David E. Larson
Impact in
- Cancer Research top 0.05%
- Cancer Genomics and Diagnostics
- Hematology top 0.1%
- Acute Myeloid Leukemia Research
Papers in
-
- Cancer Genomics and Diagnostics 21
- Genetics 27
- Genomics and Rare Diseases 11
- Genomic variations and chromosomal abnormalities 7
- Genetic Associations and Epidemiology 6
- Co-authors
- Richard K. Wilson (12 shared papers)Elaine R. Mardis (7 shared papers)Daniel C. Koboldt (8 shared papers)Ken Chen (6 shared papers)Li Ding (5 shared papers)Eugene P. DiMagno (4 shared papers)Kenneth W. Schroeder (2 shared papers)Duane D. Burton (2 shared papers)
- Journals
- Mayo Clinic Proceedings (10 papers)Nature (9 papers)Nature Communications (6 papers)New England Journal of Medicine (4 papers)Bioinformatics (4 papers)
- Partner nations
- United StatesVietnamUnited Kingdom
In The Last Decade
David E. Larson
90 papers receiving 40.2k citations
David E. Larson's Hit Papers
Peers
Comparison fields: 5 of 211
- Cancer Research 9.3k
- Hematology 5.5k
- Genetics 4.7k
- Genetics 9.6k
- Molecular Biology 18.6k
Countries citing papers authored by David E. Larson
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
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-authors
The 25 scholars most cited alongside David E. Larson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 92 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 12573 |
| 2 | Comprehensive genomic characterization defines human glioblastoma genes and core pathways Hit paper breakdown → | 2008 | 6384 |
| 3 | Somatic mutations affect key pathways in lung adenocarcinoma Hit paper breakdown → | 2008 | 2237 |
| 4 | Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome Hit paper breakdown → | 2009 | 1886 |
| 5 | DNMT3A Mutations in Acute Myeloid Leukemia Hit paper breakdown → | 2010 | 1657 |
| 6 | Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing Hit paper breakdown → | 2012 | 1645 |
| 7 | The Origin and Evolution of Mutations in Acute Myeloid Leukemia Hit paper breakdown → | 2012 | 1285 |
| 8 | BreakDancer: an algorithm for high-resolution mapping of genomic structural variation Hit paper breakdown → | 2009 | 1112 |
| 9 | VarScan: variant detection in massively parallel sequencing of individual and pooled samples Hit paper breakdown → | 2009 | 1056 |
| 10 | DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome Hit paper breakdown → | 2008 | 1050 |
| 11 | Genome remodelling in a basal-like breast cancer metastasis and xenograft Hit paper breakdown → | 2010 | 991 |
| 12 | The Next-Generation Sequencing Revolution and Its Impact on Genomics Hit paper breakdown → | 2013 | 774 |
| 13 | Percutaneous endoscopic gastrostomy Hit paper breakdown → | 1987 | 707 |
| 14 | Clonal Architecture of Secondary Acute Myeloid Leukemia Hit paper breakdown → | 2012 | 641 |
| 15 | 2011 | 490 | |
| 16 | 2011 | 484 | |
| 17 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 476 |
| 18 | CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer Hit paper breakdown → | 2017 | 441 |
| 19 | DGIdb: mining the druggable genome Hit paper breakdown → | 2013 | 414 |
| 20 | 2015 | 286 |
About David E. Larson
David E. Larson is a scholar working on Cancer Research, Genetics, Hematology, Molecular Biology and Nutrition and Dietetics, having authored 92 papers that have together received 41.2k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (21 papers), Genomics and Phylogenetic Studies (12 papers), Genomics and Rare Diseases (11 papers), Acute Myeloid Leukemia Research (11 papers), Genomic variations and chromosomal abnormalities (7 papers), Clinical Nutrition and Gastroenterology (6 papers), Genetic Associations and Epidemiology (6 papers) and Esophageal and GI Pathology (5 papers). The work is most often cited by research in Cancer Research (9.3k citations), Hematology (5.5k citations), Genetics (4.7k citations), Genetics (9.6k citations) and Molecular Biology (18.6k citations). David E. Larson has collaborated with scholars based in United States, Vietnam and United Kingdom. Frequent co-authors include Richard K. Wilson, Elaine R. Mardis, Daniel C. Koboldt, Ken Chen, Li Ding, Eugene P. DiMagno, Kenneth W. Schroeder, Duane D. Burton, Michael D. McLellan and Karyn Meltz Steinberg. Their work appears in journals such as Mayo Clinic Proceedings, Nature, Nature Communications, New England Journal of Medicine and Bioinformatics.
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.