Delphine Simon
Impact in
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- Genetic Neurodegenerative Diseases
- Cell Biology top 5%
- Endoplasmic Reticulum Stress and Disease
Papers in
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- Mitochondrial Function and Pathology 3
- Ubiquitin and proteasome pathways 2
- Genetics 4
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Michel Kœnig (3 shared papers)Hélène Puccio (3 shared papers)Pierre Rustin (2 shared papers)Francesco Danilo Tiziano (1 shared paper)Judith Melki (1 shared paper)Mireille Cossée (1 shared paper)C. Hindelang (1 shared paper)H. Seznec (2 shared papers)
- Journals
- European Journal of Human Genetics (2 papers)Human Molecular Genetics (2 papers)Human Mutation (1 paper)Nature Genetics (1 paper)Pigment Cell & Melanoma Research (1 paper)
- Partner nations
- FranceMoroccoUnited States
In The Last Decade
Delphine Simon
13 papers receiving 1.2k citations
Delphine Simon's Hit Papers
Peers
Comparison fields: 5 of 91
- Cellular and Molecular Neuroscience 630
- Cell Biology 221
- Molecular Biology 925
- Developmental Biology 25
- Clinical Biochemistry 77
Countries citing papers authored by Delphine Simon
This map shows the geographic impact of Delphine Simon'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 Delphine Simon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Delphine Simon more than expected).
Fields of papers citing papers by Delphine Simon
This network shows the impact of papers produced by Delphine Simon. 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 Delphine Simon. The network helps show where Delphine Simon may publish in the future.
Co-authors
The 25 scholars most cited alongside Delphine Simon, 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 | Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits Hit paper breakdown → | 2001 | 588 |
| 2 | 2004 | 181 | |
| 3 | 2004 | 151 | |
| 4 | 2010 | 77 | |
| 5 | 2007 | 33 | |
| 6 | 2009 | 30 | |
| 7 | 2016 | 27 | |
| 8 | 2009 | 25 | |
| 9 | 2004 | 23 | |
| 10 | 2013 | 21 | |
| 11 | 2009 | 19 | |
| 12 | 2023 | 4 | |
| 13 | 2006 | 2 |
About Delphine Simon
Delphine Simon is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Cell Biology and Plant Science, having authored 13 papers that have together received 1.2k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (3 papers), Genetic Neurodegenerative Diseases (3 papers), Mitochondrial Function and Pathology (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Congenital limb and hand anomalies (2 papers), Ubiquitin and proteasome pathways (2 papers), Microtubule and mitosis dynamics (1 paper) and Plant Disease Resistance and Genetics (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (630 citations), Cell Biology (221 citations), Molecular Biology (925 citations), Developmental Biology (25 citations) and Clinical Biochemistry (77 citations). Delphine Simon has collaborated with scholars based in France, Morocco and United States. Frequent co-authors include Michel Kœnig, Hélène Puccio, Pierre Rustin, Francesco Danilo Tiziano, Judith Melki, Mireille Cossée, C. Hindelang, H. Seznec, Daniel Metzger and Anne Gansmüller. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, Human Mutation, Nature Genetics and Pigment Cell & Melanoma Research.
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.