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 2021-11-01 to 2025-11-01.)
ArticleCitations
64. A rare finding of triple KRAS mutations with OmniSeq® INSIGHT in a patient with colorectal adenocarcinoma291
43. Challenges of classifying variants associated with disorders of somatic mosaicism and guideline creation101
40. Prioritization of defining and supportive diagnostic variants in pediatric tumors67
LncRNA FOXD2-AS1 promotes the growth, invasion and migration of OSCC cells by regulating the MiR-185–5p/PLOD1/Akt/mTOR pathway46
Exploring the role of transcription factor TWIST1 in bladder cancer progression39
2. Diagnostic next generation sequencing to detect MYD88 L265P in lymphoplasmacytic lymphoma compared to ddPCR39
Detection of VHL variant on multigene panel testing for hereditary breast cancer: Implications for genetic counselling36
Upregulation of Uracil DNA Glycosylase (UNG) in Prostate Cancer30
135. Tumor deconvolution using comprehensive single-cell RNA sequencing cell type signatures29
13. HPV forms chimeric virus-human transcripts that affect host gene expression in cervical tumors24
27. Five-year experience of evaluating individuals at-risk for underlying genetic predisposition to hematologic malignancy23
116. Integrating methylation profiling into adult brain tumor diagnostics - the Australian experience21
96. A unique case presentation of pediatric spinal ependymoma with chromothripsis of chromosome 6: case report20
58. Improving the molecular diagnosis of SBDS-related disorders by identifying rare gene conversion events.19
Molecular determinants of clinical outcomes for anaplastic lymphoma kinase–positive non-small cell lung cancer in Chinese patients: A retrospective study18
17. Multi-consortia initiative to standardize the representation and curation of oncogenic fusions17
49. Clinical validation of Infinium CytoSNP-850K SNP-Array for routine copy number profiling of hematological malignancies17
0.097985982894897