| Homozygosity mapping of depressive disorder in a large family from Pakistan: Significant linkage on chromosome 6 and 9 |
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| Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder |
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| Association of dopamine transporter gene variants with childhood ADHD features in bipolar disorder |
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| Increased risk of major depression by childhood abuse is not modified by <i>CNR1</i> genotype |
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| No evidence that common genetic risk variation is shared between schizophrenia and autism |
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| Phenotype refinement for comorbid attention deficit hyperactivity disorder and reading disability |
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| Replication and refinement of the role of rs548181 in schizophrenia: Results from a family based study |
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| Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH |
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| Reply to: ZNF804A and schizophrenia: An open peer commentary |
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| <i>ZNF804A</i> and schizophrenia: An open peer commentary |
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| Neurobehavioral phenotype observed in KBG syndrome caused by <i>ANKRD11</i> mutations |
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| No association of genetic variants in <i>BDNF</i> with major depression: A meta‐ and gene‐based analysis |
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| Erratum: Association of CRHR1 and CRHR2 with major depressive disorder and panic disorder in a Japanese population |
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✓ |
✓ |
Japanese population |
| Comparative study of regional homogeneity in schizophrenia and major depressive disorder |
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| <i>TCF4</i> (<i>e2‐2; ITF2</i>): A schizophrenia‐associated gene with pleiotropic effects on human disease |
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| <i>ANK3</i> as a risk gene for schizophrenia: New data in han Chinese and meta analysis |
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✓ |
✓ |
Han Chinese |
| Effectiveness of a web‐based protocol for the screening and phenotyping of individuals with tourette syndrome for genetic studies |
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| Molecular genetics research in ADHD: Ethical considerations concerning patients' benefit and resource allocation |
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| Maternal prenatal smoking and offspring emotional problems: No moderating effect of maternal or child 5‐HTTLPR genotype |
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| Gene expression changes in peripheral blood from chinese han patients with tourette syndrome |
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| Methylenetetrahydrofolate reductase (<i>MTHFR</i>) C677T polymorphism and age at onset of schizophrenia: No consistent evidence for an association in the nordic population |
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✓ |
✓ |
Scandinavian population; Nordic population; Scandinavian samples; Nordic samples; other populations |
| Genetic studies indicate a potential target 5‐HTR<sub>3B</sub> for Drug Therapy in Schizophrenia Patients |
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| Association of <i>KIBRA</i> with episodic and working memory: A meta‐analysis |
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✓ |
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| Genetic variant in<i>KIAA0319</i>, but not in<i>DYX1C1</i>, is associated with risk of dyslexia: An integrated meta‐analysis |
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| Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, ift27 and parvalbumin |
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| <i>CSF1R</i> mutations identified in three families with autosomal dominantly inherited leukoencephalopathy |
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| Genetic variants in the catechol‐<i>o</i>‐methyltransferase gene are associated with impulsivity and executive function: Relevance for major depression |
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| An association and haplotype analysis of porcine maternal infanticide: A model for human puerperal psychosis? |
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| Tau phosphorylation pathway genes and cerebrospinal fluid tau levels in Alzheimer's disease |
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| Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not? |
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| A common <i>TPH2</i> haplotype regulates the neural processing of a cognitive control demand |
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| Dissecting the Genetic Heterogeneity of Depression Through Age at Onset |
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| Meta‐analysis argues for a female‐specific role of <i>MAOA</i>‐uVNTR in panic disorder in four European populations |
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✓ |
✓ |
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|
four European populations; European (Estonian, German, Italian, and Polish) |
| Brain‐derived neurotrophic factor gene Val66Met polymorphism and cognitive function in obsessive–compulsive disorder |
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| Detecting anxiety symptoms in children and youths with neurofibromatosis type I |
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| Autistic disorder phenotype associated to a complex 15q intrachromosomal rearrangement |
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| Rare variants in <i>TMEM132D</i> in a case–control sample for panic disorder |
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✓ |
✓ |
different ethnic origins |
| Genome‐wide association analysis of eating disorder‐related symptoms, behaviors, and personality traits |
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✓ |
|
|
European ancestry |
| Association of genetic variations in <i>DTNBP1</i> with cognitive function in schizophrenia patients and healthy subjects |
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| <i>ZNF804A</i> and schizophrenia susceptibility in Asian populations |
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✓ |
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|
populations of European ancestries; Europeans; European samples |
| The mitochondrial genome and psychiatric illness |
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| Refining psychiatric phenotypes for response to treatment: Contribution of LPHN3 in ADHD |
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| Biochemical and genetic analyses of childhood attention deficit/hyperactivity disorder |
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| Investigation of allelic heterogeneity of the CCK‐A receptor gene in paranoid schizophrenia |
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✓ |
✓ |
Chinese |
| Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders |
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| The association of TGF‐β1 codon 10 polymorphism with suicide behavior |
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| Effect of <i>DISC1</i> SNPs on brain structure in healthy controls and patients with a history of psychosis |
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| A systematic review and meta‐analysis on the association between BDNF val<sup>66</sup>met and hippocampal volume—A genuine effect or a winners curse? |
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| GSK3β reduces risk of sporadic Parkinson's disease in ethnic Chinese |
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✓ |
✓ |
ethnic Chinese; Han Chinese |
| Genetics of dementia: Update and guidelines for the clinician |
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| Identification of two inherited copy number variants in a male with autism supports two‐hit and compound heterozygosity models of autism |
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| Serotonin transporter<i>5‐HTTLPR</i>genotype moderates the effects of childhood adversity on posttraumatic stress disorder risk: A replication study |
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|
✓ |
✓ |
✓ |
European Americans (EAs); African Americans (AAs) |
| Defining genetically meaningful language and personality traits in relatives of individuals with fragile X syndrome and relatives of individuals with autism |
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| The role of <i>ECE1</i> variants in cognitive ability in old age and Alzheimer's disease risk |
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| Genome‐wide association uncovers shared genetic effects among personality traits and mood states |
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|
✓ |
|
|
European cohorts |
| Genome‐wide association study of neurocognitive impairment and dementia in HIV‐infected adults |
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| Genetic heterogeneity according to age at onset in bipolar disorder: A combined positional cloning and candidate gene approach |
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| Prevalence of CGG expansions of the <i>FMR1</i> gene in a US population‐based sample |
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| Prevalence and heritability of skin picking in an adult community sample: A twin study |
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| The brain‐derived neurotrophic‐factor (<i>BDNF</i>) val66met polymorphism is associated with geriatric depression: A meta‐analysis |
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| Paternal age effect on age of onset in bipolar I disorder is mediated by sex and family history |
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| Mild cognitive impairment identified in older individuals with down syndrome by reduced telomere signal numbers and shorter telomeres measured in microns |
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| A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder |
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| Genetic and environmental causes of variation in perceived loneliness in young people |
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| Reduced fractional anisotropy in the uncinate fasciculus in patients with major depression carrying the met‐allele of the Val66Met brain‐derived neurotrophic factor genotype |
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| Different gene sets contribute to different symptom dimensions of depression and anxiety |
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| Depression and anxiety symptoms among women who carry the <i>FMR1</i> premutation: Impact of raising a child with fragile X syndrome is moderated by <i>CRHR1</i> polymorphisms |
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| Meta‐analysis of genetic association studies on bipolar disorder |
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| Addendum: Genome‐wide association study in German patients with attention deficit/hyperactivity disorder |
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|
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| The relationship of the serotonin transporter (SLC6A4) extra long variant to gene expression in an African American sample |
|
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|
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|
|
✓ |
|
African American |
| The interaction between BDNF and DRD2 in Bipolar II disorder but not in bipolar i disorder |
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|
|
| Identification of a <i>CACNA2D4</i> deletion in late onset bipolar disorder patients and implications for the involvement of voltage‐dependent calcium channels in psychiatric disorders |
|
|
|
|
|
✓ |
|
|
European decent |
| No associations found between the genes situated at 6p22.1, <i>HIST1H2BJ</i>, <i>PRSS16</i>, and <i>PGBD1</i> in Japanese patients diagnosed with schizophrenia |
|
|
|
|
|
|
✓ |
✓ |
Japanese |
| Association between serotonin transporter gene polymorphism and eating disorders outcome: A 6‐year follow‐up study |
|
✓ |
|
|
|
|
✓ |
✓ |
Italian |
| ASTN1 and alcohol dependence: Family‐based association analysis in multiplex alcohol dependence families |
|
|
|
|
|
|
|
|
HapMap CEU population |
| A re‐review of the association between the <i>NOTCH4</i> locus and schizophrenia |
|
|
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|
|
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|
|
| The 5‐HTTLPR polymorphism moderates the effect of stressful life events on drinking behavior in college students of African descent |
|
|
|
|
|
✓ |
✓ |
✓ |
European‐American (EA) college students; African descent; Historically Black University; Black |
| Genome‐wide search for replicable risk gene regions in alcohol and nicotine co‐dependence |
|
|
|
|
|
✓ |
✓ |
✓ |
European‐American (EA); African‐American (AA) |
| Association study of neuregulin 1 gene polymorphisms with auditory p300 in schizophrenia |
|
|
|
|
|
|
✓ |
✓ |
Chinese Han |
| No evidence that major mtDNA European haplogroups confer risk to schizophrenia |
|
|
|
|
✓ |
✓ |
|
|
European mtDNA phylogeny; European branches of the mtDNA phylogeny; European mtDNA haplogroups |
| Association of CRHR1 and CRHR2 with major depressive disorder and panic disorder in a Japanese population |
|
|
|
|
|
|
✓ |
✓ |
Japanese population |
| Genetic overlap of schizophrenia and bipolar disorder in a high‐density linkage survey in the Portuguese Island population |
|
|
|
|
|
|
✓ |
✓ |
Portuguese Island population |
| Functional genetic variation at the <i>NRGN</i> gene and schizophrenia: Evidence from a gene‐based case–control study and gene expression analysis |
|
|
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|
|
|
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|
|
| Evidence for a genetic overlap between body dysmorphic concerns and obsessive–compulsive symptoms in an adult female community twin sample |
|
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|
|
| Impact of the Reelin signaling cascade (Ligands–Receptors–Adaptor Complex) on cognition in schizophrenia |
|
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|
|
| Addendum: Novel pathogenic mutations and copy number variations in the VPS13A gene in patients with chorea‐acanthocytosis. A. Tomiyasu, M. Nakamura, M. Ichiba, S. Ueno, S. Saiki, M. Morimoto, J. Kobal |
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|
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|
|
|
|
|
|
| Association of Catechol‐<i>O</i>‐methyltransferase gene polymorphisms with schizophrenia and negative symptoms in a Chinese population |
|
|
|
|
|
|
✓ |
✓ |
Chinese; Han Chinese |
| Autosomal linkage scan for loci predisposing to comorbid dependence on multiple substances |
|
|
|
|
|
✓ |
|
|
European American (EA) |
| Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample |
|
|
|
|
|
|
✓ |
✓ |
German |
| Mutations in<i>NRXN1</i>in a family multiply affected with brain disorders:<i>NRXN1</i>mutations and brain disorders |
|
|
|
|
|
|
|
|
|
| A study of the combined effects of the EHD3 and FREM3 genes in patients with major depressive disorder |
|
|
|
|
|
|
✓ |
✓ |
Chinese Han population |
| Effects of a mis‐sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia |
|
|
|
|
|
|
|
|
|
| Erratum: Neuropsychological intra‐individual variability explains unique genetic variance of adhd and shows suggestive linkage to chromosomes 12, 13, and 17 |
|
|
|
|
|
|
|
|
|
| Sequencing of the <i>ANKYRIN 3</i> gene (<i>ANK3</i>) encoding ankyrin G in bipolar disorder reveals a non‐conservative amino acid change in a short isoform of ankyrin G |
|
|
|
|
|
|
✓ |
✓ |
ancestral populations |
| Lack of association of the 5‐HT<sub>3A</sub> receptor with schizophrenia |
|
|
|
|
|
|
|
|
|
| Moderation of adult depression by the serotonin transporter promoter variant (5‐HTTLPR), childhood abuse and adult traumatic events in a general population sample |
|
✓ |
|
|
|
|
|
|
|
| Support for involvement of glutamate decarboxylase 1 and neuropeptide y in anxiety susceptibility |
|
|
|
|
|
|
✓ |
✓ |
Finnish population-based Health 2000 sample |
| Genome‐wide supported psychosis risk variant in ZNF804A gene and impact on cortico–limbic WM integrity in schizophrenia |
|
|
|
|
|
|
✓ |
✓ |
Chinese |
| Additive effects of serotonergic and dopaminergic polymorphisms on trait impulsivity |
|
✓ |
|
|
|
|
|
|
|
| Maternal smoking during pregnancy and child emotional problems: The relevance of maternal and child 5‐HTTLPR genotype |
|
|
|
|
|
|
|
|
|
| Multivariate analysis of anxiety disorders yields further evidence of linkage to chromosomes 4q21 and 7p in panic disorder families |
|
|
|
|
|
|
|
|
|
| The neuroanatomy of genetic subtype differences in Prader–Willi syndrome |
|
|
|
|
|
|
|
|
|
| Advances in tryptophan hydroxylase‐2 gene expression regulation: New insights into serotonin–stress interaction and clinical implications |
|
|
|
|
|
|
|
|
|
| Tests of linkage and allelic association between markers in the 1p36 PRKCZ (Protein Kinase C Zeta) gene region and bipolar affective disorder |
|
|
|
|
|
|
|
|
|
| Beyond the patient: The broader impact of genetic discrimination among individuals at risk of Huntington disease |
|
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|
|
|
|
|
|
| Coordinated changes in AHRR methylation in lymphoblasts and pulmonary macrophages from smokers |
|
|
|
|
|
|
|
|
|
| Clinical improvement of the aggressive neurobehavioral phenotype in a patient with a deletion of <i>PITX3</i> and the absence of <scp>L</scp>‐DOPA in the cerebrospinal fluid |
|
|
|
|
|
|
|
|
|
| Neuropsychological intra‐individual variability explains unique genetic variance of ADHD and shows suggestive linkage to chromosomes 12, 13, and 17 |
|
|
|
|
|
|
|
|
|
| Alpha‐5 and ‐3 nicotinic receptor gene variants predict nicotine dependence but not cessation: Findings from the COMMIT cohort |
|
|
|
|
|
✓ |
|
|
European‐American |