about
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohortsHeritability of obesity-related traits among Nigerians, Jamaicans and US black peopleGenetic structure, self-identified race/ethnicity, and confounding in case-control association studiesA candidate gene study of obstructive sleep apnea in European Americans and African AmericansGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskMeta-analysis of correlated traits via summary statistics from GWASs with an application in hypertensionMultivariate Analysis of Anthropometric Traits Using Summary Statistics of Genome-Wide Association Studies from GIANT ConsortiumTrans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.Directional dominance on stature and cognition in diverse human populationsSingle-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection.The landscape of recombination in African Americans.Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium.A test of transmission/disequilibrium for quantitative traits in pedigree data, by multiple regressionGene, pathway and network frameworks to identify epistatic interactions of single nucleotide polymorphisms derived from GWAS data.A variance component based multi-marker association test using family and unrelated data.Whole genome sequencing data from pedigrees suggests linkage disequilibrium among rare variants created by population admixture.A genome-wide linkage and association study using COGA data.Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry.Admixture mapping provides evidence of association of the VNN1 gene with hypertensionA genome-wide linkage study of GAW15 gene expression data.GEE-based SNP set association test for continuous and discrete traits in family-based association studiesGene-gene and gene-environment interactions in ulcerative colitis.Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traitsGenome-wide association of anthropometric traits in African- and African-derived populationsLinkage analysis of a complex disease through use of admixed populations.Linkage and association analysis of angiotensin I-converting enzyme (ACE)-gene polymorphisms with ACE concentration and blood pressureDe novo mutations discovered in 8 Mexican American families through whole genome sequencing.Discovery of common sequences absent in the human reference genome using pooled samples from next generation sequencing.Identifying rare variants from exome scans: the GAW17 experience.Evaluation of a LASSO regression approach on the unrelated samples of Genetic Analysis Workshop 17.Capability of common SNPs to tag rare variants.The association of the vanin-1 N131S variant with blood pressure is mediated by endoplasmic reticulum-associated degradation and loss of function.Interrogating local population structure for fine mapping in genome-wide association studies.Admixture mapping for hypertension loci with genome-scan markers.Association of genetic loci with sleep apnea in European Americans and African-Americans: the Candidate Gene Association Resource (CARe).
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description
researcher ORCID 0000-0003-0037-411X
@en
name
Xiaofeng Zhu
@ast
Xiaofeng Zhu
@en
Xiaofeng Zhu
@nl
type
label
Xiaofeng Zhu
@ast
Xiaofeng Zhu
@en
Xiaofeng Zhu
@nl
prefLabel
Xiaofeng Zhu
@ast
Xiaofeng Zhu
@en
Xiaofeng Zhu
@nl
P106
P2456
P31
P496
0000-0003-0037-411X