Failure to replicate a genetic association may provide important clues about genetic architecture
about
Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birthDiverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factorsEpistasis and quantitative traits: using model organisms to study gene-gene interactionsSystems analysis of high-throughput dataAssociation of Long Runs of Homozygosity With Alzheimer Disease Among African American IndividualsTransdisciplinary approaches enhance the production of translational knowledgeThe association between endothelial nitric oxide synthase gene G894T polymorphism and hypertension in Han Chinese: a case-control study and an updated meta-analysisContextual sensitivity in scientific reproducibilityAppetite regulation genes are associated with body mass index in black South African adolescents: a genetic association studyEvolving hard problems: Generating human genetics datasets with a complex etiologyEtiology of Obesity Over the Life Span: Ecological and Genetic Highlights from Asian Countries.SNP-SNP interactions dominate the genetic architecture of candidate genes associated with left ventricular mass in African-Americans of the GENOA study.Computational genetics analysis of grey matter density in Alzheimer's disease.Multifactor dimensionality reduction for graphics processing units enables genome-wide testing of epistasis in sporadic ALS.Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity.Pure and Confounded Effects of Causal SNPs on Longevity: Insights for Proper Interpretation of Research Findings in GWAS of Populations with Different Genetic Structures.Methods of integrating data to uncover genotype-phenotype interactions.A replication study confirms the association of dendritic cell immunoreceptor (DCIR) polymorphisms with ACPA - negative RA in a large Asian cohortA meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level.FAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals.Bioinformatics challenges for genome-wide association studies.Survival dimensionality reduction (SDR): development and clinical application of an innovative approach to detect epistasis in presence of right-censored data.Association of Parkinson disease risk loci with mild parkinsonian signs in older persons.Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography.Methods for investigating gene-environment interactions in candidate pathway and genome-wide association studies.Clustering by genetic ancestry using genome-wide SNP data.Improved detection of gene-microbe interactions in the mouse skin microbiota using high-resolution QTL mapping of 16S rRNA transcripts.Model-based multifactor dimensionality reduction for detecting epistasis in case-control data in the presence of noise.Why epistasis is important for tackling complex human disease genetics.Association of ADIPOQ gene variants with body weight, type 2 diabetes and serum adiponectin concentrations: the Finnish Diabetes Prevention Study.Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and ArgentinaEpistatic Networks Jointly Influence Phenotypes Related to Metabolic Disease and Gene Expression in Diversity Outbred Mice.A survey of putative anxiety-associated genes in panic disorder patients with and without bladder symptomsGene--environment-wide association studies: emerging approachesPathways of distinction analysis: a new technique for multi-SNP analysis of GWAS data.Analysis of gene-gene interactions using gene-trait similarity regression.Performance analysis of novel methods for detecting epistasis.Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes.C8orf13-BLK is a genetic risk locus for systemic sclerosis and has additive effects with BANK1: results from a large french cohort and meta-analysis.Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.
P2860
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P2860
Failure to replicate a genetic association may provide important clues about genetic architecture
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունիսին 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
Failure to replicate a genetic ...... ues about genetic architecture
@ast
Failure to replicate a genetic ...... ues about genetic architecture
@en
type
label
Failure to replicate a genetic ...... ues about genetic architecture
@ast
Failure to replicate a genetic ...... ues about genetic architecture
@en
prefLabel
Failure to replicate a genetic ...... ues about genetic architecture
@ast
Failure to replicate a genetic ...... ues about genetic architecture
@en
P2860
P50
P1433
P1476
Failure to replicate a genetic ...... ues about genetic architecture
@en
P2093
Nadia M Penrod
P2860
P356
10.1371/JOURNAL.PONE.0005639
P407
P577
2009-06-02T00:00:00Z