Journal Report

Human Molecular Genetics

Download PDF
Journal Information
Journal Title
Human Molecular Genetics
Publisher
Oxford University Press
ISSN
0964-6906
E-ISSN
1460-2083
Database
SCOPUS
Domain
Health Sciences, Life Sciences, Physical Sciences, Social 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
Leveraging academic medical biobanks for recall-by-genotype deep phenotyping studies
Yi-An Ko, Giselle Fisher, Eleonora Scorletti et al.
2026-4-1
DOI: 10.1093/hmg/ddaf162
Subtle cellular phenotypes inform pathological and benign genetic mutants in the Iduronate-2 sulfatase gene
Anushka Viswanathan, Serena Elia, Steven Q Le et al.
2026 Vol. 35 Issue 5
DOI: 10.1093/hmg/ddag014
Specific knockout of kidney homogentisate 1,2-dioxygenase reveals that local metabolism of tyrosine and homogentisic acid is negligible in alkaptonuria
Dominic A Rutland, Brendan P Norman, Juliette H Hughes et al.
2026 Vol. 35 Issue 8
DOI: 10.1093/hmg/ddag036
Molecular analysis of individuals with suspected 46,XY differences of sex development in a homogenous and understudied population
Firman P Idris, Tara Hussein Tayeb, Gorjana Robevska et al.
2026 Vol. 35 Issue 19
DOI: 10.1093/hmg/ddag089
Viral vector-mediated <i>SLC9A6</i> gene replacement reduces cerebellar motor and molecular abnormalities in the <i>shaker</i> rat model of Christianson syndrome
Collin J Anderson, Karla P Figueroa, Sharan Paul et al.
2026 Vol. 35 Issue 6
DOI: 10.1093/hmg/ddag021
Ultra-rare variants in <i>LAMA2</i> are risk factors for frontotemporal dementia and motor neuron disease
Hiu Chuen Lok, Carol Dobson-Stone, Marianne Hallupp et al.
2026 Vol. 35 Issue 8
DOI: 10.1093/hmg/ddag034
Modeling patient variants of <i>Cnot1</i> and <i>Cdc42bpb</i> results in distinct forms of congenital diaphragmatic hernia in mice
Eric L Bogenschutz, Cynthia Carpenter, Ameleen Wong et al.
2026 Vol. 35 Issue 21
DOI: 10.1093/hmg/ddag106
KATNAL2 dysfunction impairs microtubule dynamics and contributes to syndromic neurodevelopmental disease
Ece Sönmezler, Semra Hız Kurul, Ozlem Erez et al.
2026 Vol. 35 Issue 21
DOI: 10.1093/hmg/ddag102
DDX3X syndrome mutations lock DDX3X-RNA conformational states to drive persistent pathological condensation and neuronal death
Poulami Ghosh, Shivani Krishna Kapuganti, Sabhyata Gopal et al.
2026 Vol. 35 Issue 15
DOI: 10.1093/hmg/ddag066
PONG 2.0: allele imputation for the killer cell immunoglobulin-like receptors
Suraju A Sadeeq, Laura A Leaton, Katherine M Kichula et al.
2026 Vol. 35 Issue 17
DOI: 10.1093/hmg/ddag075
Articles retrieved from Crossref.
Green Journals | https://www.green-journals.com | info@green-journals.com
Printed: November 11, 2026 23:29