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David E Larson
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Cited by
Year
A genomic case study of mixed fibrolamellar hepatocellular carcinoma
OL Griffith, M Griffith, K Krysiak, V Magrini, A Ramu, ZL Skidmore, ...
Annals of Oncology 27 (6), 1148-1154, 2016
262016
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease
X Zhang, C Zhu, G Beecham, BN Vardarajan, Y Ma, D Lancour, JJ Farrell, ...
Alzheimer's & Dementia 15 (3), 441-452, 2019
392019
Abstract PR11: Genomic approaches for risk assessment in acute myeloid leukemia
JM Klco, CA Miller, M Griffith, A Petti, DH Spencer, S Ketkar-Kulkarni, ...
Cancer Research 75 (22_Supplement_1), PR11-PR11, 2015
2015
ADSP family study design. Approximately 1,400
GW Beecham, JC Bis, ER Martin, SH Choi, AL DeStefano, CM van Duijn, ...
Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers
CA Miller, Y Gindin, C Lu, OL Griffith, M Griffith, D Shen, J Hoog, T Li, ...
Nature Communications 7, 2016
822016
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
3812015
Association of structural variation with cardiometabolic traits in Finns
L Chen, HJ Abel, I Das, DE Larson, L Ganel, KL Kanchi, AA Regier, ...
The American Journal of Human Genetics 108 (4), 583-596, 2021
262021
Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells
MA Young, DE Larson, CW Sun, DR George, L Ding, CA Miller, L Lin, ...
Cell stem cell 10 (5), 570-582, 2012
2552012
Bam-readcount-rapid generation of basepair-resolution
A Khanna, DE Larson, SN Srivatsan, OL Griffith, M Griffith, CA Miller
Bam-readcount-rapid generation of basepair-resolution sequence metrics
A Khanna, DE Larson, SN Srivatsan, M Mosior, TE Abbott, S Kiwala, ...
ArXiv, 2021
582021
Bioconda: Sustainable and comprehensive software distribution for the life sciences
R Dale, B Grüning, A Sjödin, J Rowe, BA Chapman, CH Tomkins-Tinch, ...
Nature Methods 15 (7), 475-476, 2018
8542018
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
16372009
BreakDancer: Identification of Genomic Structural Variation from Paired‐End Read Mapping
X Fan, TE Abbott, D Larson, K Chen
Current protocols in bioinformatics 45 (1), 15.6. 1-15.6. 11, 2014
1932014
Cell positioning in the Drosophila pupal retina
DE Larson
Washington University in St. Louis, 2007
12007
Cellular behavior in the developing Drosophila pupal retina
DE Larson, Z Liberman, RL Cagan
Mechanisms of development 125 (3-4), 223-232, 2008
492008
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), 170-174, 2017
5542017
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
9772012
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
25312012
CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data
Q Zhang, L Ding, DE Larson, DC Koboldt, MD McLellan, K Chen, X Shi, ...
Bioinformatics 26 (4), 464-469, 2010
732010
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes
J Zhang, M Griffith, CA Miller, OL Griffith, DH Spencer, JR Walker, ...
Experimental Hematology 55, 19-33, 2017
112017
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