David E Larson
Title
Cited by
Cited by
Year
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
Cancer Genome Atlas Research Network
Nature 455 (7216), 1061, 2008
54672008
VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing
DC Koboldt, Q Zhang, DE Larson, D Shen, MD McLellan, L Lin, CA Miller, ...
Genome research 22 (3), 568-576, 2012
31852012
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
29002013
Somatic mutations affect key pathways in lung adenocarcinoma
L Ding, G Getz, DA Wheeler, ER Mardis, MD McLellan, K Cibulskis, ...
Nature 455 (7216), 1069, 2008
26112008
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
22222009
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, 2012
19542012
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
18912010
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome
TJ Ley, ER Mardis, L Ding, B Fulton, MD McLellan, K Chen, D Dooling, ...
Nature 456 (7218), 66, 2008
13542008
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
13322012
BreakDancer: an algorithm for high-resolution mapping of genomic structural variation
K Chen, JW Wallis, MD McLellan, DE Larson, JM Kalicki, CS Pohl, ...
Nature Methods 6 (9), 677-681, 2009
13302009
Genome remodelling in a basal-like breast cancer metastasis and xenograft
L Ding, MJ Ellis, S Li, DE Larson, K Chen, JW Wallis, CC Harris, ...
Nature 464 (7291), 999-1005, 2010
11952010
VarScan: variant detection in massively parallel sequencing of individual and pooled samples
DC Koboldt, K Chen, T Wylie, DE Larson, MD McLellan, ER Mardis, ...
Bioinformatics 25 (17), 2283-2285, 2009
10992009
The next-generation sequencing revolution and its impact on genomics
DC Koboldt, KM Steinberg, DE Larson, RK Wilson, ER Mardis
Cell 155 (1), 27-38, 2013
9162013
Clonal architecture of secondary acute myeloid leukemia
MJ Walter, D Shen, L Ding, J Shao, DC Koboldt, K Chen, DE Larson, ...
New England Journal of Medicine 366 (12), 1090-1098, 2012
7802012
Endocrine-therapy-resistant ESR1 variants revealed by genomic characterization of breast-cancer-derived xenografts
S Li, D Shen, J Shao, R Crowder, W Liu, A Prat, X He, S Liu, J Hoog, C Lu, ...
Cell reports 4 (6), 1116-1130, 2013
5022013
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
4932012
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, 2011
4932011
DGIdb: mining the druggable genome
M Griffith, OL Griffith, AC Coffman, JV Weible, JF McMichael, NC Spies, ...
Nature methods 10 (12), 1209-1210, 2013
3462013
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
2762015
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer
M Griffith, NC Spies, K Krysiak, JF McMichael, AC Coffman, AM Danos, ...
Nature genetics 49 (2), 170, 2017
2722017
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