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Immune checkpoint inhibition for hypermutant glioblastoma multiforme resulting from germline biallelic mismatch repair deficiency E Bouffet, V Larouche, BB Campbell, D Merico, R De Borja, M Aronson, ... Journal of clinical oncology 34 (19), 2206-2211, 2016 | 830 | 2016 |
The genomic landscape of hypodiploid acute lymphoblastic leukemia L Holmfeldt, L Wei, E Diaz-Flores, M Walsh, J Zhang, L Ding, ... Nature genetics 45 (3), 242-252, 2013 | 785 | 2013 |
Prospective genomic profiling of prostate cancer across disease states reveals germline and somatic alterations that may affect clinical decision making W Abida, J Armenia, A Gopalan, R Brennan, M Walsh, D Barron, D Danila, ... JCO precision oncology 1, 1-16, 2017 | 500 | 2017 |
Microsatellite instability is associated with the presence of Lynch syndrome pan-cancer A Latham, P Srinivasan, Y Kemel, J Shia, C Bandlamudi, D Mandelker, ... Journal of clinical oncology 37 (4), 286, 2019 | 497 | 2019 |
Mutation detection in patients with advanced cancer by universal sequencing of cancer-related genes in tumor and normal DNA vs guideline-based germline testing D Mandelker, L Zhang, Y Kemel, ZK Stadler, V Joseph, A Zehir, ... Jama 318 (9), 825-835, 2017 | 449 | 2017 |
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Germline variants in targeted tumor sequencing using matched normal DNA KA Schrader, DT Cheng, V Joseph, M Prasad, M Walsh, A Zehir, A Ni, ... JAMA oncology 2 (1), 104-111, 2016 | 322 | 2016 |
Telomere length is a determinant of emphysema susceptibility JK Alder, N Guo, F Kembou, EM Parry, CJ Anderson, AI Gorgy, MF Walsh, ... American journal of respiratory and critical care medicine 184 (8), 904-912, 2011 | 294 | 2011 |
Retinoblastoma and neuroblastoma predisposition and surveillance J Kamihara, F Bourdeaut, WD Foulkes, JJ Molenaar, YP Mossé, ... Clinical Cancer Research 23 (13), e98-e106, 2017 | 202 | 2017 |
The genomic landscape of pediatric myelodysplastic syndromes JR Schwartz, J Ma, T Lamprecht, M Walsh, S Wang, V Bryant, G Song, ... Nature communications 8 (1), 1557, 2017 | 183 | 2017 |
Conflicting interpretation of genetic variants and cancer risk by commercial laboratories as assessed by the prospective registry of multiplex testing J Balmaña, L Digiovanni, P Gaddam, MF Walsh, V Joseph, ZK Stadler, ... Journal of Clinical Oncology 34 (34), 4071, 2016 | 180 | 2016 |
Cancer surveillance in Gorlin syndrome and rhabdoid tumor predisposition syndrome WD Foulkes, J Kamihara, DGR Evans, L Brugières, F Bourdeaut, ... Clinical Cancer Research 23 (12), e62-e67, 2017 | 176 | 2017 |
Baseline surveillance in Li-Fraumeni syndrome using whole-body magnetic resonance imaging: a meta-analysis ML Ballinger, A Best, PL Mai, PP Khincha, JT Loud, JA Peters, MI Achatz, ... JAMA oncology 3 (12), 1634-1639, 2017 | 171 | 2017 |
Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome M Rusch, J Nakitandwe, S Shurtleff, S Newman, Z Zhang, MN Edmonson, ... Nature communications 9 (1), 3962, 2018 | 169 | 2018 |
Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia S Topka, J Vijai, MF Walsh, L Jacobs, A Maria, D Villano, P Gaddam, ... PLoS genetics 11 (6), e1005262, 2015 | 167 | 2015 |
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Prevalence of germline mutations in cancer susceptibility genes in patients with advanced renal cell carcinoma MI Carlo, S Mukherjee, D Mandelker, J Vijai, Y Kemel, L Zhang, ... JAMA oncology 4 (9), 1228-1235, 2018 | 153 | 2018 |