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Christopher C Harris
Christopher C Harris
Unknown affiliation
Verified email at mskcc.org
Title
Cited by
Cited by
Year
Integrated genomic analyses of ovarian carcinoma
Cancer Genome Atlas Research Network
Nature 474 (7353), 609, 2011
51472011
Mutations in the p53 Tumor Suppressor Gene: Clues to Cancer Etiology and Molecular Pathogenesis
MS Greenblatt, WP Bennett, M Hollstein, CC Harris
Cancer research 54 (18), 4855-4878, 1994
50971994
Recurring mutations found by sequencing an acute myeloid leukemia genome
ER Mardis, L Ding, DJ Dooling, DE Larson, MD McLellan, K Chen, ...
New England Journal of Medicine 361 (11), 1058-1066, 2009
25592009
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
23592012
DNMT3A Mutations in Acute Myeloid Leukemia
TJ Ley, L Ding, MJ Walter, MD McLellan, T Lamprecht, DE Larson, ...
New England Journal of Medicine 363 (25), 2424-2433, 2010
22362010
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
16912012
The genetic basis of early T-cell precursor acute lymphoblastic leukaemia
J Zhang, L Ding, L Holmfeldt, G Wu, SL Heatley, D Payne-Turner, ...
Nature 481 (7380), 157-163, 2012
16762012
Database of p53 gene somatic mutations in human tumors and cell lines.
M Hollstein, K Rice, MS Greenblatt, T Soussi, R Fuchs, T Sørlie, E Hovig, ...
Nucleic acids research 22 (17), 3551, 1994
13391994
Genome remodelling in a basal-like breast cancer metastasis and xenograft
LI Ding, MJ Ellis, S Li, DE Larson, K Chen, JW Wallis, CC Harris, ...
Nature 464 (7291), 999-1005, 2010
13202010
Whole-genome analysis informs breast cancer response to aromatase inhibition
MJ Ellis, L Ding, D Shen, J Luo, VJ Suman, JW Wallis, BA Van Tine, ...
Nature 486 (7403), 353-360, 2012
11402012
Landscape of somatic retrotransposition in human cancers
E Lee, R Iskow, L Yang, O Gokcumen, P Haseley, LJ Luquette III, JG Lohr, ...
Science 337 (6097), 967-971, 2012
7462012
Somatic Point Mutations in the p53 Gene of Human Tumors and Cell Lines: Updated Compilation
M Hollstein, B Shomer, M Greenblatt, T Soussi, E Hovig, R Montesano, ...
Nucleic acids research 24 (1), 141-146, 1996
6731996
TP53 mutations and hepatocellular carcinoma: insights into the etiology and pathogenesis of liver cancer
SP Hussain, J Schwank, F Staib, XW Wang, CC Harris
Oncogene 26 (15), 2166-2176, 2007
6722007
SomaticSniper: identification of somatic point mutations in whole genome sequencing data
DE Larson, CC Harris, K Chen, DC Koboldt, TE Abbott, DJ Dooling, ...
Bioinformatics 28 (3), 311-317, 2012
6312012
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes
TA Graubert, D Shen, L Ding, T Okeyo-Owuor, CL Lunn, J Shao, K Krysiak, ...
Nature genetics 44 (1), 53-57, 2012
6152012
IARC Database of p53 gene mutations in human tumors and cell lines: updated compilation, revised formats and new visualisation tools
P Hainaut, T Hernandez, A Robinson, P Rodriguez-Tome, T Flores, ...
Nucleic acids research 26 (1), 205-213, 1998
5631998
CREST maps somatic structural variation in cancer genomes with base-pair resolution
J Wang, CG Mullighan, J Easton, S Roberts, SL Heatley, J Ma, MC Rusch, ...
Nature methods 8 (8), 652-654, 2011
5402011
Frequent mutation of the p53 gene in human esophageal cancer.
MC Hollstein, RA Metcalf, JA Welsh, R Montesano, CC Harris
Proceedings of the National Academy of Sciences 87 (24), 9958-9961, 1990
5391990
Developing stable fine–grain microstructures by large strain deformation
FJ Humphreys, PB Prangnell, JR Bowen, A Gholinia, C Harris
Philosophical Transactions of the Royal Society of London. Series A …, 1999
4771999
Prospective genomic profiling of prostate cancer across disease states reveals germline and somatic alterations that may affect clinical decision making
W Abida, J Armenia, A Gopalan, R Brennan, M Walsh, D Barron, D Danila, ...
JCO precision oncology 1, 1-16, 2017
4012017
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