| Organoid profiling identifies common responders to chemotherapy in pancreatic cancer H Tiriac, P Belleau, DD Engle, D Plenker, A Deschênes, TDD Somerville, ... Cancer discovery 8 (9), 1112-1129, 2018 | 792 | 2018 |
| The mutational landscape of human somatic and germline cells L Moore, A Cagan, THH Coorens, MDC Neville, R Sanghvi, MA Sanders, ... Nature 597 (7876), 381-386, 2021 | 213 | 2021 |
| Inherent mosaicism and extensive mutation of human placentas THH Coorens, TRW Oliver, R Sanghvi, U Sovio, E Cook, R Vento-Tormo, ... Nature 592 (7852), 80-85, 2021 | 154 | 2021 |
| Extensive phylogenies of human development inferred from somatic mutations THH Coorens, L Moore, PS Robinson, R Sanghvi, J Christopher, ... Nature 597 (7876), 387-392, 2021 | 102 | 2021 |
| Organoid profiling identifies common responders to chemotherapy in pancreatic cancer. Cancer Discov. 2018; 8: 1112–1129. doi: 10.1158/2159-8290 H Tiriac, P Belleau, DD Engle, D Plenker, A Deschênes, TDD Somerville, ... CD-18-0349.[Europe PMC free article][Abstract][CrossRef][Google Scholar], 0 | 98 | |
| Genetic and chemotherapeutic influences on germline hypermutation J Kaplanis, B Ide, R Sanghvi, M Neville, P Danecek, T Coorens, ... Nature 605 (7910), 503-508, 2022 | 46 | 2022 |
| Deep whole-genome sequencing of 3 cancer cell lines on 2 sequencing platforms K Arora, M Shah, M Johnson, R Sanghvi, J Shelton, K Nagulapalli, ... Scientific reports 9 (1), 19123, 2019 | 41 | 2019 |
| A recurrent novel MGA–NUTM1 fusion identifies a new subtype of high-grade spindle cell sarcoma D Diolaiti, FSD Cruz, G Gundem, N Bouvier, M Boulad, Y Zhang, AJ Chou, ... Molecular Case Studies 4 (6), a003194, 2018 | 31 | 2018 |
| Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers RV Sanghvi, CJ Buhay, BC Powell, EA Tsai, MO Dorschner, CS Hong, ... Genetics in Medicine 20 (8), 855-866, 2018 | 30 | 2018 |
| Somatic whole genome dynamics of precancer in Barrett’s esophagus reveals features associated with disease progression TG Paulson, PC Galipeau, KM Oman, CA Sanchez, MK Kuhner, LP Smith, ... Nature communications 13 (1), 2300, 2022 | 18* | 2022 |
| Human genome meeting 2016: houston, TX, USA. 28 February-2 March 2016 AK Srivastava, Y Wang, R Huang, C Skinner, T Thompson, L Pollard, ... Human genomics 10, 1-40, 2016 | 17 | 2016 |
| Cynomolgus and pigtail macaque IgG subclasses: characterization of IGHG genes and computational analysis of IgG/Fc receptor binding affinity DC Nguyen, R Sanghvi, F Scinicariello, J Pulit-Penaloza, N Hill, ... Immunogenetics 66, 361-377, 2014 | 15 | 2014 |
| Genetic and chemotherapeutic causes of germline hypermutation J Kaplanis, B Ide, R Sanghvi, M Neville, P Danecek, T Coorens, ... bioRxiv, 2021.06. 01.446180, 2021 | 9* | 2021 |
| Clonal diversification and histogenesis of malignant germ cell tumours TRW Oliver, L Chappell, R Sanghvi, L Deighton, N Ansari-Pour, ... Nature Communications 13 (1), 4272, 2022 | 6 | 2022 |
| Signatures of mutational processes in human DNA evolution H Hamidi, H Alinejad-Rokny, T Coorens, R Sanghvi, SJ Lindsay, ... bioRxiv, 2021.01. 09.426041, 2021 | 4 | 2021 |
| A naturally occurring variant of MBD4 causes maternal germline hypermutation in primates AM Stendahl, R Sanghvi, S Peterson, K Ray, AC Lima, R Rahbari, ... Genome Research 33 (12), 2053-2059, 2023 | 3 | 2023 |
| Replacing procarbazine with dacarbazine in escalated BEACOPP reduces clinical toxicity with no loss of efficacy yet protects stem cells from excess somatic mutational damage A Santarsieri, E Mitchell, R Sanghvi, H Lee‐Six, K Sturgess, P Brice, ... Hematological Oncology 41, 356-357, 2023 | | 2023 |
| Identification and electronic health record incorporation of clinically actionable pharmacogenomic variants using prospective targeted sequencing S Scherer, X Qin, R Sanghvi, K Walker, T Chiang, D Muzny, L Wang, ... HUMAN GENOMICS 10, 2016 | | 2016 |
| Rapid capture methods for clinical sequencing J Hu, K Walker, C Buhay, X Liu, Q Wang, R Sanghvi, H Doddapaneni, ... HUMAN GENOMICS 10, 2016 | | 2016 |
| The Exome Coverage and Identification (ExCID) Report: a gene survey tool for clinical sequencing applications Christian Buhay, Rashesh Sanghvi, Qiaoyan Wang, Kimberly Walker, Harsha ... Sequencing, Finishing and Analysis in the Future (SFAF), 2015 | | 2015 |
