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Shashikant Kulkarni (Shashi)
Shashikant Kulkarni (Shashi)
Professor & Vice Chairman, Baylor College of Medicine; CSO & SVP Baylor Genetics
Verified email at bcm.edu - Homepage
Title
Cited by
Cited by
Year
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
Cancer Genome Atlas Research Network
New England Journal of Medicine 368 (22), 2059-2074, 2013
45832013
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
L Ding, TJ Ley, DE Larson, CA Miller, DC Koboldt, JS Welch, JK Ritchey, ...
Nature 481 (7382), 506-510, 2012
25062012
The origin and evolution of mutations in acute myeloid leukemia
JS Welch, TJ Ley, DC Link, CA Miller, DE Larson, DC Koboldt, ...
Cell 150 (2), 264-278, 2012
18112012
Standards and guidelines for the interpretation and reporting of sequence variants in cancer: a joint consensus recommendation of the Association for Molecular Pathology …
MM Li, M Datto, EJ Duncavage, S Kulkarni, NI Lindeman, S Roy, ...
The Journal of molecular diagnostics 19 (1), 4-23, 2017
15302017
Pathogenic germline variants in 10,389 adult cancers
K Huang, RJ Mashl, Y Wu, DI Ritter, J Wang, C Oh, M Paczkowska, ...
Cell 173 (2), 355-370. e14, 2018
6932018
Assuring the quality of next-generation sequencing in clinical laboratory practice
AS Gargis, L Kalman, MW Berry, DP Bick, DP Dimmock, T Hambuch, F Lu, ...
Nature biotechnology 30 (11), 1033-1036, 2012
5012012
A phase 1/2 study of chemosensitization with the CXCR4 antagonist plerixafor in relapsed or refractory acute myeloid leukemia
GL Uy, MP Rettig, IH Motabi, K McFarland, KM Trinkaus, LM Hladnik, ...
Blood, The Journal of the American Society of Hematology 119 (17), 3917-3924, 2012
4252012
Association between mutation clearance after induction therapy and outcomes in acute myeloid leukemia
JM Klco, CA Miller, M Griffith, A Petti, DH Spencer, S Ketkar-Kulkarni, ...
Jama 314 (8), 811-822, 2015
3782015
Use of whole-genome sequencing to diagnose a cryptic fusion oncogene
JS Welch, P Westervelt, L Ding, DE Larson, JM Klco, S Kulkarni, J Wallis, ...
Jama 305 (15), 1577-1584, 2011
2962011
Genomic analysis of mycosis fungoides and Sézary syndrome identifies recurrent alterations in TNFR2
A Ungewickell, A Bhaduri, E Rios, J Reuter, CS Lee, A Mah, A Zehnder, ...
Nature genetics 47 (9), 1056-1060, 2015
2762015
TBX6 null variants and a common hypomorphic allele in congenital scoliosis
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, ...
New England Journal of Medicine 372 (4), 341-350, 2015
2682015
Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux
W Lu, AM Van Eerde, X Fan, F Quintero-Rivera, S Kulkarni, H Ferguson, ...
The American Journal of Human Genetics 80 (4), 616-632, 2007
2432007
Mouse dyskerin mutations affect accumulation of telomerase RNA and small nucleolar RNA, telomerase activity, and ribosomal RNA processing
Y Mochizuki, J He, S Kulkarni, M Bessler, PJ Mason
Proceedings of the National Academy of Sciences 101 (29), 10756-10761, 2004
2382004
Clinical next‐generation sequencing in patients with non–small cell lung cancer
IS Hagemann, S Devarakonda, CM Lockwood, DH Spencer, K Guebert, ...
Cancer 121 (4), 631-639, 2015
2332015
Optimizing cancer genome sequencing and analysis
M Griffith, CA Miller, OL Griffith, K Krysiak, ZL Skidmore, A Ramu, ...
Cell systems 1 (3), 210-223, 2015
2172015
Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML
DC Link, LG Schuettpelz, D Shen, J Wang, MJ Walter, S Kulkarni, ...
Jama 305 (15), 1568-1576, 2011
2092011
Validation of a next-generation sequencing assay for clinical molecular oncology
CE Cottrell, H Al-Kateb, AJ Bredemeyer, EJ Duncavage, DH Spencer, ...
The Journal of molecular diagnostics 16 (1), 89-105, 2014
1982014
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA
J Zhang, J Li, JB Saucier, Y Feng, Y Jiang, J Sinson, AK McCombs, ...
Nature medicine 25 (3), 439-447, 2019
1942019
Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t (8; 13)(p11; q12) myeloproliferative syndrome
A Reiter, J Sohal, S Kulkarni, A Chase, DHC Macdonald, RCT Aguiar, ...
Blood, The Journal of the American Society of Hematology 92 (5), 1735-1742, 1998
1881998
Good laboratory practice for clinical next-generation sequencing informatics pipelines
AS Gargis, L Kalman, DP Bick, C Da Silva, DP Dimmock, BH Funke, ...
Nature biotechnology 33 (7), 689-693, 2015
1632015
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