Impact Factor
2.71
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
1.69
150 total citations
h5-index
14
h5 depth signal
Cited share
56.7%
51 of 90
Total citations
150
Citation footprint
Metric signal
1.87
External metric anchor
Self-citation
0.7%
1 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
China
111
United States
61
United Kingdom
53
India
29
Brazil
24
Citing Fields of Research
Genetics & Genomics
266
Cytogenetics
55
Musculoskeletal Disorders
23
Congenital Disorders
21
Hematology
20
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
3,857
Articles tracked across the journal lifetime
Indexed publication set
90
51 cited publications
Last 12 months
36
3.3 publications/month
Open access share
16.7%
6 OA publications in the last year
Leading citing country
China
111 citing publications
Leading citing field
Genetics & Genomics
266 citing publications
Latest tracked publication
18 October 2026
10 recent records available
Coverage & Indexing History
v29n2,Nov. 1965-
v29n2,Nov. 1965-
Active Coverage
Active Coverage
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
Issuing & Sponsoring Bodies
Contributor
Galton Laboratory
Broad Categories
Genetics, Medical
Genetics & Genomics
MeSH Descriptors
Eugenics
Genetics, Medical
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1111/ahg.70064
Open DOI
MYLK c.4079G>A, p.(Gly1360Asp) Variant Associated With Hereditary Thoracic Aortic Diseases and Early Onset Aortic Dissection
Aims: Thoracic aortic aneurysms and dissections are major causes of sudden cardiovascular death. We aimed to evaluate the clinical significance of the MYLK c.4079G>A, p.(Gly1360Asp) variant in Finnish families with heritable thoracic aor...
02
DOI 10.1111/ahg.70063
Open DOI
Evidence for Reduced Somatic T‐Cell Receptor Sequence Diversity Profiles Among Midwestern Amish in an Aging Cohort Study
Background: The causes of late onset Alzheimer disease (LOAD) are not known but several recent lines of evidence implicate the adaptive immune system. Objective: To characterize the adaptive immune system among Midwestern Amish participa...
03
DOI 10.1111/ahg.70062
Open DOI
Issue Information
04
DOI 10.1111/ahg.70060
Open DOI
Report on the 29th Human Genome Meeting: ‘Bringing Our Genomes to Medicine’
05
DOI 10.1111/ahg.70061
Open DOI
Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses
Background: Hearing impairment is a genetically heterogeneous disorder and represents a significant health concern, particularly in consanguineous populations where autosomal recessive forms are more prevalent. Pakistani families provide...
06
DOI 10.1111/ahg.70053
Open DOI
What Uniparental Lineages Tell Us About the Prehistoric Human Colonization of the Americas
Objectives: From the perspective of uniparental markers, the view of the human prehistoric settlement of America is that it resulted from a single main migration after the Last Glacial Maximum, following a long or short period of genetic...
07
DOI 10.1111/ahg.70058
Open DOI
Genomic Structural Equation Modeling Identifies a Shared Inflammatory Genetic Dimension Across Inflammatory Arthritis Phenotypes and Biomarkers
Background: Inflammatory arthritis (IA), including rheumatoid arthritis (RA), psoriatic arthritis (PsA) and gout, shares systemic inflammatory features indexed by C‐reactive protein (CRP) and interleukin‐6 (IL‐6), yet the extent of their...
08
09
DOI 10.1111/ahg.70057
Open DOI
Genetically Proxied Leukocyte Telomere Length and Epigenetic Age Acceleration in Relation to Healthspan: A Mendelian Randomization Study
Background: Leukocyte telomere length (LTL) and epigenetic age acceleration (EAA) are widely studied biomarkers of biological aging, but their potential roles in healthspan remain unclear. We evaluated whether genetically proxied LTL and...
10
DOI 10.1111/ahg.70056
Open DOI
Decoding the Genetic and Phenotypic Spectrum of MT‐TI Mitochondrial Diseases
Background: Variants in the MT‐TI gene, which encodes mitochondrial transfer RNA for isoleucine, have been associated with neuromuscular, cardiac, auditory, renal, and metabolic disorders, but their clinical interpretation remains diffic...
Bibliographical & Catalog Notes
Also issued online.
Indexes: Vols. 15-19, 1950/51-1954/55, in v. 19.
Vol. 47, no. 1 (1983)19920824 Notice not published Printed on acid-free paper