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「"Schaid DJ "[Author]」の検索結果

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Targeted Sequencing Study to Uncover Shared Genetic Susceptibility Between Peripheral Artery Disease and Coronary Heart Disease.

An expanded variant list and assembly annotation identifies multiple novel coding and noncoding genes for prostate cancer risk using a normal prostate tissue eQTL data set.

Sex Differences in Older Adults' Immune Responses to Seasonal Influenza Vaccination.

A phenome-wide association study to discover pleiotropic effects of , , and .

Familial recurrence risk with varying amount of family history.

Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry.

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.

A review of kernel methods for genetic association studies.

Current perspectives in assessing humoral immunity after measles vaccination.

Germline variation at 8q24 and prostate cancer risk in men of European ancestry.

A small-sample kernel association test for correlated data with application to microbiome association studies.

Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.

From genome-wide associations to candidate causal variants by statistical fine-mapping.

Multivariate generalized linear model for genetic pleiotropy.

Polymorphisms in the Wilms Tumor Gene Are Associated With Interindividual Variations in Rubella Virus-Specific Cellular Immunity After Measles-Mumps-Rubella II Vaccination.

Network-directed cis-mediator analysis of normal prostate tissue expression profiles reveals downstream regulatory associations of prostate cancer susceptibility loci.

Breast cancer chemoprevention pharmacogenomics: Deep sequencing and functional genomics of the ZNF423 and CTSO genes.

A DAB2IP genotype: sex interaction is associated with abdominal aortic aneurysm expansion.

Fast and robust adjustment of cell mixtures in epigenome-wide association studies with SmartSVA.

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