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Cancer Genetics|September 6, 2025
Comprehensive analysis of oncogenic determinants across tumor types via multi-omics integrationSaba Ubaid, Rashmi Kushwaha, Mohammad Kashif, et al.Cancer Genetics|May 23, 2020
Myeloid neoplasm with a novel cryptic PDGFRB rearrangement detected by next-generation sequencingNives Zimmermann, Mehdi Nassiri, Jiehao Zhou, et al.Cancer Genetics|September 6, 2021
Germline mutation in the NBR1 gene involved in autophagy detected in a family with renal tumorsFlorine Adolphe, Sophie Ferlicot, Virginie Verkarre, et al.Cancer Genetics|June 13, 2020
Genetic progression of post-transplant Burkitt-like lymphoma case with 11q-Gain/Loss and MYC amplificationBeata Grygalewicz, Renata Woroniecka, Grzegorz Rymkiewicz, et al.Cancer Genetics|January 19, 2023
Rare and potentially fatal - Cytogenetically cryptic TNIP1::PDGFRB and PCM1::FGFR1 fusion leading to myeloid/lymphoid neoplasms with eosinophilia in childrenAnn-Cathrine Berking, Tim Flaadt, Yvonne Lisa Behrens, et al.Cancer Genetics|December 25, 2022
Clinical impact of 5'MYC or 3'MYC gain/loss detected by FISH in patients with aggressive B-cell lymphomasGuilin Tang, Shaoying Li, Gokce A Toruner, et al.Cancer Genetics|June 22, 2021
Molecular follow-up of first-line treatment by osimertinib in lung cancer: Importance of using appropriate tools for detecting EGFR resistance mutation C797SY Fanjat, H Barazzutti, I Di Mauro, et al.Cancer Genetics|June 21, 2021
Whole-exome sequencing in osteosarcoma with distinct prognosis reveals disparate genetic heterogeneityWeifeng Liu, Renxian Wang, Yanrui Zhang, et al.Cancer Genetics|July 5, 2021
A pediatric BAL case with double Ph chromosomes and trisomy 5Gulcin Gunden, Sevgi Isik, Canan Ozdemir, et al.Cancer Genetics|June 13, 2021
A hereditary ovarian cancer family with rare pathogenic splicing mutation: Implications for variant interpretationKe Wang, Yingnan Ye, Lewen Bao, et al.Pageof 113