Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
- Authors
- Lesch, Klaus-Peter; Timmesfeld, Nina; Renner, Tobias J; Halperin, Rebecca; RΓΆser, Christoph; Nguyen, T Trang; Craig, David W; Romanos, Jasmin; Heine, Monika; Meyer, Jobst; Freitag, Christine; Warnke, Andreas; Romanos, Marcel; SchΓ€fer, Helmut; Walitza, Susanne; Reif, Andreas; Stephan, Dietrich A; Jacob, Christian
- Year
- 2008
- Journal
- Journal of neural transmission (Vienna, Austria : 1996)
- PMID
- 18839057
- DOI
- 10.1007/s00702-008-0119-3
A genome-wide association (GWA) study with pooled DNA in adult attention-deficit/hyperactivity disorder (ADHD) employing approximately 500K SNP markers identifies novel risk genes and reveals remarkable overlap with findings from recent GWA scans in substance use disorders. Comparison with results from our previously reported high-resolution linkage scan in extended pedigrees confirms several chromosomal loci, including 16q23.1-24.3 which also reached genome-wide significance in a recent meta-analysis of seven linkage studies (Zhou et al. in Am J Med Genet Part B, 2008). The findings provide additional support for a common effect of genes coding for cell adhesion molecules (e.g., CDH13, ASTN2) and regulators of synaptic plasticity (e.g., CTNNA2, KALRN) despite the complex multifactorial etiologies of adult ADHD and addiction vulnerability.
No figures extracted from this document.
No chunks β full text not yet ingested.
No entities extracted from this document yet.
No uploaded files.
No citations found.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Bi-allelic variants in neuronal adhesion molecule astrotactin 1 gene ASTN1 cause diverse neurodevelopmental disorders. | Levine JM et al. | β | 2026 | β |
| Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 Patients. | Goleva SB et al. | β | 2026 | β |
| Preliminary exploration of the role and mechanism of BAIAP2 in learning and memory impairment in ADHD. | Tian T et al. | β | 2026 | β |
| Uncovering the molecular logic of cortical wiring between neuronal subtypes across development through ligand-receptor inference. | Mathieu R et al. | β | 2026 | β |
| A Decoy Oligodeoxynucleotides Disturbing Forkhead Box O3 Mediated ctnna2 Transcriptional Repression Prevents Postoperative Neurocognitive Disorder in Mice. | Wu Z et al. | β | 2025 | β |
| A phenotypic journey into NT5DC proteins in cancer and other diseases. | Cros-Perrial E et al. | β | 2025 | β |
| Attention-Deficit Hyperactivity Disorder (ADHD): A Comprehensive Overview of the Mechanistic Insights from Human Studies to Animal Models. | Yacoub MW et al. | β | 2025 | β |
| Developmental pyrethroid exposure disrupts molecular pathways for MAP kinase and circadian rhythms in mouse brain. | Nguyen JH et al. | β | 2025 | β |
| Drug-related suicidal ideation in the K-12 population: a real-world pharmacovigilance study of the FDA adverse event reporting system (FAERS) database. | Ju Y et al. | β | 2025 | β |
| Insights into the Neurobiology of Behavioral Inhibition from Nonhuman Primate Models. | Campos LJ et al. | β | 2025 | β |
| Gene-environment interactions in the influence of maternal education on adolescent neurodevelopment using ABCD study. | Shi R et al. | β | 2024 | β |
| Novel pharmacological targets for GABAergic dysfunction in ADHD. | Ferranti AS et al. | β | 2024 | β |
| Somatic mosaicism in schizophrenia brains reveals prenatal mutational processes. | Maury EA et al. | β | 2024 | β |
| Association analysis of polymorphisms of candidate genes for laying traits in Yangzhou geese. | Zhang Y et al. | β | 2023 | β |
| Association of the <i>CDH13</i> gene variant rs9940180 with schizophrenia risk in North Indian population. | Gupta S et al. | β | 2023 | β |
| Astrotactin 2 (ASTN2) regulates emotional and cognitive functions by affecting neuronal morphogenesis and monoaminergic systems. | Ito T et al. | β | 2023 | β |
| Evaluating the Genetic Effects of Gut Microbiota on the Development of Neuroticism and General Happiness: A Polygenic Score Analysis and Interaction Study Using UK Biobank Data. | Jia Y et al. | β | 2023 | β |
| Genetics of psycho-emotional well-being: genome-wide association study and polygenic risk score analysis. | Yakovchik AY et al. | β | 2023 | β |
| Modulation effect of non-invasive transcranial ultrasound stimulation in an ADHD rat model. | Wang M et al. | β | 2023 | β |
| A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. | Li C et al. | β | 2022 | β |
| Astroblastomas exhibit radial glia stem cell lineages and differential expression of imprinted and X-inactivation escape genes. | Lehman NL et al. | β | 2022 | β |
| Genetics of glutamate and its receptors in autism spectrum disorder. | Nisar S et al. | β | 2022 | β |
| Myelin-associated oligodendrocyte basic protein rs616147 polymorphism as a risk factor for Parkinson's disease. | Siokas V et al. | β | 2022 | β |
| Neuroprotection in late life attention-deficit/hyperactivity disorder: A review of pharmacotherapy and phenotype across the lifespan. | Dutta CN et al. | β | 2022 | β |
| Whole-genome sequencing reveals the genetic mechanisms of domestication in classical inbred mice. | Liu M et al. | β | 2022 | β |
| A Common <i>CDH13</i> Variant Is Associated with Low Agreeableness and Neural Responses to Working Memory Tasks in ADHD. | Ziegler GC et al. | β | 2021 | β |
| Altered dopaminergic firing pattern and novelty response underlie ADHD-like behavior of SorCS2-deficient mice. | Olsen D et al. | β | 2021 | β |
| Astrocyte-induced synapse formation and ischemic stroke. | Yamagata K | β | 2021 | β |
| Catenin Alpha 2 May Be a Biomarker or Potential Drug Target in Psychiatric Disorders with Perseverative Negative Thinking. | Eszlari N et al. | β | 2021 | β |
| Deep learning model reveals potential risk genes for ADHD, especially Ephrin receptor gene EPHA5. | Liu L et al. | β | 2021 | β |
| Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People. | Lo YH et al. | β | 2021 | β |
| Do gene expression findings from mouse models of cocaine use recapitulate human cocaine use disorder in reward circuitry? | Huggett SB et al. | β | 2021 | β |
| Dynamic transcriptome landscape in the song nucleus HVC between juvenile and adult zebra finches. | Shi Z et al. | β | 2021 | β |
| Identification of novel risk loci with shared effects on alcoholism, heroin, and methamphetamine dependence. | Sun Y et al. | β | 2021 | β |
| Integrating genomics and transcriptomics: Towards deciphering ADHD. | Pujol-Gualdo N et al. | β | 2021 | β |
| Knockdown of the ADHD Candidate Gene <i>Diras2</i> in Murine Hippocampal Primary Cells. | GrΓΌnewald L et al. | β | 2021 | β |
| Neuropsychiatric Adverse Events of Montelukast: An Analysis of Real-World Datasets and drug-gene Interaction Network. | Umetsu R et al. | β | 2021 | β |
| Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American Ancestry. | Liu Y et al. | β | 2021 | β |
| Serotonin-specific neurons differentiated from human iPSCs form distinct subtypes with synaptic protein assembly. | Jansch C et al. | β | 2021 | β |
| Stick around: Cell-Cell Adhesion Molecules during Neocortical Development. | de AgustΓn-DurΓ‘n D et al. | β | 2021 | β |
| Super-variants identification for brain connectivity. | Li T et al. | β | 2021 | β |
| A study combining whole-exome sequencing and structural neuroimaging analysis for major depressive disorder. | Han KM et al. | β | 2020 | β |
| From man to fly - convergent evidence links FBXO25 to ADHD and comorbid psychiatric phenotypes. | Harich B et al. | β | 2020 | β |
| Genetic Influence on Efficacy of Pharmacotherapy for Pediatric Attention-Deficit/Hyperactivity Disorder: Overview and Current Status of Research. | Elsayed NA et al. | β | 2020 | β |
| Genetic Intersections of Language and Neuropsychiatric Conditions. | Koomar T et al. | β | 2020 | β |
| Genetics of ADHD: What Should the Clinician Know? | Grimm O et al. | β | 2020 | β |
| Genome-wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders. | Price KM et al. | β | 2020 | β |
| Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing. | Corominas J et al. | β | 2020 | β |
| Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk. | Nudel R et al. | β | 2020 | β |
| Large epigenome-wide association study of childhood ADHD identifies peripheral DNA methylation associated with disease and polygenic risk burden. | Mooney MA et al. | β | 2020 | β |
| Maternal antenatal depression and child mental health: Moderation by genomic risk for attention-deficit/hyperactivity disorder. | Chen LM et al. | β | 2020 | β |
| Rare variants and biological pathways identified in treatment-refractory depression. | McClain LL et al. | β | 2020 | β |
| Shared genetic background between children and adults with attention deficit/hyperactivity disorder. | Rovira P et al. | β | 2020 | β |
| Sodium hydrogen exchanger 9 NHE9 (SLC9A9) and its emerging roles in neuropsychiatric comorbidity. | Patak J et al. | β | 2020 | β |
| The stress-Wnt-signaling axis: a hypothesis for attention-deficit hyperactivity disorder and therapy approaches. | Yde Ohki CM et al. | β | 2020 | β |
| Early-life stress impairs developmental programming in Cadherin 13 (CDH13)-deficient mice. | Kiser DP et al. | β | 2019 | β |
| Epigenome-wide association study of leukocyte telomere length. | Lee Y et al. | β | 2019 | β |
| Genetics of attention deficit hyperactivity disorder. | Faraone SV et al. | β | 2019 | β |
| Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. | Howard DM et al. | β | 2019 | β |
| GWAS of Behavioral Traits. | Mehta D et al. | β | 2019 | β |
| Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot study. | Waltes R et al. | β | 2019 | β |
| Neuropsychological Performance Patterns of Adult ADHD Subtypes. | LeRoy A et al. | β | 2019 | β |
| Pain and gastrointestinal dysfunction are significant associations with psychiatric disorders in patients with Ehlers-Danlos syndrome and hypermobility spectrum disorders: a retrospective study. | Wasim S et al. | β | 2019 | β |
| Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease. | VΓ©lez JI et al. | β | 2019 | β |
| The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis. | GrΓΌnblatt E et al. | β | 2019 | β |
| Zebrafish models for attention deficit hyperactivity disorder (ADHD). | Fontana BD et al. | β | 2019 | β |
| A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene. | Hawi Z et al. | β | 2018 | β |
| A Schizophrenia-Linked KALRN Coding Variant Alters Neuron Morphology, Protein Function, and Transcript Stability. | Russell TA et al. | β | 2018 | β |
| ASTN2 modulates synaptic strength by trafficking and degradation of surface proteins. | Behesti H et al. | β | 2018 | β |
| Common and specific genes and peripheral biomarkers in children and adults with attention-deficit/hyperactivity disorder. | Bonvicini C et al. | β | 2018 | β |
| Emerging role of miRNA in attention deficit hyperactivity disorder: a systematic review. | Srivastav S et al. | β | 2018 | β |
| Expression of the ADHD candidate gene Diras2 in the brain. | GrΓΌnewald L et al. | β | 2018 | β |
| Functional analysis of a triplet deletion in the gene encoding the sodium glucose transporter 3, a potential risk factor for ADHD. | SchΓ€fer N et al. | β | 2018 | β |
| Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions | Howard DM et al. | β | 2018 | β |
| Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder. | Pagerols M et al. | β | 2018 | β |
| Interplay Between Amphetamine and Activity Level in Gene Networks of the Mouse Striatum. | Goncalves TM et al. | β | 2018 | β |
| Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan. | Franke B et al. | β | 2018 | β |
| Methylomic changes in response to micronutrient supplementation and MTHFR genotype. | Stevens AJ et al. | β | 2018 | β |
| Methylphenidate enhances neuronal differentiation and reduces proliferation concomitant to activation of Wnt signal transduction pathways. | GrΓΌnblatt E et al. | β | 2018 | β |
| Mice Lacking Glypican 4 Display Juvenile Hyperactivity and Adult Social Interaction Deficits. | Dowling C et al. | β | 2018 | β |
| Recent developments in the genetics of attention-deficit hyperactivity disorder. | Grimm O et al. | β | 2018 | β |
| Sex Differences in Psychiatric Disease: A Focus on the Glutamate System. | Wickens MM et al. | β | 2018 | β |
| The role of cadherin genes in five major psychiatric disorders: A literature update. | Hawi Z et al. | β | 2018 | β |
| Transcriptome Analysis Identifies Multifaceted Regulatory Mechanisms Dictating a Genetic Switch from Neuronal Network Establishment to Maintenance During Postnatal Prefrontal Cortex Development. | Kroeze Y et al. | β | 2018 | β |
| Alpha-1 antitrypsin inhibits RANKL-induced osteoclast formation and functions. | Akbar MA et al. | β | 2017 | β |
| Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder. | Shinwari JMA et al. | β | 2017 | β |
| Astrocyte-Secreted Glypican 4 Regulates Release of Neuronal Pentraxin 1 from Axons to Induce Functional Synapse Formation. | Farhy-Tselnicker I et al. | β | 2017 | β |
| Attention deficit hyperactivity disorder (ADHD) in phenotypically similar neurogenetic conditions: Turner syndrome and the RASopathies. | Green T et al. | β | 2017 | β |
| Attention-deficit/hyperactivity disorder associated with KChIP1 rs1541665 in Kv channels accessory proteins. | Yuan FF et al. | β | 2017 | β |
| Brain imaging genetics in ADHD and beyond - Mapping pathways from gene to disorder at different levels of complexity. | Klein M et al. | β | 2017 | β |
| Cadherin-13 Deficiency Increases Dorsal Raphe 5-HT Neuron Density and Prefrontal Cortex Innervation in the Mouse Brain. | Forero A et al. | β | 2017 | β |
| Cdh13 and AdipoQ gene knockout alter instrumental and Pavlovian drug conditioning. | King CP et al. | β | 2017 | β |
| Cleave but not leave: Astrotactin proteins in development and disease. | Chang H | β | 2017 | β |
| Family-based association study of DRD4 gene in methylphenidate-responded Attention Deficit/Hyperactivity Disorder. | Leung PW et al. | β | 2017 | β |
| Fundamental Elements in Autism: From Neurogenesis and Neurite Growth to Synaptic Plasticity. | Gilbert J et al. | β | 2017 | β |
| Genetic Approaches to Understanding Psychiatric Disease. | Michaelson JJ | β | 2017 | β |
| Genetic Variant of <i>Kalirin</i> Gene Is Associated with Ischemic Stroke in a Chinese Han Population. | Li H et al. | β | 2017 | β |
| Imaging genetics in neurodevelopmental psychopathology. | Klein M et al. | β | 2017 | β |
| Long-term prenatal exposure to paracetamol is associated with DNA methylation differences in children diagnosed with ADHD. | Gervin K et al. | β | 2017 | β |
| Neurodevelopmental MACPFs: The vertebrate astrotactins and BRINPs. | Berkowicz SR et al. | β | 2017 | β |
| No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson's disease in nine ADHD candidate SNPs. | Geissler JM et al. | β | 2017 | β |
| Regulating the Regulators in Attention-Deficit/Hyperactivity Disorder: A Genetic Association Study of microRNA Biogenesis Pathways. | Karakas U et al. | β | 2017 | β |
| Repurposing a pore: highly conserved perforin-like proteins with alternative mechanisms. | Ni T et al. | β | 2017 | β |
| Role of neurotrophic factors in attention deficit hyperactivity disorder. | Tsai SJ | β | 2017 | β |
| Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder. | Kim DS et al. | β | 2017 | β |
| The SNP-set based association study identifies ITGA1 as a susceptibility gene of attention-deficit/hyperactivity disorder in Han Chinese. | Liu L et al. | β | 2017 | β |
| An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder. | Lima Lde A et al. | β | 2016 | β |
| Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies. | Bonvicini C et al. | β | 2016 | β |
| Cadherin 13: human <i>cis</i>-regulation and selectively-altered addiction phenotypes and cerebral cortical dopamine in knockout mice. | Drgonova J et al. | β | 2016 | β |
| Decoding the non-coding genome: elucidating genetic risk outside the coding genome. | Barr CL et al. | β | 2016 | β |
| Exome chip analyses in adult attention deficit hyperactivity disorder. | Zayats T et al. | β | 2016 | β |
| Functional Impact of An ADHD-Associated DIRAS2 Promoter Polymorphism. | GrΓΌnewald L et al. | β | 2016 | β |
| Genetics of attention-deficit/hyperactivity disorder: an update. | Akutagava-Martins GC et al. | β | 2016 | β |
| Genome-wide haplotype association analysis identifies SERPINB9, SERPINE2, GAK, and HSP90B1 as novel risk genes for oral squamous cell carcinoma. | Sun W et al. | β | 2016 | β |
| Guanfacine Extended Release: A New Pharmacological Treatment Option in Europe. | Huss M et al. | β | 2016 | β |
| HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease. | Ward LD et al. | β | 2016 | β |
| HMGB4 is expressed by neuronal cells and affects the expression of genes involved in neural differentiation. | Rouhiainen A et al. | β | 2016 | β |
| MAP1B and NOS1 genes are associated with working memory in youths with attention-deficit/hyperactivity disorder. | Salatino-Oliveira A et al. | β | 2016 | β |
| Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis. | Tsetsos F et al. | β | 2016 | β |
| Mice Lacking <i>Brinp2</i> or <i>Brinp3</i>, or Both, Exhibit Behaviors Consistent with Neurodevelopmental Disorders. | Berkowicz SR et al. | β | 2016 | β |
| Mouse and Human Genetic Analyses Associate Kalirin with Ventral Striatal Activation during Impulsivity and with Alcohol Misuse. | PeΓ±a-Oliver Y et al. | β | 2016 | β |
| Moving towards causality in attention-deficit hyperactivity disorder: overview of neural and genetic mechanisms. | Gallo EF et al. | β | 2016 | β |
| Paternal Aging Affects Behavior in Pax6 Mutant Mice: A Gene/Environment Interaction in Understanding Neurodevelopmental Disorders. | Yoshizaki K et al. | β | 2016 | β |
| Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach. | Mooney MA et al. | β | 2016 | β |
| Regulation of neuronal migration, an emerging topic in autism spectrum disorders. | Reiner O et al. | β | 2016 | β |
| Regulation of Tlx3 by Pax6 is required for the restricted expression of ChrnΞ±3 in Cerebellar Granule Neuron progenitors during development. | Divya TS et al. | β | 2016 | β |
| Separating the wheat from the chaff: systematic identification of functionally relevant noncoding variants in ADHD. | Tong JH et al. | β | 2016 | β |
| Single nucleotide polymorphisms in the REG-CTNNA2 region of chromosome 2 and NEIL3 associated with impulsivity in a Native American sample. | Ehlers CL et al. | β | 2016 | β |
| Structure of astrotactin-2: a conserved vertebrate-specific and perforin-like membrane protein involved in neuronal development. | Ni T et al. | β | 2016 | β |
| Testing candidate genes for attention-deficit/hyperactivity disorder in fruit flies using a high throughput assay for complex behavior. | Rohde PD et al. | β | 2016 | β |
| Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits. | Pinto R et al. | β | 2016 | β |
| The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits. | Freitag CM et al. | β | 2016 | β |
| Whole-Exome Sequencing Reveals Increased Burden ofΒ Rare Functional and Disruptive Variants in CandidateΒ Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder. | Demontis D et al. | β | 2016 | β |
| Annual research review: The (epi)genetics of neurodevelopmental disorders in the era of whole-genome sequencing--unveiling the dark matter. | Kiser DP et al. | β | 2015 | β |
| A novel relationship for schizophrenia, bipolar and major depressive disorder Part 7: A hint from chromosome 7 high density association screen. | Chen X et al. | β | 2015 | β |
| Attention deficit hyperactivity disorder and developmental coordination disorder: Two separate disorders or do they share a common etiology. | Goulardins JB et al. | β | 2015 | β |
| Cadherin-13, a risk gene for ADHD and comorbid disorders, impacts GABAergic function in hippocampus and cognition. | Rivero O et al. | β | 2015 | β |
| Cadherin-13 gene is associated with hyperactive/impulsive symptoms in attention/deficit hyperactivity disorder. | Salatino-Oliveira A et al. | β | 2015 | β |
| Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder. | SΓ‘nchez-Mora C et al. | β | 2015 | β |
| Converging evidence does not support GIT1 as an ADHD risk gene. | Klein M et al. | β | 2015 | β |
| Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease. | Yokoyama JS et al. | β | 2015 | β |
| Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorder. | SΓ‘nchez-Mora C et al. | β | 2015 | β |
| Duplications in ADHD patients harbour neurobehavioural genes that are co-expressed with genes associated with hyperactivity in the mouse. | Taylor A et al. | β | 2015 | β |
| Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE. | Jacobsen KK et al. | β | 2015 | β |
| Further evidence for the association of the NPSR1 gene A/T polymorphism (Asn107Ile) with impulsivity and hyperactivity. | Laas K et al. | β | 2015 | β |
| Genome-wide analysis of attention deficit hyperactivity disorder in Norway. | Zayats T et al. | β | 2015 | β |
| Genome-wide haplotype association study identify TNFRSF1A, CASP7, LRP1B, CDH1 and TG genes associated with Alzheimer's disease in Caribbean Hispanic individuals. | Shang Z et al. | β | 2015 | β |
| Genomic structural variants are linked with intellectual disability. | Bulayeva K et al. | β | 2015 | β |
| Identification of Laying-Related SNP Markers in Geese Using RAD Sequencing. | Yu S et al. | β | 2015 | β |
| Integrative analysis of 111 reference human epigenomes. | Roadmap Epigenomics Consortium et al. | β | 2015 | β |
| Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders. | Eicher JD et al. | β | 2015 | β |
| Neural Zinc Finger Factor/Myelin Transcription Factor Proteins: Metal Binding, Fold, and Function. | Besold AN et al. | β | 2015 | β |
| New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder. | Alemany S et al. | β | 2015 | β |
| Pathway-Based Genome-Wide Association Studies for Plasma Triglycerides in Obese Females and Normal-Weight Controls. | Jiao H et al. | β | 2015 | β |
| Polymorphisms within ASTN2 gene are associated with age at onset of Alzheimer's disease. | Wang KS et al. | β | 2015 | β |
| Synapse assembly and neurodevelopmental disorders. | Washbourne P | β | 2015 | β |
| The molecular genetic architecture of attention deficit hyperactivity disorder. | Hawi Z et al. | β | 2015 | β |
| The Physiology of BDNF and Its Relationship with ADHD. | Liu DY et al. | β | 2015 | β |
| Abnormal kalirin signaling in neuropsychiatric disorders. | Remmers C et al. | β | 2014 | β |
| Advances in molecular genetic studies of attention deficit hyperactivity disorder in China. | Gao Q et al. | β | 2014 | β |
| A functional NPSR1 gene variant and environment shape personality and impulsive action: a longitudinal study. | Laas K et al. | β | 2014 | β |
| Applying imaging genetics to ADHD: the promises and the challenges. | Wu Z et al. | β | 2014 | β |
| Characterization of biological pathways associated with a 1.37 Mbp genomic region protective of hypertension in Dahl S rats. | Cowley AW et al. | β | 2014 | β |
| Decreased serum levels of adiponectin in adult attention deficit hyperactivity disorder. | Mavroconstanti T et al. | β | 2014 | β |
| Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. | Lionel AC et al. | β | 2014 | β |
| DNA methylation changes in the postmortem dorsolateral prefrontal cortex of patients with schizophrenia. | Numata S et al. | β | 2014 | β |
| Functional gene-set analysis does not support a major role for synaptic function in attention deficit/hyperactivity disorder (ADHD). | Hammerschlag AR et al. | β | 2014 | β |
| Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. | BΓΈrglum AD et al. | β | 2014 | β |
| Internalizing and externalizing behavior in adult ADHD. | Jacob C et al. | β | 2014 | β |
| Molecular genetic studies of ADHD and its candidate genes: a review. | Li Z et al. | β | 2014 | β |
| Nonenzymatic domains of Kalirin7 contribute to spine morphogenesis through interactions with phosphoinositides and Abl. | Ma XM et al. | β | 2014 | β |
| Role of COMT in ADHD: a systematic meta-analysis. | Sun H et al. | β | 2014 | β |
| SorCS2 regulates dopaminergic wiring and is processed into an apoptotic two-chain receptor in peripheral glia. | Glerup S et al. | β | 2014 | β |
| SPOCK3, a risk gene for adult ADHD and personality disorders. | Weber H et al. | β | 2014 | β |
| The neurobiological link between OCD and ADHD. | Brem S et al. | β | 2014 | β |
| Acetylcholine-metabolizing butyrylcholinesterase (BCHE) copy number and single nucleotide polymorphisms and their role in attention-deficit/hyperactivity syndrome. | Jacob CP et al. | β | 2013 | β |
| Advances in osteoarthritis genetics. | Panoutsopoulou K et al. | β | 2013 | β |
| Association of genetic risk severity with ADHD clinical characteristics. | Kotte A et al. | β | 2013 | β |
| A study of the possible association between adenosine A2A receptor gene polymorphisms and attention-deficit hyperactivity disorder traits. | Molero Y et al. | β | 2013 | β |
| Atomoxetine affects transcription/translation of the NMDA receptor and the norepinephrine transporter in the rat brain--an in vivo study. | Udvardi PT et al. | β | 2013 | β |
| Attention-deficit/hyperactivity disorder in a chronic care paradigm. | Culpepper L et al. | β | 2013 | β |
| BAIAP2 exhibits association to childhood ADHD especially predominantly inattentive subtype in Chinese Han subjects. | Liu L et al. | β | 2013 | β |
| Clinical significance of de novo and inherited copy-number variation. | Vulto-van Silfhout AT et al. | β | 2013 | β |
| Dances with black widow spiders: dysregulation of glutamate signalling enters centre stage in ADHD. | Lesch KP et al. | β | 2013 | β |
| Ephrin-A5 deficiency alters sensorimotor and monoaminergic development. | Sheleg M et al. | β | 2013 | β |
| Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients. | Mavroconstanti T et al. | β | 2013 | β |
| Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort. | Ward-Caviness C et al. | β | 2013 | β |
| Genetics of attention-deficit/hyperactivity disorder: current findings and future directions. | Akutagava-Martins GC et al. | β | 2013 | β |
| Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated German multi-generation families. | Lin MK et al. | β | 2013 | β |
| Impact of the ADHD-susceptibility gene CDH13 on development and function of brain networks. | Rivero O et al. | β | 2013 | β |
| KCNIP4 as a candidate gene for personality disorders and adult ADHD. | WeiΓflog L et al. | β | 2013 | β |
| Peter Riederer "70th birthday" neurobiological foundations of modern addiction treatment. | Jacob C | β | 2013 | β |
| Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants. | Yang L et al. | β | 2013 | β |
| The comorbidity of ADHD and autism spectrum disorder. | Antshel KM et al. | β | 2013 | β |
| Toward developmental models of psychiatric disorders in zebrafish. | Norton WH | β | 2013 | β |
| Unbiased discovery of glypican as a receptor for LRRTM4 in regulating excitatory synapse development. | de Wit J et al. | β | 2013 | β |
| ADHD and autism: differential diagnosis or overlapping traits? A selective review. | Taurines R et al. | β | 2012 | β |
| ADHDgene: a genetic database for attention deficit hyperactivity disorder. | Zhang L et al. | β | 2012 | β |
| A discovery resource of rare copy number variations in individuals with autism spectrum disorder. | Prasad A et al. | β | 2012 | β |
| A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. | Casey JP et al. | β | 2012 | β |
| Association of APC and REEP5 gene polymorphisms with major depression disorder and treatment response to antidepressants in a Han Chinese population. | Yang Z et al. | β | 2012 | β |
| ASTN1 and alcohol dependence: family-based association analysis in multiplex alcohol dependence families. | Hill SY et al. | β | 2012 | β |
| Astrocyte glypicans 4 and 6 promote formation of excitatory synapses via GluA1 AMPA receptors. | Allen NJ et al. | β | 2012 | β |
| Behavioral genetics of affective and anxiety disorders. | Domschke K et al. | β | 2012 | β |
| Behavioural genetics of childhood disorders. | Freitag CM et al. | β | 2012 | β |
| Biomarkers for attention-deficit/hyperactivity disorder (ADHD). A consensus report of the WFSBP task force on biological markers and the World Federation of ADHD. | Thome J et al. | β | 2012 | β |
| Cadherins and neuropsychiatric disorders. | Redies C et al. | β | 2012 | β |
| Cadherins in brain morphogenesis and wiring. | Hirano S et al. | β | 2012 | β |
| Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients. | Tsai YC et al. | β | 2012 | β |
| Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. | Williams NM et al. | β | 2012 | β |
| Genome-wide association study of comorbid depressive syndrome and alcohol dependence. | Edwards AC et al. | β | 2012 | β |
| Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13). | Hart AB et al. | β | 2012 | β |
| Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. | Stergiakouli E et al. | β | 2012 | β |
| Kalirin, a key player in synapse formation, is implicated in human diseases. | Mandela P et al. | β | 2012 | β |
| Kalirin signaling: implications for synaptic pathology. | Penzes P et al. | β | 2012 | β |
| Kalrn plays key roles within and outside of the nervous system. | Mandela P et al. | β | 2012 | β |
| Long-term perturbation of spine plasticity results in distinct impairments of cognitive function. | Vanleeuwen JE et al. | β | 2012 | β |
| Modeling the functional genomics of autism using human neurons. | Konopka G et al. | β | 2012 | β |
| Pharmacotherapy for attention-deficit/hyperactivity disorder: from cells to circuits. | Minzenberg MJ | β | 2012 | β |
| PPP2R2C as a candidate gene of a temperament and character trait-based endophenotype of ADHD. | Jacob C et al. | β | 2012 | β |
| Quantitative and molecular genetics of ADHD. | Asherson P et al. | β | 2012 | β |
| Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy. | Kim DS et al. | β | 2012 | β |
| Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148. | Dharmadhikari AV et al. | β | 2012 | β |
| Targeted pharmacogenetic analysis of antipsychotic response in the CATIE study. | Liu Q et al. | β | 2012 | β |
| The ADHD-susceptibility gene lphn3.1 modulates dopaminergic neuron formation and locomotor activity during zebrafish development. | Lange M et al. | β | 2012 | β |
| The genetics of attention deficit/hyperactivity disorder in adults, a review. | Franke B et al. | β | 2012 | β |
| What causes attention deficit hyperactivity disorder? | Thapar A et al. | β | 2012 | β |
| What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations. | Panagiotou OA et al. | β | 2012 | β |
| ADHD in Dutch adults: heritability and linkage study. | Saviouk V et al. | β | 2011 | β |
| ADRA2A polymorphisms and ADHD in adults: possible mediating effect of personality. | de Cerqueira CC et al. | β | 2011 | β |
| A lifetime of attention-deficit/hyperactivity disorder: diagnostic challenges, treatment and neurobiological mechanisms. | Geissler J et al. | β | 2011 | β |
| Cross-disorder analysis of bipolar risk genes: further evidence of DGKH as a risk gene for bipolar disorder, but also unipolar depression and adult ADHD. | Weber H et al. | β | 2011 | β |
| DCDC2, KIAA0319 and CMIP are associated with reading-related traits. | Scerri TS et al. | β | 2011 | β |
| DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders. | Reif A et al. | β | 2011 | β |
| Dissection of genetic associations with language-related traits in population-based cohorts. | Paracchini S | β | 2011 | β |
| Electrophysiological markers of genetic risk for attention deficit hyperactivity disorder. | Tye C et al. | β | 2011 | β |
| Genome-wide association study in German patients with attention deficit/hyperactivity disorder. | Hinney A et al. | β | 2011 | β |
| Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree. | Lesch KP et al. | β | 2011 | β |
| Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. | Elia J et al. | β | 2011 | β |
| Integrated genome-wide association study findings: identification of a neurodevelopmental network for attention deficit hyperactivity disorder. | Poelmans G et al. | β | 2011 | β |
| Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. | Newbury DF et al. | β | 2011 | β |
| Kalrn promoter usage and isoform expression respond to chronic cocaine exposure. | Mains RE et al. | β | 2011 | β |
| Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. | Terracciano A et al. | β | 2011 | β |
| Modulation of cell adhesion systems by prenatal nicotine exposure in limbic brain regions of adolescent female rats. | Cao J et al. | β | 2011 | β |
| Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. | Lionel AC et al. | β | 2011 | β |
| The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia. | HΓ₯vik B et al. | β | 2011 | β |
| Val/Val genotype of brain-derived neurotrophic factor (BDNF) ValβΆβΆMet polymorphism is associated with a better response to OROS-MPH in Korean ADHD children. | Kim BN et al. | β | 2011 | β |
| A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. | Butler AW et al. | β | 2010 | β |
| A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. | Wang KS et al. | β | 2010 | β |
| Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum. | Lantieri F et al. | β | 2010 | β |
| Animal models of attention deficit/hyperactivity disorder (ADHD): a critical review. | Sontag TA et al. | β | 2010 | β |
| Astn2, a novel member of the astrotactin gene family, regulates the trafficking of ASTN1 during glial-guided neuronal migration. | Wilson PM et al. | β | 2010 | β |
| Case-control genome-wide association study of attention-deficit/hyperactivity disorder. | Neale BM et al. | β | 2010 | β |
| Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. | Mick E et al. | β | 2010 | β |
| Fitting the pieces together: current research on the genetic basis of attention-deficit/hyperactivity disorder (ADHD). | Stergiakouli E et al. | β | 2010 | β |
| Genetic advances in the study of speech and language disorders. | Newbury DF et al. | β | 2010 | β |
| Genome-wide association studies: a powerful tool for neurogenomics. | Cowperthwaite MC et al. | β | 2010 | β |
| Genome-wide haplotype association analysis and gene prioritization identify CCL3 as a risk locus for rheumatoid arthritis. | Zhang R et al. | β | 2010 | β |
| Genome-wide linkage analysis in a Dutch multigenerational family with attention deficit hyperactivity disorder. | Vegt R et al. | β | 2010 | β |
| Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations. | SΓ‘nchez-Mora C et al. | β | 2010 | β |
| Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. | Neale BM et al. | β | 2010 | β |
| [Methylphenidate. Therapy option for adults with ADHD and comorbid substance use disorder?]. | Paslakis G et al. | β | 2010 | β |
| miRNA genes and the brain: implications for psychiatric disorders. | Forero DA et al. | β | 2010 | β |
| Molecular genetics of attention deficit hyperactivity disorder. | Faraone SV et al. | β | 2010 | β |
| Molecular genetics of attention-deficit/hyperactivity disorder: an overview. | Banaschewski T et al. | β | 2010 | β |
| Owner reports of attention, activity, and impulsivity in dogs: a replication study. | Lit L et al. | β | 2010 | β |
| Recent advances in the genetics of language impairment. | Newbury DF et al. | β | 2010 | β |
| Separation of cognitive impairments in attention-deficit/hyperactivity disorder into 2 familial factors. | Kuntsi J et al. | β | 2010 | β |
| The structure and function of mammalian membrane-attack complex/perforin-like proteins. | Kondos SC et al. | β | 2010 | β |
| Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHD. | Arcos-Burgos M et al. | β | 2010 | β |
| Voxelwise genome-wide association study (vGWAS). | Stein JL et al. | β | 2010 | β |
| 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. | β | 2009 | β |
| Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorder. | RibasΓ©s M et al. | β | 2009 | β |
| CMIP and ATP2C2 modulate phonological short-term memory in language impairment. | Newbury DF et al. | β | 2009 | β |
| [Comorbidity of substance use disorders and attention-deficit hyperactivity disorders: pathogenesis and therapy]. | Fallgatter AJ et al. | β | 2009 | β |
| Genetics of attention-deficit hyperactivity disorder (ADHD). | Sharp SI et al. | β | 2009 | β |
| Genome-wide association studies in ADHD. | Franke B et al. | β | 2009 | β |
| Kalirin regulates cortical spine morphogenesis and disease-related behavioral phenotypes. | Cahill ME et al. | β | 2009 | β |
| Understanding genes, environment and their interaction in attention-deficit hyperactivity disorder: is there a role for neuroimaging? | Plomp E et al. | β | 2009 | β |