Tanja Smith
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 16
- Genetic Associations and Epidemiology 16
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- Acute Myeloid Leukemia Research 2
- Journals
- Nature Communications (7 papers)Nature Genetics (5 papers)Nature (4 papers)Nature Methods (2 papers)Nature Computational Science (1 paper)
- Partner nations
- United StatesFinland
In The Last Decade
Tanja Smith
22 papers receiving 3.1k citations
Tanja Smith's Hit Papers
Peers
Comparison fields: 5 of 104
- Genetics 1.5k
- Hematology 558
- Aging 19
- Cancer Research 134
- Genetics 74
Countries citing papers authored by Tanja Smith
This map shows the geographic impact of Tanja Smith'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 Tanja Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tanja Smith more than expected).
Fields of papers citing papers by Tanja Smith
This network shows the impact of papers produced by Tanja Smith. 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 Tanja Smith. The network helps show where Tanja Smith may publish in the future.
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All Works
Showing the 20 most-cited of 22 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 | 89 | |
| 9 | 2023 | 75 | |
| 10 | 2022 | 67 | |
| 11 | 2022 | 47 | |
| 12 | 2021 | 35 | |
| 13 | 2022 | 33 | |
| 14 | 2022 | 31 | |
| 15 | 2021 | 22 | |
| 16 | 2021 | 22 | |
| 17 | 2021 | 16 | |
| 18 | 2025 | 15 | |
| 19 | 2023 | 13 | |
| 20 | 2025 | 7 |
About Tanja Smith
Tanja Smith is a scholar working on Genetics, Hematology, Physiology, Hepatology and Surgery, having authored 22 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (16 papers), Acute Myeloid Leukemia Research (2 papers), Lipoproteins and Cardiovascular Health (2 papers), Asthma and respiratory diseases (2 papers), Epigenetics and DNA Methylation (1 paper), Liver physiology and pathology (1 paper), Liver Disease Diagnosis and Treatment (1 paper) and Obstructive Sleep Apnea Research (1 paper). The work is most often cited by research in Genetics (1.5k citations), Hematology (558 citations), Aging (19 citations), Cancer Research (134 citations) and Genetics (74 citations). Tanja Smith has collaborated with scholars based in United States and Finland. Their work appears in journals such as Nature Communications, Nature Genetics, Nature, Nature Methods and Nature Computational Science.
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.