Impact Factor
3.61
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
3.69
608 total citations
h5-index
30
h5 depth signal
Cited share
83.5%
147 of 176
Total citations
608
Citation footprint
Metric signal
3.07
External metric anchor
Self-citation
3.6%
22 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
399
United Kingdom
66
Germany
62
Canada
58
Netherlands
52
Citing Fields of Research
Genetics & Genomics
406
Cytogenetics
111
Neurodevelopmental Disorders
38
Cell Differentiation & Development
35
Congenital Disorders
31
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
546
Articles tracked across the journal lifetime
Indexed publication set
176
147 cited publications
Last 12 months
135
11.3 publications/month
Open access share
99.3%
134 OA publications in the last year
Leading citing country
United States
399 citing publications
Leading citing field
Genetics & Genomics
406 citing publications
Latest tracked publication
1 October 2026
10 recent records available
Coverage & Indexing History
v4n1, Jan. 2023-
v1n1, Oct. 2020-
Active Coverage
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
Issuing & Sponsoring Bodies
sponsoring body
American Society of Human Genetics
Broad Categories
Genetics
Genetics & Genomics
MeSH Descriptors
Genetic Phenomena
Genetic Research
Genomics
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1016/j.xhgg.2026.100677
Open DOI
EndoPRS-SS: Summary-statistic based incorporation of endophenotypes to improve risk prediction
02
03
04
05
DOI 10.1016/j.xhgg.2026.100672
Open DOI
Trio-based GWAS reveals loci associated with different forms of isolated cleft lip
06
07
DOI 10.1016/j.xhgg.2026.100670
Open DOI
Cyclin C nuclear release and mitochondrial dysfunction define molecular signatures of MED13L syndrome
08
DOI 10.1016/j.xhgg.2026.100671
Open DOI
Inherited predisposition to increased systemic inflammation predicts a broad class of disease phenotypes
09
DOI 10.1016/j.xhgg.2026.100667
Open DOI
Elucidating shared genetic signals between type 2 diabetes and three neurodegenerative dementia phenotypes
10
DOI 10.1016/j.xhgg.2026.100668
Open DOI