| Fine mapping and association studies in a candidate region for autism on chromosome 2q31–q32 |
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✓ |
✓ |
Irish sample |
| The TGM2 gene is associated with schizophrenia in a British population |
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| Misinterpreting schizophrenia relatives' impairments |
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| <i>MAOA</i> exon 8 941T > G <i>Fnu</i>4HI polymorphism: Actual rs number |
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| Interspecies comparisons of functional genetic variations and their implications in neuropsychiatry |
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| A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin‐1 gene and risk of Alzheimer's disease; Extra‐short alleles and accumulated allele homozygosity |
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| <i>G72/G30</i> (<i>DAOA</i>) and juvenile‐onset mood disorders |
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| Association of major depression with rare functional variants in norepinephrine transporter and serotonin<sub>1A</sub>receptor genes |
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| Identification of a CREB‐dependent serotonergic pathway and neuronal circuit regulating foraging behavior in <i>Caenorhabditis elegans</i>: A useful model for mental disorders and their treatments? |
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| No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder |
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| Convergent functional genomics of genome‐wide association data for bipolar disorder: Comprehensive identification of candidate genes, pathways and mechanisms |
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| Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan |
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| Genome‐wide association scan of attention deficit hyperactivity disorder |
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| Familial dyskinesia and facial myokymia (FDFM): Follow‐up of a large family and linkage to chromosome 3p21‐3q21 |
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| Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder |
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| In Memoriam |
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| Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: Suggestive linkage to 3q13 |
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| Lack of association of the serotonin transporter gene promoter region polymorphism,<i>5‐HTTLPR</i>, including<i>rs25531</i>with cigarette smoking and alcohol consumption |
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| A preliminary study of dopamine D4 receptor genotype and structural brain alterations in adults with ADHD |
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| Perspective on the genetics of attention deficit/hyperactivity disorder |
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| Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study |
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✓ |
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a European cohort |
| Genome‐wide association scan of the time to onset of attention deficit hyperactivity disorder |
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| Replication of a rare protective allele in the noradrenaline transporter gene and ADHD |
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✓ |
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|
multi‐centre European sample (the IMAGE project) |
| Association of the steroid sulfatase (<i>STS</i>) gene with attention deficit hyperactivity disorder |
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| Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples |
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✓ |
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| Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: A preliminary study |
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| A comparison of molecular alterations in environmental and genetic rat models of ADHD: A pilot study |
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| Genome‐wide association study of response to methylphenidate in 187 children with attention‐deficit/hyperactivity disorder |
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| Genome‐wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations |
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| SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families |
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| Association between Catechol O‐methyltransferase (<i>COMT</i>) haplotypes and severity of hyperactivity symptoms in Adults |
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| Association of the dopamine transporter (<i>SLC6A3/DAT1</i>) gene 9–6 haplotype with adult ADHD |
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| A common haplotype at the dopamine transporter gene 5′ region is associated with attention‐deficit/hyperactivity disorder |
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| The impact of individual and methodological factors in the variability of response to methylphenidate in ADHD pharmacogenetic studies from four different continents |
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✓ |
✓ |
ethnicity |
| Detailed analysis of the serotonin transporter gene (<i>SLC6A4</i>) shows no association with bipolar disorder in the Northern Swedish population |
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✓ |
✓ |
Northern Swedish population |
| Systemic and psychiatric disorders associated with polymorphisms of the P2RX7 gene |
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| Gene expression and association analyses of the phosphodiesterase 4B (PDE4B) gene in major depressive disorder in the Japanese population |
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| Letter to the editor in response to Dr. Kapoor's comments “systemic and psychiatric disorders associated with polymorphisms of the P2RX7 gene” |
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| Genome‐wide linkage of cotinine pharmacokinetics suggests candidate regions on chromosomes 9 and 11 |
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| Prepulse inhibition in fragile X syndrome: Feasibility, reliability, and implications for treatment |
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| Variability of AChE, BChE, and ChAT genes in the late‐onset form of Alzheimer's disease and relationships with response to treatment with Donepezil and Rivastigmine |
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| Association studies of 22 candidate SNPs with late‐onset Alzheimer's disease |
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✓ |
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| Attention deficit hyperactivity disorder in obese melanocortin‐4‐receptor (MC4R) deficient subjects: A newly described expression of MC4R deficiency |
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| Genetic predictors of depressive symptoms in cardiac patients |
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| Failure to confirm genetic association of the <i>CHI3L1</i> gene with schizophrenia in Japanese and Chinese populations |
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| Brain derived neurotrophic factor (BDNF) genetic polymorphism (Val66Met) in suicide: A study of 512 cases |
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| Positive association between SAT‐1 −1415T/C polymorphism and anxiety |
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| Age of onset and death in inherited prion disease are heritable |
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| A review and analysis of the relationship between neuropsychological measures and <i>DAT1</i> in ADHD |
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| Differential association between <i>MAOA</i>, ADHD and neuropsychological functioning in boys and girls |
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| Interaction between gene variants of the serotonin transporter promoter region (5‐HTTLPR) and catechol <i>O</i>‐methyltransferase (COMT) in borderline personality disorder |
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✓ |
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| Genetic variation in the serotonin 2A receptor and suicidal ideation in a sample of 270 Irish high‐density schizophrenia families |
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| Repeat instability in the 27–39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications |
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| Association of <i>SLITRK1</i> to Gilles de la Tourette Syndrome |
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| Candidate region linkage analysis in twins discordant or concordant for depression symptomatology |
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| Do the estrogen receptors 1 gene variants influence the temperament and character inventory scores in suicidal attempters and healthy subjects? |
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| Association of ADHD with genetic variants in the 5′‐region of the dopamine transporter gene: Evidence for allelic heterogeneity |
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| Polymorphisms in the 3′ UTR of the serotonin transporter are associated with cognitive flexibility in rhesus macaques |
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| Non‐random error in genotype calling procedures: Implications for family‐based and case–control genome‐wide association studies |
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| Characterization of a glucocorticoid receptor gene (<i>GR</i>, <i>NR3C1</i>) promoter polymorphism reveals functionality and extends a haplotype with putative clinical relevance |
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| Letter to Editor in response to: “Linkage studies in familial idiopathic basal ganglia calcification: Separating the wheat from the chaff” by Oliveria et al. (AJMB 08‐0193) |
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| Linkage studies in familial idiopathic basal ganglia calcification: Separating the wheat from the chaff |
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✓ |
✓ |
American, Spanish/Spain, Australian, Italian, Tyrolean, Japanese; phrases: 'population isolate', 'It |
| Association of the PIK4CA schizophrenia‐susceptibility gene in adults with the 22q11.2 deletion syndrome |
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| Interspecies genetics of eating disorder traits |
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| High‐activity variants of the uMAOA polymorphism increase the risk for depression in a large primary care sample |
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| Familial aggregation of quantitative autistic traits in multiplex versus simplex autism |
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| SLC6A4 variation and citalopram response |
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✓ |
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| Association of single nucleotide polymorphisms in a glutamate receptor gene (<i>GRM8</i>) with theta power of event‐related oscillations and alcohol dependence |
|
✓ |
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| Misgenotyping of dopamine receptor D1 gene −48A/G polymorphism |
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| Failure to confirm the association between the <i>PIK4CA</i> gene and schizophrenia in a Japanese population |
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✓ |
|
Japanese population |
| COMT val158met modulates association between brain white matter architecture and IQ |
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| Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression |
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| Novel de novo SHANK3 mutation in autistic patients |
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| DRD2 C32806T modifies the effect of child‐rearing environment on adulthood novelty seeking |
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✓ |
✓ |
Finns; population-based sample |
| Risk of cognitive impairment in female premutation carriers of fragile X premutation: Analysis by means of robust segmented linear regression models |
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| Pharmacogenetics of methylphenidate response in attention deficit/hyperactivity disorder: Association with the dopamine transporter gene (<i>SLC6A3</i>) |
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| The XVth world congress of psychiatric genetics, october 7–11, 2007: Rapporteur summaries of oral presentations |
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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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| Family‐based association study between NOS‐I and ‐IIA polymorphisms and autism spectrum disorders in Korean trios |
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| The impact of genetic variation in DRD2 and SLC6A3 on smoking cessation in a cohort of participants 1 year after enrollment in a lung cancer screening study |
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| Mood and anxiety disorders in females with the FMR1 premutation |
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| Dopamine transporter polymorphism modulates oculomotor function and DAT1 mRNA expression in schizophrenia |
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| Recent adaptive selection at <i>MAOB</i> and ancestral susceptibility to schizophrenia |
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| Response to letter to editor by Dr. Das and Dr. Mukhopadhyay |
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| Analysis of genetic variations in the <i>RGS9</i> gene and antipsychotic‐induced tardive dyskinesia in schizophrenia |
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| A searchable database of genetic evidence for psychiatric disorders |
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| Association between depression and the Gln460Arg polymorphism of P2RX7 Gene: A dimensional approach |
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| A polymorphism of the neuregulin 1 gene (SNP8NRG243177/rs6994992) affects reactivity to expressed emotion in schizophrenia |
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| Mitochondrial DNA haplogroup analysis in patients with bipolar disorder |
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| 5‐HTTLPR genotype and anxiety‐related personality traits: A meta‐analysis and new data |
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✓ |
✓ |
Finnish population |
| Semantic but not phonological verbal fluency associated with BDNF Val66Met polymorphism in schizophrenia |
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| Emotional symptoms in children: The effect of maternal depression, life events, and COMT genotype |
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| Analysis of human alternative first exons and copy number variation of the <i>GJA12</i> gene in patients with Pelizaeus–Merzbacher‐like disease |
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| Association study between the<i>PIK4CA</i>gene and methamphetamine use disorder in a Japanese population |
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✓ |
✓ |
Dutch population; Japanese population |
| Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion |
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| Angiotensin I‐converting enzyme I/D polymorphism and suicidal behaviors |
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| The tryptophan hydroxylase‐1 A218C polymorphism is associated with diagnosis, but not suicidal behavior, in borderline personality disorder |
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|
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| Analysis of genetic variations in the human <i>Par‐4</i> (<i>PAWR</i>) gene and tardive dyskinesia in schizophrenia |
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|
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| Methionine sulfoxide reductase: A novel schizophrenia candidate gene |
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✓ |
✓ |
Hispanic population |
| No association between tagging SNPs of SNARE complex genes (STX1A, VAMP2 and SNAP25) and schizophrenia in a Japanese population |
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| Ordered subsets linkage analysis of antisocial behavior in substance use disorder among participants in the collaborative study on the genetics of alcoholism |
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| The positives, protocols, and perils of genome‐wide association |
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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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| Cyclooxygenase‐2 polymorphisms in Parkinson's disease |
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| Criteria for validating mouse models of psychiatric diseases |
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| <i>PPP2R2B</i> CAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implications |
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|
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| Polymorphisms in the <i>GRIA1</i> gene region in psychotic bipolar disorder |
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|
|
| Effect of 5‐HT1A gene polymorphisms on antidepressant response in major depressive disorder |
|
|
|
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|
|
✓ |
✓ |
Japanese |
| Polymorphisms in the angiotensin‐converting enzyme gene region predict coping styles in healthy adults and depressed patients |
|
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|
|
| Early‐phase ERK activation as a biomarker for metabolic status in fragile X syndrome |
|
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|
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| Association analysis of dynamin‐binding protein (<i>DNMBP</i>) on chromosome 10q with late onset Alzheimer's disease in a large caucasian UK sample |
✓ |
✓ |
|
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|
|
| No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder |
|
|
|
|
|
|
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|
|
| Association and linkage analysis of candidate genes GRP, GRPR, CRHR1, and TACR1 in panic disorder |
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|
|
| Association of reading disability on chromosome 6p22 in the Afrikaner population |
|
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|
✓ |
✓ |
Afrikaner population; founding population in the Afrikaner population |
| A novel non‐parametric regression reveals linkage on chromosome 4 for the number of externalizing symptoms in sib‐pairs |
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| MAOA methylation is associated with nicotine and alcohol dependence in women |
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| The influence of sex chromosome aneuploidy on brain asymmetry |
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| Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region |
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|
|
| Association study of the estrogen receptor alpha gene (<i>ESR1</i>) and childhood‐onset mood disorders |
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|
|
| The validity of the family history screen for assessing family history of mental disorders |
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| Lack of association between DRD3 gene polymorphism and response to clozapine in Turkish schizoprenia patients |
|
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|
✓ |
✓ |
Turkish |
| Association study between the genetic polymorphisms of glutathione‐related enzymes and schizophrenia in a Japanese population |
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|
|
| Support for schizophrenia susceptibility locus on chromosome 2q detected in a Swedish isolate using a dense map of microsatellites and SNPs |
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|
✓ |
✓ |
Swedish isolate |
| Genome screen of late‐onset Alzheimer's extended pedigrees identifies TRPC4AP by haplotype analysis |
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|
|
| Genome‐wide scan in 124 Indonesian sib‐pair families with schizophrenia reveals genome‐wide significant linkage to a locus on chromosome 3p26‐21 |
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|
|
| Bipolar disorder in the Bulgarian Gypsies: Genetic heterogeneity in a young founder population |
|
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|
|
✓ |
✓ |
Gypsies |
| Additional functional variation at the SLC6A4 gene |
|
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|
|
| Neurotransmission and bipolar disorder: A systematic family‐based association study |
|
✓ |
|
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|
|
| Neurotrophic factor‐related gene polymorphisms and adult attention deficit hyperactivity disorder (ADHD) score in a high‐risk male population |
|
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| Gender differences in genetic linkage and association on 11p15 in obsessive–compulsive disorder families |
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|
| <i>PRNP</i> mutations in a series of apparently sporadic neurodegenerative dementias in China |
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| Genetic association between α‐synuclein and idiopathic parkinson's disease |
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|
|
| <i>FBXL21</i> association with schizophrenia in irish family and case–control samples |
|
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|
|
✓ |
✓ |
Irish |
| Association analysis of schizophrenia on 18 genes involved in neuronal migration: <i>MDGA1</i> as a new susceptibility gene |
|
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|
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|
|
✓ |
✓ |
Scandinavian origin |
| Dementia in fragile X‐associated tremor/ataxia syndrome (FXTAS): Comparison with Alzheimer's disease |
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|
|
| Association study of candidate variants of COMT with neuroticism, anxiety and depression |
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|
|
| Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder |
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|
|
| Social support in older individuals: The role of the BDNF Val66Met polymorphism |
|
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|
|
| A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting <i>RAB11FIP5</i> identifies a potential candidate gene for autism spectrum disorder |
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|
|
| Twin study refining psychotic symptom dimensions as phenotypes for genetic research |
|
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|
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| No pathogenic rearrangement within the <i>DISC 1</i> gene in psychosis |
|
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|
|
| Analysis of the gastrin‐releasing peptide receptor gene in Italian patients with autism spectrum disorders |
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|
| Pharmacogenetics of parkinsonism, rigidity, rest tremor, and bradykinesia in African‐Caribbean inpatients: Differences in association with dopamine and serotonin receptors |
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|
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| Longitudinal follow‐up of late‐onset Alzheimer disease families |
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| Genetic influences on the broad spectrum of autism: Study of proband‐ascertained twins |
|
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| Array comparative genomic hybridization in global developmental delay |
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|
| Candidate genes for schizophrenia: A survey of association studies and gene ranking |
|
|
|
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|
|
✓ |
✓ |
ethnic populations |
| Exclusion of linkage to chromosome 14q in a large South Tyrolean family with idiopathic basal ganglia calcification (IBGC) |
|
|
|
|
|
|
✓ |
✓ |
South Tyrolean; Italian; population isolate |
| A genome‐wide linkage scan provides evidence for both new and previously reported loci influencing common migraine |
|
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|
|
| Analysis of X chromosome inactivation in autism spectrum disorders |
|
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| Calibration of credibility of agnostic genome‐wide associations |
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|
|
| A reanalysis of 409 European‐Ancestry and African American schizophrenia pedigrees reveals significant linkage to 8p23.3 with evidence of locus heterogeneity |
|
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|
✓ |
✓ |
✓ |
✓ |
European-Ancestry; "European (EA: 263 pedigrees)"; African-American; "African‐American (AA: 146 pedigrees)" |
| Gene expression profiling in porcine maternal infanticide: A model for puerperal psychosis |
|
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| Association of <i>PTPRB</i> gene polymorphism with drug addiction |
|
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|
|
✓ |
|
|
European‐American |
| Family based association study of pediatric bipolar disorder and the dopamine transporter gene (<i>SLC6A3</i>) |
|
|
|
|
|
✓ |
|
|
CEU (European) population of the International HapMap project (www.hapmap.org) |
| Absence of the 7‐repeat variant of the DRD4 VNTR is associated with drifting sustained attention in children with ADHD but not in controls |
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| Transmission disequilibrium testing of the chromosome 15q11‐q13 region in autism |
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| Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene |
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|
| DRD3, but not COMT or DRD2, genotype affects executive functions in healthy and first‐episode psychosis adolescents |
|
✓ |
|
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|
|
|
|
|
| Comments on “Novelty seeking and the dopamine D4 receptor gene (DRD4) revisited in Asians: Haplotype characterization and relevance of the 2‐repeat allele” by C. Reist et al. Am J Med Genet B Neuropsy |
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✓ |
|
Asians |
| A functional polymorphism, rs6280, in<i>DRD3</i>is significantly associated with nicotine dependence in European‐American smokers |
|
|
|
|
✓ |
✓ |
✓ |
✓ |
European‐Americans (EAs); African‐Americans (AAs) |
| An analysis of candidate autism loci on chromosome 2q24–q33: Evidence for association to the <i>STK39</i> gene |
|
|
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|
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| Association of PIP5K2A with schizophrenia: A study in an indonesian family sample |
|
✓ |
|
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|
✓ |
|
|
non‐European descent |
| A simulated genetic structure for bipolar illness |
|
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|
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| Comprehensive analysis of tagging sequence variants in <i>DTNBP1</i> shows no association with schizophrenia or with its composite neurocognitive endophenotypes |
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|
|
✓ |
✓ |
✓ |
European populations; Anglo‐Irish ancestry; Irish |
| Possible association of the alpha‐2A‐adrenergic receptor gene with response time variability in attention deficit hyperactivity disorder |
|
|
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|
|
✓ |
✓ |
Korean subjects |
| Beckwith Weidemann syndrome: A behavioral phenotype–genotype study |
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|
| The XVth World Congress of Psychiatric Genetics, October 7–11, 2007: Rapporteur summaries of oral presentations |
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| Externalizing disorders in American Indians: Comorbidity and a genome wide linkage analysis |
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| Reduced hippocampal volumes associated with the long variant of the tri‐ and diallelic serotonin transporter polymorphism in major depression |
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|
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| Unipolar depression and hippocampal volume: Impact of DNA sequence variants of the glucocorticoid receptor gene |
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|
|
✓ |
✓ |
German |
| Cognitive dysfunction in mice deficient for TNF‐ and its receptors |
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|
|
| Evidence for potential relationship between SLC1A1 and a putative genetic linkage region on chromosome 14q to obsessive‐compulsive disorder with compulsive hoarding |
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| Association study of brain‐derived neurotrophic factor (<i>BDNF</i>) and <i>LIN‐7</i> homolog (<i>LIN‐7</i>) genes with adult attention‐deficit/hyperactivity disorder |
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|
✓ |
✓ |
ethnically matched controls |
| The neuregulin 1 promoter polymorphism rs6994992 is not associated with chronic schizophrenia or neurocognition |
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|
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| Autism and serotonin transporter gene polymorphisms: A systematic review and meta‐analysis |
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|
✓ |
✓ |
✓ |
European samples; Asian samples; US mixed population samples; ethnicity |
| Worldwide genetic variation in dopamine and serotonin pathway genes: Implications for association studies |
|
|
|
|
|
|
✓ |
✓ |
ethnic differences; worldwide populations; continental regions; HapMap populations |
| A family‐ and population‐based study of the UFD1L gene for schizophrenia |
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|
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|
|
✓ |
✓ |
Han descent; Italian and Canadian samples |
| Genetic analyses of <i>Roundabout</i> (<i>ROBO</i>) axon guidance receptors in autism |
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|
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| <i>DISC1</i> mRNA expression is not influenced by common <i>Cis</i>‐acting regulatory polymorphisms or imprinting |
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|
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| Catechol‐<i>O</i>‐methyltransferase (<i>COMT</i>) gene variants: Possible association of the Val158Met variant with opiate addiction in hispanic women |
|
✓ |
|
|
|
|
✓ |
✓ |
Hispanics, African Americans |
| Phenomic, Convergent Functional Genomic, and biomarker studies in a stress‐reactive genetic animal model of bipolar disorder and co‐morbid alcoholism |
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| Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm |
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| Autism spectrum conditons in myotonic dystrophy type 1: A study on 57 individuals with congenital and childhood forms |
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| Serotonin transporter gene and adverse life events in adult ADHD |
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| Catechol‐<i>O</i>‐methyltransferase Val158Met polymorphism is associated with methylphenidate response in ADHD children |
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|
|
| Lack of association of the dopamine transporter gene in a French ADHD sample |
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|
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|
|
✓ |
✓ |
French |
| Genetic association study of BDNF in depression: Finding from two cohort studies and a meta‐analysis |
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|
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| A DRD1 haplotype is associated with risk for autism spectrum disorders in male‐only affected sib‐pair families |
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|
|
| Failure to replicate effect of kibra on human memory in two large cohorts of European origin |
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|
✓ |
✓ |
|
|
European origin; European genetic origin |
| Initial association of <i>NR2E1</i> with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing |
|
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|
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| Association of the cannabinoid receptor gene (CNR1) with ADHD and post‐traumatic stress disorder |
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|
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| Association between trypotphan hydroxylase 2, performance on a continuance performance test and response to methylphenidate in ADHD participants |
|
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|
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| Putative role of the COMT gene polymorphism (Val158Met) on verbal working memory functioning in a healthy population |
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| Effects of the G(‐656)A variant on <i>CREB1</i> promoter activity in a glial cell line: Interactions with gonadal steroids and stress |
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|
|
| Multiple <i>OPR</i> genes influence personality traits in substance dependent and healthy subjects in two American populations |
|
|
|
|
|
✓ |
✓ |
✓ |
European‐Americans (EAs); African‐Americans (AAs) |
| Diabetes and overweight associate with non‐APOE4 genotype in an alzheimer's disease population |
|
|
|
|
|
|
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|
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| Further evidence for shared genetic effects between psychotic bipolar disorder and P50 suppression: A combined twin and family study |
|
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|
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| DSM‐IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkage |
|
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|
|
| A genomic scan for age at onset of alzheimer's disease in 437 families from the NIMH genetic initiative |
|
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|
|
| Polymorphisms in the catechol‐<i>O</i>‐methyltransferase (COMT) gene influence plasma total homocysteine levels |
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|
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| Lithium response and genetic variation in the CREB family of genes |
|
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|
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| No evidence for involvement of genetic variants in the X‐linked neuroligin genes <i>NLGN3</i> and <i>NLGN4X</i> in probands with autism spectrum disorder on high functioning level |
|
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|
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| Cannabinoid receptor 1 gene (CNR1) and susceptibility to a quantitative phenotype for hebephrenic schizophrenia |
|
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|
|
| Interactive effects of COMT Val108/158Met and MTHFR C677T on executive function in schizophrenia |
|
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|
|
|
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|
|
| No association between the protein tyrosine phosphatase, receptor‐type, Z Polypeptide 1 (<i>PTPRZ1</i>) gene and schizophrenia in the Japanese population |
|
✓ |
|
|
|
|
✓ |
✓ |
Japanese population |
| Association of the serotonin transporter polymorphism and obsessive‐compulsive disorder: Systematic review |
|
✓ |
|
|
|
|
✓ |
✓ |
Asian |
| Association study of the 15q11‐q13 maternal expression domain in Japanese autistic patients |
|
|
|
|
|
|
|
|
|
| Association study between polymorphisms in glutathione‐related genes and methamphetamine use disorder in a Japanese population |
|
|
|
|
|
|
✓ |
✓ |
Japanese population |
| Increased longevity in offspring of mothers with alzheimer's disease |
|
|
|
|
|
|
|
|
|
| Does <i>APOE</i> explain the linkage of Alzheimer's disease to chromosome 19q13? |
|
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|
|
| An investigation of mitochondrial haplogroups in autism |
|
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|
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|
|
| Evidence for a heritable unidimensional symptom factor underlying obsessionality |
|
|
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|
|
|
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|
|
| A linkage analysis of cigarette and alcohol consumption in an unselected Mexican American population |
|
|
|
|
|
|
✓ |
✓ |
Mexican American population |
| Variation in GABA‐A subunit gene copy number in an autistic patient with mosaic 4 p duplication (p12p16) |
|
|
|
|
|
|
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|
|
| The utility of SELENBP1 gene expression as a biomarker for major psychotic disorders: Replication in schizophrenia and extension to bipolar disorder with psychosis |
|
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|
|
| No association with the 5,10‐methylenetetrahydrofolate reductase gene and major depressive disorder: Results of the depression case control (DeCC) study and a meta‐analysis |
|
|
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|
|
|
|
|
|
| Do mood symptoms subdivide the schizophrenia phenotype? association of the GMP6A gene with a depression subgroup |
|
|
|
|
|
|
|
|
|
| Association of complement factor H Y402H gene polymorphism with Alzheimer's disease |
|
✓ |
|
|
|
|
|
|
|
| Identification of pharmacogenetic markers in smoking cessation therapy |
|
|
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|
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|
|
| Association analysis of 528 intra‐genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease |
|
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|
|
| Identification of FMRP‐associated mRNAs using yeast three‐hybrid system |
|
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|
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|
|
| Regulation of a novel αN‐catenin splice variant in schizophrenic smokers |
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|
|
| Association of DAO and G72(DAOA)/G30 genes with bipolar affective disorder |
|
|
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|
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|
|
| Different‐sized duplications of Xq28, including <i>MECP2</i>, in three males with mental retardation, absent or delayed speech, and recurrent infections |
|
|
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|
|
|
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|
|
| Impact of the Fragile X mental retardation 1 (<i>FMR1</i>) gene premutation on neuropsychiatric functioning in adult males without fragile X‐associated Tremor/Ataxia syndrome: A controlled study |
|
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|
|
|
|
|
|
| Two methylenetetrahydrofolate reductase gene (<i>MTHFR</i>) polymorphisms, schizophrenia and bipolar disorder: An association study |
|
|
|
|
|
|
✓ |
✓ |
Scandinavian; Norwegian |
| Replication of linkage with bipolar disorder on chromosome 16p in the eastern Quebec population |
|
|
|
|
|
|
|
|
|
| Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients |
|
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|
|
|
|
|
|
| Associations of <i>ATF4</i> gene polymorphisms with schizophrenia in male patients |
|
|
|
|
|
|
✓ |
✓ |
Han Chinese |
| Pharmacogenetic study of atypical antipsychotic drug response: Involvement of the norepinephrine transporter gene |
|
✓ |
|
|
|
|
|
|
|
| Haplotype analysis of the IGF2‐INS‐TH gene cluster in Parkinson's disease |
|
✓ |
|
|
|
|
|
|
|
| No association between prostate apoptosis response 4 gene (PAWR) in schizophrenia and mood disorders in a japanese population |
|
|
|
|
|
|
✓ |
✓ |
Japanese population |
| A first stage genome‐wide screen for regions shared identical‐by‐descent in hutterite families with multiple sclerosis |
|
|
|
|
|
|
|
|
|
| A loss‐of‐function mutation in the <i>FTSJ1</i> gene causes nonsyndromic X‐linked mental retardation in a japanese family |
|
|
|
|
|
✓ |
|
|
"European and North American countries"; "in Europeans" |
| Heritability of obsessive‐compulsive symptom dimensions |
|
|
|
|
|
|
|
|
|
| The −1021 C/T DBH polymorphism is associated with neuropsychological performance among children and adolescents with ADHD |
|
|
|
|
|
|
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|
|
| Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette Syndrome |
|
|
|
|
|
|
|
|
|
| Differential methylation of the X‐chromosome is a possible source of discordance for bipolar disorder female monozygotic twins |
|
|
|
|
|
|
|
|
|
| <i>Cis</i>‐acting factors promoting the CAG intergenerational instability in Machado–Joseph disease |
|
|
|
|
|
|
|
|
|
| The association between DRD2/ANKK1, 5‐HTTLPR gene, and specific personality trait on antisocial alcoholism among Han Chinese in Taiwan |
|
|
|
|
|
|
✓ |
✓ |
Han Chinese |
| Association of 5‐HT1B receptor polymorphisms with the loudness dependence of auditory evoked potentials in a community‐based sample of healthy volunteers |
|
|
|
|
|
|
|
|
|
| Dopaminergic mutations: Within‐family association and linkage in multiplex alcohol dependence families |
|
✓ |
|
|
|
|
|
|
|
| Defining key features of the broad autism phenotype: A comparison across parents of multiple‐ and single‐incidence autism families |
|
|
|
|
|
|
|
|
|
| Chromosome 4q31‐34 panic disorder risk locus: Association of neuropeptide Y Y5 receptor variants |
|
|
|
|
|
|
✓ |
✓ |
German |
| Association of the ENGRAILED 2 (<i>EN2</i>) gene with autism in Chinese Han population |
|
|
|
|
|
|
✓ |
✓ |
Chinese Han |
| <i>EFHC2</i> SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome |
|
|
|
|
|
|
|
|
|
| Association of dopamine, serotonin, and nicotinic gene polymorphisms with methylphenidate response in ADHD |
|
|
|
|
|
|
|
|
|
| Absence of <i>OLIG2</i> mutations in patients presenting with a severe Pelizaeus‐Merzbacher‐like leukodystrophy associated with motor neuron dysfunction |
|
|
|
|
|
|
|
|
|
| BDNF Val66Met variant and age of onset in schizophrenia |
|
|
|
|
|
|
✓ |
✓ |
African‐American |
| Associations between an alpha 2a adrenergic receptor gene polymorphism and adolescent personality |
|
|
|
|
|
|
✓ |
✓ |
Estonian |