| A twin study of schizoaffective‐mania, schizoaffective‐depression, and other psychotic syndromes |
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| Longevity candidate genes and their association with personality traits in the elderly |
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| <i>PLA2G6</i> mutations in PARK14‐linked young‐onset parkinsonism and sporadic Parkinson's disease |
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✓ |
✓ |
Han Chinese |
| Mutations in <i>MECP2</i> exon 1 in classical rett patients disrupt <i>MECP2_e1</i> transcription, but not transcription of <i>MECP2_e2</i> |
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| No evidence of non‐homologous insertions in mouse model of MDD created by replacement of homologous mouse DNA sequence with pathogenic 6‐base human <i>CREB1</i> promoter sequence |
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| Summaries from the XIX world congress of psychiatric genetics, Washington, DC, September 10–14, 2011 |
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| Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and At‐Risk for psychosis |
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| Association study of serotonin pathway genes in attempted suicide |
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| Genetic and environmental contributions to self‐reported thoughts of self‐harm and suicide |
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| Evaluation of conserved and ultra‐conserved non‐genic sequences in chromosome 15q15‐linked periodic catatonia |
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| SNP variants within the vanilloid<i>TRPV1</i>and<i>TRPV3</i>receptor genes are associated with migraine in the Spanish population |
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✓ |
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| Study of a possible role of the monoamine oxidase A (<i>MAOA</i>) gene in paranoid schizophrenia among a Chinese population |
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| No association of brain‐derived neurotrophic factor Val66Met polymorphism with anorexia nervosa in Japanese |
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| Association of SNPs linked to increased expression of <i>SLC1A1</i> with schizophrenia |
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✓ |
✓ |
Japanese population; Japanese individuals; Japanese control subjects |
| Homeobox genes in obsessive‐compulsive disorder |
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| Lack of association between p.Ser167Asn variant of Parkin and Parkinson's disease: A meta‐analysis of 15 studies involving 2,280 cases and 2,459 controls |
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| Mutation screening of the <i>HDC</i> gene in Chinese Han patients with Tourette syndrome |
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| Evidence for involvement of <i>GNB1L</i> in autism |
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| Sex differences in repetitive stereotyped behaviors in autism: Implications for genetic liability |
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| Phenotypic psychiatric characterization of children with Williams syndrome and response of those with ADHD to methylphenidate treatment |
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| GRIK4/KA1 protein expression in human brain and correlation with bipolar disorder risk variant status |
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| Genome‐wide association study in German patients with attention deficit/hyperactivity disorder |
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✓ |
✓ |
German (e.g., "German young patients", "independent German families") |
| A<i>CRHR1</i>haplotype moderates the effect of adverse childhood experiences on lifetime risk of major depressive episode in African‐American women |
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✓ |
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European‐Americans (EAs) |
| Genetic variation in <i>CNTNAP2</i> alters brain function during linguistic processing in healthy individuals |
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| Interaction between genetic variants of<i>DLGAP3</i>and<i>SLC1A1</i>Affecting the Risk of Atypical Antipsychotics‐Induced Obsessive–Compulsive Symptoms |
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| The genetics of antipsychotic induced tremors: A genome‐wide pathway analysis on the STEP‐BD SCP sample |
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| Association analysis of <i>ANK3</i> gene variants in nordic bipolar disorder and schizophrenia case–control samples |
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✓ |
✓ |
Scandinavian; Icelandic; Nordic |
| Similarities and differences in peripheral blood gene‐expression signatures of individuals with schizophrenia and their first‐degree biological relatives |
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| Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia |
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| Sleep apnea in fragile X premutation carriers with and without FXTAS |
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| Transcriptome‐wide gene expression in a rat model of attention deficit hyperactivity disorder symptoms: Rats developmentally exposed to polychlorinated biphenyls |
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| Association of <i>GRIN1</i> and <i>GRIN2A‐D</i> With schizophrenia and genetic interaction with maternal herpes simplex virus‐2 infection affecting disease risk |
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| Positive association of Phencyclidine‐responsive genes, <i>PDE4A</i> and <i>PLAT</i>, with schizophrenia |
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| What should be said to the lay public regarding ADHD etiology based on unbiased systematic quantitative empirical evidence |
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| What should be said to the lay public regarding ADHD etiology |
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| <i>SLC9A9</i> mutations, gene expression, and protein–protein interactions in rat models of attention‐deficit/hyperactivity disorder |
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| Indexing disease progression at study entry with individuals at‐risk for Huntington disease |
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| RE: Butler AW et al. 2010. A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. Am J Med genet part B 153B(8):1465–1473. |
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| Response to the letter from Dr. Maher and colleagues Re. Linkage on suicidality |
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| Mutation screening of the 3q29 microdeletion syndrome candidate genes <i>DLG1</i> and <i>PAK2</i> in schizophrenia |
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| Erratum to “Genome‐wide association analysis of age at onset and psychotic symptoms in bipolar disorder”, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics”, April 1; 156(3):370–3 |
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| Borderline personality traits and adult attention‐deficit hyperactivity disorder symptoms: A genetic analysis of comorbidity |
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| Association between <i>TCF4</i> and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing <i>cis</i>‐acting regulation of mRNA expression in adult human brain |
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| Genome scan of age‐at‐onset in the NIMH Alzheimer disease sample uncovers multiple loci, along with evidence of both genetic and sample heterogeneity |
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| Distinct <i>De Novo</i> deletions in a brother–sister pair with RTT: A case report |
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| No evidence that extended tracts of homozygosity are associated with Alzheimer's disease |
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| Linkage analyses of stimulant dependence, craving, and heavy use in American Indians |
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✓ |
✓ |
American Indian |
| A loss‐of‐function mutation in the <i>SLC9A6</i> gene causes X‐linked mental retardation resembling Angelman syndrome |
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| Genomic architecture of aggression: Rare copy number variants in intermittent explosive disorder |
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| Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the <i>CA8</i> gene, encoding carbonic anhydrase (CA) VIII |
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| Dopamine β‐hydroxylase gene associates with stroop color‐word task performance in Han Chinese children with attention deficit/hyperactivity disorder |
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✓ |
✓ |
Han Chinese |
| Association analyses of <i>MAOA</i> in Chinese Han subjects with attention‐deficit/hyperactivity disorder: Family‐based association test, case–control study, and quantitative traits of impulsivity |
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✓ |
✓ |
Chinese Han |
| Association between polymorphisms of <i>DRD2</i> and <i>DRD4</i> and opioid dependence: Evidence from the current studies |
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| Sleep quality and diurnal preference in a sample of young adults: Associations with <i>5HTTLPR</i>, <i>PER3</i>, and <i>CLOCK 3111</i> |
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| Differential immune system DNA methylation and cytokine regulation in post‐traumatic stress disorder |
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| ATP13A2 variability in Taiwanese Parkinson's disease |
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| Functional assessment of a promoter polymorphism in S100B, a putative risk variant for bipolar disorder |
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✓ |
✓ |
Irish and German subjects |
| No association observed between schizophrenia and non‐HLA coeliac disease genes: Integration with the initial MYO9B association with coeliac disease |
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| Genome‐wide association analysis of age at onset in schizophrenia in a European‐American sample |
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|
✓ |
✓ |
|
|
European‐American sample |
| No association between a common single nucleotide polymorphism, rs4141463, in the <i>MACROD2</i> gene and autism spectrum disorder |
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| Association between polymorphisms in catechol‐<i>O</i>‐methyltransferase (<i>COMT</i>) and cocaine‐induced paranoia in European‐American and African‐American populations |
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|
✓ |
✓ |
|
|
European‐American (EA) |
| A follow‐up case–control association study of tractable (druggable) genes in recurrent major depression |
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✓ |
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✓ |
✓ |
white German origin; ethnically matched controls |
| Misunderstandings of the genetics and neurobiology of ADHD: Moving beyond anachronisms |
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| Hypomethylation of the serotonin receptor type‐2A Gene (HTR2A) at T102C polymorphic site in DNA derived from the saliva of patients with schizophrenia and bipolar disorder |
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| Replacement of homologous mouse DNA sequence with pathogenic 6‐base human <i>CREB1</i> promoter sequence creates murine model of major depressive disorder |
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| Novel pathogenic mutations and copy number variations in the <i>VPS13A</i> Gene in patients with chorea‐acanthocytosis |
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| Converging evidence implicates the dopamine D3 receptor gene in vulnerability to schizophrenia |
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|
✓ |
✓ |
✓ |
European populations; East Asian population; Han Chinese population |
| Ethnic disparities in the perception of ethical risks from psychiatric genetic studies |
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✓ |
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| Exploring <i>DRD4</i> and its interaction with <i>SLC6A3</i> as possible risk factors for adult ADHD: A meta‐analysis in four European populations |
|
✓ |
|
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✓ |
✓ |
|
|
four European populations; from four European countries |
| Association study of Nogo‐related genes with schizophrenia in a Japanese case–control sample |
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|
✓ |
✓ |
Japanese population; different populations |
| The relationship of deiodinase 1 genotype and thyroid function to lifetime history of major depression in three independent populations |
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✓ |
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| Common genetic influences on depression, alcohol, and substance use disorders in Mexican‐American families |
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|
✓ |
✓ |
Mexican-American; Mexican ancestry |
| The familial association of tourette's disorder and ADHD: The impact of OCD symptoms |
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| Analysis of neurogranin (<i>NRGN</i>) in schizophrenia |
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| Replication study of genome‐wide associated SNPs with late‐onset Alzheimer's disease |
|
✓ |
|
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✓ |
✓ |
Caucasian Americans |
| A twin study of genetic and environmental determinants of abnormal persistence of psychotic experiences in young adulthood |
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| Using linkage information to weight a genome‐wide association of bipolar disorder |
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| Non‐syndromic language delay in a child with disruption in the Protocadherin11X/Y gene pair |
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| Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21 |
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| In memoriam: Terje Sagvolden |
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| Comprehensive family‐based association study of the glutamate transporter gene SLC1A1 in obsessive‐compulsive disorder |
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|
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| Association of <i>CHRNA4</i> polymorphisms with smoking behavior in two populations |
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|
✓ |
✓ |
✓ |
European‐Americans (EAs); African‐Americans (AAs); race |
| White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism |
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| DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls |
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| <i>P2RX7</i> gene is associated consistently with mood disorders and predicts clinical outcome in three clinical cohorts |
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| Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activity |
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| Association of <i>RGS2</i> variants with panic disorder in a Japanese population |
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| Dysfunctional gene splicing as a potential contributor to neuropsychiatric disorders |
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| Absence of association between specific common variants of the obesity‐related FTO gene and psychological and behavioral eating disorder phenotypes |
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| The association between family history of mental disorder and delusional‐like experiences: A general population study |
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| <i>PARK2</i> copy number aberrations in two children presenting with autism spectrum disorder: Further support of an association and possible evidence for a new microdeletion/microduplication syndrome |
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| Association of catechol‐<i>O</i>‐methyl transferase (COMT) gene −287A/G polymorphism with susceptibility to obsessive–compulsive disorder in Chinese Han population |
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|
|
| Dysbindin‐1 gene contributes differentially to early‐ and adult‐onset forms of functional psychosis |
|
✓ |
|
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|
|
| Genome‐wide association analysis of age at onset and psychotic symptoms in bipolar disorder |
|
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| Age at onset of psychotic disorder: Cannabis, BDNF Val66Met, and sex‐specific models of gene–environment interaction |
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| ADHD in Dutch adults: Heritability and linkage study |
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| Familial transmission of schizophrenia in Palau: A 20‐year genetic epidemiological study in three generations |
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| Variation in <i>NGFB</i> is associated with primary affective disorders in women |
|
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|
|
✓ |
|
|
European‐Americans (EAs) |
| Markers in the 15q24 nicotinic receptor subunit gene cluster (CHRNA5‐A3‐B4) predict severity of nicotine addiction and response to smoking cessation therapy |
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| Association of GWAS loci with PD in China |
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| Mutations in the <i>TSGA14</i> gene in families with autism spectrum disorders |
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| Evaluation of risk loci for schizophrenia derived from genome-wide association studies in a German population |
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| Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia |
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| Influence of a genetic variant of the neuronal growth associated protein Stathmin 1 on cognitive and affective control processes: An event‐related potential study |
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| Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder |
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| Mutational analysis reveals the <i>FUS</i> homolog <i>TAF15</i> as a candidate gene for familial amyotrophic lateral sclerosis |
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| Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and age of onset in schizophrenia: A combined analysis of independent samples |
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| Effect of model choice in genetic association studies: DRD4 exon III VNTR and cigarette use in young adults |
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| Autism spectrum disorders and autistic traits: A decade of new twin studies |
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| Association of <i>ANK3</i> with bipolar disorder confirmed in East Asia |
|
✓ |
|
|
|
|
✓ |
✓ |
Asian; Korean; Japanese; Han‑Chinese; Taiwan; ethnicities |
| Glucocorticoid receptor haplotype is associated with a decreased risk of delirium in the elderly |
|
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| A phenotype‐based genetic association study reveals the contribution of neuregulin1 gene variants to age of onset and positive symptom severity in schizophrenia |
|
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|
✓ |
✓ |
Icelandic; comparable ethnicity |
| Narrowing the critical deletion region for autism spectrum disorders on 16p11.2 |
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