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
Somatic mosaicism and longitudinal genotype-phenotype spectrum of ARR3-associated early-onset myopia in seven families
Mengya Han, Wenlong Hao, Zhenbang Ruan et al.
2026-11-11
DOI: 10.1038/s10038-026-01527-1
Expanding mutational landscape and clinical phenotype of the CASK-related neurological disorders
Mert Pekerbas, Kutay Bulut, Ayca Yigit et al.
2026-11-6
DOI: 10.1038/s10038-026-01523-5
Clinical genetics and genetic counseling in the era of disease-modifying therapies for dementia: lessons from Japan
Katsuya Nakamura, Yoshiki Sekijima
2026-11-4
DOI: 10.1038/s10038-026-01526-2
A homozygous C2ORF78 variant is associated with mTOR hyperactivation and neurodevelopmental defects in focal cortical dysplasia
S Rehan Ahmad, Md. Zeyaullah, Yousef Zahrani et al.
2026-11-4
DOI: 10.1038/s10038-026-01524-4
Asymmetric Y-chromosomal and mitochondrial haplogroup structure in two pastoralist Tibetan communities of the Sanjiangyuan region
An Zhou, Qingyao Wang, Wen Qi et al.
2026-10-31
DOI: 10.1038/s10038-026-01525-3
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
Articles retrieved from Crossref.
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Printed: November 13, 2026 22:51