Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans. Read more about Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.
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.
DLX4 is associated with orofacial clefting and abnormal jaw development. Read more about DLX4 is associated with orofacial clefting and abnormal jaw development.
The active Hsc70/tau complex can be exploited to enhance tau turnover without damaging microtubule dynamics. Read more about The active Hsc70/tau complex can be exploited to enhance tau turnover without damaging microtubule dynamics.
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. Read more about Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.
SRY interference of normal regulation of the RET gene suggests a potential role of the Y-chromosome gene in sexual dimorphism in Hirschsprung disease. Read more about SRY interference of normal regulation of the RET gene suggests a potential role of the Y-chromosome gene in sexual dimorphism in Hirschsprung disease.
