Uncovering the roles of rare variants in common disease through whole-genome sequencing.
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Implication of next-generation sequencing on association studiesRapid-throughput skeletal phenotyping of 100 knockout mice identifies 9 new genes that determine bone strengthFine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritabilityWhat have we learnt about the causes of ADHD?Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic EpidemiologyA genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer diseaseIntegrative cancer epidemiology--the next generationGenetic advances in the study of speech and language disordersBeyond the fourth wave of genome-wide obesity association studiesGenes and chronic obstructive pulmonary diseaseDownregulated kynurenine 3-monooxygenase gene expression and enzyme activity in schizophrenia and genetic association with schizophrenia endophenotypes.AMD and the alternative complement pathway: genetics and functional implicationsGenetic causes of cancer predisposition in children and adolescentsImpact of New Genomic Technologies on Understanding Adverse Drug ReactionsNew insights from monogenic diabetes for "common" type 2 diabetesGenetic prediction of common diseases. Still no help for the clinical diabetologist!Personalized medicine and human genetic diversityMedical genomics: The intricate path from genetic variant identification to clinical interpretationTwo-phase and family-based designs for next-generation sequencing studiesFollowing the genes: a framework for animal modeling of psychiatric disordersGenetics of impulsive behaviourRare-variant association analysis: study designs and statistical testsChild development and molecular genetics: 14 years laterThe molecular pathogenesis of migraine: new developments and opportunitiesSecond malignant neoplasms and cardiovascular disease following radiotherapy.The role of host genetics in susceptibility to influenza: a systematic reviewCopy number variants in obesity-related syndromes: review and perspectives on novel molecular approachesCellular hyperproliferation and cancer as evolutionary variablesGenetic variants at the IFNL3 locus and their association with hepatitis C virus infections reveal novel insights into host-virus interactionsCurrent concepts on primary open-angle glaucoma genetics: a contribution to disease pathophysiology and future treatmentAmish revisited: next-generation sequencing studies of psychiatric disorders among the Plain peopleHidden disease susceptibility and sexual dimorphism in the heterozygous knockout of Cyp51 from cholesterol synthesisTrends in Next-Generation Sequencing and a New Era for Whole Genome SequencingOmics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism InvestigationsSystematic analysis and functional annotation of variations in the genome of an Indian individualImputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohortMosaic PPM1D mutations are associated with predisposition to breast and ovarian cancerIdentifying disease mutations in genomic medicine settings: current challenges and how to accelerate progressCombining family- and population-based imputation data for association analysis of rare and common variants in large pedigreesAberrant gene expression in humans
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Uncovering the roles of rare variants in common disease through whole-genome sequencing.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on June 2010
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
@en
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
@nl
type
label
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
@en
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
@nl
prefLabel
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
@en
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
@nl
P356
P1476
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
@en
P2093
David B Goldstein
P2888
P304
P356
10.1038/NRG2779
P577
2010-06-01T00:00:00Z