Jonas Mandel
Impact in
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- Hereditary Neurological Disorders
- Surgery top 10%
- Lipoproteins and Cardiovascular Health
Papers in
- Surgery 8
- Lipoproteins and Cardiovascular Health 8
-
- Hereditary Neurological Disorders 3
- Co-authors
- Helen Martina Colhoun (3 shared papers)Lawrence A. Leiter (5 shared papers)Maja Bujas‐Bobanovic (5 shared papers)Alexia Letierce (5 shared papers)Rita Samuel (4 shared papers)Francisco José Tinahones (3 shared papers)Kausik Kumar Ray (3 shared papers)Stefano Del Prato (3 shared papers)
- Journals
- Orphanet Journal of Rare Diseases (3 papers)Diabetes Obesity and Metabolism (2 papers)Diabetic Medicine (1 paper)European Heart Journal (1 paper)Cardiovascular Diabetology (1 paper)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Jonas Mandel
15 papers receiving 596 citations
Peers
Comparison fields: 5 of 36
- Cellular and Molecular Neuroscience 133
- Surgery 273
- Nephrology 22
- Genetics 8
- Pathology and Forensic Medicine 14
Countries citing papers authored by Jonas Mandel
This map shows the geographic impact of Jonas Mandel'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 Jonas Mandel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonas Mandel more than expected).
Fields of papers citing papers by Jonas Mandel
This network shows the impact of papers produced by Jonas Mandel. 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 Jonas Mandel. The network helps show where Jonas Mandel may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonas Mandel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 122 | |
| 2 | 2014 | 92 | |
| 3 | 2018 | 92 | |
| 4 | 2014 | 78 | |
| 5 | 2017 | 66 | |
| 6 | 2010 | 41 | |
| 7 | 2019 | 34 | |
| 8 | 2018 | 22 | |
| 9 | 2018 | 18 | |
| 10 | 2018 | 17 | |
| 11 | 2015 | 16 | |
| 12 | 2016 | 13 | |
| 13 | 2020 | 7 | |
| 14 | 2015 | 6 | |
| 15 | 2022 | 1 |
About Jonas Mandel
Jonas Mandel is a scholar working on Surgery, Cellular and Molecular Neuroscience, Pathology and Forensic Medicine, Genetics and Molecular Biology, having authored 15 papers that have together received 625 indexed citations. Recurring topics across this work include Lipoproteins and Cardiovascular Health (8 papers), Hereditary Neurological Disorders (3 papers), Breast Lesions and Carcinomas (1 paper), Gene expression and cancer classification (1 paper) and Genetic Associations and Epidemiology (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (133 citations), Surgery (273 citations), Nephrology (22 citations), Genetics (8 citations) and Pathology and Forensic Medicine (14 citations). Jonas Mandel has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Helen Martina Colhoun, Lawrence A. Leiter, Maja Bujas‐Bobanovic, Alexia Letierce, Rita Samuel, Francisco José Tinahones, Kausik Kumar Ray, Stefano Del Prato, Dirk Müller‐Wieland and Bertrand Cariou. Their work appears in journals such as Orphanet Journal of Rare Diseases, Diabetes Obesity and Metabolism, Diabetic Medicine, European Heart Journal and Cardiovascular Diabetology.
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.