Jennifer E. Huffman
Impact in
- Genetics top 10%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Ophthalmology top 5%
- Glaucoma and retinal disorders
Papers in
- Genetics 20
- Genetic Associations and Epidemiology 17
- Genetic Mapping and Diversity in Plants and Animals 6
- Genetic and phenotypic traits in livestock 5
- Diabetes and associated disorders 2
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- Glycosylation and Glycoproteins Research 4
- Co-authors
- Caroline Hayward (15 shared papers)Véronique Vitart (12 shared papers)Igor Rudan (13 shared papers)James F. Wilson (10 shared papers)Harry Campbell (8 shared papers)Pau Navarro (9 shared papers)Alan F. Wright (10 shared papers)Ozren Polašek (8 shared papers)
- Journals
- PLoS ONE (4 papers)Human Molecular Genetics (3 papers)Nature Communications (3 papers)PLoS Genetics (2 papers)Journal of Thrombosis and Haemostasis (2 papers)
- Partner nations
- United StatesUnited KingdomCroatia
In The Last Decade
Jennifer E. Huffman
37 papers receiving 883 citations
Peers
Comparison fields: 5 of 92
- Genetics 266
- Ophthalmology 54
- Internal Medicine 19
- Radiology, Nuclear Medicine and Imaging 113
- Immunology 95
Countries citing papers authored by Jennifer E. Huffman
This map shows the geographic impact of Jennifer E. Huffman'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 Jennifer E. Huffman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jennifer E. Huffman more than expected).
Fields of papers citing papers by Jennifer E. Huffman
This network shows the impact of papers produced by Jennifer E. Huffman. 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 Jennifer E. Huffman. The network helps show where Jennifer E. Huffman may publish in the future.
Co-authors
The 25 scholars most cited alongside Jennifer E. Huffman, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 99 | |
| 2 | 2022 | 65 | |
| 3 | 2019 | 59 | |
| 4 | 2020 | 56 | |
| 5 | 2013 | 53 | |
| 6 | 2012 | 51 | |
| 7 | 2016 | 46 | |
| 8 | 2022 | 38 | |
| 9 | 2012 | 33 | |
| 10 | 2012 | 31 | |
| 11 | 2012 | 27 | |
| 12 | 2023 | 26 | |
| 13 | 2017 | 25 | |
| 14 | 2010 | 25 | |
| 15 | 2015 | 23 | |
| 16 | 2015 | 22 | |
| 17 | 2018 | 19 | |
| 18 | 2021 | 19 | |
| 19 | 2010 | 19 | |
| 20 | 2011 | 17 |
About Jennifer E. Huffman
Jennifer E. Huffman is a scholar working on Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine, Hematology and Surgery, having authored 39 papers that have together received 889 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (17 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers), Genetic and phenotypic traits in livestock (5 papers), Glycosylation and Glycoproteins Research (4 papers), Lipid metabolism and disorders (3 papers), Diabetes and associated disorders (2 papers), Blood groups and transfusion (2 papers) and Liver Disease Diagnosis and Treatment (2 papers). The work is most often cited by research in Genetics (266 citations), Ophthalmology (54 citations), Internal Medicine (19 citations), Radiology, Nuclear Medicine and Imaging (113 citations) and Immunology (95 citations). Jennifer E. Huffman has collaborated with scholars based in United States, United Kingdom and Croatia. Frequent co-authors include Caroline Hayward, Véronique Vitart, Igor Rudan, James F. Wilson, Harry Campbell, Pau Navarro, Alan F. Wright, Ozren Polašek, Chris Haley and Nicholas D. Hastie. Their work appears in journals such as PLoS ONE, Human Molecular Genetics, Nature Communications, PLoS Genetics and Journal of Thrombosis and Haemostasis.
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.