Tara Schmidlen
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Pharmacology top 5%
- Pharmacogenetics and Drug Metabolism
Papers in
- Genetics 20
- BRCA gene mutations in cancer 16
- Genomics and Rare Diseases 11
- Genetic Associations and Epidemiology 5
- Nutrition, Genetics, and Disease 3
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- Pharmacogenetics and Drug Metabolism 8
- Co-authors
- Amy C. Sturm (13 shared papers)Michael F. Christman (16 shared papers)Erynn S. Gordon (15 shared papers)M. Schwartz (6 shared papers)H. Lester Kirchner (4 shared papers)Neda Gharani (9 shared papers)Laura Scheinfeldt (15 shared papers)Margaret Keller (6 shared papers)
- Journals
- Journal of Personalized Medicine (5 papers)Genetics in Medicine (4 papers)Patient Education and Counseling (1 paper)npj Genomic Medicine (1 paper)Pharmacogenomics (1 paper)
- Partner nations
- United StatesSwitzerlandCanada
In The Last Decade
Tara Schmidlen
35 papers receiving 745 citations
Peers
Comparison fields: 5 of 75
- Genetics 399
- Pharmacology 114
- Health Informatics 8
- Pediatrics, Perinatology and Child Health 64
- Public Health, Environmental and Occupational Health 85
Countries citing papers authored by Tara Schmidlen
This map shows the geographic impact of Tara Schmidlen'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 Tara Schmidlen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tara Schmidlen more than expected).
Fields of papers citing papers by Tara Schmidlen
This network shows the impact of papers produced by Tara Schmidlen. 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 Tara Schmidlen. The network helps show where Tara Schmidlen may publish in the future.
Co-authors
The 25 scholars most cited alongside Tara Schmidlen, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 104 | |
| 2 | 2020 | 82 | |
| 3 | 2010 | 56 | |
| 4 | 2022 | 47 | |
| 5 | 2011 | 35 | |
| 6 | 2013 | 34 | |
| 7 | 2020 | 31 | |
| 8 | 2015 | 30 | |
| 9 | 2015 | 28 | |
| 10 | 2014 | 26 | |
| 11 | 2015 | 24 | |
| 12 | 2018 | 23 | |
| 13 | 2022 | 23 | |
| 14 | 2017 | 23 | |
| 15 | 2014 | 19 | |
| 16 | 2017 | 17 | |
| 17 | 2016 | 16 | |
| 18 | 2016 | 16 | |
| 19 | 2020 | 16 | |
| 20 | 2023 | 15 |
About Tara Schmidlen
Tara Schmidlen is a scholar working on Genetics, Pharmacology, Cognitive Neuroscience, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 37 papers that have together received 762 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (16 papers), Genomics and Rare Diseases (11 papers), Pharmacogenetics and Drug Metabolism (8 papers), Autism Spectrum Disorder Research (6 papers), Genetic Associations and Epidemiology (5 papers), Pharmaceutical studies and practices (4 papers), Nutrition, Genetics, and Disease (3 papers) and Statistical Methods in Clinical Trials (3 papers). The work is most often cited by research in Genetics (399 citations), Pharmacology (114 citations), Health Informatics (8 citations), Pediatrics, Perinatology and Child Health (64 citations) and Public Health, Environmental and Occupational Health (85 citations). Tara Schmidlen has collaborated with scholars based in United States, Switzerland and Canada. Frequent co-authors include Amy C. Sturm, Michael F. Christman, Erynn S. Gordon, M. Schwartz, H. Lester Kirchner, Neda Gharani, Laura Scheinfeldt, Margaret Keller, Catharine B. Stack and Norman P. Gerry. Their work appears in journals such as Journal of Personalized Medicine, Genetics in Medicine, Patient Education and Counseling, npj Genomic Medicine and Pharmacogenomics.
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.