Leveraging diverse genomic data to guide equitable carrier screening: Insights from gnomAD v.4.1.0. Read more about Leveraging diverse genomic data to guide equitable carrier screening: Insights from gnomAD v.4.1.0.
Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variants. Read more about Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variants.
Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications. Read more about Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications.
Genetic determinants of IgG antibody response to COVID-19 vaccination. Read more about Genetic determinants of IgG antibody response to COVID-19 vaccination.
Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans. Read more about Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans.
Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry. Read more about Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.
The immunogenetics of viral antigen response is associated with subtype-specific glioma risk and survival. Read more about The immunogenetics of viral antigen response is associated with subtype-specific glioma risk and survival.
Trans-ancestral fine-mapping of MHC reveals key amino acids associated with spontaneous clearance of hepatitis C in HLA-DQβ1. Read more about Trans-ancestral fine-mapping of MHC reveals key amino acids associated with spontaneous clearance of hepatitis C in HLA-DQβ1.
Conceptualization of utility in translational clinical genomics research. Read more about Conceptualization of utility in translational clinical genomics research.
