Impact Factor
3.87
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
4.47
861 total citations
h5-index
41
h5 depth signal
Cited share
87.3%
179 of 205
Total citations
861
Citation footprint
Metric signal
4.00
External metric anchor
Self-citation
1.4%
12 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
494
China
231
United Kingdom
156
Germany
131
France
113
Citing Fields of Research
Genetics & Genomics
710
Cytogenetics
254
Auditory Loss
102
Cell Differentiation & Development
64
Congenital Disorders
60
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
12,146
Articles tracked across the journal lifetime
Indexed publication set
205
179 cited publications
Last 12 months
95
7.9 publications/month
Open access share
49.5%
47 OA publications in the last year
Leading citing country
United States
494 citing publications
Leading citing field
Genetics & Genomics
710 citing publications
Latest tracked publication
17 October 2026
10 recent records available
Coverage & Indexing History
v31n1,Jan. 28, 1976-
v31n1,Jan. 28, 1976-
Active Coverage
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
Broad Categories
Genetics, Medical
Genetics & Genomics
MeSH Descriptors
Genetics, Medical
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1007/s00439-026-02877-8
Open DOI
Gene-based association analysis of depression risk among European ancestry Parkinson’s disease patients
Depression is one of the most common and disabling non-motor symptoms in Parkinson’s disease (PD), yet its genetic basis remains poorly understood. Here, we investigate the genetic contributions to depression in PD by estimating the burd...
02
DOI 10.1007/s00439-026-02886-7
Open DOI
Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics
Constitutional chromosomal heteromorphisms are common cytogenetic variants involving constitutive heterochromatin and acrocentric short-arm structures whose visual identification and classification remain challenging in routine cytogenet...
03
DOI 10.1007/s00439-026-02887-6
Open DOI
A genome-wide association study of cognitive impairment in a Chinese cohort of 1,040 individuals
While genetic heritability plays a major role in the development of cognitive impairment, most genetic risk factors are identified from studies of European populations. We conducted a genome-wide association study (GWAS) on cognitive imp...
04
05
DOI 10.1007/s00439-026-02881-y
Open DOI
Clinical and molecular spectrum of congenital disorders of glycosylation in 80 Egyptian patients
06
DOI 10.1007/s00439-026-02869-8
Open DOI
Geographic barrier contributed to the diversity of maternal and paternal lineages in New Guinea Island
07
08
DOI 10.1007/s00439-026-02879-6
Open DOI
Clinical, immunological, and molecular characteristics of severe combined immune deficiency in China
09
DOI 10.1007/s00439-026-02876-9
Open DOI
Association of apolipoprotein E gene with risk, cognition, and prognosis of epilepsy
10
Bibliographical & Catalog Notes
Also issued online.
Articles in English or German with summaries in English or in both languages.
Continues Humangenetik.
(1988)19890818 Notice published Printed on acid-free paper