| Comparing the utility of homogeneous subtypes of cocaine use and related behaviors with DSM‐IV cocaine dependence as traits for genetic association analysis |
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✓ |
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European‐Americans |
| <i>ALDH2</i> is associated to alcohol dependence and is the major genetic determinant of “daily maximum drinks” in a GWAS study of an isolated rural chinese sample |
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✓ |
✓ |
Chinese |
| In search of biomarkers in psychiatry: EEG‐based measures of brain function |
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| Contribution of congenital heart disease to neuropsychiatric outcome in school‐age children with 22q11.2 deletion syndrome |
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| Significant study of population stratification, sensitivity analysis and trim and fill analyses on <i>GBA</i> mutation and parkinson's disease |
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| Genome‐wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition |
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✓ |
✓ |
Mexican American |
| Genetic susceptibility for bipolar disorder and response to antidepressants in major depressive disorder |
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| Neurophysiologic effect of GWAS derived schizophrenia and bipolar risk variants |
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| Impaired response inhibition is associated with self‐reported symptoms of depression, anxiety, and ADHD in female<i>FMR1</i>premutation carriers |
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| HLA associations in schizophrenia: Are we re‐discovering the wheel? |
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| Sex differences in the genetic risk for schizophrenia: History of the evidence for sex‐specific and sex‐dependent effects |
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| Association of genetic risk severity with ADHD clinical characteristics |
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✓ |
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| The New England family study high‐risk project: Neurological impairments among offspring of parents with schizophrenia and other psychoses |
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| Festschrift celebrating the career of Ming T. Tsuang |
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| Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From Taiwan |
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| Can sodium/hydrogen exchange inhibitors be repositioned for treating attention deficit hyperactivity disorder? An in silico approach |
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| Sex‐specific association of a common variant of the XG gene with autism spectrum disorders |
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✓ |
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families of European ancestry |
| Disorders and borders: Psychiatric genetics and nosology |
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| Gene‐environment interaction of ApoE genotype and combat exposure on PTSD |
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| Next‐generation sequencing in schizophrenia and other neuropsychiatric disorders |
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| Genetics of brain structure: Contributions from the vietnam era twin study of aging |
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| Taiwan schizophrenia linkage study: Lessons learned from endophenotype‐based genome‐wide linkage scans and perspective |
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| A review of neuroimaging studies of young relatives of individuals with schizophrenia: A developmental perspective from schizotaxia to schizophrenia |
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| On the outside, looking in: A review and evaluation of the comparability of blood and brain “‐omes” |
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| Heterogeneity of schizophrenia: Genetic and symptomatic factors |
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✓ |
✓ |
✓ |
European‐American cohort; African‐American cohort; European‐American cohort |
| A network medicine approach to psychiatric genetics |
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| Genome‐wide association study of atypical psychosis |
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| What can we learn about schizophrenia from studying the human model, drug‐induced psychosis? |
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| Development of liability syndromes for schizophrenia: Where did they come from and where are they going? |
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| Association study of 83 candidate genes for bipolar disorder in chromosome 6q selected using an evidence‐based prioritization algorithm |
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| Effects of neuregulin‐1 genetic variation and depression symptom severity on longitudinal patterns of psychotic symptoms in primary care attendees |
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| How might <i>ZNF804A</i> variants influence risk for schizophrenia and bipolar disorder? A literature review, synthesis, and bioinformatic analysis |
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| The XY gene hypothesis of psychosis: Origins and current status |
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| Methylenetetrahydrofolate reductase (<i>MTHFR</i>) genetic variation and major depressive disorder prognosis: A five‐year prospective cohort study of primary care attendees |
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| A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability |
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✓ |
✓ |
Scottish |
| Sequence analysis of 17<i>NRXN1</i>deletions |
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| Genome‐wide copy number scan identifies disruption of <i>PCDH11X</i> in developmental dyslexia |
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| Genetic predictors of risk and resilience in psychiatric disorders: A cross‐disorder genome‐wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizoph |
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✓ |
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Participants of European‐American descent (N = 2,246) |
| Epigenetic studies in Alzheimer's disease: Current findings, caveats, and considerations for future studies |
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| <i>SOX12</i> and <i>NRSN2</i> are candidate genes for 20p13 subtelomeric deletions associated with developmental delay |
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| Reaffirmation of GAK, but not HLA‐DRA, as a Parkinson's disease susceptibility gene in a Taiwanese population |
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✓ |
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✓ |
✓ |
Taiwanese population |
| Haplotype co‐segregation with attention deficit‐hyperactivity disorder in unrelated german multi‐generation families |
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German descent |
| High rates of comorbid depressive and anxiety disorders among women with premutation of the FMR1 gene |
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| Mood disorders in individuals with distal 18q deletions |
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| Alterations of brain anatomy in mouse model of MDD created by replacement of homologous mouse DNA sequence with an illness‐associated 6‐base human<i>CREB1</i>promoter sequence |
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| High frequency of intermediate alleles on huntington disease‐associated haplotypes in British Columbia's general population |
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| Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities |
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| Genome‐wide association analysis accounting for environmental factors through propensity‐score matching: Application to stressful live events in major depressive disorder |
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✓ |
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European individuals |
| Pharmacogenetics of antidepressant drugs: An update after almost 20 years of research |
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| Neural effects of the <scp><i>CSMD</i></scp><i>1</i> genome‐wide associated schizophrenia risk variant rs10503253 |
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| Association of BDNF gene polymorphisms with schizophrenia and clinical symptoms in a Chinese population |
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✓ |
✓ |
Han Chinese population |
| Association between <i>DRD2</i>/<i>DRD4</i> interaction and conduct disorder: A potential developmental pathway to alcohol dependence |
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| Replication of Genome‐Wide association studies (<scp>GWAS</scp>) loci for sleep in the British G1219 cohort |
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| Allele‐specific expression of the serotonin transporter and its transcription factors following lamotrigine treatment in vitro |
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| Partial duplication of the <scp><i>PARK</i></scp>2 gene in a child with developmental delay and her normal mother: A second report |
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| SNCA rs356219 variant increases risk of sporadic Parkinson's disease in ethnic Chinese |
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✓ |
✓ |
Han Chinese; Asian population; USA and Europe |
| <i>FMR1</i> CGG expansions: Prevalence and sex ratios |
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| Response to Mariani Et al.: A second report of <scp><i>PARK2</i></scp> duplication and developmental delay |
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| A prospective study of the effects of breastfeeding and FADS2 polymorphisms on cognition and hyperactivity/attention problems |
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| Convergent functional genomics of psychiatric disorders |
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| Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome‐wide association study of both common and rare variants |
|
✓ |
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✓ |
✓ |
✓ |
European Ancestry ADHD samples; Han Chinese |
| A genome‐wide association study of sleep habits and insomnia |
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| Principal components methods for narrow‐sense heritability in the analysis of multidimensional longitudinal cognitive phenotypes |
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| Association of aggression with a novel microRNA binding site polymorphism in the wolframin gene |
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| Autism spectrum disorders: The quest for genetic syndromes |
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| Substantial genetic link between iq and working memory: Implications for molecular genetic studies on schizophrenia. the european twin study of schizophrenia (EUTwinsS) |
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|
✓ |
✓ |
|
|
European Twin Study Network on Schizophrenia (EUTwinsS); "two centers within the European Twin Study |
| Blood‐based gene‐expression predictors of PTSD risk and resilience among deployed marines: A pilot study |
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| The genomic psychiatry cohort: Partners in discovery |
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| Meta‐analysis of association between obsessive‐compulsive disorder and the 3′ region of neuronal glutamate transporter gene <i>SLC1A1</i> |
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| Common obesity risk alleles in childhood attention‐deficit/hyperactivity disorder |
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| Molecular and clinical characterization of 25 individuals with exonic deletions of <i>NRXN1</i> and comprehensive review of the literature |
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| Overlap and specificity of genetic and environmental influences on excessive acquisition and difficulties discarding possessions: Implications for hoarding disorder |
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| Sex dependent influence of a functional polymorphism in steroid 5‐α‐reductase type 2 (<i>SRD5A2</i>) on post‐traumatic stress symptoms |
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✓ |
✓ |
African-American |
| <i>ADCYAP1R1</i> genotype associates with post‐traumatic stress symptoms in highly traumatized African‐American females |
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| Identification of rare copy number variants in high burden schizophrenia families |
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| Response to the letter “Actigraphic evaluation for patients with attention deficit/hyperactivity disorder” |
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| Catechol‐<i>O</i>‐methyltransferase gene <i>val</i>158<i>met</i> polymorphism and depressive symptoms during early childhood |
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| Testing the diathesis‐stress model: 5‐HTTLPR, childhood emotional maltreatment, and vulnerability to social anxiety disorder |
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| Actigraphic evaluation for patients with attention deficit/hyperactivity disorder |
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| A meta‐analysis of the relationship of the Parkin p.Val380Leu polymorphism to Parkinson's disease |
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| <i>DISC1</i> in adult ADHD patients: An association study in two European samples |
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✓ |
|
✓ |
✓ |
two European samples; controls of Norwegian ancestry; Spanish adult ADHD sample |
| Mitochondrial DNA (mtDNA) in brain samples from patients with major psychiatric disorders: Gene expression profiles, MtDNA content and presence of the MtDNA common deletion |
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| The evolutionary paradox and the missing heritability of schizophrenia |
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| Genome scan in familial late‐onset Alzheimer's disease: A locus on chromosome 6 contributes to age‐at‐onset |
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| A family‐based association analysis and meta‐analysis of the reading disabilities candidate gene <i>DYX1C1</i> |
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| Deletion at the SLC1A1 glutamate transporter gene co‐segregates with schizophrenia and bipolar schizoaffective disorder in a 5‐generation family |
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✓ |
✓ |
Palauan |
| Selected rapporteur summaries from the XX world congress of psychiatric genetics, Hamburg, Germany, october 14–18, 2012 |
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| Brain‐derived neurotrophic factor Val66Met polymorphism and early life adversity affect hippocampal volume |
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| Schizophrenia two‐hit hypothesis in velo‐cardio facial syndrome |
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| A combined study of genetic association and brain imaging on the <i>DAOA</i> gene in schizophrenia |
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| Associations of the 5‐hydroxytryptamine (serotonin) Receptor 1B gene (<i>HTR1B</i>) with alcohol, cocaine, and heroin abuse |
|
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|
✓ |
✓ |
✓ |
European, Asian, African, and Hispanic populations; non-Europeans; Asian, African, and Hispanic populations; non-Europeans |