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Cancer Genetics|May 22, 2019
Prognostic significance of CDC25C in lung adenocarcinoma: An analysis of TCGA dataZengfei Xia, Wen Ou-Yang, Ting Hu, et al.Cancer Genetics|May 11, 2019
PTPRD copy number variants and Ewing's sarcoma: Strengthening the association and therapeutic implicationsAvi Saskin, Kimberly Seath, Frederique Tihy, et al.Cancer Genetics|May 13, 2019
FANCM, RAD1, CHEK1 and TP53I3 act as BRCA-like tumor suppressors and are mutated in hereditary ovarian cancerJaime L Lopes, Sophia Chaudhry, Guilherme S Lopes, et al.Cancer Genetics|May 21, 2018
Female-specific association among I, J and K mitochondrial genetic haplogroups and cancer: A longitudinal cohort studyClaudio Luchini, Alessia Nottegar, Alberto Vaona, et al.Cancer Genetics|July 17, 2022
Complex karyotype with double Philadelphia chromosome and T315I mutation results in blastic phase and extensive extramedullary infiltration in a chronic myeloid leukemia patientEren Arslan Davulcu, Mert Pekerbas, Emin Karaca, et al.Cancer Genetics|February 21, 2022
Necessity of multiplex ligation probe amplification in genetic tests: Germline variant analysis of the APC gene in familial adenomatous polyposis patientsJong Kwon Lee, Won Kyung Kwon, Sung Noh Hong, et al.Cancer Genetics|February 12, 2022
Lynch syndrome caused by a novel deletion of the promoter and exons 1-13 of MLH1 geneJialing Huang, Victoria Stinnett, Liqun Jiang, et al.Cancer Genetics|April 2, 2022
Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusionsJason Saliba, Alanna J Church, Shruti Rao, et al.Cancer Genetics|March 25, 2022
TRK inhibitor activity and resistance in TRK fusion-positive cancers in adultsGuilherme Harada, Alexander DrilonPageof 113