Daniel Harris
Impact in
- Genetics top 1%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Forensic and Genetic Research
- Hematology top 2%
- Acute Myeloid Leukemia Research
Papers in
- Genetics 21
- Genetic Associations and Epidemiology 19
- Forensic and Genetic Research 3
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- Acute Myeloid Leukemia Research 2
- Co-authors
- Timothy D. O’Connor (3 shared papers)Heinner Guio (2 shared papers)Michael D. Kessler (2 shared papers)Amol Carl Shetty (2 shared papers)César Sánchez (1 shared paper)Omar Cáceres (1 shared paper)Carlos Padilla (1 shared paper)Marco Galarza (1 shared paper)
- Journals
- Nature Communications (7 papers)Nature Genetics (5 papers)Nature (5 papers)Proceedings of the National Academy of Sciences (3 papers)Nature Methods (2 papers)
- Partner nations
- United StatesPeruNew Zealand
In The Last Decade
Daniel Harris
29 papers receiving 3.4k citations
Daniel Harris's Hit Papers
Peers
Comparison fields: 5 of 112
- Genetics 1.7k
- Hematology 560
- Aging 21
- Cancer Research 145
- Genetics 74
Countries citing papers authored by Daniel Harris
This map shows the geographic impact of Daniel Harris'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 Harris with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Harris more than expected).
Fields of papers citing papers by Daniel Harris
This network shows the impact of papers produced by Daniel Harris. 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 Harris. The network helps show where Daniel Harris may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel Harris, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program Hit paper breakdown → | 2021 | 1363 |
| 2 | Inherited causes of clonal haematopoiesis in 97,691 whole genomes Hit paper breakdown → | 2020 | 555 |
| 3 | Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data Hit paper breakdown → | 2022 | 229 |
| 4 | 2020 | 166 | |
| 5 | Clonal haematopoiesis and risk of chronic liver disease Hit paper breakdown → | 2023 | 151 |
| 6 | 2018 | 135 | |
| 7 | 2021 | 132 | |
| 8 | 2018 | 122 | |
| 9 | 2018 | 89 | |
| 10 | 2023 | 75 | |
| 11 | 2020 | 72 | |
| 12 | 2022 | 67 | |
| 13 | 2022 | 47 | |
| 14 | 2019 | 41 | |
| 15 | 2020 | 35 | |
| 16 | 2021 | 35 | |
| 17 | 2022 | 33 | |
| 18 | 2022 | 31 | |
| 19 | 2021 | 22 | |
| 20 | 2021 | 22 |
About Daniel Harris
Daniel Harris is a scholar working on Genetics, Hematology, Physiology, Anthropology and Hepatology, having authored 29 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (19 papers), Forensic and Genetic Research (3 papers), Acute Myeloid Leukemia Research (2 papers), Lipoproteins and Cardiovascular Health (2 papers), Pleistocene-Era Hominins and Archaeology (2 papers), Asthma and respiratory diseases (2 papers), Epigenetics and DNA Methylation (1 paper) and Liver physiology and pathology (1 paper). The work is most often cited by research in Genetics (1.7k citations), Hematology (560 citations), Aging (21 citations), Cancer Research (145 citations) and Genetics (74 citations). Daniel Harris has collaborated with scholars based in United States, Peru and New Zealand. Frequent co-authors include Timothy D. O’Connor, Heinner Guio, Michael D. Kessler, Amol Carl Shetty, César Sánchez, Omar Cáceres, Carlos Padilla, Marco Galarza, Eduardo Tarazona‐Santos and Víctor Borda. Their work appears in journals such as Nature Communications, Nature Genetics, Nature, Proceedings of the National Academy of Sciences and Nature Methods.
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.