Associated Papers
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error.
Musolf AM et al.
Communications Biology, 2023
36596879 (PubMed )
Supplement: 42003_2022_4323_MOESM7_ESM.xlsx › SData33
Rare coding variants and breast cancer risk: evaluation of susceptibility Loci identified in genome-wide association studies.
Zhang Y et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2014
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