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 France. David E. Larson's co-authors include Richard K. Wilson, Elaine R. Mardis, Daniel C. Koboldt, Li Ding, Michael D. McLellan, Qunyuan Zhang, Christopher A. Miller, Dong Shen, 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

VarScan 2: Somatic mutati... 1987 2026 2000 2013 2012 2009 2009 2013 1987 1000 2.0k 3.0k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
David E. Larson 4.2k 2.4k 2.2k 1.0k 954 50 8.9k
André Franke 6.5k 1.6× 3.7k 1.5× 1.1k 0.5× 773 0.8× 918 1.0× 377 14.9k
Qunyuan Zhang 5.7k 1.4× 2.0k 0.8× 3.4k 1.5× 1.3k 1.3× 2.3k 2.4× 41 10.4k
Thomas J. Hudson 10.0k 2.4× 5.8k 2.4× 1.7k 0.8× 1.1k 1.1× 1.6k 1.6× 227 20.1k
P Vassalli 6.1k 1.5× 1.7k 0.7× 1.7k 0.7× 1.8k 1.8× 2.1k 2.2× 209 22.4k
Christopher S. Potten 7.0k 1.7× 2.8k 1.1× 1.9k 0.9× 1.5k 1.5× 6.2k 6.4× 235 16.4k
D. Stephen Charnock‐Jones 6.7k 1.6× 1.3k 0.5× 1.3k 0.6× 949 0.9× 1.2k 1.3× 308 18.8k
John P. Sundberg 7.4k 1.8× 3.0k 1.2× 1.3k 0.6× 1.3k 1.3× 1.6k 1.6× 422 18.4k
Donna M. Muzny 5.1k 1.2× 2.7k 1.1× 987 0.4× 409 0.4× 481 0.5× 163 8.9k
Martin J. Aryee 14.7k 3.5× 3.5k 1.4× 1.7k 0.7× 1.1k 1.0× 1.0k 1.1× 92 17.9k
Michael Baseler 6.0k 1.4× 1.3k 0.5× 1.6k 0.7× 902 0.9× 1.4k 1.5× 99 17.1k

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

20 of 20 papers shown
1.
Abel, Haley, David E. Larson, Allison Regier, et al.. (2020). Mapping and characterization of structural variation in 17,795 human genomes. Nature. 583(7814). 83–89. 148 indexed citations
2.
Larson, David E., Haley Abel, Colby Chiang, et al.. (2019). svtools: population-scale analysis of structural variation. Bioinformatics. 35(22). 4782–4787. 33 indexed citations
3.
Regier, Allison, Yossi Farjoun, David E. Larson, et al.. (2018). Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects. Nature Communications. 9(1). 4038–4038. 73 indexed citations
4.
Koboldt, Daniel C., Krishna Kanchi, Bin Gui, et al.. (2016). Rare Variation in TET2 Is Associated with Clinically Relevant Prostate Carcinoma in African Americans. Cancer Epidemiology Biomarkers & Prevention. 25(11). 1456–1463. 19 indexed citations
5.
Miller, Christopher A., Yevgeniy Gindin, Charles Lu, et al.. (2016). Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers. Nature Communications. 7(1). 12498–12498. 51 indexed citations
6.
Koboldt, Daniel C., David E. Larson, Lori S. Sullivan, et al.. (2014). Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders. The American Journal of Human Genetics. 94(3). 373–384. 30 indexed citations
7.
Koboldt, Daniel C., David E. Larson, Lori S. Sullivan, et al.. (2013). Variant prioritization and linkage mapping using whole-exome sequencing data for families with autosomal dominant retinitis pigmentosa (adRP). Investigative Ophthalmology & Visual Science. 54(15). 3357–3357. 1 indexed citations
8.
Koboldt, Daniel C., Karyn Meltz Steinberg, David E. Larson, Richard K. Wilson, & Elaine R. Mardis. (2013). The Next-Generation Sequencing Revolution and Its Impact on Genomics. Cell. 155(1). 27–38. 665 indexed citations breakdown →
9.
Koboldt, Daniel C., Qunyuan Zhang, David E. Larson, et al.. (2012). VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Research. 22(3). 568–576. 3093 indexed citations breakdown →
10.
Koboldt, Daniel C., David E. Larson, Ken Chen, Li Ding, & Richard K. Wilson. (2011). Massively Parallel Sequencing Approaches for Characterization of Structural Variation. Methods in molecular biology. 838. 369–384. 35 indexed citations
11.
Larson, David E., Ruth I. Johnson, Maciej Swat, et al.. (2010). Computer Simulation of Cellular Patterning Within the Drosophila Pupal Eye. PLoS Computational Biology. 6(7). e1000841–e1000841. 20 indexed citations
12.
Koboldt, Daniel C., Ken Chen, Todd Wylie, et al.. (2009). VarScan: variant detection in massively parallel sequencing of individual and pooled samples. Bioinformatics. 25(17). 2283–2285. 917 indexed citations breakdown →
13.
Larson, David E., Zoe Liberman, & Ross Cagan. (2007). Cellular behavior in the developing Drosophila pupal retina. Mechanisms of Development. 125(3-4). 223–232. 38 indexed citations
14.
Vidal, Marcos, David E. Larson, & Ross Cagan. (2006). Csk-Deficient Boundary Cells Are Eliminated from Normal Drosophila Epithelia by Exclusion, Migration, and Apoptosis. Developmental Cell. 10(1). 33–44. 153 indexed citations
15.
Hinz, Aaron, David E. Larson, Christopher Smith, & Yves V. Brun. (2003). The Caulobacter crescentus polar organelle development protein PodJ is differentially localized and is required for polar targeting of the PleC development regulator. Molecular Microbiology. 47(4). 929–941. 87 indexed citations
16.
Nawaz, Haq, et al.. (2001). Self-reported weight and height. American Journal of Preventive Medicine. 20(4). 294–298. 237 indexed citations
17.
Larson, David E.. (1996). Mayo Clinic family health book. 12 indexed citations
18.
Sandborn, William J., et al.. (1993). High-Volume Postobstructive Choleresis After Transhepatic External Biliary Drainage Resolves with Conversion to Internal Drainage. Journal of Clinical Gastroenterology. 17(1). 42–45. 5 indexed citations
19.
Mauch, Peter, David E. Larson, R T Osteen, et al.. (1990). Prognostic factors for positive surgical staging in patients with Hodgkin's disease.. Journal of Clinical Oncology. 8(2). 257–265. 82 indexed citations
20.
Larson, David E., et al.. (1989). Tetanus: An Uncommon Cause of Dysphagia. Mayo Clinic Proceedings. 64(3). 335–338. 14 indexed citations

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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