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American Journal of Human Genetics|April 4, 2020
DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex GenesSanaa Choufani, William T Gibson, Andrei L Turinsky, et al.American Journal of Human Genetics|December 24, 2022
Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?David A Mackey, Jue-Sheng Ong, Stuart MacGregor, et al.American Journal of Human Genetics|January 7, 2023
Leveraging drug perturbation to reveal genetic regulators of hepatic gene expression in African AmericansYizhen Zhong, Tanima De, Mrinal Mishra, et al.American Journal of Human Genetics|October 1, 1987
The effects of genetic screening and assortative mating on lethal recessive-allele frequencies and homozygote incidenceR B CampbellAmerican Journal of Human Genetics|January 17, 2023
Epigenome-wide meta-analysis of BMI in nine cohorts: Examining the utility of epigenetically predicted BMIWhitney L Do, Dianjianyi Sun, Karlijn Meeks, et al.American Journal of Human Genetics|February 1, 1987
Glucose dehydrogenase polymorphism among ethnic groups of Singapore--with report of two additional alleles (GDH4 and GDH5)N Saha, S P Bhattacharyya, S C Yeoh, et al.American Journal of Human Genetics|June 6, 2022
The importance of universal ethical standards in scienceAmerican Journal of Human Genetics|June 6, 2022
Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?Paul S Appelbaum, Wylie Burke, Erik Parens, et al.American Journal of Human Genetics|December 2, 2022
A minimal role for synonymous variation in human diseaseRyan S Dhindsa, Quanli Wang, Dimitrios Vitsios, et al.American Journal of Human Genetics|December 2, 2022
Functional characterization of 5p15.33 risk locus in uveal melanoma reveals rs452384 as a functional variant and NKX2.4 as an allele-specific interactorAnne-Céline Derrien, Alexandre Houy, Olivier Ganier, et al.Pageof 981