G. Imbert
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Autism Spectrum Disorder Research
Papers in
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- DNA Repair Mechanisms 1
- Mitochondrial Function and Pathology 1
- Genetics 2
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Jean‐Louis Mandel (3 shared papers)Didier Devys (2 shared papers)Dominique Heitz (1 shared paper)Christine Kretz (1 shared paper)J. Beckmann (1 shared paper)Yvon Trottier (2 shared papers)Malin Karlsson (1 shared paper)Mark E. Schmidt (1 shared paper)
- Journals
- Pharmacogenomics (1 paper)Genomics (1 paper)Journal of Medical Genetics (1 paper)Alzheimer s & Dementia (1 paper)PubMed (1 paper)
- Partner nations
- FranceSwitzerlandUnited States
In The Last Decade
G. Imbert
6 papers receiving 231 citations
Peers
Comparison fields: 5 of 39
- Genetics 136
- Cognitive Neuroscience 79
- Cellular and Molecular Neuroscience 59
- Molecular Biology 133
- Neurology 19
Countries citing papers authored by G. Imbert
This map shows the geographic impact of G. 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 G. Imbert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G. Imbert more than expected).
Fields of papers citing papers by G. Imbert
This network shows the impact of papers produced by G. 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 G. Imbert. The network helps show where G. Imbert may publish in the future.
Co-authors
The 25 scholars most cited alongside G. 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 | 1992 | 142 | |
| 2 | 1994 | 55 | |
| 3 | 2009 | 24 | |
| 4 | 2005 | 17 | |
| 5 | 1993 | 3 | |
| 6 | 2004 | 1 |
About G. Imbert
G. Imbert is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 6 papers that have together received 242 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (2 papers), Autism Spectrum Disorder Research (1 paper), DNA Repair Mechanisms (1 paper), Alzheimer's disease research and treatments (1 paper), Pharmacogenetics and Drug Metabolism (1 paper), Immunotherapy and Immune Responses (1 paper), Mitochondrial Function and Pathology (1 paper) and Statistical Methods in Clinical Trials (1 paper). The work is most often cited by research in Genetics (136 citations), Cognitive Neuroscience (79 citations), Cellular and Molecular Neuroscience (59 citations), Molecular Biology (133 citations) and Neurology (19 citations). G. Imbert has collaborated with scholars based in France, Switzerland and United States. Frequent co-authors include Jean‐Louis Mandel, Didier Devys, Dominique Heitz, Christine Kretz, J. Beckmann, Yvon Trottier, Malin Karlsson, Mark E. Schmidt, Mats Bergström and Patrick D. Maguire. Their work appears in journals such as Pharmacogenomics, Genomics, Journal of Medical Genetics, Alzheimer s & Dementia and PubMed.
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.