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Cancer Genetics|January 22, 2020
hsa_circ_0062389 promotes the progression of non-small cell lung cancer by sponging miR-103a-3p to mediate CCNE1 expressionYahui She, Yuanyuan Han, Guangting Zhou, et al.Cancer Genetics|November 4, 2019
High-resolution copy number analysis of clear cell endometrial carcinomaAndrea J O'Hara, Matthieu Le Gallo, Meghan L Rudd, et al.Cancer Genetics|February 7, 2018
SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq)Sarah H Johnson, James B Smadbeck, Stephanie A Smoley, et al.Cancer Genetics|February 7, 2018
Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasmRoberto R Capela de Matos, Moneeb A K Othman, Gerson M Ferreira, et al.Cancer Genetics|February 7, 2018
Survey of gynecological carcinosarcomas in families with breast and ovarian cancer predispositionCarla B Ripamonti, Siranoush Manoukian, Bernard Peissel, et al.Cancer Genetics|January 10, 2018
A leukemic double-hit follicular lymphoma associated with a complex variant translocation, t(8;14;18)(q24;q32;q21), involving BCL2, MYC, and IGHDaisuke Minakata, Kazuya Sato, Takashi Ikeda, et al.Cancer Genetics|May 14, 2022
High incidence of PI3K pathway gene mutations in South Indian cervical cancersMathew Maria Rose, Shankar Dhamodharan, Sundaramoorthy Revathidevi, et al.Cancer Genetics|May 25, 2022
Jumping translocation involving chromosome 13q in a patient with Crohn's Disease and inv(16)(p13.1q22)/CBFB-MYH11 acute myeloid leukemiaSarah Clarke, Rebecca de Kraa, Hun Chuah, et al.Cancer Genetics|July 8, 2021
BRCA1 and BRCA2 whole cDNA analysis in unsolved hereditary breast/ovarian cancer patientsGemma Montalban, Sandra Bonache, Vanessa Bach, et al.Cancer Genetics|December 4, 2019
Utility of copy number variants in the classification of intracranial ependymomaMichael Evenson, Chunyu Cai, Vishwanathan Hucthagowder, et al.Pageof 114