Human Molecular Genetics : Impact Factor & More
eISSN: 1460-2083pISSN: 0964-6906
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Aims and Scope of Human Molecular Genetics
Human Molecular Genetics, first published in 1992, is a semimonthly peer reviewed, scientific journal, published by The Oxford University Press. The journal's focus is research papers on all topics related to human molecular genetics. In addition, two "special review" issues are published each year. There are four professors who share the title of Executive Editor for this journal: Professor Kay Davies from the University of Oxford, Professor Anthony Wynshaw-Boris from Case Western Reserve University, Timothy M. Frayling from the University of Exeter, and Eleftheria Zeggini from Helmholtz Zentrum München. Less
Key Metrics
CiteScore 
10.3
Eigenfactor
0.01 - 0.05
Impact Factor
< 5
Scite Index
0.92 5-Year SI
SJR
Q1Genetics
SNIP
1.38
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Topics Covered on Human Molecular Genetics
Human Molecular Genetics Journal Specifications
| Overview | |
| Publisher | OXFORD UNIV PRESS |
| Language | English |
| Frequency | Fortnightly |
| General Details | |
| Language | English |
| Frequency | Fortnightly |
| Publication Start Year | 1992 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in Human Molecular Genetics
A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.
- 28 Jul 2026
- Human molecular genetics
The potential regulatory relationship between hsa_circ_0000973 and MBOAT2 in hypertriglyceridemia with abnormal glucose metabolism.
- 28 Jul 2026
- Human molecular genetics
Neurodevelopmental alterations are key drivers of SPG56.
- 28 Jul 2026
- Human molecular genetics
NRAS mutation in a central conducting lymphatic anomaly and PPFIBP1::ROS1 fusion in a Gorham-stout disease patient.
- 28 Jul 2026
- Human molecular genetics
Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.
- 28 Jul 2026
- Human molecular genetics
Single-cell transcriptomic integrated with machine learning reveals human retinal cell-specific biomarkers in diabetic retinopathy.
- 28 Jul 2026
- Human molecular genetics
A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.
- 28 Jul 2026
- Human molecular genetics
The potential regulatory relationship between hsa_circ_0000973 and MBOAT2 in hypertriglyceridemia with abnormal glucose metabolism.
- 28 Jul 2026
- Human molecular genetics
Neurodevelopmental alterations are key drivers of SPG56.
- 28 Jul 2026
- Human molecular genetics
NRAS mutation in a central conducting lymphatic anomaly and PPFIBP1::ROS1 fusion in a Gorham-stout disease patient.
- 28 Jul 2026
- Human molecular genetics
Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.
- 28 Jul 2026
- Human molecular genetics
Single-cell transcriptomic integrated with machine learning reveals human retinal cell-specific biomarkers in diabetic retinopathy.
- 28 Jul 2026
- Human molecular genetics
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