Eli and Edythe L. Broad Institute of MIT and Harvard

Mutations in WDR4 as a new cause of Galloway–Mowat syndrome (2018) Braun DA, Shril S, Sinha A, Schneider R, Tan W, Ashraf S, Hermle T, et al. Journal article Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract (2018) Van Der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, et al. Journal article GAPVD1 and ANKFY1 mutations implicate RAB5 regulation in nephrotic syndrome (2018) Hermle T, Schneider R, Schapiro D, Braun DA, Van Der Ven AT, Warejko JK, Daga A, et al. Journal article Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas. (2018) Way GP, Sanchez-Vega F, La K, Armenia J, Chatila WK, Luna A, Sander C, et al. Journal article Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas. (2018) Knijnenburg TA, Wang L, Zimmermann MT, Chambwe N, Gao GF, Cherniack AD, Fan H, et al. Journal article Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018) Bailey MH, Tokheim C, Porta-Pardo E, Sengupta S, Bertrand D, Weerasinghe A, Colaprico A, et al. Journal article Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics. (2018) Ding L, Bailey MH, Porta-Pardo E, Thorsson V, Colaprico A, Bertrand D, Gibbs DL, et al. Journal article Genomic and Functional Approaches to Understanding Cancer Aneuploidy. (2018) Taylor AM, Shih J, Ha G, Gao GF, Zhang X, Berger AC, Schumacher SE, et al. Journal article Comparative Molecular Analysis of Gastrointestinal Adenocarcinomas. (2018) Liu Y, Sethi NS, Hinoue T, Schneider BG, Cherniack AD, Sanchez-Vega F, Seoane JA, et al. Journal article Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer. (2018) Hoadley KA, Yau C, Hinoue T, Wolf DM, Lazar AJ, Drill E, Shen R, et al. Journal article