Associated Papers
A dominant variant in apoptosis-related gene XKR8 is relevant to hereditary auditory neuropathy.
Chen K et al.
Journal of Translational Medicine, 2023
37101210 (PubMed )
Supplement: 12967_2023_4139_MOESM1_ESM.xlsx › all.byhand.hg19
Harnessing the paradoxical phenotypes of APOE ɛ2 and APOE ɛ4 to identify genetic modifiers in Alzheimer's disease.
Kim YW et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2021
33576571 (PubMed )
Supplement: ALZ-17-831-s002.xlsx › Table_S4
Whole-exome sequencing of over 4100 men of African ancestry and prostate cancer risk.
Rand KA et al.
Human Molecular Genetics, 2016
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