Cancer Analysis

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Frank TS, Sun X, Zhang Y, Yang J, Fisher WE, Gingras M-C, et al.. Genomic profiling guides the choice of molecular targeted therapy of pancreatic cancer. Cancer Lett. 2015 ;363(1):1-6.

Mayle R, Campbell IM, Beck CR, Yu Y, Wilson M, Shaw CA, et al.. DNA REPAIR. Mus81 and converging forks limit the mutagenicity of replication fork breakage. Science. 2015 ;349(6249):742-7.

Day FR, Ruth KS, Thompson DJ, Lunetta KL, Pervjakova N, Chasman DI, et al.. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat Genet. 2015 ;47(11):1294-1303.

Jonsson P, Coarfa C, Mesmar F, Raz T, Rajapakshe K, Thompson JF, et al.. Single-Molecule Sequencing Reveals Estrogen-Regulated Clinically Relevant lncRNAs in Breast Cancer. Mol Endocrinol. 2015 ;29(11):1634-45.

Scollon S, Bergstrom K, McCullough LB, McGuire AL, Gutierrez S, Kerstein R, et al.. Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject. J Law Med Ethics. 2015 ;43(3):529-37.

Ciupek A, Rechoum Y, Gu G, Gelsomino L, Beyer AR, Brusco L, et al.. Androgen receptor promotes tamoxifen agonist activity by activation of EGFR in ERα-positive breast cancer. Breast Cancer Res Treat. 2015 ;154(2):225-37.

Roy A, Kumar V, Zorman B, Fang E, Haines KM, Doddapaneni H, et al.. Recurrent internal tandem duplications of BCOR in clear cell sarcoma of the kidney. Nat Commun. 2015 ;6:8891.

Dogruluk T, Tsang YHuen, Espitia M, Chen F, Chen T, Chong Z, et al.. Identification of Variant-Specific Functions of PIK3CA by Rapid Phenotyping of Rare Mutations. Cancer Res. 2015 ;75(24):5341-54.

Alioto TS, Buchhalter I, Derdak S, Hutter B, Eldridge MD, Hovig E, et al.. A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing. Nat Commun. 2015 ;6:10001.

Wang L, Wheeler DA. Genomic sequencing for cancer diagnosis and therapy. Annu Rev Med. 2014 ;65:33-48.