| Genetic heterogeneity in ADHD: <i>DAT1</i> gene only affects probands without CD |
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| Gene copy number variation in schizophrenia |
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✓ |
✓ |
large ethnic differences cannot be excluded |
| PRODH gene is associated with executive function in schizophrenic families |
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| Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): Analysis of data from the international multicenter ADHD genetics (IMAGE) program |
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| Association study of two polymorphisms of the serotonin‐2A receptor gene and suicide attempts |
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| New functional single nucleotide polymorphism (Ala72Ser) in the COMT gene is associated with aggressive behavior in male schizophrenia |
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| Family‐based SNP association study on 8q24 in bipolar disorder |
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| Association study between the serotonin 1A receptor (HTR1A) gene and neuroticism, major depression, and anxiety disorders |
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| Association of the dopamine transporter gene and ADHD symptoms in a Canadian population‐based sample of same‐age twins |
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| Suggestive linkage of a chromosomal locus on 18p11 to cyclothymic temperament in bipolar disorder families |
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| Genetic analyses of dopamine related genes in adult ADHD patients suggest an association with the DRD5‐microsatellite repeat, but not with DRD4 or SLC6A3 VNTRs |
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|
✓ |
✓ |
Norwegian; ethnically matched controls |
| Linkage analysis of attention deficit hyperactivity disorder |
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| Up‐regulation of<i>ADM</i>and<i>SEPX1</i>in the lymphoblastoid cells of patients in monozygotic twins discordant for schizophrenia |
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✓ |
✓ |
Japanese population |
| Association study for genes at chromosome 5p13‐q11 in attention deficit hyperactivity disorder |
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| Evidence for association between genetic variants of <i>p75 neurotrophin receptor</i> (<i>p75</i><sup><i>NTR</i></sup>) gene and antidepressant treatment response in chinese major depressive disorder |
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| No association of genetic variants of liver X receptor‐β with alzheimer's disease risk |
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✓ |
✓ |
Spanish |
| Comprehensive evaluation of positional candidates in the IL‐18 pathway reveals suggestive associations with schizophrenia and herpes virus seropositivity |
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| Controlling false discoveries in genetic studies |
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| Catechol‐<i>O</i>‐methyltransferase<i>Val158Met</i>polymorphism and clinical characteristics in first episode non‐affective psychosis |
|
✓ |
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| The new neuropsychiatric genetics |
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| A twin study of the common vulnerability between heightened sensitivity to hypercapnia and panic disorder |
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| No evidence for interaction between <i>MAOA</i> and childhood adversity for antisocial behavior |
|
✓ |
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| A phenotype for genetic studies of successful cognitive aging* |
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| Psychiatric genetic testing: Attitudes and intentions among future users and providers |
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| Intelligence in DSM‐IV combined type attention‐deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention‐d |
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| The relationship of <i>5HTT</i> (<i>SLC6A4</i>) methylation and genotype on mRNA expression and liability to major depression and alcohol dependence in subjects from the Iowa Adoption Studies |
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| A genome‐wide linkage study in families with major depression and co‐morbid unexplained swelling |
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| Gene–Environment interactions in the development of combined type ADHD: Evidence for a synapse‐based model |
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| Divergent backward masking performance in schizophrenia and bipolar disorder: Association with COMT |
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| The association analysis of RELN and GRM8 genes with autistic spectrum disorder in chinese han population |
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✓ |
✓ |
chinese han population |
| Response to methylphenidate in adults with ADHD is associated with a polymorphism in <i>SLC6A3 (DAT1)</i> |
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| A polymorphism at the 3′‐untranslated region of the <i>CLOCK</i> gene is associated with adult attention‐deficit hyperactivity disorder |
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| Replication study and meta‐analysis of the genetic association of GRM3 gene polymorphisms with schizophrenia in a large Japanese case‐control population |
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✓ |
✓ |
Japanese, Chinese |
| Heterogeneous association between engrailed‐2 and autism in the CPEA network |
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✓ |
✓ |
similar ethnicity |
| Dopa decarboxylase and tyrosine hydroxylase gene variants in suicidal behavior |
|
✓ |
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✓ |
✓ |
German |
| Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease |
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| No evidence for genetic association between DARPP‐32 (<i>PP1R1B</i>) polymorphisms and attention deficit hyperactivity disorder |
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| Is MYO9B the missing link between schizophrenia and celiac disease? |
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| Association study of the brain‐derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder |
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| The monoamine oxidase B gene exhibits significant association to ADHD |
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| Genetic and environmental contributions to stability in loneliness throughout childhood |
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✓ |
✓ |
Dutch |
| Alpha‐synuclein promoter haplotypes and dementia in Parkinson's Disease |
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|
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| <i>ADH7</i> variation modulates extraversion and conscientiousness in substance‐dependent subjects |
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|
✓ |
✓ |
✓ |
European‐Americans (EAs); European‐Americans (EAs); African‐Americans (AAs); ancestry‐informative markers |
| The functional polymorphism of the hemoglobin‐binding protein haptoglobin influences susceptibility to idiopathic Parkinson's disease |
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| Genetic Association of Neurotrophic Tyrosine Kinase Receptor Type 2 (<i>NTRK2</i>) With Alzheimer's Disease |
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| Meta‐study on association between the monoamine oxidase A gene (<i>MAOA</i>) and schizophrenia |
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| Association of the <i>SLC1A1</i> glutamate transporter gene and obsessive‐compulsive disorder |
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| Autism‐related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism |
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| An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD |
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| Haplotype analysis confirms association of the serotonin transporter (5‐HTT) gene with schizophrenia but not with major depression |
|
✓ |
|
|
|
✓ |
|
|
North European Caucasians |
| Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib‐pair collection |
|
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|
|
✓ |
✓ |
Dutch |
| Executive function and genetic predisposition to schizophrenia—the Maudsley family study |
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| Genetics of tension‐type headache: A population based twin study |
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| Dopamine beta‐hydroxylase (DBH) activity and ‐1021C/T polymorphism of <i>DBH</i> gene in combat‐related post‐traumatic stress disorder |
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| Sequence variants within exon 1 of <i>MECP2</i> occur in females with mental retardation. Am J Medical Genetics Part B (Neuropsychiatric Genetic) 144B:355–360 (2007) |
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| Genome‐wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13 |
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|
|
✓ |
✓ |
Arab Israeli |
| Lack of supporting evidence for a genetic association of the <i>FKBP5</i> polymorphism and response to antidepressant treatment |
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| A coalescent simulation of marker selection strategy for candidate gene association studies |
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| An association study of RGS4 polymorphisms with clinical phenotypes of schizophrenia in a Chinese population |
|
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|
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|
|
✓ |
✓ |
Han Chinese descent |
| Dissocial behavior, the 5HTTLPR polymorphism, and maltreatment in women with bulimic syndromes |
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|
|
| No association between common variants in glyoxalase 1 and autism spectrum disorders |
|
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|
|
|
|
✓ |
✓ |
Finnish population |
| Evidence of normal hearing laterality in familial schizophrenic patients and their relatives |
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|
| The ADHD resource: Creation of an online tool for attention deficit hyperactivity disorder information and research |
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| Zhang F, Sarginson J, Crombie C, Walker N, StClair D, Shaw D. Genetic Association Between Schizophrenia and the DISC1 Gene in the Scottish Population. Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5 |
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| Heritability of cognitive functions in families with bipolar disorder |
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|
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| Genetic association studies of the chromosome 15 GABA‐A receptor cluster in migraine with aura |
|
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|
|
| Autism in African American Families: Clinical‐phenotypic findings |
|
✓ |
|
|
|
|
✓ |
✓ |
African American; racial‐ethnic groups; ethnic‐racial groups |
| Polymorphisms TaqI A of the DRD2, BalI of the DRD3, exon III repeat of the DRD4, and 3′ UTR VNTR of the DAT: Association with childhood ADHD in male African‐Caribbean cocaine dependents? |
|
|
|
|
|
|
✓ |
✓ |
African‑Caribbean |
| Gene‐based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: Association with <i>HMG2L1</i> and <i>TOM1</i> |
|
|
|
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|
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|
|
| Autosomal linkage analysis of a Japanese single multiplex schizophrenia pedigree reveals two candidate loci on chromosomes 4q and 3q |
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|
|
| Association study between gilles de la tourette syndrome and two genes in the robo‐slit pathway located in the chromosome 11q24 linked/associated region |
|
|
|
|
|
|
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|
|
| No association between the DAT1 10‐repeat allele and ADHD in the Iranian population |
|
|
|
|
|
|
✓ |
✓ |
Iranian population |
| The glycine transporter 1 gene (<i>GLYT1</i>) is associated with methamphetamine‐use disorder |
|
|
|
|
|
|
|
|
|
| NOS‐I and ‐III gene variants are differentially associated with facets of suicidal behavior and aggression‐related traits |
|
✓ |
|
|
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|
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|
|
| No association of migraine to the GABA‐A receptor complex on chromosome 15 |
|
|
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|
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|
|
| Family‐based association analysis of a statistically derived quantitative traits for ADHD reveal an association in<i>DRD4</i>with inattentive symptoms in ADHD individuals |
|
|
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|
|
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|
|
| Mutational screening analysis of <i>DHCR24</i>/<i>seladin‐1</i> gene in Italian familial Alzheimer's disease |
|
|
|
|
|
|
✓ |
✓ |
Italian; Italian population |
| The BDNF Val<sup>66</sup>Met × 5‐HTTLPR × child adversity interaction and depressive symptoms: An attempt at replication |
|
|
|
|
|
|
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|
|
| Is the <i>5‐HTTLPR</i> polymorphism associated with bipolar disorder or with suicidal behavior of bipolar disorder patients? |
|
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|
|
| Testing for gene × environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior |
|
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|
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|
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|
|
| Relationship between VNTR polymorphisms of the human dopamine transporter gene and expression in post‐mortem midbrain tissue |
|
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|
|
| Preliminary report of familial clustering of EEG measures in ADHD |
|
|
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|
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|
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|
|
| Exploring candidate gene associations with neuropsychological performance |
|
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|
|
|
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|
|
| Decomposing the autism phenotype into familial dimensions |
|
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|
|
| Polymorphisms in the homeobox gene <i>OTX2</i> may be a risk factor for bipolar disorder |
|
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|
|
| Whole genome association studies: Deciding when persistence becomes perseveration |
|
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|
|
| Possible association of the pro‐melanin‐concentrating hormone gene with <i>a greater</i> body mass index as a side effect of the antipsychotic olanzapine |
|
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|
|
|
|
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|
|
| The effect of genetic variation of the serotonin 1B receptor gene on impulsive aggressive behavior and suicide |
|
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|
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|
|
| Molecular genetic studies of<i>DMT1</i>on 12q in French‐Canadian restless legs syndrome patients and families |
|
|
|
|
|
|
✓ |
✓ |
French‐Canadian |
| The association study between <i>DHCR24</i> polymorphisms and Alzheimer's disease |
|
|
|
|
|
|
✓ |
✓ |
Finnish |
| The 3111T/C polymorphism of the CLOCK gene confers a predisposition to a lifetime lower body weight in patients with anorexia nervosa and bulimia nervosa: A preliminary study |
|
|
|
|
|
|
|
|
|
| Prediction of psychosis onset in Alzheimer disease: The role of depression symptom severity and the HTR2A T102C polymorphism |
|
✓ |
|
|
|
|
|
|
|
| Analysis of DRD4 and DAT polymorphisms and behavioral inhibition in healthy adults: Implications for impulsivity |
|
|
|
|
|
|
|
|
|
| Evidence that the COMT<sup>Val158Met</sup> polymorphism moderates sensitivity to stress in psychosis: An experience‐sampling study |
|
|
|
|
|
|
|
|
|
| Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth |
|
|
|
|
|
|
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|
|
| Candidate gene analysis of 21q22: Support for S100B as a susceptibility gene for bipolar affective disorder with psychosis |
|
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|
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|
|
| The importance of genetic counseling for individuals with schizophrenia and their relatives: Potential clients' opinions and experiences |
|
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|
|
| Meta‐analyses suggest association between COMT, but not HTR1B, alleles, and suicidal behavior |
|
|
|
|
|
|
|
|
|
| Familiality and diagnostic patterns of subphenotypes in the National Institutes of Mental Health Bipolar sample |
|
|
|
|
|
|
|
|
|
| Investigating the role of <i>p11</i> (<i>S100A10</i>) sequence variation in susceptibility to major depression |
|
|
|
|
|
|
|
|
|
| Association of genetic variants of ABCA1 with Alzheimer's disease risk |
|
|
|
|
|
|
✓ |
✓ |
Spanish |
| Dopaminergic candidate genes in Tourette syndrome: Association between tic severity and 3′ UTR polymorphism of the dopamine transporter gene |
|
|
|
|
|
|
|
|
|
| A review of association and linkage studies for genetical analyses of learning disorders |
|
|
|
|
|
|
|
|
|
| Catechol‐<i>O</i>‐methyltransferase polymorphism (<i>COMT</i>) in suicide attempters: A possible gender effect on anger traits |
|
|
|
|
|
|
|
|
|
| The influence of urban/rural residency on depressive symptoms is moderated by the serotonin receptor 2A gene |
|
|
|
|
|
|
✓ |
✓ |
Finnish |
| The Val66Met polymorphism of the brain‐derived neurotrophic factor gene is associated with psychotic feature and suicidal behavior in Japanese major depressive patients |
|
|
|
|
|
|
✓ |
✓ |
Japanese population |
| A novel intronic polymorphism of <i>ABCA1</i> gene reveals risk for sporadic Alzheimer's disease in Chinese |
|
|
|
|
|
|
✓ |
✓ |
Chinese |
| Effect of interleukin‐1β gene functional polymorphism on dorsolateral prefrontal cortex activity in schizophrenic patients |
|
|
|
|
|
|
✓ |
✓ |
Spanish origin |
| Family‐based association study of neuregulin‐1 gene and psychosis in a Spanish sample |
|
|
|
|
|
✓ |
✓ |
✓ |
European and Asian populations; Icelandic population; Spanish population; Asian populations |
| Dopamine beta‐hydroxylase gene polymorphisms and psychotic symptoms in schizophrenia |
|
|
|
|
|
|
|
|
|
| Porcine maternal infanticide as a model for puerperal psychosis |
|
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|
|
|
|
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|
|
| Cytogenetic and molecular characterization of <i>A2BP1</i>/<i>FOX1</i> as a candidate gene for autism |
|
|
|
|
|
|
|
|
|
| No evidence for a preferential transmission of the methylenetetrahydrofolate reductase 677T allele in families with schizophrenia offspring |
|
|
|
|
|
|
|
|
|
| A subgroup of Tourette's patients overexpress specific natural killer cell genes in blood: A preliminary report |
|
|
|
|
|
|
|
|
|
| Choline acetyltransferase variants and their influence in schizophrenia and olanzapine response |
|
|
|
|
|
|
✓ |
✓ |
Basque; Spanish |
| The opioid system in alcohol and drug dependence: Family‐based association study |
|
|
|
|
|
✓ |
|
|
European Americans |
| Alzheimer's disease: Case‐control association study of polymorphisms in ACHE, CHAT, and BCHE genes in a Sardinian sample |
|
|
|
|
|
|
✓ |
✓ |
Sardinian ancestry |
| Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description |
|
|
|
|
|
|
|
|
|
| Genetic susceptibility to environmental toxicants in ALS |
|
|
|
|
|
|
|
|
|
| Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis |
|
|
|
|
|
|
|
|
|
| Is the Wisconsin card sorting test a useful neurocognitive endophenotype? |
|
|
|
|
|
|
|
|
|
| Evidence for association and epistasis at the DAOA/G30 and <scp>D</scp>‐amino acid oxidase loci in an Irish schizophrenia sample |
|
✓ |
|
|
|
|
✓ |
✓ |
Irish; Republic of Ireland |
| Novelty seeking and the dopamine D4 receptor gene (<i>DRD4</i>) revisited in Asians: Haplotype characterization and relevance of the 2‐repeat allele |
|
✓ |
|
|
|
|
|
|
|
| Expression of multiple catechol‐o‐methyltransferase (COMT) mRNA variants in human brain |
|
|
|
|
|
|
|
|
|
| Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: A unique case of γ‐hydroxybutyric aciduria and Williams syndrome |
|
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|
|
|
|
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|
|
| Non‐verbal deficits in young children with a genetic metabolic disorder: WPPSI‐III performance in cystinosis |
|
|
|
|
|
|
|
|
|
| Genome‐wide scan of bipolar disorder and investigation of population stratification effects on linkage: Support for susceptibility loci at 4q21, 7q36, 9p21, 12q24, 14q24, and 16p13 |
|
|
|
|
|
|
✓ |
✓ |
Irish population |
| Relationship of 5‐HTTLPR genotypes and depression risk in the presence of trauma in a female twin sample |
|
|
|
|
|
|
|
|
|
| Polymorphisms in dopamine receptor DRD1 and DRD2 genes and psychopathological and extrapyramidal symptoms in patients on long‐term antipsychotic treatment |
|
|
|
|
|
|
|
|
|
| Investigation of variation in <i>SNAP‐25</i> and ADHD and relationship to co‐morbid major depressive disorder |
|
|
|
|
|
|
|
|
|
| No interaction between the serotonin transporter polymorphism (5‐HTTLPR) and childhood adversity or recent stressful life events on symptoms of depression: Results from two community surveys |
|
|
|
|
|
|
|
|
|
| Variance in facial recognition performance associated with BDNF in schizophrenia |
|
|
|
|
|
|
|
|
|
| Evaluation of candidate genes for <i>DYX1</i> and <i>DYX2</i> in families with dyslexia |
|
|
|
|
|
|
|
|
|
| Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations |
|
|
|
|
|
|
✓ |
✓ |
Italian origin |
| Tachykinin receptor 1 variants associated with aggression in suicidal behavior |
|
✓ |
|
|
|
|
|
|
|
| Gene–lifecourse interaction for alcohol consumption in adolescence and young adulthood: Five monoamine genes |
|
|
|
|
|
|
|
|
|
| Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder |
|
|
|
|
|
|
|
|
|
| Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early‐onset parkinsonism |
|
|
|
|
|
|
✓ |
✓ |
Taiwanese/Ethnic Chinese; ethnic Chinese; Chinese |
| Obsessive–compulsive symptoms in sibling pairs concordant for obsessive–compulsive disorder |
|
|
|
|
|
|
|
|
|
| Mitochondrial DNA haplogroups and age at onset of schizophrenia |
|
|
|
|
|
✓ |
✓ |
✓ |
major European haplogroups (hgs); Italian origin |
| Understanding comorbidity: A twin study of reading disability and attention‐deficit/hyperactivity disorder |
|
|
|
|
|
|
|
|
|
| Neurocognitive deficits in first‐episode schizophrenic patients and their first‐degree relatives |
|
|
|
|
|
|
|
|
|
| Association analysis of GABA receptor subunit genes on 5q33 with heroin dependence in a Chinese male population |
|
|
|
|
|
|
✓ |
✓ |
Han Chinese |
| A meta‐analysis of association studies between the 10‐repeat allele of a VNTR polymorphism in the 3′‐UTR of dopamine transporter gene and attention deficit hyperactivity disorder |
|
|
|
|
|
|
|
|
|
| Interaction between the <i>ADAM12</i> and <i>SH3MD1</i> genes may confer susceptibility to late‐onset Alzheimer's disease |
|
|
|
|
|
|
|
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| Candidate gene association study of insulin signaling genes and Alzheimer's disease: Evidence for <i>SOS2</i>, <i>PCK1</i>, and <i>PPARγ</i> as susceptibility loci |
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| Anorexia nervosa, perfectionism, and dopamine D4 receptor (<i>DRD4</i>) |
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| Acrodysostosis with unusual iridal color changing with age |
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| <i>DAT1</i> 3′‐UTR 9R allele: Preferential transmission in Indian children with attention deficit hyperactivity disorder |
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✓ |
✓ |
Indian |
| Mutation screening of the <i>PTEN</i> gene in patients with autism spectrum disorders and macrocephaly |
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| Association studies testing for risk for late‐onset Alzheimer's disease with common variants in the β‐amyloid precursor protein (APP) |
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| <i>MECP2</i> coding sequence and 3′UTR variation in 172 unrelated autistic patients |
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✓ |
✓ |
Portuguese autistic population |
| Low brain‐derived neurotrophic factor (BDNF) levels in serum of Huntington's disease patients |
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| Sustained attention and response inhibition in boys with fragile X syndrome: Measures of continuous performance |
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| Investigation of parent‐of‐origin effects in ADHD candidate genes |
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| Monoamine oxidase A gene polymorphism predicts adolescent outcome of attention‐deficit/hyperactivity disorder |
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✓ |
✓ |
ethnic or geographic groups; other populations |
| Nuclear receptor <i>NR4A2</i> IVS6 +18insG and brain derived neurotrophic factor (<i>BDNF</i>) V66M polymorphisms and risk of Taiwanese parkinson's disease |
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✓ |
✓ |
Taiwanese |
| A genome‐wide linkage analysis for the personality trait neuroticism in the Irish affected sib‐pair study of alcohol dependence |
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| CGG repeat length correlates with age of onset of motor signs of the fragile X‐associated tremor/ataxia syndrome (FXTAS) |
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| Identification of two risk haplotypes for schizophrenia and bipolar disorder in the synaptic vesicle monoamine transporter gene (SVMT) |
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| Association analysis of <i>COMT</i> polymorphisms and schizophrenia in a Chinese Han population: A case‐control study |
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| Association of the neuropilin‐2 (<i>NRP2</i>) gene polymorphisms with autism in Chinese Han population |
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|
✓ |
✓ |
Chinese Han |
| Why do young women smoke? IV. Role of genetic variation in the dopamine transporter and lifetime traumatic experience |
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| Erratum |
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| Erratum |
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| Response to lithium prophylaxis: Interaction between serotonin transporter and <i>BDNF</i> genes |
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| Human Kappa opioid receptor gene (OPRK1) polymorphism is associated with opiate addiction |
|
✓ |
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✓ |
|
|
West European |
| A primate model for Alzheimer's disease: Investigation of the apolipoprotein E profile of the vervet monkey of St. Kitts |
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| No evidence for association between 19 cholinergic genes and bipolar disorder |
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| Association studies of 23 positional/functional candidate genes on chromosome 10 in late‐onset Alzheimer's disease |
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| p75<sup>NTR</sup> gene and suicide attempts in young adults with a history of childhood‐onset mood disorder |
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| Association between cytochrome P450 (CYP) 2C19 polymorphisms and harm avoidance in Japanese |
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| Meta‐analysis of COMT val158met in panic disorder: Ethnic heterogeneity and gender specificity |
|
✓ |
|
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|
✓ |
✓ |
Asian |
| Increase in <i>GSK3β</i> gene copy number variation in bipolar disorder |
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| SNP fine mapping of chromosome 8q24 in bipolar disorder |
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| Dysregulation of X‐linked gene expression in Klinefelter's syndrome and association with verbal cognition |
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| Transcriptional profiling of lymphoblast lines from subjects with panic disorder |
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| Transcriptional profiling of subjects from the Iowa adoption studies |
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| The association of the HOPA<sup>12bp</sup> polymorphism with schizophrenia in the NIMH genetics initiative for schizophrenia sample |
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|
✓ |
|
|
European ancestry |
| The fatty acid amide hydrolase C385A (P129T) missense variant in cannabis users: Studies of drug use and dependence in caucasians |
✓ |
✓ |
|
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|
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| Heritability and clinical features of multigenerational families with obsessive‐compulsive disorder and hoarding |
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| Association study of dysbindin gene with clinical and outcome measures in a representative cohort of Italian schizophrenic patients |
|
✓ |
|
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|
|
✓ |
✓ |
Italian |
| Positive association of the <i>Disrupted‐in‐Schizophrenia‐1</i> gene (<i>DISC1</i>) with schizophrenia in the Chinese han population |
|
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|
|
✓ |
✓ |
Chinese han; Chinese Han Population |
| Towards understanding the schizophrenia code: An expanded convergent functional genomics approach |
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| A genome‐wide scan for modifier loci in schizophrenia |
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| Family‐based and case‐control studies reveal no association of<i>lipocalin‐type prostaglandin D2 synthase</i>with schizophrenia |
|
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|
|
| Association of the neuronal nicotinic receptor β2 subunit gene (CHRNB2) with subjective responses to alcohol and nicotine |
|
✓ |
|
|
|
|
✓ |
✓ |
ethnically diverse young adults |
| Association of adenomatous polyposis coli (<i>APC</i>) gene polymorphisms with autism spectrum disorder (ASD) |
|
|
|
|
|
|
✓ |
✓ |
Swedish |
| Association study of polymorphisms in the glutamate transporter genes <i>SLC1A1</i>, <i>SLC1A3</i>, and <i>SLC1A6</i> with schizophrenia |
|
|
|
|
|
|
✓ |
✓ |
Japanese |
| Differential expression and parent‐of‐origin effect of the <i>5‐HT2A</i> receptor gene C102T polymorphism: Analysis of suicidality in schizophrenia and bipolar disorder |
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| Genetic analysis of SCA 27 in ataxia and childhood onset postural tremor |
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| Actimetric evidence that CLOCK 3111 T/C SNP influences sleep and activity patterns in patients affected by bipolar depression |
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| Association of a serotonin receptor 2A gene polymorphism with cognitive functions in patients with schizophrenia |
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| The influence of four serotonin‐related genes on decision‐making in suicide attempters |
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| Informative phenotypes for genetic studies of psychiatric disorders |
|
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| “No one else sees the difference: ”family members' perceptions of changes in persons with preclinical Huntington disease |
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| Absence of the Arg441His polymorphism in the tryptophan hydroxylase 2 gene in adults with anxiety disorders and depression |
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