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Discoveries on the Genetics of ADHD in the 21st Century: New Findings and Their Implications
54/54 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
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The 54 checked references that resolve
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Who says this is a modern disorder? The early history of attention deficit hyperactivity disorder
resolves10.1111/j.1469-7610.2012.02611.x
Practitioner Review: What have we learnt about the causes of ADHD?
resolves10.1007/s10802-008-9278-9
A Common Genetic Factor Explains the Covariation Among ADHD ODD and CD Symptoms in 9–10 Year Old Boys and Girls
resolves10.1017/S0033291709990274
Neurodevelopmental disorders: Cluster 2 of the proposed meta-structure for DSM-V and ICD-11
resolves10.1038/mp.2017.17
The familial co-aggregation of ASD and ADHD: a register-based cohort study
resolves10.1038/ng.3792
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
resolves10.1001/jamapsychiatry.2016.1831
Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia
resolves10.1016/j.jaac.2016.11.011
The Familial Co-Aggregation of Attention-Deficit/Hyperactivity Disorder and Intellectual Disability: A Register-Based Family Study
resolves10.1016/S0140-6736(10)61109-9
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
resolves10.1176/appi.ajp.2013.13070864
Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome
resolves10.1016/j.neuron.2017.06.010
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
resolves10.1038/ng.1013
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
resolves10.1176/appi.ajp.2011.11060822
Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
resolves10.1126/scitranslmed.3002464
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD
resolves10.1038/mp.2012.161
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder
resolves10.1056/NEJMoa0802828
A Functional Genetic Link between Distinct Developmental Language Disorders
resolves10.1016/j.biopsych.2017.11.026
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
resolves10.1016/S0140-6736(12)62129-1
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
resolves10.1192/bjp.bp.112.120808
Risk of bipolar disorder and schizophrenia in relatives of people with attention-deficit hyperactivity disorder
resolves10.1002/ajmg.b.32411
Genetic and environmental influences on the relationship between ADHD symptoms and internalizing problems: A Chinese twin study
resolves10.1001/jamapsychiatry.2014.363
Common Etiological Factors of Attention-Deficit/Hyperactivity Disorder and Suicidal Behavior
resolves10.1017/S0033291714000361
Genetic and environmental influences on the relationship between adult ADHD symptoms and self-reported problem drinking in 6024 Dutch twins
resolves10.1016/j.biopsych.2016.02.018
Medication for Attention-Deficit/Hyperactivity Disorder and Risk for Depression: A Nationwide Longitudinal Cohort Study
resolves10.1093/hmg/ddu328
Mendelian randomization: genetic anchors for causal inference in epidemiological studies
resolves10.1111/jcpp.12475
The opposite end of the attention deficit hyperactivity disorder continuum: genetic and environmental aetiologies of extremely low
<scp>ADHD</scp>
traits
resolves10.1016/j.biopsych.2014.02.013
Genetic Risk for Attention-Deficit/Hyperactivity Disorder Contributes to Neurodevelopmental Traits in the General Population
resolves10.1016/j.jaac.2014.06.014
Attention-Deficit/Hyperactivity Disorder Polygenic Risk Scores Predict Attention Problems in a Population-Based Sample of Children
resolves10.1016/j.jaac.2015.01.010
Shared Genetic Influences Between Attention-Deficit/Hyperactivity Disorder (ADHD) Traits in Children and Clinical ADHD
resolves10.1016/j.jaac.2016.05.025
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts
resolves10.1111/jcpp.12336
Neurocognitive abilities in the general population and composite genetic risk scores for attention‐deficit hyperactivity disorder
resolves10.1016/j.jaac.2017.12.013
Working Memory and Vigilance as Multivariate Endophenotypes Related to Common Genetic Risk for Attention-Deficit/Hyperactivity Disorder
resolves10.1001/jamapsychiatry.2015.0469
Genetic and Environmental Influences on the Developmental Course of Attention-Deficit/Hyperactivity Disorder Symptoms From Childhood to Adolescence
resolves10.1001/jamapsychiatry.2016.2817
Association of Genetic Risk Variants With Attention-Deficit/Hyperactivity Disorder Trajectories in the General Population
resolves10.1017/S0033291713002493
The heritability of clinically diagnosed attention deficit hyperactivity disorder across the lifespan
resolves10.1016/j.jpsychires.2013.10.022
Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder
resolves10.1038/npp.2014.267
Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder
resolves10.1038/mp.2011.138
The genetics of attention deficit/hyperactivity disorder in adults, a review
resolves10.1038/s41467-017-02244-2
Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling
resolves10.1038/nn.4618
Analysis of genome-wide association data highlights candidates for drug repositioning in psychiatry
resolves10.1038/ng.3863
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
resolves10.1097/00004583-200207000-00012
Cytogenetic Abnormalities in Attention-Deficit/Hyperactivity Disorder
resolves10.1038/ng.2579
Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies
The 4 references without a DOI — listed, not checked
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no DOI — not checkedB28
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