Cancer Genetics

Papers
(The H4-Index of Cancer Genetics is 17. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-05-01 to 2026-05-01.)
ArticleCitations
84. Continued utility of chromosome analysis for plasma cell disorders451
94. Novel rare atypical e8a2 BCR::ABL1 fusion transcript detected in a patient with chronic myeloid leukemia (CML)131
93. Enhancing cytogenetic abnormality detection through flow cytometry-guided B-Cell stimulated cultures83
34. Best practices for testing low-level mosaic variants:Recommendations from CGC somatic overgrowth and vascular anomalies working group61
77. Cytogenomic characterization of ALK-negative ALCL cell lines DL-40 and Fe-PD45
24. Prediction of gene expression in NSCLC tumors and their microenvironment using an explainable machine learning model45
26. An ATIC::ALK fusion created by balanced insertion rather than inversion of chromosome 2 in an ALK+ anaplastic large cell lymphoma41
13. HPV forms chimeric virus-human transcripts that affect host gene expression in cervical tumors33
135. Tumor deconvolution using comprehensive single-cell RNA sequencing cell type signatures33
27. Five-year experience of evaluating individuals at-risk for underlying genetic predisposition to hematologic malignancy30
96. A unique case presentation of pediatric spinal ependymoma with chromothripsis of chromosome 6: case report27
58. Improving the molecular diagnosis of SBDS-related disorders by identifying rare gene conversion events.26
116. Integrating methylation profiling into adult brain tumor diagnostics - the Australian experience25
64. A rare finding of triple KRAS mutations with OmniSeq® INSIGHT in a patient with colorectal adenocarcinoma22
43. Challenges of classifying variants associated with disorders of somatic mosaicism and guideline creation21
40. Prioritization of defining and supportive diagnostic variants in pediatric tumors18
Expression and clinical significance of the imprinted gene PHLDA2 in colorectal cancer17
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