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Shashikant Kulkarni (Shashi)
Shashikant Kulkarni (Shashi)
Professor & Vice Chairman, Baylor College of Medicine; CSO & SVP Baylor Genetics
Подтвержден адрес электронной почты в домене bcm.edu - Главная страница
Название
Процитировано
Процитировано
Год
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
46232013
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
25162012
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
18242012
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
15542017
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
7072018
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
5022012
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
4272012
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
3792015
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
2772015
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
2732015
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
2442007
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
2392004
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
2352015
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
2182015
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
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
1982019
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
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
1891998
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
1642015
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