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Exome sequencing identifies DLG1 as a novel gene for potential susceptibility to Crohn's disease in a Chinese family studyGenetic architecture of body size in mammalsJumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic EpidemiologyCancer pharmacogenomics: strategies and challengesSystematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitusWhat Is a Genome?Systems psychopharmacology: A network approach to developing novel therapiesImportance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene FunctionsProgress and promise in understanding the genetic basis of common diseasesEntering the second century of maize quantitative geneticsDevelopments in our understanding of the genetic basis of birth defectsThe advantages and limitations of trait analysis with GWAS: a reviewRare-variant association analysis: study designs and statistical testsThe Human Genome Project, and recent advances in personalized genomicsThe association of attempted suicide with genetic variants in the SLC6A4 and TPH genes depends on the definition of suicidal behavior: a systematic review and meta-analysisCopy number variants in obesity-related syndromes: review and perspectives on novel molecular approachesLate-Onset Alzheimer's Disease Genes and the Potentially Implicated PathwaysHeritability in the genome-wide association eraComplex genetic architecture of cardiac disease in a wild type inbred strain of Drosophila melanogasterQuantitative magnetic resonance imaging traits as endophenotypes for genetic mapping in epilepsyUnderstanding rare and common diseases in the context of human evolutionAssociation Analysis in Rice: From Application to UtilizationThe genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discoveryStrategies for Imputing and Analyzing Rare Variants in Association StudiesMapping asthma-associated variants in admixed populationsEnvironmental epigenetics and its implication on disease risk and health outcomesCombining family- and population-based imputation data for association analysis of rare and common variants in large pedigreesSystems biology approach reveals genome to phenome correlation in type 2 diabetesProgress in methods for rare variant associationAdvances in the genetic dissection of plant cell walls: tools and resources available in MiscanthusRank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populationsSystematic localization of common disease-associated variation in regulatory DNAEvolution and functional impact of rare coding variation from deep sequencing of human exomesA conservative assessment of the major genetic causes of idiopathic chronic pancreatitis: data from a comprehensive analysis of PRSS1, SPINK1, CTRC and CFTR genes in 253 young French patientsMendelian randomization in cardiometabolic disease: challenges in evaluating causality.Dissecting the genetics of complex traits using summary association statisticsRegularized Machine Learning in the Genetic Prediction of Complex TraitsElectrophysiological Endophenotypes for SchizophreniaHigh-specificity detection of rare alleles with Paired-End Low Error Sequencing (PELE-Seq).Functional analysis of a chromosomal deletion associated with myelodysplastic syndromes using isogenic human induced pluripotent stem cells.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Rare and common variants: twenty arguments.
@ast
Rare and common variants: twenty arguments.
@en
type
label
Rare and common variants: twenty arguments.
@ast
Rare and common variants: twenty arguments.
@en
prefLabel
Rare and common variants: twenty arguments.
@ast
Rare and common variants: twenty arguments.
@en
P2860
P356
P1476
Rare and common variants: twenty arguments.
@en
P2093
Greg Gibson
P2860
P2888
P304
P356
10.1038/NRG3118
P577
2011-02-01T00:00:00Z
P6179
1001779725