Journal Report

JOURNAL OF HUMAN GENETICS

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Journal Information
Journal Title
JOURNAL OF HUMAN GENETICS
Publisher
SPRINGERNATURE
ISSN
1434-5161
E-ISSN
1435-232X
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
Neuromuscular junction pathology in amyotrophic lateral sclerosis and emerging molecular therapeutic strategies
Kazuki Okoshi, Yoshitsugu Aoki
2026-10-27
DOI: 10.1038/s10038-026-01522-6
Genotype–phenotype variability in TRMT10A deficiency: divergent developmental outcomes associated with biallelic loss-of-function variants
Zeynep Esener, Dilan Genç-Akdağ, Canberk Toprak et al.
2026-10-8
DOI: 10.1038/s10038-026-01519-1
Integrated genetic and epigenetic diagnosis of facioscapulohumeral muscular dystrophy using Oxford Nanopore long-read sequencing
Xinrong Xu, Liangliang Qiu, Minghui Zeng et al.
2026-10-5
DOI: 10.1038/s10038-026-01521-7
MC1R variants in four Chinese children with red hair and hypopigmentation
Yingzi Zhang, Qiaorong Huang, Xiaojing Chen et al.
2026-9-30
DOI: 10.1038/s10038-026-01520-8
Uptake of cascade testing and the factors affecting its implementation among patients in Japan with Lynch syndrome
Yoshimi Kiyozumi, Hiroyuki Matsubayashi, Nobuhiro Kado et al.
2026-9-29
DOI: 10.1038/s10038-026-01518-2
Variable phenotypic manifestations of two splice-site variants in DNAJB2: insights from two families and a systematic review
Fatemeh Ghermezcheshmeh, Nazila Malekian, Aida Ghasemi et al.
2026-9-28
DOI: 10.1038/s10038-026-01516-4
Riddle syndrome with RNF168 mutation in first Asian family cluster exhibiting pulmonary fibrosis and achalasia
Ting-Wei Kao, Jung-Yien Chien, Jo-Yu Chen et al.
2026-9-28
DOI: 10.1038/s10038-026-01517-3
Which R2 should be used to benchmark polygenic score performance against heritability?
Ciaran Michael Kelly
2026-9-28
DOI: 10.1038/s10038-026-01515-5
Characterising the motif composition and allele length distribution of ZFHX3 GGC repeat expansions in amyotrophic lateral sclerosis
Zoe N. Zussa, Andrew N. Smith, Joke J.F.A van Vugt et al.
2026-9-15
DOI: 10.1038/s10038-026-01513-7
Novel SLC6A9 variants in an adult presenting with GlyT1 encephalopathy
Mark Mencias, Meneka Kanagaratnam, Emma Matthews
2026-9-11 Vol. 71 Issue 11 Pages 761-765
DOI: 10.1038/s10038-026-01497-4
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Printed: October 31, 2026 01:54