| An investigation of the neurotrophic factor genes <i>GDNF</i>, <i>NGF</i>, and <i>NT3</i> in susceptibility to ADHD |
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| <i>HTR2C</i> and <i>HTR1A</i> gene variants in German and Italian suicide attempters and completers |
|
✓ |
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|
✓ |
✓ |
German; Italian |
| Tumor necrosis factor‐α promoter polymorphism is associated with the risk of Parkinson's disease |
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| Association study between the TNXB locus and schizophrenia in a Japanese population |
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| Association of dopamine transporter genotype with disruptive behavior disorders in an eight‐year longitudinal study of children and adolescents |
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| The <i>MAOA</i> T941G polymorphism and short‐term treatment response to mirtazapine and paroxetine in major depression |
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| Synaptotagmin XI as a candidate gene for susceptibility to schizophrenia |
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| Sensory gating and alpha‐7 nicotinic receptor gene allelic variants in schizoaffective disorder, bipolar type |
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| Effect of 5‐haplotype of dysbindin gene (<i>DTNBP1</i>) polymorphisms for the susceptibility to bipolar I disorder |
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| Linkage of schizophrenia with chromosome 1q32 in Korean multiplex families' |
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✓ |
✓ |
Korean population |
| Association analysis of the protein phosphatase 1 regulatory subunit 1B (<i>PPP1R1B</i>) gene with nicotine dependence in European‐ and African‐American smokers |
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✓ |
✓ |
|
|
European‐American (EA) |
| Sequence variants within exon 1 of <i>MECP2</i> occur in females with mental retardation |
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| Oligodendroglial transcription factor (OLIG1 and OLIG2) mutations are not associated with Pelizaeus–Merzbacher‐like leukodystrophy |
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| Cyclooxygenase‐2 polymorphisms in Parkinson's disease |
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✓ |
✓ |
Swedish population |
| Association of the dopamine receptor D4 (<i>DRD4</i>) gene 7‐repeat allele with children with attention‐deficit/hyperactivity disorder (ADHD): An update |
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| Preliminary evidence for linkage to chromosome 1q31‐32, 10q23.3, and 16p13.3 in a South African cohort with bipolar disorder |
|
✓ |
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|
✓ |
✓ |
Afrikaner and British origin |
| Dopaminergic polymorphisms in Tourette syndrome: Association with the DAT gene (<i>SLC6A3</i>) |
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| <i>HOXA1</i> gene variants influence head growth rates in humans |
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| No significant association between response to methylphenidate and genes of the dopaminergic and serotonergic systems in a sample of Brazilian children with attention‐deficit/hyperactivity disorder |
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| No association between the Ser9Gly polymorphism of the dopamine D3 receptor gene and schizophrenia in a Spanish sample |
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|
✓ |
✓ |
Spanish |
| Association between the 120‐bp duplication of the dopamine D4 receptor gene and attention deficit hyperactivity disorder: Genetic and molecular analyses |
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| Evaluation of association of SNPs in the TNF alpha gene region with schizophrenia |
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| The serotonin 5‐HT1D receptor gene and attention‐deficit hyperactivity disorder in Chinese Han subjects |
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✓ |
✓ |
Chinese Han; Chinese ethnicity |
| Addiction molecular genetics: 639,401 SNP whole genome association identifies many “cell adhesion” genes |
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| Obsessive‐compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene |
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| Homozygosity of the interleukin‐10 receptor 1 G330R allele is associated with schizophrenia |
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✓ |
✓ |
Austrian; German |
| Haplotype association study between <i>DRD1</i> gene and bipolar type I affective disorder in two samples from Canada and Sardinia |
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✓ |
✓ |
Sardinian origin; samples originating from different ethnic backgrounds; samples from Canada and Sar |
| A resistance gene in disguise for schizophrenia? |
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| Synergistic association of mitochondrial uncoupling protein (UCP) genes with schizophrenia |
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| The 5‐HTTLPR s/s genotype at the serotonin transporter gene (SLC6A4) increases the risk for depression in a large cohort of primary care attendees: The PREDICT‐gene study |
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|
✓ |
✓ |
Spanish |
| Evaluation of potential gene–gene interactions for attention deficit hyperactivity disorder in the Han Chinese population |
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✓ |
✓ |
Han Chinese population |
| Family‐based association study between brain‐derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples |
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| Association between the 5q31.1 gene neurogenin1 and schizophrenia |
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✓ |
✓ |
Irish |
| Mutation screening of the <i>ARX</i> gene in patients with autism |
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| A genome‐wide scan for schizophrenia and psychosis susceptibility loci in families of Mexican and Central American ancestry |
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|
✓ |
✓ |
Mexican and Central American ancestry; emigrants from the Spanish empire |
| A promoter polymorphism (−839 C > T) at the dopamine transporter gene is associated with attention deficit/hyperactivity disorder in Brazilian children |
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| <i>IGF1</i>, growth pathway polymorphisms and schizophrenia: A pooling study |
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|
✓ |
✓ |
UK and Irish; Bulgarian |
| Persistence problem in schizophrenia and mitochondrial DNA |
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| The Palau early psychosis study: Distribution of cases by level of genetic risk |
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| Schizophrenic‐like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome |
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| No association between ADRA2A polymorphisms and schizophrenia |
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| Adolescent girls and criminal activity: Role of MAOA‐LPR genotype and psychosocial factors |
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| Follow‐up mapping supports the evidence for linkage in the candidate region at 9q22 in the NIMH Alzheimer's disease Genetics Initiative cohort |
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| Adjudicating neurocognitive endophenotypes for schizophrenia |
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| Glutathione S‐transferase polymorphisms and onset age in α‐synuclein A53T mutant Parkinson's disease |
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|
✓ |
✓ |
Italian or Greek origin |
| Mutation screen of the <i>GAD2</i> gene and association study of alcoholism in three populations |
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|
✓ |
✓ |
✓ |
European–American (EA); Russian |
| Schizotypal dimensions: An intermediate phenotype associated with the COMT high activity allele |
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| Case‐control and within‐family tests for an association between conduct disorder and 5HTTLPR |
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| Perceived parenting behavior in the childhood of cocaine users: Relationship with genotype and personality traits |
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| Positive association of schizophrenia to <i>JARID2</i> gene |
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| Association of tagSNPs in the urokinase‐plasminogen activator (PLAU) gene with Alzheimer's disease and associated quantitative traits |
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|
✓ |
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| Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins |
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| XIV World Congress on Psychiatric Genetics, October 28th–November 1st, 2006 Congress Centre Fiera Internazionate della Sardegna, Cagliari, Italy |
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| Analysis of the 5HT‐2A T102C receptor polymorphism and psychotic symptoms in Alzheimer's disease |
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| Schizophrenia is not associated with the functional candidate gene <i>ERBB3</i>: Results from a case‐control study |
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| Association of the human kainate receptor <i>GluR7</i> gene (<i>GRIK3</i>) with recurrent major depressive disorder |
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| Serotonin genes and attention deficit/hyperactivity disorder in a Brazilian sample: Preferential transmission of the HTR2A 452His allele to affected boys |
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| Evidence of linkage to psychosis on chromosome 5q33‐34 in pedigrees ascertained for bipolar disorder |
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| Autistic‐spectrum disorders in down syndrome: Further delineation and distinction from other behavioral abnormalities |
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| Family‐based association study of TPH1 and TPH2 polymorphisms in autism |
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| Allelic association of a truncation mutation of the <i>KCNMB3</i> gene with idiopathic generalized epilepsy |
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|
✓ |
✓ |
German |
| The genomic era and perceptions of psychotic disorders: Genetic risk estimation, associations with reproductive decisions and views about predictive testing |
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| The role of <i>RELN</i> in lissencephaly and neuropsychiatric disease |
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| Serotonin transporter mRNA levels are associated with the methylation of an upstream CpG island |
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| Further evidence of MAO‐A gene variants associated with bipolar disorder |
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| Recurrence risk to offspring in extended multiplex schizophrenia pedigrees from a pacific island isolate |
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|
✓ |
|
|
Western European families |
| The serotonin receptor HTR1B: Gene polymorphisms in attention deficit hyperactivity disorder |
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|
| A genetic cluster of early onset Parkinson's disease in a Colombian population |
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|
✓ |
✓ |
Spanish ancestry / Spanish immigrants / Spanish family; Spanish family; Spanish immigrants; Antioquia (Colombia) population |
| Evidence of linkage and association on 18p11.2 for psychosis |
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|
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| Association between polymorphisms in serotonin transporter gene and attention deficit hyperactivity disorder in Chinese Han subjects |
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|
✓ |
✓ |
Chinese Han |
| <i>CHMP2B</i> mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia |
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| Reelin gene polymorphisms in the Indian population: A possible paternal 5′UTR‐CGG‐repeat‐allele effect on autism |
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| Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism |
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| Cannabis receptor haplotype associated with fewer cannabis dependence symptoms in adolescents |
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| Exon 3 polymorphisms of dopamine D4 receptor (DRD4) gene and attention deficit hyperactivity disorder in Chinese children |
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|
✓ |
✓ |
Chinese |
| Catechol‐<i>O</i>‐methyltransferase and the clinical features of psychosis |
|
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|
✓ |
✓ |
Irish |
| A genome‐wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba |
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|
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| Absence of association with DAT1 polymorphism and response to methylphenidate in a sample of adults with ADHD |
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| Possible role of preproghrelin gene polymorphisms in susceptibility to bulimia nervosa |
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| Association between the interleukin‐1 receptor antagonist gene and negative symptom improvement during antipsychotic treatment† |
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|
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| Possible involvement of alpha‐2A adrenergic receptors in attention deficit hyperactivity disorder: Radioligand binding and polymorphism studies |
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|
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| Pooled association genome scanning for alcohol dependence using 104,268 SNPs: Validation and use to identify alcoholism vulnerability loci in unrelated individuals from the collaborative study on the |
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|
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| Linkage disequilibrium, haplotype and association studies of a chromosome 4 GABA receptor gene cluster: Candidate gene variants for addictions |
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|
|
| A review and re‐evaluation of an association between the NOTCH4 locus and schizophrenia |
|
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|
|
✓ |
✓ |
British population; Chinese population; ethnical backgrounds |
| Dimensional anxiety mediates linkage of <i>GABRA2</i> haplotypes with alcoholism |
|
✓ |
|
|
|
|
✓ |
✓ |
Finnish; Finns |
| Accelerated evolution of <i>Protocadherin11X/Y</i>: A candidate gene‐pair for cerebral asymmetry and language |
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|
|
| Abnormalities of cholesterol metabolism in autism spectrum disorders |
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|
|
| <i>MAOA</i> promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children |
|
|
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|
|
|
✓ |
✓ |
Indian; ethnically matched controls |
| Genome‐wide linkage analysis of heroin dependence in Han Chinese: Results from wave one of a multi‐stage study |
|
|
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|
|
|
✓ |
✓ |
Han Chinese |
| Association study of seven polymorphisms in four serotonin receptor genes on suicide victims |
|
|
|
|
|
|
✓ |
✓ |
Slovenian population |
| Gene for the serotonin transporter and ADHD: No association with two functional polymorphisms |
|
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|
|
| Rh and ABO maternal‐fetal incompatibility and risk of autism |
|
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|
|
| Interleukin‐1 Gene Complex in Schizophrenia: An Association Study* |
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|
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| PhenoChipping of psychotic disorders: A novel approach for deconstructing and quantitating psychiatric phenotypes |
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|
|
| Analysis of the dopamine beta hydroxylase gene in Gilles de la tourette syndrome |
|
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|
|
| Adult‐onset autosomal dominant leukodystrophy with autonomic symptoms restricted to 1.5 Mbp on chromosome 5q23 |
|
|
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|
|
|
✓ |
✓ |
Swedish origin |
| Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder |
|
|
|
|
|
|
✓ |
✓ |
ethnically matched healthy controls; German population |
| An association study of the brain‐derived neurotrophic factor Val66Met polymorphism and amphetamine response |
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|
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| Prevalence of psychiatric disorders in 4 to 16‐year‐olds with Williams syndrome |
|
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|
|
| Association study of CHRFAM7A copy number and 2bp deletion polymorphisms with schizophrenia and bipolar affective disorder |
|
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|
|
| Screening of subtelomeric rearrangements in autistic disorder: Identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation |
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|
|
| Exploring an interaction of adenosine A2A receptor variability with coffee and tea intake in Parkinson's disease |
|
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|
|
| Bad luck: An unappreciated limitation in the interpretation of twin studies |
|
|
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|
|
| Ethnicity‐dependent genetic association of <i>ABCA2</i> with sporadic Alzheimer's disease |
|
✓ |
|
|
|
✓ |
|
|
Western European |
| Stratification based on language‐related endophenotypes in autism: Attempt to replicate reported linkage |
|
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|
|
| Clinical and genetic uniqueness in an individual with MELAS |
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|
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| Three major haplotypes of the β<sub>2</sub> adrenergic receptor define psychological profile, blood pressure, and the risk for development of a common musculoskeletal pain disorder |
|
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|
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| Contribution of 5‐HT2A receptor gene ‐1438A>G polymorphism to outcome of attention‐deficit/hyperactivity disorder in adolescents |
|
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|
|
| An examination of the behavioral and neuropsychological correlates of three ADHD candidate gene polymorphisms (DRD4 7+, DBH TaqI A2, and DAT1 40 bp VNTR) in hyperactive and normal children followed to |
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|
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| BDNF gene variants and brain morphology in schizophrenia |
|
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|
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| Methylation of two<i>Homo sapiens</i>‐specific X‐Y homologous genes in Klinefelter's syndrome (XXY) |
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|
|
| No association between low density lipoprotein receptor genetic variants and Alzheimer's disease risk |
|
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|
|
|
✓ |
✓ |
Spanish |
| Transmission distortion of <i>BDNF</i> variants to bipolar disorder type I patients from a south american population isolate<sup>,</sup> |
|
|
|
|
|
|
✓ |
✓ |
South American population isolate (Antioquia, Colombia) |
| Chronological age, but not FMRP levels, predicts neuropsychological performance in girls with fragile X syndrome |
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|
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| Angiotensin‐converting enzyme and angiotensin II type 1 receptor gene polymorphisms in children with subacute sclerosing panencephalitis |
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|
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| Further evidence of a maternal parent‐of‐origin effect on chromosome 10 in late‐onset Alzheimer's disease |
|
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|
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| Lack of influence of COMT and NET genes variants on executive functions in schizophrenic and bipolar patients, their first‐degree relatives and controls |
|
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|
|
| A family‐based and case‐control association study of <i>SOX10</i> in schizophrenia |
|
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|
✓ |
✓ |
Japanese |
| LRRK2 G2019S and I2020T mutations are not common in Alzheimer's disease and vascular dementia |
|
|
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|
|
|
|
|
|
| Association study of the <i>CNR1</i> gene exon 3 alternative promoter region polymorphisms and substance dependence |
|
|
|
|
|
✓ |
✓ |
✓ |
European‐American; African‐American |
| Association analyses suggest <i>GPR24</i> as a shared susceptibility gene for bipolar affective disorder and schizophrenia |
|
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|
|
| Association analysis of δ‐opioid receptor gene polymorphisms in methamphetamine dependence/psychosis |
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|
|
| A Meniere's disease gene linked to chromosome 12p12.3 |
|
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|
|
✓ |
✓ |
Swedish family |
| A genome‐wide screen for nicotine dependence susceptibility loci |
|
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|
|
| Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder |
|
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|
|
|
|
✓ |
✓ |
French Canadian population |
| Klinefelter's syndrome (XXY) as a genetic model for psychotic disorders. Am J Medical Genetics Part B (Neuropsychiatric Genetics) 135B: 15–23 (2005) |
|
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| Model averaging in linkage analysis |
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|
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| When is a “Positive” association truly a “Positive” in psychiatric genetics? A commentary based on issues debated at the World Congress of Psychiatric Genetics, Boston, October 12–18, 2005 |
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|
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| Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder |
|
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|
|
| Brain derived neurotrophic factor (<i>BDNF</i>) gene variants and Alzheimer's disease, affective disorders, posttraumatic stress disorder, schizophrenia, and substance dependence |
|
|
|
|
|
✓ |
|
|
European American (EA) subjects |
| A cautionary note on the use of simulation procedures for analyzing contingency tables containing small expected cell frequencies |
|
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|
|
| Genetic overlap between P300, P50, and duration mismatch negativity |
|
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|
|
| “Association study of a functional promoter polymorphism in the <i>XBP1</i> gene and schizophrenia,” American Journal Of Medical Genetics Part B (Neuropsychiatric Genetics) 141B:71–75 (2006) |
|
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|
|
| Association of AKT1 haplotype with the risk of schizophrenia in Iranian population |
|
|
|
|
|
✓ |
|
|
Northern European origin |
| A family‐based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron‐2 (STin2) polymorphism and attention‐deficit‐hyperactivity disorder (ADHD) |
|
|
|
|
|
|
✓ |
✓ |
"Indian subjects from Kolkata" and the phrase "other ethnic groups" |
| Preliminary evidence for an association between a dopamine D3 receptor gene variant and obsessive‐compulsive personality disorder in patients with major depression |
|
|
|
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|
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|
|
| Weight gain associated with the α<sub>2a</sub>‐adrenergic receptor −1291 C/G polymorphism and olanzapine treatment |
|
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|
|
|
|
| Haplotype analysis of single nucleotide polymorphisms in <i>VEGF</i> gene for vascular dementia |
|
|
|
|
|
|
✓ |
✓ |
Koreans |
| The fourth <i>apolipoprotein E</i> haplotype found in the Yoruba of Ibadan |
|
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|
|
| Factor analysis of obsessive–compulsive disorder YBOCS‐SC symptoms and association with 5‐HTTLPR SERT polymorphism |
|
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| Comment on the use of genetic findings on schizophrenia |
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| Future ethical use of genetic findings on schizophrenia: Comments on data interpretation, and support for conclusions |
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| Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol‐O‐methyltransferase (<i>COMT</i>) gene |
|
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|
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| Association between the <i>DRD2</i> A<sub>1</sub> allele and response to methadone and buprenorphine maintenance treatments |
|
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|
|
| Suggestive evidence for association of the circadian genes <i>PERIOD3</i> and <i>ARNTL</i> with bipolar disorder |
|
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|
|
| [<sup>18</sup>F]FDOPA PET as an endophenotype for Parkinson's Disease linkage studies |
|
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|
|
|
|
✓ |
✓ |
Amish |
| The effect of dopamine D2, D5 receptor and transporter (SLC6A3) polymorphisms on the cue‐elicited heroin craving in Chinese |
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✓ |
✓ |
Chinese |
| Evaluation of <i>RGS4</i> as a candidate gene for schizophrenia |
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| Glutamate AMPA receptor subunit 1 gene (<i>GRIA1</i>) and DSM‐IV‐TR schizophrenia: A pilot case‐control association study in an Italian sample |
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| Lack of association between UBQLN1 and Alzheimer disease |
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| Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population |
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| Intergeneration CAG expansion and contraction in a Chinese HD family |
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✓ |
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| Evaluating the comparability of gene expression in blood and brain |
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| Association of the DAT1 polymorphism with attention deficit hyperactivity disorder (ADHD): A family‐based approach |
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✓ |
✓ |
Korean; Asian populations |
| Smoking cessation, weight gain, and <i>DRD4</i> −521 genotype |
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| MAOA‐uVNTR polymorphism in a Brazilian sample: Further support for the association with impulsive behaviors and alcohol dependence |
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✓ |
|
|
Brazilian alcoholics of European descent |
| Association study of the adrenergic receptors and childhood‐onset mood disorders in Hungarian families |
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| Array‐based genomic delineation of a familial duplication 11q14.1–q22.1 associated with recurrent depression |
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| Validation of population‐based ADHD subtypes and identification of three clinically impaired subtypes |
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| The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura |
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| Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G‐protein signaling 4 protein (<i>RGS4</i>) |
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| Haplotype‐based systematic association studies of <i>ATP1A2</i> in migraine with aura |
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| Association of mitochondrial complex I subunit gene <i>NDUFV2</i> at 18p11 with schizophrenia in the Japanese population |
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✓ |
✓ |
Japanese population / Japanese |
| Absence of coding mutations in the X‐linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection |
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| A gender‐moderated effect of a functional <i>COMT</i> polymorphism on prefrontal brain morphology and function in velo‐cardio‐facial syndrome (22q11.2 deletion syndrome) |
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| A point mutation at the calreticulin gene core promoter conserved sequence in a case of schizophrenia |
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| Evidence that variation in the peripheral benzodiazepine receptor <i>(PBR)</i> gene influences susceptibility to panic disorder |
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| The OCD collaborative genetics study: Methods and sample description |
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| Negative perceived paternal parenting is associated with dopamine D<sub>2</sub> receptor exon 8 and GABA(A) alpha 6 receptor variants: An explorative study |
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| Investigation of the phenylalanine hydroxylase gene and tardive dyskinesia |
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| No association between VNTR polymorphisms of dopamine transporter gene and attention deficit hyperactivity disorder in Chinese children |
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|
✓ |
✓ |
Chinese |
| The involvement of <i>ErbB4</i> with schizophrenia: Association and expression studies |
|
✓ |
|
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✓ |
✓ |
Ashkenazi |
| A novel homeobox mutation in the<i>PITX2</i>gene in a family with Axenfeld‐Rieger syndrome associated with brain, ocular, and dental phenotypes |
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| Comments on MCP‐1 gene (<i>SCYA2</i>) and schizophrenia: A case‐control association study |
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| A genome‐wide linkage analysis of dementia in the Amish |
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✓ |
✓ |
Amish population; North American Amish community; relatively isolated, genetically homogeneous, Amis |
| Possible association of the alpha‐2A adrenergic receptor gene (<i>ADRA2A</i>) with symptoms of attention‐deficit/hyperactivity disorder |
|
✓ |
|
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|
✓ |
✓ |
Han Chinese population; Chinese |
| Association between tryptophan hydroxylase gene polymorphisms and attention deficit hyperactivity disorder in Chinese Han population |
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✓ |
✓ |
Chinese Han population |
| Hyperprolinemia is not associated with childhood onset schizophrenia |
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| CAG repeats in restless legs syndrome |
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| The Val66Met polymorphism of the brain‐derived neurotrophic factor gene is associated with risk for psychosis: Evidence from a family‐based association study |
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| Characteristics of the broader phenotype in autism: A study of siblings using the children's communication checklist‐2 |
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| The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database |
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| TPH gene polymorphism and aging: Indication of combined effect on the predisposition to violent suicide |
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✓ |
✓ |
Slavic (Croatian) origin |
| The Cys allele of the <i>DRD2</i> Ser311Cys polymorphism has a dominant effect on risk for schizophrenia: Evidence from fixed‐ and random‐effects meta‐analyses |
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| Genetic association between schizophrenia and the DISC1 gene in the Scottish population |
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✓ |
✓ |
Scottish population |
| XYY chromosome abnormality in sexual homicide perpetrators |
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