Chip Stewart
Chip Stewart
The Broad Institute
Verified email at broadinstitute.org
TitleCited byYear
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
64952010
Observation of the top quark
S Abachi, B Abbott, M Abolins, BS Acharya, I Adam, DL Adams, M Adams, ...
Physical Review Letters 74 (14), 2632, 1995
35271995
Mutational heterogeneity in cancer and the search for new cancer-associated genes
MS Lawrence, P Stojanov, P Polak, GV Kryukov, K Cibulskis, ...
Nature 499 (7457), 214, 2013
29552013
The DØ detector
S Abachi, M Abolins, BS Acharya, I Adam, S Ahn, H Aihara, G Alvarez, ...
Nuclear Instruments and Methods in Physics Research Section A: Accelerators …, 1994
17041994
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia
DA Landau, SL Carter, P Stojanov, A McKenna, K Stevenson, ...
Cell 152 (4), 714-726, 2013
10062013
Integrated genomic characterization of papillary thyroid carcinoma
N Agrawal, R Akbani, BA Aksoy, A Ally, H Arachchi, SL Asa, JT Auman, ...
Cell 159 (3), 676-690, 2014
9592014
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59, 2011
9402011
The molecular taxonomy of primary prostate cancer
A Abeshouse, J Ahn, R Akbani, A Ally, S Amin, CD Andry, M Annala, ...
Cell 163 (4), 1011-1025, 2015
8402015
Prospective derivation of a living organoid biobank of colorectal cancer patients
M van de Wetering, HE Francies, JM Francis, G Bounova, F Iorio, A Pronk, ...
Cell 161 (4), 933-945, 2015
6352015
The genetic landscape of high-risk neuroblastoma
TJ Pugh, O Morozova, EF Attiyeh, S Asgharzadeh, JS Wei, D Auclair, ...
Nature genetics 45 (3), 279, 2013
5672013
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity
AM Dulak, P Stojanov, S Peng, MS Lawrence, C Fox, C Stewart, S Bandla, ...
Nature genetics 45 (5), 478, 2013
5152013
Whole-genome sequencing and variant discovery in C. elegans
LDW Hillier, GT Marth, AR Quinlan, D Dooling, G Fewell, D Barnett, P Fox, ...
Nature methods 5 (2), 183, 2008
5052008
Mutations driving CLL and their evolution in progression and relapse
DA Landau, E Tausch, AN Taylor-Weiner, C Stewart, JG Reiter, J Bahlo, ...
Nature 526 (7574), 525, 2015
4382015
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
4352011
Landscape of genomic alterations in cervical carcinomas
AI Ojesina, L Lichtenstein, SS Freeman, CS Pedamallu, ...
Nature 506 (7488), 371, 2014
4162014
Genomic correlates of immune-cell infiltrates in colorectal carcinoma
M Giannakis, XJ Mu, SA Shukla, ZR Qian, O Cohen, R Nishihara, S Bahl, ...
Cell reports 15 (4), 857-865, 2016
3082016
Rapid whole-genome mutational profiling using next-generation sequencing technologies
DR Smith, AR Quinlan, HE Peckham, K Makowsky, W Tao, B Woolf, ...
Genome research 18 (10), 1638-1642, 2008
2992008
A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers
RS Lee, C Stewart, SL Carter, L Ambrogio, K Cibulskis, C Sougnez, ...
The Journal of clinical investigation 122 (8), 2983-2988, 2012
2612012
Top quark search with the D0 1992–1993 data sample
S Abachi, B Abbott, M Abolins, BS Acharya, I Adam, DL Adams, M Adams, ...
Physical Review D 52 (9), 4877, 1995
2441995
Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation
M Costello, TJ Pugh, TJ Fennell, C Stewart, L Lichtenstein, JC Meldrim, ...
Nucleic acids research 41 (6), e67-e67, 2013
2432013
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