| Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature |
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| Cover Image, Volume 174B, Number 1, January 2017 |
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| Issue Information ‐ TOC |
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| Genomic variants, genes, and pathways of Alzheimer's disease: An overview |
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| <i>APOE</i>gene and neuropsychiatric disorders and endophenotypes: A comprehensive review |
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| The discovery of <i>LRRK2</i> p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot |
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| Identification of extreme motor phenotypes in Huntington's disease |
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| Blood transcriptomic comparison of individuals with and without autism spectrum disorder: A combined‐samples mega‐analysis |
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| Genetic and environmental contributions to the inverse association between specific autistic traits and experience seeking in adults |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 171B, Number 8, December 2016 |
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| Genetic variants associated with risk of Alzheimer's disease contribute to cognitive change in midlife: The Atherosclerosis Risk in Communities Study |
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| Genetic factors in neurodegenerative diseases |
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| Psychopathology in 7‐year‐old children: Differences in maternal and paternal ratings and the genetic epidemiology |
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| Paternal age and psychiatric disorders: A review |
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| Methamphetamine‐induced psychosis is associated with DNA hypomethylation and increased expression of <i>AKT1</i> and key dopaminergic genes |
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| Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression |
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Irish |
| Sex‐specific linkage scans in opioid dependence |
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European‐American (EA); African‐American (AA) |
| Personality traits in Huntington's disease: An exploratory study of gene expansion carriers and non‐carriers |
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| Replication analyses of four chromosomal deletions with schizophrenia via independent large‐scale meta‐analyses |
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| Highly polygenic architecture of antidepressant treatment response: Comparative analysis of SSRI and NRI treatment in an animal model of depression |
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| Family, twin, and adoption studies of childhood onset psychiatric and neurodevelopmental disorders |
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| Cover Image, Volume 171B, Number 7, October 2016 |
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| Issue Information ‐ TOC |
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| Genetic analysis of <i>CHCHD2</i> gene in Chinese Parkinson's disease |
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Chinese, Japanese, Asian, Asian populations, mainland China |
| IQ and hemizygosity for the Val<sup>158</sup>Met functional polymorphism of <i>COMT</i> in 22q11DS |
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| Psychiatric disorders among women with the fragile X premutation without children affected by fragile X syndrome |
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| Apolipoprotein E genotypes and plasma levels in mild cognitive impairment conversion to Alzheimer's disease: A follow‐up study |
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| Two‐stage additional evidence support association of common variants in the <i>HDAC3</i> with the increasing risk of schizophrenia susceptibility |
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Han Chinese |
| Mutations modifying sporadic Alzheimer's disease age of onset |
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| Recurrent 15q11.2 BP1‐BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders |
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| <i>GAD1</i> gene polymorphisms are associated with hyperactivity in Attention‐Deficit/Hyperactivity Disorder |
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| Issue Information ‐ TOC |
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| Associations of rare nicotinic cholinergic receptor gene variants to nicotine and alcohol dependence |
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| Cover Image, Volume 171B, Number 6, September 2016 |
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| A current snapshot of common genomic variants contribution in psychiatric disorders |
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| Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort |
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| A targeted sequencing study of glutamatergic candidate genes in suicide attempters with bipolar disorder |
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| Heritability of major depressive and comorbid anxiety disorders in multi‐generational families at high risk for depression |
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| Whole genome sequencing of a dizygotic twin suggests a role for the serotonin receptor <i>HTR7</i> in autism spectrum disorder |
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| Reduced gamma‐aminobutyric acid is associated with emotional and behavioral problems in Prader–Willi syndrome |
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| Genetic variation in the endocannabinoid system and response to Cognitive Behavior Therapy for child anxiety disorders |
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| Fragile X syndrome screening in pregnant women and women planning pregnancy shows a remarkably high <i>FMR1</i> premutation prevalence in the Balearic Islands |
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Spanish population; Balearic Islands |
| GWAS‐identified schizophrenia risk SNPs at <i>TSPAN18</i> are highly diverged between Europeans and East Asians |
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European and East Asian descent; Europeans; East Asians; East Asian; East Asians; Han Chinese |
| Issue Information ‐ TOC |
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| Cover Image, Volume 171B, Number 5, July 2016 |
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| A novel <i>CCM2</i> variant in a family with non‐progressive cognitive complaints and cerebral microbleeds |
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| A balanced translocation disrupting <i>BCL2L10</i> and <i>PNLDC1</i> segregates with affective psychosis |
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| Common variants in <i>CACNA1C</i> and MDD susceptibility: A comprehensive meta‐analysis |
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one European GWAS; reanalyzing the data according to ethnicity |
| Whole‐exome sequencing implicates<i>DGKH</i>as a risk gene for panic disorder in the Faroese population |
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outbred European populations; more outbreed European populations |
| Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits |
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| Whole‐gene sequencing investigation of<i>SAT1</i>in attempted suicide |
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| The genetics of anxiety‐related negative valence system traits |
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| <i>FKBP5</i> genotype interacts with early life trauma to predict heavy drinking in college students |
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| Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic <i>NTRK1‐</i>mutation due to uniparental disomy |
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| The role of protein intrinsic disorder in major psychiatric disorders |
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| Cover Image, Volume 171B, Number 4, June 2016 |
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| Issue Information ‐ TOC |
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| Genetic counseling and testing for Huntington's disease: A historical review |
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| The <i>ANK3</i> gene and facial affect processing: An ERP study |
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| Preliminary examination of microRNA expression profiling in bipolar disorder I patients during antipsychotic treatment |
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| <i>PARK16</i> is associated with PD in the Malaysian population |
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European |
| Genome‐wide association study of generalized anxiety symptoms in the Hispanic Community Health Study/Study of Latinos |
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| The discovery of <i>LRRK2</i> p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot |
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| Polymorphisms of the <i>TCF4</i> gene are associated with the risk of schizophrenia in the Han Chinese |
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Han Chinese |
| Transcriptome analysis of genes and gene networks involved in aggressive behavior in mouse and zebrafish |
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| The genetics of aggression: Where are we now? |
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| Genome‐wide analyses of aggressiveness in attention‐deficit hyperactivity disorder |
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| Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach |
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| Genome‐wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered <i>cis</i>‐regulation of <i>BORCS7</i>, <i>AS3MT</i>, and <i>NT5C2</i> in the human brain |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 171B, Number 3, April 2016 |
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| LINE1 insertions as a genomic risk factor for schizophrenia: Preliminary evidence from an affected family |
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| Unusually long duration and delayed penetrance in a family with FTD and mutation in <i>MAPT</i> (V337M) |
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| Rare <i>UNC13B</i> variations and risk of schizophrenia: Whole‐exome sequencing in a multiplex family and follow‐up resequencing and a case–control study |
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Japanese population |
| Meta‐analysis of the serotonin transporter promoter variant (<i>5‐HTTLPR</i>) in relation to adverse environment and antisocial behavior |
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| An examination of the language construct in NIMH's research domain criteria: Time for reconceptualization! |
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| 15q13.3 duplication in two patients with childhood‐onset schizophrenia |
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| <i>COMT</i> genotype is associated with differential expression of muscarinic M1 receptors in human cortex |
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| Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion |
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| Multimarker analysis suggests the involvement of BDNF signaling and microRNA biosynthesis in suicidal behavior |
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| Understanding the covariation of tics, attention‐deficit/hyperactivity, and obsessive‐compulsive symptoms: A population‐based adult twin study |
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| Discovery of biochemical biomarkers for aggression: A role for metabolomics in psychiatry |
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| A pilot integrative genomics study of GABA and glutamate neurotransmitter systems in suicide, suicidal behavior, and major depressive disorder |
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| The contribution of protein intrinsic disorder to understand the role of genetic variants uncovered by autism spectrum disorders exome studies |
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| Physical and verbal aggressive behavior and <i>COMT</i> genotype: Sensitivity to the environment |
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Swedish population‐based cohort |
| Genetic association between <i>NRG1</i> and schizophrenia, major depressive disorder, bipolar disorder in Han Chinese population |
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Han Chinese population |
| Comparative mRNA analysis of behavioral and genetic mouse models of aggression |
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| Issue Information ‐ TOC |
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| Adult neurogenesis and neurodegenerative diseases: A systems biology perspective |
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| A comprehensive meta‐analysis of <i>ZNF804A</i> SNPs in the risk of schizophrenia among Asian populations |
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Europeans; European GWAS risk single nucleotide polymorphism (SNP) |
| The ethics of complexity. Genetics and autism, a literature review |
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| Surface‐based morphometry reveals distinct cortical thickness and surface area profiles in Williams syndrome |
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| Reinforcing the association between distal <i>1q</i> CNVs and structural brain disorder: A case of a complex <i>1q43‐q44</i> CNV and a review of the literature |
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| Association of copy number polymorphisms at the promoter and translated region of <i>COMT</i> with Japanese patients with schizophrenia |
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| Novel variants in <i>ZNF34</i> and other brain‐expressed transcription factors are shared among early‐onset MDD relatives |
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| Variants in <i>TERT</i> influencing telomere length are associated with paranoid schizophrenia risk |
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| Smoking during pregnancy and ADHD risk: A genetically informed, multiple‐rater approach |
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| Longitudinal heritability of childhood aggression |
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| Executive functioning deficits in children with neurofibromatosis type 1: The influence of intellectual and social functioning |
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| Aggressive behavior in humans: Genes and pathways identified through association studies |
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| The 22q11 <i>PRODH/DGCR6</i> deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD |
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| Longitudinal predictors of cannabis use and dependence in offspring from families at ultra high risk for alcohol dependence and in control families |
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| The impact of <i>CACNA1C</i> allelic variation on regional gray matter volume in Chinese population |
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European populations; Han Chinese; Chinese population |
| Autism spectrum disorder traits in<i>Slc9a9</i>knock‐out mice |
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| Genetics of psychosis of Alzheimer disease |
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