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
Recommended pre-submission checks
Powered by 

Topics Covered on American Journal of Human Genetics
American Journal of Human Genetics Journal Specifications
Indexed in the following public directories
Web of Science
Scopus
SJR
| Overview | |
| Publisher | CELL PRESS |
| Language | English |
| Frequency | Monthly |
| General Details | |
| Language | English |
| Frequency | Monthly |
| Publication Start Year | 1948 |
| Publisher URL | Visit website |
| Website URL | Visit website |
View less
Planning to publish in American Journal of Human Genetics ?
Upload your Manuscript to get
- Degree of match
- Common matching concepts
- Additional journal recommendations

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