Benoît Funalot
Impact in
-
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Papers in
-
- Hereditary Neurological Disorders 24
- Genetic Neurodegenerative Diseases 8
- Neurology 25
- Neurological diseases and metabolism 10
- Amyotrophic Lateral Sclerosis Research 7
- Co-authors
- Jean‐Michel Vallat (16 shared papers)Franck G. Sturtz (15 shared papers)Philippe Couratier (5 shared papers)Laurence Richard (13 shared papers)Gérard Lucotte (3 shared papers)Kumaraswamy Sivakumar (2 shared papers)Victor V. Ionasescu (2 shared papers)Jean‐Claude Desport (2 shared papers)
- Journals
- Neurology (5 papers)Orphanet Journal of Rare Diseases (5 papers)Journal of Medical Genetics (4 papers)The American Journal of Human Genetics (4 papers)ESC Heart Failure (4 papers)
- Partner nations
- FranceUnited StatesAustralia
In The Last Decade
Benoît Funalot
115 papers receiving 4.2k citations
Peers
Comparison fields: 5 of 114
- Cellular and Molecular Neuroscience 1.1k
- Clinical Biochemistry 360
- Neurology 767
- Neurology 351
- Genetics 391
Countries citing papers authored by Benoît Funalot
This map shows the geographic impact of Benoît Funalot'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 Benoît Funalot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Benoît Funalot more than expected).
Fields of papers citing papers by Benoît Funalot
This network shows the impact of papers produced by Benoît Funalot. 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 Benoît Funalot. The network helps show where Benoît Funalot may publish in the future.
Co-authors
The 25 scholars most cited alongside Benoît Funalot, 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 123 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 471 | |
| 2 | 2017 | 427 | |
| 3 | 2011 | 226 | |
| 4 | 2009 | 187 | |
| 5 | 2006 | 164 | |
| 6 | 2008 | 141 | |
| 7 | 2008 | 125 | |
| 8 | 2016 | 116 | |
| 9 | 2005 | 110 | |
| 10 | 2014 | 107 | |
| 11 | 2017 | 107 | |
| 12 | 2009 | 97 | |
| 13 | 2010 | 96 | |
| 14 | 2014 | 91 | |
| 15 | 2010 | 82 | |
| 16 | 2008 | 75 | |
| 17 | 2017 | 65 | |
| 18 | 2002 | 64 | |
| 19 | 2012 | 58 | |
| 20 | 2004 | 54 |
About Benoît Funalot
Benoît Funalot is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Neurology and Genetics, having authored 123 papers that have together received 4.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (24 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (19 papers), Mitochondrial Function and Pathology (19 papers), Neurological diseases and metabolism (10 papers), Metabolism and Genetic Disorders (9 papers), Genetic Neurodegenerative Diseases (8 papers), Amyotrophic Lateral Sclerosis Research (7 papers) and Neurogenetic and Muscular Disorders Research (7 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.1k citations), Clinical Biochemistry (360 citations), Neurology (767 citations), Neurology (351 citations) and Genetics (391 citations). Benoît Funalot has collaborated with scholars based in France, United States and Australia. Frequent co-authors include Jean‐Michel Vallat, Franck G. Sturtz, Philippe Couratier, Laurence Richard, Gérard Lucotte, Kumaraswamy Sivakumar, Victor V. Ionasescu, Jean‐Claude Desport, Kenneth H. Fischbeck and Kyproula Christodoulou. Their work appears in journals such as Neurology, Orphanet Journal of Rare Diseases, Journal of Medical Genetics, The American Journal of Human Genetics and ESC Heart Failure.
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.