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American Journal of Human Genetics|October 1, 1986
Frequent deletion and duplication of the steroid 21-hydroxylase genesJ W Werkmeister, M I New, B Dupont, et al.American Journal of Human Genetics|August 5, 2026
Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological featuresMarina Boon, Meghan R Mulligan, Jolijn J A Verseput, et al.American Journal of Human Genetics|August 12, 2026
Anthropometric and cardio-metabolic trait variation and genetic associations in sub-Saharan AfricaMatthew E B Hansen, Ujani Hazra, Michelle Kim, et al.American Journal of Human Genetics|May 6, 2022
Response to Wyckelsma et al.: Loss of α-actinin-3 during human evolution provides superior cold resilience and muscle heat generationAlexander Mörseburg, Luca Pagani, Boris Malyarchuk, et al.American Journal of Human Genetics|December 9, 2022
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14Haloom Rafehi, Justin Read, David J Szmulewicz, et al.American Journal of Human Genetics|October 8, 2020
Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European AncestriesKatherine A Owen, Andrew Price, Hannah Ainsworth, et al.American Journal of Human Genetics|October 14, 2020
Probabilistic Estimation of Identity by Descent Segment Endpoints and Detection of Recent SelectionSharon R Browning, Brian L BrowningAmerican Journal of Human Genetics|December 1, 1988
Clinical, genetic, and epidemiological factors in neural tube defectsJ G Hall, J M Friedman, B A Kenna, et al.American Journal of Human Genetics|December 1, 1988
Inheritance of low-density lipoprotein subclass patterns: results of complex segregation analysisM A Austin, M C King, K M Vranizan, et al.American Journal of Human Genetics|December 1, 1988
Protein variants in Hiroshima and Nagasaki: tales of two citiesJ V Neel, C Satoh, P Smouse, et al.Pageof 979