Journal Report

AMERICAN JOURNAL OF HUMAN GENETICS

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Journal Information
Journal Title
AMERICAN JOURNAL OF HUMAN GENETICS
Publisher
CELL PRESS
ISSN
0002-9297
E-ISSN
1537-6605
Database
Clarivate
Domain
Health Sciences, Life Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓ ✓
2018 ✓
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Recent Articles
Loss of the human BRIP1 C terminus does not cause Fanconi anemia
Anja Droste, Alexandra Sobeck, Jost Knaup et al.
2026-10
DOI: 10.1016/j.ajhg.2026.09.009
Robust cis-by-trans epistasis in the human plasma proteome highlights an ABO-centered interaction network
Jinghui Li, Xuanyao Liu
2026-10 Vol. 113 Issue 10 Pages 2068-2081
DOI: 10.1016/j.ajhg.2026.09.003
Distinct cochlear cell types associated with genetic susceptibility to sensory and metabolic hearing loss in older adults
Samah Ahmed, Kenneth I. Vaden, Judy R. Dubno et al.
2026-10 Vol. 113 Issue 10 Pages 2195-2201
DOI: 10.1016/j.ajhg.2026.08.018
This month in The Journal
Paul W. Hook, Alyson B. Barnes
2026-10 Vol. 113 Issue 10 Pages 2023-2024
DOI: 10.1016/j.ajhg.2026.09.004
MMACHC burden variants are associated with higher circulating vitamin B12 in the All of Us cohort
Ling Cai, Ralph J. DeBerardinis
2026-10 Vol. 113 Issue 10 Pages 2202-2204
DOI: 10.1016/j.ajhg.2026.08.015
International experiences of genomic newborn screening: Lessons from over 10,800 newborns
Zornitza Stark, Sebastian Lunke, François Boemer et al.
2026-10 Vol. 113 Issue 10 Pages 2025-2033
DOI: 10.1016/j.ajhg.2026.09.002
Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk
Olivier Quenez, Catherine Schramm, Kévin Cassinari et al.
2026-10 Vol. 113 Issue 10 Pages 2099-2117
DOI: 10.1016/j.ajhg.2026.07.013
Phenome- and laboratory-wide meta-analyses of sickle cell trait reveal multi-system disease associations
Micah R. Hysong, Megan M. Shuey, Tyne W. Miller-Fleming et al.
2026-10 Vol. 113 Issue 10 Pages 2082-2098
DOI: 10.1016/j.ajhg.2026.08.010
Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features
Susan M. Hiatt, Wenjing Zhao, Zhongqing Wang et al.
2026-10 Vol. 113 Issue 10 Pages 2165-2177
DOI: 10.1016/j.ajhg.2026.08.013
Functional characterization of the 9q34.13 locus identifies RAPGEF1 as a candidate gene modulating risk for melanoma and nevi via RAS activation
Rohit Thakur, Mai Xu, Alexandra M. Thornock et al.
2026-10 Vol. 113 Issue 10 Pages 2140-2164
DOI: 10.1016/j.ajhg.2026.08.014
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Printed: November 1, 2026 14:54