Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls - Wikidata - awgldk - TriplyDB

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

http://www.wikidata.org/entity/Q24628710

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Genome-wide copy number analysis uncovers a new HSCR gene: NRG3 CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems Human genetics and genomics a decade after the release of the draft sequence of the human genome Detection of identity by descent using next-generation whole genome sequencing data Recent Insights Into the Genetics of Inflammatory Bowel Disease Personalized medicine: hope or hype?ESPRESSO: taking into account assessment errors on outcome and exposures in power analysis for association studies Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls Rare deletions at the neurexin 3 locus in autism spectrum disorder SHANK1 Deletions in Males with Autism Spectrum Disorder Diversity of human copy number variation and multicopy genes Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis Mapping copy number variation by population-scale genome sequencing A map of human genome variation from population-scale sequencing Direct measure of the de novo mutation rate in autism and schizophrenia cohorts Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder Human IRGM regulates autophagy and cell-autonomous immunity functions through mitochondria Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes Rheumatoid arthritis susceptibility genes: An overview Complexity of gene expression evolution after duplication: protein dosage rebalancing Child development and molecular genetics: 14 years later Proceedings: consideration of genetics in the design of induced pluripotent stem cell-based models of complex disease Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approaches Human molecular cytogenetics: From cells to nucleotides The impact of human copy number variation on gene expression Regulation of ribosomal DNA amplification by the TOR pathway.Complex and multi-allelic copy number variation in human disease A copy number variation map of the human genome Immunologic manifestations of autophagy Exploring the role of copy number variants in human adaptation Abnormal dosage of ultraconserved elements is highly disfavored in healthy cells but not cancer cells Impact of changing drug treatment and malaria endemicity on the heritability of malaria phenotypes in a longitudinal family-based cohort study The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation CNVs leading to fusion transcripts in individuals with autism spectrum disorder Schizophrenia, "Just the Facts" 6. Moving ahead with the schizophrenia concept: from the elephant to the mouse Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24 Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants The genetic effect of copy number variations on the risk of type 2 diabetes in a Korean population Genome-wide analysis of copy number variation in type 1 diabetes IRGM Governs the Core Autophagy Machinery to Conduct Antimicrobial Defense

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

http://www.wikidata.org/entity/Q24628710

description

2010 nî lūn-bûn

@nan

2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Genome-wide association study ...... ases and 3,000 shared controls

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Genome-wide association study ...... ases and 3,000 shared controls

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Genome-wide association study ...... ases and 3,000 shared controls

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Genome-wide association study ...... ases and 3,000 shared controls

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Genome-wide association study ...... ases and 3,000 shared controls

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Abiodun Onipinla

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Alison J Coffey

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Anne Phillips

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P2860

The diploid genome sequence of an individual human

Finding the missing heritability of complex diseases

Mapping and sequencing of structural variation from eight human genomes

Rare chromosomal deletions and duplications increase risk of schizophrenia

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Strong association of de novo copy number mutations with autism

Copy number variation at 1q21.1 associated with neuroblastoma

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

Large recurrent microdeletions associated with schizophrenia

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10.1038/NATURE08979

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464

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Andrew Tym Hattersley

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Alastair Compston

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1003788883

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genome-wide association study

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