Simple estimates of haplotype relative risks in case-control data.
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Meta-analysis of haplotype-association studies: comparison of methods and empirical evaluation of the literatureVariation in eicosanoid genes, non-fatal myocardial infarction and ischemic stroke.IL1B genetic variation and plasma C-reactive protein level among young adults: the CARDIA study.Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.Discovering novel risk factors for venous thrombosis: a candidate-gene approach.Genetic variation in a4GnT in relation to Helicobacter pylori serology and gastric cancer risk.A comprehensive analysis of common genetic variation in MUC1, MUC5AC, MUC6 genes and risk of stomach cancerPolymorphisms of the IL12B and IL23R genes are associated with psoriasis.Matrix metalloproteinase-3 (MMP3) and MMP9 genes and risk of myocardial infarction, ischemic stroke, and hemorrhagic stroke.Complete effect-profile assessment in association studies with multiple genetic and multiple environmental factors.Pathway-guided identification of gene-gene interactionsGenetic variation in IGF2 and HTRA1 and breast cancer risk among BRCA1 and BRCA2 carriersNon-iterative, regression-based estimation of haplotype associations with censored survival outcomes.Cervical and vulvar cancer risk in relation to the joint effects of cigarette smoking and genetic variation in interleukin 2.Variation in inflammation-related genes and risk of incident nonfatal myocardial infarction or ischemic stroke.CYP1B1 variants are associated with prostate cancer in non-Hispanic and Hispanic CaucasiansCytokine and cytokine receptor single-nucleotide polymorphisms predict risk for non-small cell lung cancer among women.Single and multivariate associations of MSR1, ELAC2, and RNASEL with prostate cancer in an ethnic diverse cohort of men.Association of chromosome 8q variants with prostate cancer risk in Caucasian and Hispanic menGenetic variation in insulin-like growth factor signaling genes and breast cancer risk among BRCA1 and BRCA2 carriersEvaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis?The use of inferred haplotypes in downstream analyses.A comprehensive approach to haplotype-specific analysis by penalized likelihood.Coagulation factor VII gene haplotypes, obesity-related traits, and cardiovascular risk in young women.Validation of PPP1R12B as a candidate gene for childhood asthma in Russians.
P2860
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P2860
Simple estimates of haplotype relative risks in case-control data.
description
2006 nî lūn-bûn
@nan
2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Simple estimates of haplotype relative risks in case-control data.
@ast
Simple estimates of haplotype relative risks in case-control data.
@en
type
label
Simple estimates of haplotype relative risks in case-control data.
@ast
Simple estimates of haplotype relative risks in case-control data.
@en
prefLabel
Simple estimates of haplotype relative risks in case-control data.
@ast
Simple estimates of haplotype relative risks in case-control data.
@en
P2093
P356
P1433
P1476
Simple estimates of haplotype relative risks in case-control data.
@en
P2093
Alexander P Reiner
Benjamin French
Kenneth M Rice
Lucia A Hindorff
Stephanie A Monks
Thomas Lumley
P304
P356
10.1002/GEPI.20161
P577
2006-09-01T00:00:00Z