Jennifer E. Below
Impact in
- Genetics top 2%
- Genetic Associations and Epidemiology
- Diabetes and associated disorders
- Ophthalmology top 5%
Papers in
- Genetics 32
- Genetic Associations and Epidemiology 22
- Genomics and Rare Diseases 5
- Diabetes and associated disorders 3
- Genetic Mapping and Diversity in Plants and Animals 3
-
- Metabolism, Diabetes, and Cancer 3
- Co-authors
- Nancy J. Cox (17 shared papers)Graeme I. Bell (6 shared papers)Joseph R. Testa (2 shared papers)Anna Pluzhnikov (4 shared papers)Masaki Nasu (1 shared paper)Mika Tanji (1 shared paper)Mitchell Cheung (1 shared paper)Giovanni Gaudino (1 shared paper)
- Journals
- The American Journal of Human Genetics (9 papers)Diabetes (4 papers)Human Molecular Genetics (3 papers)Alzheimer s & Dementia (3 papers)PLoS ONE (2 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Jennifer E. Below
61 papers receiving 2.6k citations
Jennifer E. Below's Hit Papers
Peers
Comparison fields: 5 of 127
- Genetics 854
- Ophthalmology 142
- Pulmonary and Respiratory Medicine 487
- Endocrinology, Diabetes and Metabolism 221
- Surgery 546
Countries citing papers authored by Jennifer E. Below
This map shows the geographic impact of Jennifer E. Below'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. Below 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. Below more than expected).
Fields of papers citing papers by Jennifer E. Below
This network shows the impact of papers produced by Jennifer E. Below. 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. Below. The network helps show where Jennifer E. Below may publish in the future.
Co-authors
The 25 scholars most cited alongside Jennifer E. Below, 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 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Germline BAP1 mutations predispose to malignant mesothelioma Hit paper breakdown → | 2011 | 728 |
| 2 | 2007 | 425 | |
| 3 | 2016 | 121 | |
| 4 | 2011 | 114 | |
| 5 | 2007 | 92 | |
| 6 | 2011 | 89 | |
| 7 | 2014 | 87 | |
| 8 | 2009 | 82 | |
| 9 | 2011 | 82 | |
| 10 | 2017 | 53 | |
| 11 | 2012 | 52 | |
| 12 | 2014 | 47 | |
| 13 | 2012 | 44 | |
| 14 | 2021 | 42 | |
| 15 | 2010 | 39 | |
| 16 | 2010 | 38 | |
| 17 | 2011 | 37 | |
| 18 | 2012 | 36 | |
| 19 | 2014 | 32 | |
| 20 | 2015 | 31 |
About Jennifer E. Below
Jennifer E. Below is a scholar working on Genetics, Molecular Biology, Surgery, Clinical Psychology and Epidemiology, having authored 65 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (22 papers), Stuttering Research and Treatment (6 papers), Pancreatic function and diabetes (5 papers), Genomics and Rare Diseases (5 papers), Language Development and Disorders (4 papers), Diabetes and associated disorders (3 papers), Metabolism, Diabetes, and Cancer (3 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). The work is most often cited by research in Genetics (854 citations), Ophthalmology (142 citations), Pulmonary and Respiratory Medicine (487 citations), Endocrinology, Diabetes and Metabolism (221 citations) and Surgery (546 citations). Jennifer E. Below has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Nancy J. Cox, Graeme I. Bell, Joseph R. Testa, Anna Pluzhnikov, Masaki Nasu, Mika Tanji, Mitchell Cheung, Giovanni Gaudino, A. Umran Doğan and Jianming Pei. Their work appears in journals such as The American Journal of Human Genetics, Diabetes, Human Molecular Genetics, Alzheimer s & Dementia and PLoS ONE.
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.