Impact Factor
3.01
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
2.74
184 total citations
h5-index
16
h5 depth signal
Cited share
62.2%
46 of 74
Total citations
184
Citation footprint
Metric signal
2.39
External metric anchor
Self-citation
2.7%
5 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
57
China
57
Brazil
54
Germany
29
Japan
24
Citing Fields of Research
Cytogenetics
481
Genetics & Genomics
125
DNA Damage
51
Crop Science
27
Hematology
27
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
8,705
Articles tracked across the journal lifetime
Indexed publication set
74
46 cited publications
Last 12 months
29
2.9 publications/month
Open access share
3.4%
1 OA publications in the last year
Leading citing country
United States
57 citing publications
Leading citing field
Cytogenetics
481 citing publications
Latest tracked publication
13 October 2026
10 recent records available
Coverage & Indexing History
v96n1-4, 2002-
v96n1-4, 2002-
Active Coverage
Research Focus & Classification
Indexed Subjects
Cytogenetics
Broad Categories
Genetics
Cytogenetics
MeSH Descriptors
Cytogenetics
Genomics
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1159/cgr/achag009
Open DOI
Quality Gaps in Cytogenetic Reporting: A Single-Center Retrospective Audit of 225 Bone Marrow Karyotype Reports in Hematologic Malignancies
Introduction: Cytogenetic findings are essential for diagnosis and prognostic risk stratification in hematologic malignancies. However, the extent to which routine karyotype reports incorporate clinically relevant interpretation remains ...
02
DOI 10.1159/cgr/achag010
Open DOI
Three-Way Chromosomal Translocation Involving KMT2A::MLLT3 in AML: A Case Report and Genomic Characterization
Introduction: Complex chromosomal translocations can obscure the identification of pathogenic rearrangements involving KMT2A in acute myeloid leukemia (AML). Case Presentation: We report a 20-year-old female with AML harboring a novel th...
03
DOI 10.1159/cgr/achag011
Open DOI
A novel microdeletion syndrome involving 17q23.3 region in a child with short stature and multiple congenital anomalies: A Case Report
Microdeletion syndromes are rare chromosomal abnormalities causing diverse clinical features due to gene dosage imbalances. Deletions in chromosome 17q23.3 have been linked to neurodevelopmental and growth disorders, although the genotyp...
04
DOI 10.1159/cgr/achag006
Open DOI
Chromosomal location of repetitive DNA supports the Robertsonian fusion hypothesis in the carpenter ant Camponotus rufipes (Fabricius, 1775)
Introduction: Camponotus is a diverse ant genus with over 1,500 described taxa and notable ecological and chromosomal variation. Some species display polymorphism of chromosome number, such as Camponotus rufipes which has individuals wit...
05
DOI 10.1159/cgr/achag008
Open DOI
A Familial 22.59 Mb Deletion of the 10q11.21q21.3 Region on the Neocentromeric Chromosome 10 with Coexistence of Small Marker Chromosome (10): Case Report and Review of Literature
Introduction: We report a boy with intellectual disability and dysmorphic features carrying an interstitial 22.59 Mb deletion of the 10q11.21q21.3 region that contains 95 coding genes. Case Presentation: The 8-year-old-male patient is th...
06
DOI 10.1159/cgr/achag005
Open DOI
Comparative cytogenetics of Crocidura species: C. kegoensis, C. dracula and C.sibirica (Soricidae, Eulipotyphla)
Cytogenetic variation and chromosomal evolution in Palearctic white-toothed shrews (Crocidura) remain poorly understood, particularly within the Asian clade. Here, we provide the first cytogenetic characterization of Crocidura kegoensis ...
07
DOI 10.1159/cgr/achag004
Open DOI
Comparative Analysis of the Karyotypes of Equus caballus and Equus asinus in the Context of Contemporary Genomic Data
Background: Karyotypes of species within the genus Equus display considerable variation in chromosome number and are characterised by numerous structural rearrangements that have played a pivotal role in their evolutionary divergence and...
08
DOI 10.1159/cgr/achag003
Open DOI
Paternal Transmission of Angelman Syndrome via a Mosaic Small Supernumerary Marker Chromosome 15: A Rare Case of Germline Epigenetic Reset Failure and Somatic Rescue
Introduction: Angelman syndrome (AS) is an imprinting disorder that arises almost exclusively through maternal mechanisms; most commonly maternal 15q11.2-q13 deletion; less often, paternal uniparental disomy (UPD) of chromosome 15. Pater...
09
DOI 10.1159/000552480
Open DOI
Clone-Specific Cytogenetic Features Revealed by a New Repetitive Marker in Dojo Loach
Introduction: Most fish reproduce sexually, but some species reproduce asexually through gynogenesis. Gynogenetic species are thought to provide important insight into the evolution of sexual reproduction, and investigations into their o...
10
DOI 10.1159/cgr/achag002
Open DOI
Integrating Optical Genome Mapping into the Genetic Diagnostic Algorithm: Clinical Utility in Unresolved Autosomal Recessive Disorders from a Large Cohort
Introduction: The identification of precise genetic etiologies is indispensable for the clinical management of monogenic disorders. However, conventional diagnostic methods and exome sequencing (ES) frequently fail to identify complex st...
Bibliographical & Catalog Notes
Title from cover.
Each vol. consists of 4 numbers; 4 vols. per year.
Also available online.