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) study. Read more about 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) study.
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies. Read more about Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.
Isl1 mediates mesenchymal expansion in the developing external genitalia via regulation of Bmp4, Fgf10 and Wnt5a. Read more about Isl1 mediates mesenchymal expansion in the developing external genitalia via regulation of Bmp4, Fgf10 and Wnt5a.
The Y-located proto-oncogene TSPY exacerbates and its X-homologue TSPX inhibits transactivation functions of androgen receptor and its constitutively active variants. Read more about The Y-located proto-oncogene TSPY exacerbates and its X-homologue TSPX inhibits transactivation functions of androgen receptor and its constitutively active variants.
Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci. Read more about Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.
Modeling craniofacial and skeletal congenital birth defects to advance therapies. Read more about Modeling craniofacial and skeletal congenital birth defects to advance therapies.
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes. Read more about Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes.
Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors. Read more about Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors.
A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome. Read more about A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome.
Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions. Read more about Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions.
