Takip et
Sumit Middha
Sumit Middha
Bilinmeyen bağlantı
umn.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients
A Zehir, R Benayed, RH Shah, A Syed, S Middha, HR Kim, P Srinivasan, ...
Nature medicine 23 (6), 703-713, 2017
28922017
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
NM Ioannidis, JH Rothstein, V Pejaver, S Middha, SK McDonnell, ...
The American Journal of Human Genetics 99 (4), 877-885, 2016
17282016
The Genomic Landscape of Endocrine-Resistant Advanced Breast Cancers
P Razavi, MT Chang, G Xu, C Bandlamudi, DS Ross, N Vasan, Y Cai, ...
Cancer cell 34 (3), 427-438. e6, 2018
7822018
Clinical sequencing defines the genomic landscape of metastatic colorectal cancer
R Yaeger, WK Chatila, MD Lipsyc, JF Hechtman, A Cercek, ...
Cancer cell 33 (1), 125-136. e3, 2018
6712018
Analysis of the prevalence of microsatellite instability in prostate cancer and response to immune checkpoint blockade
W Abida, ML Cheng, J Armenia, S Middha, KA Autio, HA Vargas, ...
JAMA oncology 5 (4), 471-478, 2019
5272019
Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides
JB Egan, CX Shi, W Tembe, A Christoforides, A Kurdoglu, S Sinari, ...
Blood, The Journal of the American Society of Hematology 120 (5), 1060-1066, 2012
5002012
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), 286-295, 2019
4852019
Genetic diversity of tumors with mismatch repair deficiency influences anti–PD-1 immunotherapy response
R Mandal, RM Samstein, KW Lee, JJ Havel, H Wang, C Krishna, ...
Science 364 (6439), 485-491, 2019
4342019
The human gut microbiome: current knowledge, challenges, and future directions
M Dave, PD Higgins, S Middha, KP Rioux
Translational Research 160 (4), 246-257, 2012
4332012
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
CJ Klein, MV Botuyan, Y Wu, CJ Ward, GA Nicholson, S Hammans, ...
Nature genetics 43 (6), 595-600, 2011
4282011
Integrated genomic characterization reveals novel, therapeutically relevant drug targets in FGFR and EGFR pathways in sporadic intrahepatic cholangiocarcinoma
MJ Borad, MD Champion, JB Egan, WS Liang, R Fonseca, AH Bryce, ...
PLoS genetics 10 (2), e1004135, 2014
3552014
MAP-RSeq: Mayo analysis pipeline for RNA sequencing
KR Kalari, AA Nair, JD Bhavsar, DR O’Brien, JI Davila, MA Bockol, J Nie, ...
BMC bioinformatics 15, 1-11, 2014
3142014
Genetic Predictors of Response to Systemic Therapy in Esophagogastric CancerGenomic Biomarkers in Esophagogastric Adenocarcinoma
YY Janjigian, F Sanchez-Vega, P Jonsson, WK Chatila, JF Hechtman, ...
Cancer discovery 8 (1), 49-58, 2018
3082018
Reliable Pan-Cancer Microsatellite Instability Assessment by Using Targeted Next-Generation Sequencing Data
S Middha, L Zhang, K Nafa, G Jayakumaran, D Wong, HR Kim, ...
JCO Precision Oncology 1, 1-17, 2017
3052017
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants
F Zou, HS Chai, CS Younkin, M Allen, J Crook, VS Pankratz, ...
PLoS genetics 8 (6), e1002707, 2012
2482012
Reliable detection of mismatch repair deficiency in colorectal cancers using mutational load in next-generation sequencing panels
ZK Stadler, F Battaglin, S Middha, JF Hechtman, C Tran, A Cercek, ...
Journal of Clinical Oncology 34 (18), 2141, 2016
2412016
The genetic landscape of endometrial clear cell carcinomas
DF DeLair, KA Burke, P Selenica, RS Lim, SN Scott, S Middha, ...
The Journal of pathology 243 (2), 230-241, 2017
2062017
3'tag digital gene expression profiling of human brain and universal reference RNA using Illumina Genome Analyzer
YW Asmann, EW Klee, EA Thompson, EA Perez, S Middha, AL Oberg, ...
BMC genomics 10, 1-11, 2009
1992009
Novel late-onset Alzheimer disease loci variants associate with brain gene expression
M Allen, F Zou, HS Chai, CS Younkin, J Crook, VS Pankratz, ...
Neurology 79 (3), 221-228, 2012
1782012
CAP-miRSeq: a comprehensive analysis pipeline for microRNA sequencing data
Z Sun, J Evans, A Bhagwate, S Middha, M Bockol, H Yan, JP Kocher
BMC genomics 15 (1), 1-10, 2014
1772014
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