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 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Loss of the human BRIP1 C terminus does not cause Fanconi anemia
Anja Droste, Alexandra Sobeck, Jost Knaup et al.
2026-11 Vol. 113 Issue 11 Pages 2354-2362
DOI: 10.1016/j.ajhg.2026.09.009
Deep CRISPR mutagenesis predicts cancer risk in Li-Fraumeni syndrome
Judith Penkert, Anika Großhennig, Christina M. Dutzmann et al.
2026-11
DOI: 10.1016/j.ajhg.2026.09.016
Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy
Mingxi Deng, Mengqi Ma, Vanessa Andrea Gomez et al.
2026-11 Vol. 113 Issue 11 Pages 2291-2309
DOI: 10.1016/j.ajhg.2026.09.005
Integrating clinical diagnostics with interventional genetics for neurodevelopmental disorders
Julia Macintosh, Khadijé Jizi, Ying Zhang et al.
2026-11 Vol. 113 Issue 11 Pages 2310-2323
DOI: 10.1016/j.ajhg.2026.09.006
Population-scale genomics reveals divergent pathogenicity of variant classes across paralogous collagen IV genes
Konstantinos Tzoumkas, Gabriel T. Doctor, Omid Sadeghi-Alavijeh et al.
2026-11
DOI: 10.1016/j.ajhg.2026.10.002
Genetic data sharing by clinical laboratories in Canada: A position statement by the Canadian College of Medical Geneticists
Jordan Lerner-Ellis, Yael Fisher, Ma’n H. Zawati et al.
2026-11 Vol. 113 Issue 11 Pages 2207-2221
DOI: 10.1016/j.ajhg.2026.09.001
Recurrent de novo ABI2 p.Tyr491Cys variants define a neurodevelopmental syndrome with corpus callosum hypoplasia and white matter abnormalities
Emanuela Argilli, Caleb Yang, Carolyn Le et al.
2026-11
DOI: 10.1016/j.ajhg.2026.10.003
De novo MAP2K4 variants cause a neurodevelopmental syndrome and impaired JNK signaling in iPSC-derived neurons
Tomoki T. Nomakuchi, Alyssa L. Rippert, Sabrina A. Santos De León et al.
2026-11 Vol. 113 Issue 11 Pages 2363-2373
DOI: 10.1016/j.ajhg.2026.09.014
Accurate detection of sub-1% frequency somatic mutations by whole-genome sequencing
Yeongjun Jang, Stephanie Gardiner, Yifan Wang et al.
2026-11 Vol. 113 Issue 11 Pages 2239-2253
DOI: 10.1016/j.ajhg.2026.09.010
Genomic Analyses Reveal Mutational Signatures and Frequently Altered Genes in Esophageal Squamous Cell Carcinoma
Ling Zhang, Yong Zhou, Caixia Cheng et al.
2026-11 Vol. 113 Issue 11 Pages 2374
DOI: 10.1016/j.ajhg.2026.09.012
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Printed: November 8, 2026 11:25