Impact Factor
4.32
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
12.75
423 total citations
h5-index
36
h5 depth signal
Cited share
97.2%
35 of 36
Total citations
423
Citation footprint
Metric signal
9.25
External metric anchor
Self-citation
0.5%
2 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
145
United Kingdom
37
Canada
19
France
8
South Africa
7
Citing Fields of Research
Genetics & Genomics
152
Cytogenetics
24
Medical Ethics
18
Cell Differentiation & Development
13
Cell Biology
10
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
526
Articles tracked across the journal lifetime
Indexed publication set
36
35 cited publications
Last 12 months
20
3.3 publications/month
Open access share
95.0%
19 OA publications in the last year
Leading citing country
United States
145 citing publications
Leading citing field
Genetics & Genomics
152 citing publications
Latest tracked publication
15 June 2026
10 recent records available
Coverage & Indexing History
v1, 2000-
v1, 2000-
Active Coverage
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
Broad Categories
Genetics
Genetics, Medical
Genetics & Genomics
MeSH Descriptors
Chromosome Mapping
Genetics, Medical
Genome
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1146/annurev-genom-120324-032239
Open DOI
Common Principles Underlie Mitochondrial DNA Heteroplasmy Dynamics in the Germline and Soma
Heteroplasmy is the mixture of mutant and wild-type mitochondrial DNA (mtDNA) within each of our cells. Heteroplasmy levels in cells, tissues, and organisms change over time, thus contributing to mitochondrial disease, aging, and evoluti...
02
DOI 10.1146/annurev-genom-020525-014813
Open DOI
Human Sex Chromosome Biology in the Genomic Era
Recent research has significantly advanced our understanding of how variation in the genome shapes human biology, yet the sex chromosomes remain among its least explored regions. Technical and conceptual challenges have historically limi...
03
DOI 10.1146/annurev-genom-020525-015843
Open DOI
Beyond TADs and Compartments: Mesoscale Chromatin Folding and Its Dynamics in Transcriptional Regulation
Below the scale of long-range compartments and topologically associating domains (TADs) lie a diverse set of local chromatin organization features. Recent maps and single-molecule assays reveal modular sub-TAD units, nucleosome clutches,...
04
DOI 10.1146/annurev-gg-26-052726-200001
Open DOI
Erratum: Emerging Functions of the Repeat Genome in Nuclear Structure: A View from the Human Karyotype
05
DOI 10.1146/annurev-genom-111124-024627
Open DOI
Experimental and Computational Approaches to Identify Noncoding Pathogenic Variation in Rare Disease
Noncoding variants occur within noncoding genes as well as within the regulatory nontranslated regions of protein-coding genes. It is important to be aware that these variants have been increasingly implicated in developmental disease th...
06
DOI 10.1146/annurev-genom-020525-025811
Open DOI
How Studying Rare Disease Leads to Mechanistic Insights and Therapeutic Development: Lessons from Nonmammalian Models
Though individually rare, rare diseases collectively affect nearly 1 out of 30 individuals, highlighting the continued need for and importance of research on these disorders. We argue that the recent work in identifying and diagnosing pr...
07
DOI 10.1146/annurev-genom-120324-123022
Open DOI
Synthetic Regulatory Genomics
The genomics era has yielded high-quality genome assemblies, comprehensive atlases of biochemical signatures of gene regulation, and genetic associations for thousands of common human diseases and traits. These dramatic advances in obser...
08
DOI 10.1146/annurev-genom-020525-034046
Open DOI
Community Engagement in Genomic Research: Where We Have Been and Where We Should Go
Community engagement in science has a long history but is particularly important for genomics because of the legacy of eugenics and the importance of diversity and representation in population genetics. In this article, I describe the ro...
09
DOI 10.1146/annurev-genom-020525-034901
Open DOI
Revisiting Founder Populations in an Age of Global Biobanks
Founder populations have played a pivotal role in human genetics, enabling the discovery of causal variants for disease and providing insight into population history and dynamics. The rapid expansion of global genomic databases has revea...
10
DOI 10.1146/annurev-genom-120324-010100
Open DOI
Unraveling Non-B DNA Structures in the Era of Telomere-to-Telomere Genomes
Telomere-to-telomere (T2T) genome assemblies now provide a complete representation of genomic sequences, enabling unprecedented exploration of non-B DNA structures—secondary conformations distinct from canonical B-DNA. These fully resolv...
Bibliographical & Catalog Notes
Also issued online.
v. 1 (2000)20011126 Notice published Printed on acid-free paper that meets the full ANSI standard for Permanent Paper