Shashikant Kulkarni (Shashi)

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	Hepsi	2020 yılından bugüne
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Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

Eric DuncavageProfessor of Pathology and Immunology, Washington University School of Medicinewustl.edu üzerinde doğrulanmış e-posta adresine sahip
NCP CrossUniversity of Southamptonsoton.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Deborah RitterBaylor College of Medicinebcm.edu üzerinde doğrulanmış e-posta adresine sahip
Michael TomassonProfessor, University of Iowauiowa.edu üzerinde doğrulanmış e-posta adresine sahip
Christina M LockwoodAssociate Professor of Laboratory Medicine, University of Washingtonuw.edu üzerinde doğrulanmış e-posta adresine sahip
Subha MadhavanGeorgetown Universitygeorgetown.edu üzerinde doğrulanmış e-posta adresine sahip
Geoffrey L. UyProfessor of Medicine, Washington University School of Medicinewustl.edu üzerinde doğrulanmış e-posta adresine sahip
Shruti RaoCedars-Sinai Precision Biomarker Laboratories | Innovation Center For Biomedical Informaticsgeorgetown.edu üzerinde doğrulanmış e-posta adresine sahip
Michael DattoMedical Director and Associate Vice President of Clinical Laboratories, Duke Universityduke.edu üzerinde doğrulanmış e-posta adresine sahip
TJ LeyProfessor of Medicine and Genetics, Washington University School of Medicinewustl.edu üzerinde doğrulanmış e-posta adresine sahip
john s welchWashington Universitywustl.edu üzerinde doğrulanmış e-posta adresine sahip
Malachi GriffithAssociate Professor, Medicine, Washington University School of Medicinewustl.edu üzerinde doğrulanmış e-posta adresine sahip
Obi L. GriffithAssociate Professor, Washington University School of Medicinewustl.edu üzerinde doğrulanmış e-posta adresine sahip
Richard K. Wilson, Ph.D.Nationwide Children's Hospital; Ohio State UniversityNationwideChildrens.org üzerinde doğrulanmış e-posta adresine sahip
Elaine MardisOhio State Universitynationwidechildrens.org üzerinde doğrulanmış e-posta adresine sahip
Dmitriy SonkinNCInih.gov üzerinde doğrulanmış e-posta adresine sahip
Marwan ShinawiProfessor of Pediatricskids.wustl.edu üzerinde doğrulanmış e-posta adresine sahip
Philip MasonCHOPemail.chop.edu üzerinde doğrulanmış e-posta adresine sahip
Jeffery KlcoSt Jude Children's Research Hospitalstjude.org üzerinde doğrulanmış e-posta adresine sahip
Andrew Bredemeyer, PhDPierianDxpieriandx.com üzerinde doğrulanmış e-posta adresine sahip

Takip et

Shashikant Kulkarni (Shashi)

Professor & Vice Chairman, Molecular Pathology & Cytogenetics, MD Anderson Cancer Center, Houston Th

mdanderson.org üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa

Precision Medicine using genomic and integrated multi-omic tools Cancer Genomics Clinical Genomics


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
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	4999	2013
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	2609	2012
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	1908	2012
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	1829	2017
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	787	2018
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	518	2012
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	443	2012
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	403	2015
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	309	2015
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	306	2011
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	303	2015
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	248	2007
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	245	2004
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	236	2015
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	227	2015
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	226	2019
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	212	2011
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	203	2014
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	191	1998
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	175	2015

Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.

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