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Human Genetics : Impact Factor & More

eISSN: 1432-1203pISSN: 0340-6717

Aims and Scope of Human Genetics

Human Genetics is a peer-reviewed medical journal covering all aspects of human genetics, including legal and social issues. It was established in 1964 by Arno Motulsky and Friedrich Vogel as the German-language Humangenetik, obtaining its current title in 1976. It is published by Springer Science+Business Media. Its editors-in-chief are David N. Cooper (Cardiff University) and Thomas J. Hudson (Ontario Institute for Cancer Research). According to the Journal Citation Reports, the journal has a 2018 impact factor of 5.20. Less

Key Metrics

CiteScore
7.8
Eigenfactor
0.005 - 0.01
H-Index
148
Impact Factor
5 - 10
SJR
Q1Genetics
SNIP
1.46
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Topics Covered on Human Genetics

Human Genetics Journal Specifications

Indexed in the following public directories

  • Web of Science Web of Science
  • Scopus Scopus
  • SJR SJR
Overview
Publisher SPRINGER
Language English
Frequency Monthly
General Details
LanguageEnglish
FrequencyMonthly
Publication Start Year1976
Publisher URLVisit website
Website URLVisit website
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Recently Published Papers in Human Genetics

Clinical validation of artificial intelligence-assisted karyotyping on peripheral blood in a cytogenetic diagnostic laboratory.
  • 10 Nov 2025
  • Human genetics
Deficiency of SCAMP5 causes Parkinson's disease due to loss of dopamine neurons.
  • 4 Nov 2025
  • Human genetics
Unfolding the genetic map of monogenic liver diseases in Egypt.
  • 30 Oct 2025
  • Human genetics
Development and validation of an MPS-based 513-Plex SNP identity panel for degraded forensic samples.
  • 27 Oct 2025
  • Human genetics
Non-recurrent duplications on chromosome 4p16.1 involving cis-regulatory elements affecting neural crest development in patients with isolated bilateral microtia.
  • 27 Oct 2025
  • Human genetics
Polygenic risk scores in healthcare contexts: what's the scope? An interview study of European healthcare providers and researchers' perspectives on ethical challenges.
  • 27 Oct 2025
  • Human genetics
Clinical validation of artificial intelligence-assisted karyotyping on peripheral blood in a cytogenetic diagnostic laboratory.
  • 10 Nov 2025
  • Human genetics
Deficiency of SCAMP5 causes Parkinson's disease due to loss of dopamine neurons.
  • 4 Nov 2025
  • Human genetics
Unfolding the genetic map of monogenic liver diseases in Egypt.
  • 30 Oct 2025
  • Human genetics
Development and validation of an MPS-based 513-Plex SNP identity panel for degraded forensic samples.
  • 27 Oct 2025
  • Human genetics
Non-recurrent duplications on chromosome 4p16.1 involving cis-regulatory elements affecting neural crest development in patients with isolated bilateral microtia.
  • 27 Oct 2025
  • Human genetics
Polygenic risk scores in healthcare contexts: what's the scope? An interview study of European healthcare providers and researchers' perspectives on ethical challenges.
  • 27 Oct 2025
  • Human genetics

FAQs on Human Genetics