Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. - Wikidata - wikimedia - TriplyDB

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.

http://www.wikidata.org/entity/Q34672061

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Association claims in the sequencing era In search of low-frequency and rare variants affecting complex traits Rare-variant association analysis: study designs and statistical tests Association between Stress Response Genes and Features of Diurnal Cortisol Curves in the Multi-Ethnic Study of Atherosclerosis: A New Multi-Phenotype Approach for Gene-Based Association Tests Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data.DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.The impact of population demography and selection on the genetic architecture of complex traits.Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.Bio-collections in autism research.Large-scale genomics unveils the genetic architecture of psychiatric disorders A polygenic burden of rare disruptive mutations in schizophrenia.Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses.Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders.Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.Rare autism-associated variants implicate syntaxin 1 (STX1 R26Q) phosphorylation and the dopamine transporter (hDAT R51W) in dopamine neurotransmission and behaviors.Horizons of psychiatric genetics and epigenetics: where are we and where are we heading?A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing.No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations.GWASeq: targeted re-sequencing follow up to GWAS.Identification of Human Neuronal Protein Complexes Reveals Biochemical Activities and Convergent Mechanisms of Action in Autism Spectrum Disorders Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database General framework for meta-analysis of rare variants in sequencing association studies.Meta-Analysis of Gene Expression in Autism Spectrum Disorder.Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.Comorbidity clusters in autism spectrum disorders: an electronic health record time-series analysis Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.High-throughput sequencing of autism spectrum disorders comes of age.Genomic Characteristics of Gender Dysphoria Patients and Identification of Rare Mutations in RYR3 Gene.Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics.From Common to Rare Variants: The Genetic Component of Alzheimer Disease.Absence of substantial copy number differences in a pair of monozygotic twins discordant for features of autism spectrum disorder.Rare variant association test in family-based sequencing studies.

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Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.

http://www.wikidata.org/entity/Q34672061

description

2013 nî lūn-bûn

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2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի ապրիլին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... orders and population controls

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Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... rders and population controls.

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Analysis of rare, exonic varia ...... rders and population controls.

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Alicia Hawes

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Aniko Sabo

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Benjamin M Neale

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Bernie Devlin

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Christine Stevens

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Corneliu A Bodea

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Gerard D Schellenberg

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Hillary Coon

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P2860

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

The allelic architecture of human disease genes: common disease-common variant... or not?

Are rare variants responsible for susceptibility to complex diseases?

Functional impact of global rare copy number variation in autism spectrum disorders

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

Measuring inconsistency in meta-analyses

A method and server for predicting damaging missense mutations

Principal components analysis corrects for stratification in genome-wide association studies

Patterns and rates of exonic de novo mutations in autism spectrum disorders

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10.1371/JOURNAL.PGEN.1003443

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Eric Boerwinkle

Joseph D. Buxbaum

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Mark Joseph Daly

Kaitlin E Samocha

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2013-04-11T00:00:00Z

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236207407

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23593035

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Autism spectrum

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3623759

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