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Human Molecular Genetics : Impact Factor & More

eISSN: 1460-2083pISSN: 0964-6906

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
LanguageEnglish
FrequencyFortnightly
Publication Start Year1992
Publisher URLVisit website
Website URLVisit website
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Recently Published Papers in Human Molecular Genetics

Rats lacking emerin develop muscle pathologies and molecular alterations found in humans with X-linked EDMD.
  • 15 Apr 2026
  • Human molecular genetics
Genetic insights into pulmonary nodules and lung cancer: similarities and differences revealed by GWAS studies.
  • 15 Apr 2026
  • Human molecular genetics
Genetic vitamin B6 deficiency exacerbates alcohol behavioral responses, metabolism, and toxicity in Drosophila.
  • 15 Apr 2026
  • Human molecular genetics
The p.(Leu97Ile) variant expands the genetic landscape of NEFL-associated Charcot-Marie-tooth neuropathies.
  • 15 Apr 2026
  • Human molecular genetics
Revisiting low penetrance retinoblastoma: an integrated clinical, genetic, and bioinformatic analysis
  • 4 Apr 2026
  • Human Molecular Genetics
Modification of internal RNA domains from the long non-coding RNA XIST refines roles in silencing and heterochromatin recruitment
  • 2 Apr 2026
  • Human Molecular Genetics
Rats lacking emerin develop muscle pathologies and molecular alterations found in humans with X-linked EDMD.
  • 15 Apr 2026
  • Human molecular genetics
Genetic insights into pulmonary nodules and lung cancer: similarities and differences revealed by GWAS studies.
  • 15 Apr 2026
  • Human molecular genetics
Genetic vitamin B6 deficiency exacerbates alcohol behavioral responses, metabolism, and toxicity in Drosophila.
  • 15 Apr 2026
  • Human molecular genetics
The p.(Leu97Ile) variant expands the genetic landscape of NEFL-associated Charcot-Marie-tooth neuropathies.
  • 15 Apr 2026
  • Human molecular genetics
Revisiting low penetrance retinoblastoma: an integrated clinical, genetic, and bioinformatic analysis
  • 4 Apr 2026
  • Human Molecular Genetics
Modification of internal RNA domains from the long non-coding RNA XIST refines roles in silencing and heterochromatin recruitment
  • 2 Apr 2026
  • Human Molecular Genetics

FAQs on Human Molecular Genetics