receptor polymorphisms and outcome of hepatitis C infection. | Hennig BJ et al. | — | 2002 | → |
| Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness. | Van Eerdewegh P et al. | — | 2002 | → |
| Caution on pedigree haplotype inference with software that assumes linkage equilibrium. | Schaid DJ et al. | — | 2002 | → |
| Evidence for linkage and association with reading disability on 6p21.3-22. | Kaplan DE et al. | — | 2002 | → |
| Finer linkage mapping of a primary hip osteoarthritis susceptibility locus on chromosome 6. | Loughlin J et al. | — | 2002 | → |
| Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis. | Rubio JP et al. | — | 2002 | → |
| Haplotype and linkage disequilibrium architecture for human cancer-associated genes. | Bonnen PE et al. | — | 2002 | → |
| High-density genotyping and linkage disequilibrium in the human genome using chromosome 22 as a model. | Remm M et al. | — | 2002 | → |
| Linkage disequilibrium in domestic sheep. | McRae AF et al. | — | 2002 | → |
| New insights into the role of thyroid hormone in the CNS: the microglial track. | Mallat M et al. | — | 2002 | → |
| Segmental linkage disequilibrium within the dopamine transporter gene. | Greenwood TA et al. | — | 2002 | → |
| TaqMan systems for genotyping of disease-related polymorphisms present in the gene encoding apolipoprotein E. | Koch W et al. | — | 2002 | → |
| The impact of genotyping error on haplotype reconstruction and frequency estimation. | Kirk KM et al. | — | 2002 | → |
| Extent and distribution of linkage disequilibrium in three genomic regions. | Abecasis GR et al. | — | 2001 | → |
| Haplotypes of the 5' region of the IL-4 gene and SNPs in the intergene sequence between the IL-4 and IL-13 genes are associated with atopic asthma. | Noguchi E et al. | — | 2001 | → |
| Identification of novel polymorphisms in the beta7 integrin gene: family-based association studies in inflammatory bowel disease. | van Heel DA et al. | — | 2001 | → |
| Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region. | Vorechovsky I et al. | — | 2001 | → |
| Testing for gene-gene interaction controlling total IgE in families from Barbados: evidence of sensitivity regarding linkage heterogeneity among families. | Barnes KC et al. | — | 2001 | → |
| Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association. | Tsai HJ et al. | — | 2001 | → |