Arnaud Molin
Impact in
- Nephrology top 5%
- Parathyroid Disorders and Treatments
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- Vitamin D Research Studies
Papers in
- Genetics 25
- Genomics and Rare Diseases 12
- Genetic Syndromes and Imprinting 7
- Genetic and Kidney Cyst Diseases 4
- Genomic variations and chromosomal abnormalities 3
- Nephrology 10
- Parathyroid Disorders and Treatments 9
- Co-authors
- Nicolas Richard (9 shared papers)Nadia Coudray (7 shared papers)Marie‐Laure Kottler (7 shared papers)Martin Kaufmann (7 shared papers)Glenville Jones (7 shared papers)Justine Bacchetta (13 shared papers)Harald Jüppner (2 shared papers)Marie-Laure Kottler (6 shared papers)
- Journals
- Journal of Bone and Mineral Research (4 papers)The Journal of Clinical Endocrinology & Metabolism (4 papers)Orphanet Journal of Rare Diseases (3 papers)Archives of Disease in Childhood Fetal & Neonatal (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- FranceUnited StatesCanada
In The Last Decade
Arnaud Molin
47 papers receiving 821 citations
Peers
Comparison fields: 5 of 68
- Nephrology 134
- Pathology and Forensic Medicine 305
- Orthopedics and Sports Medicine 62
- Genetics 211
- Nutrition and Dietetics 103
Countries citing papers authored by Arnaud Molin
This map shows the geographic impact of Arnaud Molin'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 Arnaud Molin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arnaud Molin more than expected).
Fields of papers citing papers by Arnaud Molin
This network shows the impact of papers produced by Arnaud Molin. 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 Arnaud Molin. The network helps show where Arnaud Molin may publish in the future.
Co-authors
The 25 scholars most cited alongside Arnaud Molin, 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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 116 | |
| 2 | 2019 | 93 | |
| 3 | 2013 | 62 | |
| 4 | 2017 | 59 | |
| 5 | 2017 | 53 | |
| 6 | 2022 | 52 | |
| 7 | 2020 | 33 | |
| 8 | 2020 | 26 | |
| 9 | 2025 | 22 | |
| 10 | 2017 | 20 | |
| 11 | 2020 | 19 | |
| 12 | 2018 | 19 | |
| 13 | 2021 | 18 | |
| 14 | 2014 | 18 | |
| 15 | 2019 | 18 | |
| 16 | 2019 | 15 | |
| 17 | 2019 | 14 | |
| 18 | 2022 | 12 | |
| 19 | 2024 | 12 | |
| 20 | 2024 | 12 |
About Arnaud Molin
Arnaud Molin is a scholar working on Genetics, Nephrology, Pathology and Forensic Medicine, Molecular Biology and Rheumatology, having authored 54 papers that have together received 842 indexed citations. Recurring topics across this work include Vitamin D Research Studies (13 papers), Genomics and Rare Diseases (12 papers), Parathyroid Disorders and Treatments (9 papers), Genetic Syndromes and Imprinting (7 papers), Congenital heart defects research (5 papers), Genetic and Kidney Cyst Diseases (4 papers), Kidney Stones and Urolithiasis Treatments (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Nephrology (134 citations), Pathology and Forensic Medicine (305 citations), Orthopedics and Sports Medicine (62 citations), Genetics (211 citations) and Nutrition and Dietetics (103 citations). Arnaud Molin has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Nicolas Richard, Nadia Coudray, Marie‐Laure Kottler, Martin Kaufmann, Glenville Jones, Justine Bacchetta, Harald Jüppner, Marie-Laure Kottler, Karl P. Schlingmann and John Christopher Gallagher. Their work appears in journals such as Journal of Bone and Mineral Research, The Journal of Clinical Endocrinology & Metabolism, Orphanet Journal of Rare Diseases, Archives of Disease in Childhood Fetal & Neonatal and Journal of Medical Genetics.
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.