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Cancer Genetics|December 4, 2019
Utility of copy number variants in the classification of intracranial ependymomaMichael Evenson, Chunyu Cai, Vishwanathan Hucthagowder, et al.Cancer Genetics|December 19, 2020
DNA damaging agents and DNA repair: From carcinogenesis to cancer therapyLarissa Costa de Almeida, Felipe Antunes Calil, João Agostinho Machado-Neto, et al.Cancer Genetics|December 20, 2020
Implementation of cytogenomic microarray with plasma cell enrichment enables better abnormality detection and risk stratification in patients with plasma cell neoplasia than conventional cytogenetics and fluorescence in situ hybridizationChuanfei Chen, Alvin Soon Tiong Lim, Lai Ching Lau, et al.Cancer Genetics|December 18, 2020
Genetic variants as biomarkers for progression and resistance in multiple myelomaRachel A Montel, Matthew Gregory, Tinchun Chu, et al.Cancer Genetics|October 23, 2020
Intrahepatic cholangiocarcinoma development in a patient with a novel BAP1 germline mutation and low exposure to asbestosG Brandi, M Deserti, A Palloni, et al.Cancer Genetics|January 14, 2021
A 10-gene-methylation-based signature for prognosis prediction of colorectal cancerDong-Hai Li, Xiao-Hui Du, Ming Liu, et al.Cancer Genetics|November 14, 2021
Tumor-intrinsic FABP5 is a novel driver for colon cancer cell growth via the HIF-1 signaling pathwayJieun Seo, JeongEun Yun, Junji Fukuda, et al.Cancer Genetics|January 2, 2022
Is 5q deletion in de novo Acute Myelogenous Leukemia (AML) with excess blasts a surrogate marker for the cryptic t(7;21)(p22;q22)? A case report and review of literatureRobert D Johnston, Farzaneh H Sayedian, Christina Mendiola, et al.Cancer Genetics|October 26, 2022
Partial tandem duplication of KMT2A gene in patient afflicted with hypereosinophilic syndrome: A case reportFaramarz Ghasemian Sorbeni, Atefeh Ansarin, Ebrahim Sakhinia, et al.Cancer Genetics|October 24, 2022
Myxoid spindle cell sarcoma with ETV6-NTRK3 fusionAnastasios Kyriazoglou, Efhtymios Dimitriadis, Luiza Mahaira, et al.Pageof 114