about
Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants.Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array.Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) studyMinority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) studyUse of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
P50
Q36068167-FB8BE36A-E55B-4CB2-B953-4D71E5E58E47Q36159275-C37C405B-4DFD-440D-BBE0-D18F4EFA5124Q36223643-FEC49283-EC0D-43B1-8620-567682478C24Q45073555-4583173F-CF9A-416C-97A4-F6ECA4D385ADQ89022168-E00393FE-5776-4C8D-B013-FD61CF789A98Q90743121-7AAE664A-7C1D-493E-8E56-FE1DF37B5376Q92206054-56FAAA7F-F2B4-4B63-B2DE-FA561053FD89
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Stephanie A Bien
@ast
Stephanie A Bien
@en
Stephanie A Bien
@es
Stephanie A Bien
@nl
type
label
Stephanie A Bien
@ast
Stephanie A Bien
@en
Stephanie A Bien
@es
Stephanie A Bien
@nl
prefLabel
Stephanie A Bien
@ast
Stephanie A Bien
@en
Stephanie A Bien
@es
Stephanie A Bien
@nl
P106
P214
104151302826548660776
P31
P496
0000-0002-8713-4583
P7859
viaf-104151302826548660776