Impact Factor
3.21
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
2.48
415 total citations
h5-index
25
h5 depth signal
Cited share
69.1%
121 of 175
Total citations
415
Citation footprint
Metric signal
2.11
External metric anchor
Self-citation
4.6%
19 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
342
Germany
121
Canada
87
China
78
Japan
73
Citing Fields of Research
Musculoskeletal & Nerve Cancer
309
Oncology
186
Hematology
144
Genetics & Genomics
135
Cytogenetics
92
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
4,383
Articles tracked across the journal lifetime
Indexed publication set
175
121 cited publications
Last 12 months
87
7.3 publications/month
Open access share
33.3%
29 OA publications in the last year
Leading citing country
United States
342 citing publications
Leading citing field
Musculoskeletal & Nerve Cancer
309 citing publications
Latest tracked publication
9 October 2026
10 recent records available
Coverage & Indexing History
v1n1,Sept. 1989-
v1n1,Sept. 1989-
Active Coverage
Research Focus & Classification
Indexed Subjects
Musculoskeletal & Nerve Cancer
Broad Categories
Molecular Biology
Neoplasms
Musculoskeletal & Nerve Cancer
MeSH Descriptors
Cell Transformation, Neoplastic
Chromosome Aberrations
Neoplasms
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1002/gcc.70177
Open DOI
Banding Karyotyping From Peripheral Blood Is a Useful Method for the Diagnostic Workup of Myelodysplastic Neoplasia and CMML
This retrospective study involving 155 patients from the Düsseldorf MDS Registry compared cytogenetic banding from peripheral blood (PB) and bone marrow (BM) in patients with myelodysplastic syndromes (MDS) and chronic myelomonocytic leu...
02
DOI 10.1002/gcc.70179
Open DOI
Dual INI1 – BRG1 ‐Deficient Pericardial Tumor With Rhabdoid Morphology and Clinical Benefit From DNA ‐Damaging Therapy
Primary pericardial SMARCB1 ‐deficient tumors with rhabdoid morphology are exceptionally rare. We present an adult case of a primary SMARCB1 ‐deficient pericardial tumor showing concurrent loss of INI1 ( SMARCB1 ) and BRG1 ( SMARCA4 ) ex...
03
DOI 10.1002/gcc.70180
Open DOI
Round‐to‐Epithelioid Mesenchymal Tumor Harboring an MN1::BEND2 Fusion: Expanding the Morphologic Spectrum
MN1::BEND2 fusion is well established in CNS tumors but exceptionally rare in extracranial mesenchymal neoplasms. We report a subcutaneous upper‐back tumor in a 41‐year‐old woman, composed of bland round‐to‐epithelioid cells with branchi...
04
DOI 10.1002/gcc.70178
Open DOI
Retrospective RNA Sequencing Reclassifies a Historical t (5;12) Eosinophilic Neoplasm From Presumed PDGFRB Rearrangement to ETV6::ACSL6
The molecular interpretation of eosinophilic neoplasms harboring t (5;12) may be challenging because cytogenetic breakpoint assignments can suggest a PDGFRB rearrangement without identifying the underlying fusion. We retrospectively inve...
05
DOI 10.1002/gcc.70176
Open DOI
Tumor Profile, Clinical Features, and Outcomes in Individuals With Constitutional Trisomy 8: A Systematic Review of Case Reports and Case Series
Background: Constitutional trisomy 8 mosaicism (CT8M) is a rare chromosomal disorder with poorly characterized cancer risk. This systematic review aimed at summarizing reported cases of malignancy and associated clinical outcomes in indi...
06
DOI 10.1002/gcc.70139
Open DOI
Issue Information
07
DOI 10.1002/gcc.70175
Open DOI
A Reproducible Transcriptomic Program of Neurofibroma‐to‐Malignant Peripheral Nerve Sheath Tumor Transformation
Malignant peripheral nerve sheath tumor (MPNST) carries the highest excess mortality of the cancers associated with neurofibromatosis Type 1, and usually arises from a neurofibroma. We asked whether the transcriptomic differences that di...
08
DOI 10.1002/gcc.70173
Open DOI
Integrated Genomic Profiling of PTEN and TP53 in Cervical Neuroendocrine Carcinoma: Synergistic Roles With HER2/KRAS/PIK3CA and Implications for Precision Oncology
Background: Neuroendocrine carcinoma (NEC) of the uterine cervix is a rare, highly aggressive malignancy with a poor prognosis. Expanding upon our previous work, which identified frequent mutations in HER2 , KRAS , and PIK3CA in this dis...
09
DOI 10.1002/gcc.70174
Open DOI
Nano‐ RAPID : Integrated Diagnosis for Sarcoma Using a Nanopore Sequencer
Pathological diagnosis of sarcoma is challenging. Although high‐throughput sequencing and methylation array aid sarcoma diagnosis and are routine in high‐income countries, access to these genetic/epigenetic analyses in many countries, in...
10
DOI 10.1002/gcc.70165
Open DOI
HPV ‐Associated Adenosquamous Carcinoma of the Oropharynx With a PARD3B :: ERBB4 Fusion
Head and neck carcinomas can be diagnostically challenging because of their diverse histologic subtypes. We report a case of a 55‐year‐old male presenting with right‐sided cervical adenopathy, in whom imaging revealed a cystic lesion tha...
Bibliographical & Catalog Notes
Title from cover.
Print issues ceased with v. 59 (2020).
Also issued online.
Vol. 12, no. 4 (1995)19950516 Notice published Printed on acid-free paper