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Cancer Genetics|March 18, 2020
Novel and recurrent germline mutations in the VHL gene in 5 Arab patients with Von Hippel-Lindau diseaseMuhammad Faiyaz-Ul-Haque, Masood Jamil, Muhammad Aslam, et al.Cancer Genetics|March 18, 2020
Integrating transcriptome-wide association study and copy number variation study identifies candidate genes and pathways for diffuse non-Hodgkin's lymphomaDi Wu, Jing Zhao, Hong Ma, et al.Cancer Genetics|July 8, 2021
Identification of KMT2A-ARHGEF12 fusion in a child with a high-grade B-cell lymphomaKristian T Schafernak, James A Williams, Benjamin I Clyde, et al.Cancer Genetics|July 3, 2022
Patient with multiple genetically distinct thyroid nodules including papillary thyroid carcinoma harboring novel YWHAG-BRAF fusionRuihe Lin, Zi-Xuan Wang, Elizabeth Cottrill, et al.Cancer Genetics|November 21, 2022
The hsa-miR-516a-5p and hsa-miR-516b-5p microRNAs reduce the migration and invasion on T98G glioblastoma cell lineÁngela Y García Fonseca, Yeimy González-Giraldo, Jannet Gonzalez Santos, et al.Cancer Genetics|June 24, 2022
Chimeric transcripts observed in non-canonical FGFR2 fusions with partner genes' breakpoint located in intergenic region in intrahepatic cholangiocarcinomaLei Yin, Zhijun Han, Meilin Feng, et al.Cancer Genetics|June 10, 2021
Differences in the mitochondrial microsatellite instability of Keratoacanthoma and cutaneous squamous cell carcinomaMohammad Rizwan Alam, Ahmad Alsulimani, Shafiul Haque, et al.Cancer Genetics|June 9, 2021
Hereditary inflammatory fibroid polyps caused by germline pathogenic variants in PDGFRA: Refining PDGFRA-mutation syndromeRachel Hodan, Gregory W Charville, Uri LadabaumCancer Genetics|January 12, 2021
Matched sequential tumor molecular profiling in solid malignancies may impact clinical practiceTiffany S Lai, Erica Manrriquez, Adam Neal, et al.Cancer Genetics|June 10, 2017
Single nucleotide polymorphisms in an Indian cohort and association of CNTN4, MMP2 and SNTB1 variants with oral cancerSubuhi Yete, Sultan Pradhan, Dhananjaya SaranathPageof 113