David E. Larson

72.8k total citations · 5 hit papers
50 papers, 8.9k citations indexed

About

David E. Larson is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, David E. Larson has authored 50 papers receiving a total of 8.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 12 papers in Surgery. Recurrent topics in David E. Larson's work include Genomics and Phylogenetic Studies (9 papers), Genomics and Rare Diseases (7 papers) and Cancer Genomics and Diagnostics (7 papers). David E. Larson is often cited by papers focused on Genomics and Phylogenetic Studies (9 papers), Genomics and Rare Diseases (7 papers) and Cancer Genomics and Diagnostics (7 papers). David E. Larson collaborates with scholars based in United States, Vietnam and United Kingdom. David E. Larson's co-authors include Richard K. Wilson, Elaine R. Mardis, Daniel C. Koboldt, Li Ding, Michael D. McLellan, Qunyuan Zhang, Dong Shen, Christopher A. Miller, Ling Lin and Ken Chen and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

David E. Larson

48 papers receiving 8.7k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing

2012 3.1k citations Daniel C. Koboldt, Qunyuan Zhang et al. Genome Research profile →
BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

2009 997 citations Ken Chen, John W. Wallis et al. Nature Methods profile →
VarScan: variant detection in massively parallel sequencing of individual and pooled samples

2009 917 citations Daniel C. Koboldt, Ken Chen et al. Bioinformatics profile →
The Next-Generation Sequencing Revolution and Its Impact on Genomics

2013 665 citations Daniel C. Koboldt, Karyn Meltz Steinberg et al. Cell profile →
Percutaneous endoscopic gastrostomy

1987 642 citations David E. Larson, Eugene P. DiMagno et al. profile →

Peers

Countries citing papers authored by David E. Larson

Since Specialization

Citations

This map shows the geographic impact of David E. Larson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by David E. Larson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David E. Larson more than expected).

Fields of papers citing papers by David E. Larson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David E. Larson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by David E. Larson. The network helps show where David E. Larson may publish in the future.

Co-authorship network of co-authors of David E. Larson

This figure shows the co-authorship network connecting the top 25 collaborators of David E. Larson. A scholar is included among the top collaborators of David E. Larson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with David E. Larson. David E. Larson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Mapping and characterization of structural variation in 17,795 human genomes 2020 ·Nature ·Haley Abel, David E. Larson, Allison Regier, Colby Chiang, Indraniel Das, Krishna Kanchi, Ryan M. Layer, Benjamin M. Neale, William Salerno, Catherine Reeves, Steven Buyske, Tara C. Matise, Donna M. Muzny, Michael C. Zody, Eric S. Lander, Susan K. Dutcher, Nathan O. Stitziel, Ira M. Hall	148
2	svtools: population-scale analysis of structural variation 2019 ·Bioinformatics ·David E. Larson, Haley Abel, Colby Chiang, (unknown), Indraniel Das, James M. Eldred, Ryan M. Layer, Ira M. Hall	33
3	Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects 2018 ·Nature Communications ·Allison Regier, Yossi Farjoun, David E. Larson, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan, (unknown), (unknown), Eric Banks, Darren C. Ames, Adam C. English, Heng Li, Jinchuan Xing, Yeting Zhang, Tara C. Matise, Gonçalo R. Abecasis, (unknown), Michael C. Zody, Benjamin M. Neale, Ira M. Hall	73
4	Rare Variation in TET2 Is Associated with Clinically Relevant Prostate Carcinoma in African Americans 2016 ·Cancer Epidemiology Biomarkers & Prevention ·Daniel C. Koboldt, Krishna Kanchi, Bin Gui, David E. Larson, Robert S. Fulton, William B. Isaacs, Aldi T. Kraja, Ingrid B. Borecki, Jia Li, Richard K. Wilson, Elaine R. Mardis, Adam S. Kibel	19
5	Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers 2016 ·Nature Communications ·Christopher A. Miller, Yevgeniy Gindin, Charles Lu, Obi L. Griffith, Malachi Griffith, Dong Shen, Jeremy Hoog, Tiandao Li, David E. Larson, Mark A. Watson, Sherri R. Davies, Kelly K. Hunt, Vera J. Suman, Jacqueline Snider, Thomas Walsh, Graham A. Colditz, Katherine DeSchryver, Richard K. Wilson, Elaine R. Mardis, Matthew J. Ellis	51
6	Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders 2014 ·The American Journal of Human Genetics ·Daniel C. Koboldt, David E. Larson, Lori S. Sullivan, Sara J. Bowne, Karyn Meltz Steinberg, Jennifer D. Churchill, (unknown), (unknown), Eric A. Pierce, Susan H. Blanton, George M. Weinstock, Richard K. Wilson, Stephen P. Daiger	30
7	Variant prioritization and linkage mapping using whole-exome sequencing data for families with autosomal dominant retinitis pigmentosa (adRP) 2013 ·Investigative Ophthalmology & Visual Science ·Daniel C. Koboldt, David E. Larson, Lori S. Sullivan, Sara J. Bowne, Robert S. Fulton, Erica Sodergren, Susan H. Blanton, Stephen P. Daiger, Richard K. Wilson, George M. Weinstock	1
8	The Next-Generation Sequencing Revolution and Its Impact on Genomics breakdown → 2013 ·Cell ·Daniel C. Koboldt, Karyn Meltz Steinberg, David E. Larson, Richard K. Wilson, Elaine R. Mardis	665
9	VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing breakdown → 2012 ·Genome Research ·Daniel C. Koboldt, Qunyuan Zhang, David E. Larson, Dong Shen, Michael D. McLellan, Ling Lin, Christopher A. Miller, Elaine R. Mardis, Li Ding, Richard K. Wilson	3093
10	Massively Parallel Sequencing Approaches for Characterization of Structural Variation 2011 ·Methods in molecular biology ·Daniel C. Koboldt, David E. Larson, Ken Chen, Li Ding, Richard K. Wilson	35
11	VarScan: variant detection in massively parallel sequencing of individual and pooled samples breakdown → 2009 ·Bioinformatics ·Daniel C. Koboldt, Ken Chen, Todd Wylie, David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding	917
12	BreakDancer: an algorithm for high-resolution mapping of genomic structural variation breakdown → 2009 ·Nature Methods ·Ken Chen, John W. Wallis, Michael D. McLellan, David E. Larson, Joelle Kalicki, Craig Pohl, Sean McGrath, Michael C. Wendl, Qunyuan Zhang, Devin P. Locke, Xiaoqi Shi, Robert S. Fulton, Timothy J. Ley, Richard K. Wilson, Li Ding, Elaine R. Mardis	997
13	Cellular behavior in the developing Drosophila pupal retina 2007 ·Mechanisms of Development ·David E. Larson, Zoe Liberman, Ross Cagan	38
14	Csk-Deficient Boundary Cells Are Eliminated from Normal Drosophila Epithelia by Exclusion, Migration, and Apoptosis 2006 ·Developmental Cell ·Marcos Vidal, David E. Larson, Ross Cagan	153
15	The Caulobacter crescentus polar organelle development protein PodJ is differentially localized and is required for polar targeting of the PleC development regulator 2003 ·Molecular Microbiology ·Aaron Hinz, David E. Larson, Christopher Smith, Yves V. Brun	87
16	Mayo Clinic family health book 1996 ·David E. Larson	12
17	High-Volume Postobstructive Choleresis After Transhepatic External Biliary Drainage Resolves with Conversion to Internal Drainage 1993 ·Journal of Clinical Gastroenterology ·William J. Sandborn, John B. Gross, David E. Larson, (unknown), Keith D. Lindor	5
18	Predictors of Outcome After Percutaneous Endoscopic Gastrostomy: A Community-Based Study 1992 ·Mayo Clinic Proceedings ·(unknown), David E. Larson, David Ballard, Larry Bergstrom, Marc D. Silverstein, Alan R. Zinsmeister, Eugene P. DiMagno	165
19	Prognostic factors for positive surgical staging in patients with Hodgkin's disease. 1990 ·Journal of Clinical Oncology ·Peter Mauch, David E. Larson, R T Osteen, B. Silver, Bu B. Yeap, G P Canellos, H Weinstein, David I. Rosenthal, Geraldine Pinkus, Maxine S. Jochelson	82
20	Tetanus: An Uncommon Cause of Dysphagia 1989 ·Mayo Clinic Proceedings ·(unknown), (unknown), (unknown), David E. Larson	14

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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