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American Journal of Human Genetics : Impact Factor & More

eISSN: 1537-6605pISSN: 0002-9297

Key Metrics

CiteScore
17
Eigenfactor
0.05 - 0.1
Impact Factor
5 - 10
Scite Index
0.91 5-Year SI
SJR
Q1Genetics
SNIP
3.01
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Topics Covered on American Journal of Human Genetics

American Journal of Human Genetics Journal Specifications

Indexed in the following public directories

  • Web of Science Web of Science
  • Scopus Scopus
  • SJR SJR
Overview
Publisher CELL PRESS
Language English
Frequency Monthly
General Details
LanguageEnglish
FrequencyMonthly
Publication Start Year1948
Publisher URLVisit website
Website URLVisit website
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Recently Published Papers in American Journal of Human Genetics

Enhanced muscle uptake of chemically optimized miR-23b antisense oligonucleotides as lead compounds for myotonic dystrophy type 1.
  • 20 Feb 2026
  • American journal of human genetics
Bi-allelic variants in FSD1L cause retinitis pigmentosa with or without neurological involvement.
  • 19 Feb 2026
  • American journal of human genetics
Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome.
  • 19 Feb 2026
  • American journal of human genetics
An endothelial RNA splicing atlas catalogs effects of IL-1β and identifies an alternative PROCR isoform with genetic links to pleiotropic vascular disease.
  • 10 Feb 2026
  • American journal of human genetics
Expanded chromatin accessibility mapping explains genetic variation associated with complex traits in liver.
  • 5 Feb 2026
  • American journal of human genetics
MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy.
  • 5 Feb 2026
  • American journal of human genetics
Enhanced muscle uptake of chemically optimized miR-23b antisense oligonucleotides as lead compounds for myotonic dystrophy type 1.
  • 20 Feb 2026
  • American journal of human genetics
Bi-allelic variants in FSD1L cause retinitis pigmentosa with or without neurological involvement.
  • 19 Feb 2026
  • American journal of human genetics
Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome.
  • 19 Feb 2026
  • American journal of human genetics
An endothelial RNA splicing atlas catalogs effects of IL-1β and identifies an alternative PROCR isoform with genetic links to pleiotropic vascular disease.
  • 10 Feb 2026
  • American journal of human genetics
Expanded chromatin accessibility mapping explains genetic variation associated with complex traits in liver.
  • 5 Feb 2026
  • American journal of human genetics
MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy.
  • 5 Feb 2026
  • American journal of human genetics

FAQs on American Journal of Human Genetics