Georges Imbert
Impact in
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Neurology top 1%
- Neurological disorders and treatments
Papers in
-
- Mitochondrial Function and Pathology 6
-
- Genetic Neurodegenerative Diseases 7
- Co-authors
- Jean‐Louis Mandel (8 shared papers)Yves Agid (5 shared papers)Frédéric Saudou (5 shared papers)C. R. Weber (4 shared papers)Yvon Trottier (5 shared papers)Didier Devys (4 shared papers)Giovanni Stévanin (4 shared papers)Géraldine Cancel‐Tassin (4 shared papers)
- Journals
- Nature Genetics (4 papers)Alzheimer s & Dementia (3 papers)Epilepsia (1 paper)Mental Retardation and Developmental Disabilities Research Reviews (1 paper)Nature (1 paper)
- Partner nations
- FranceSwitzerlandUnited States
In The Last Decade
Georges Imbert
17 papers receiving 2.9k citations
Georges Imbert's Hit Papers
Peers
Comparison fields: 5 of 90
- Cellular and Molecular Neuroscience 2.3k
- Neurology 859
- Molecular Biology 2.2k
- Neurology 175
- Biological Psychiatry 40
Countries citing papers authored by Georges Imbert
This map shows the geographic impact of Georges Imbert'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 Georges Imbert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Georges Imbert more than expected).
Fields of papers citing papers by Georges Imbert
This network shows the impact of papers produced by Georges Imbert. 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 Georges Imbert. The network helps show where Georges Imbert may publish in the future.
Co-authors
The 25 scholars most cited alongside Georges Imbert, 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 | Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats Hit paper breakdown → | 1996 | 737 |
| 2 | Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion Hit paper breakdown → | 1997 | 655 |
| 3 | Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias Hit paper breakdown → | 1995 | 572 |
| 4 | 1995 | 377 | |
| 5 | 2012 | 252 | |
| 6 | 1993 | 173 | |
| 7 | 2005 | 82 | |
| 8 | 1997 | 43 | |
| 9 | 1994 | 38 | |
| 10 | 1998 | 37 | |
| 11 | 2015 | 25 | |
| 12 | 1995 | 7 | |
| 13 | 2010 | 3 | |
| 14 | 2011 | 3 | |
| 15 | 2022 | 2 | |
| 16 | 2009 | 2 | |
| 17 | 2016 | 1 |
About Georges Imbert
Georges Imbert is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Physiology and Radiology, Nuclear Medicine and Imaging, having authored 17 papers that have together received 3.0k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (6 papers), Neurological disorders and treatments (4 papers), Alzheimer's disease research and treatments (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Monoclonal and Polyclonal Antibodies Research (3 papers), Pharmaceutical Economics and Policy (2 papers) and Autism Spectrum Disorder Research (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (2.3k citations), Neurology (859 citations), Molecular Biology (2.2k citations), Neurology (175 citations) and Biological Psychiatry (40 citations). Georges Imbert has collaborated with scholars based in France, Switzerland and United States. Frequent co-authors include Jean‐Louis Mandel, Yves Agid, Frédéric Saudou, C. R. Weber, Yvon Trottier, Didier Devys, Giovanni Stévanin, Géraldine Cancel‐Tassin, Alexis Brice and Gaël Yvert. Their work appears in journals such as Nature Genetics, Alzheimer s & Dementia, Epilepsia, Mental Retardation and Developmental Disabilities Research Reviews and Nature.
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.