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Genetic architecture of body size in mammalsHuman genetics and genomics a decade after the release of the draft sequence of the human genomeMissense mutations in the MEFV gene are associated with fibromyalgia syndrome and correlate with elevated IL-1beta plasma levelsGenomics era and complex disorders: Implications of GWAS with special reference to coronary artery disease, type 2 diabetes mellitus, and cancersAMD and the alternative complement pathway: genetics and functional implicationsAn introductory review of parallel independent component analysis (p-ICA) and a guide to applying p-ICA to genetic data and imaging phenotypes to identify disease-associated biological pathways and systems in common complex disordersGenetic prediction of common diseases. Still no help for the clinical diabetologist!Two-phase and family-based designs for next-generation sequencing studiesGenetics of impulsive behaviourPerioperative genomicsChild development and molecular genetics: 14 years laterComplex genetics of pulmonary diseases: lessons from genome-wide association studies and next-generation sequencingGenomics, personalized medicine, and pediatricsAnnotating individual human genomesInherited susceptibility for aggressive prostate cancerMolecular mechanisms of disease-causing missense mutationsSystems analysis of high-throughput dataCommon Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum DisorderUnderstanding rare and common diseases in the context of human evolutionBerberine and evodiamine influence serotonin transporter (5-HTT) expression via the 5-HTT-linked polymorphic regionEvolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseasesA comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseEvidence for the role of EPHX2 gene variants in anorexia nervosaInvestigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working populationProgress in methods for rare variant associationGene-based rare allele analysis identified a risk gene of Alzheimer's diseaseTargeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing StudyA genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysisGenome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traitsA novel genome-information content-based statistic for genome-wide association analysis designed for next-generation sequencing dataEpidemiology of cardiovascular disease: recent novel outlooks on risk factors and clinical approaches.Novel candidate genes may be possible predisposing factors revealed by whole exome sequencing in familial esophageal squamous cell carcinoma.Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderlyAssessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modelingA naturally occurring variant in human TLR9, P99L, is associated with loss of CpG oligonucleotide responsiveness.The application of naive Bayes model averaging to predict Alzheimer's disease from genome-wide dataOptimum designs for next-generation sequencing to discover rare variants for common complex disease.Secondary analysis of publicly available data reveals superoxide and oxygen radical pathways are enriched for associations between type 2 diabetes and low-frequency variants.A generalized genetic random field method for the genetic association analysis of sequencing data.The application of network label propagation to rank biomarkers in genome-wide Alzheimer's data.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Common vs. rare allele hypotheses for complex diseases
@ast
Common vs. rare allele hypotheses for complex diseases
@en
Common vs. rare allele hypotheses for complex diseases
@nl
type
label
Common vs. rare allele hypotheses for complex diseases
@ast
Common vs. rare allele hypotheses for complex diseases
@en
Common vs. rare allele hypotheses for complex diseases
@nl
prefLabel
Common vs. rare allele hypotheses for complex diseases
@ast
Common vs. rare allele hypotheses for complex diseases
@en
Common vs. rare allele hypotheses for complex diseases
@nl
P2860
P1476
Common vs. rare allele hypotheses for complex diseases
@en
P2093
Kelly A Frazer
Sarah S Murray
P2860
P304
P356
10.1016/J.GDE.2009.04.010
P577
2009-05-28T00:00:00Z