Daniel C. Koboldt
Impact in
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
- Oncology top 2%
- HER2/EGFR in Cancer Research
Papers in
- Genetics 13
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 3
- Neurogenetic and Muscular Disorders Research 2
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- RNA modifications and cancer 6
- Co-authors
- Elaine R. Mardis (7 shared papers)Cynthia X. Ma (1 shared paper)Ron Bose (1 shared paper)John D. Monsey (1 shared paper)Wei Shen (1 shared paper)Li Ding (1 shared paper)Adam B. Aronson (1 shared paper)Adam C. Searleman (1 shared paper)
- Journals
- Scientific Reports (2 papers)Neurology Genetics (2 papers)Nature Communications (2 papers)Human Mutation (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- United StatesGermanyFrance
In The Last Decade
Daniel C. Koboldt
26 papers receiving 3.6k citations
Daniel C. Koboldt's Hit Papers
Peers
Comparison fields: 5 of 106
- Cancer Research 962
- Oncology 1.2k
- Pulmonary and Respiratory Medicine 965
- Molecular Biology 1.7k
- Genetics 210
Countries citing papers authored by Daniel C. Koboldt
This map shows the geographic impact of Daniel C. Koboldt'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 Daniel C. Koboldt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel C. Koboldt more than expected).
Fields of papers citing papers by Daniel C. Koboldt
This network shows the impact of papers produced by Daniel C. Koboldt. 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 Daniel C. Koboldt. The network helps show where Daniel C. Koboldt may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel C. Koboldt, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Somatic mutations affect key pathways in lung adenocarcinoma Hit paper breakdown → | 2008 | 2237 |
| 2 | Activating HER2 Mutations in HER2 Gene Amplification Negative Breast Cancer Hit paper breakdown → | 2012 | 705 |
| 3 | 2015 | 186 | |
| 4 | 2013 | 149 | |
| 5 | 2017 | 127 | |
| 6 | 2015 | 48 | |
| 7 | 2013 | 34 | |
| 8 | 2016 | 24 | |
| 9 | 2016 | 24 | |
| 10 | 2006 | 20 | |
| 11 | 2018 | 19 | |
| 12 | 2020 | 19 | |
| 13 | 2021 | 15 | |
| 14 | 2022 | 9 | |
| 15 | 2015 | 7 | |
| 16 | 2023 | 6 | |
| 17 | 2019 | 5 | |
| 18 | 2024 | 5 | |
| 19 | 2022 | 4 | |
| 20 | 2024 | 3 |
About Daniel C. Koboldt
Daniel C. Koboldt is a scholar working on Genetics, Molecular Biology, Cancer Research, Genetics and Neurology, having authored 30 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), RNA modifications and cancer (6 papers), Genetics and Neurodevelopmental Disorders (4 papers), Cancer Genomics and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Prenatal Screening and Diagnostics (2 papers), Acute Myeloid Leukemia Research (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). The work is most often cited by research in Cancer Research (962 citations), Oncology (1.2k citations), Pulmonary and Respiratory Medicine (965 citations), Molecular Biology (1.7k citations) and Genetics (210 citations). Daniel C. Koboldt has collaborated with scholars based in United States, Germany and France. Frequent co-authors include Elaine R. Mardis, Cynthia X. Ma, Ron Bose, John D. Monsey, Wei Shen, Li Ding, Adam B. Aronson, Adam C. Searleman, Matthew Ellis and Shunqiang Li. Their work appears in journals such as Scientific Reports, Neurology Genetics, Nature Communications, Human Mutation and European Journal of Human Genetics.
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.