Delphine Simon

1.6k citations
13 papers · 1.2k · 1 hit paper · h-index 11

Impact in

Papers in

    • Mitochondrial Function and Pathology 3
    • Ubiquitin and proteasome pathways 2
    • Genomic variations and chromosomal abnormalities 3

Delphine Simon

13 papers receiving 1.2k citations

Delphine Simon's Hit Papers

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits 2001 · 626 citations
6260+8+16Years since publication200400600

Peers

Delphine Simon
Comparison fields: 5 of 88
  • Cellular and Molecular Neuroscience 664
  • Cell Biology 218
  • Molecular Biology 906
  • Clinical Biochemistry 77
  • Developmental Biology 25
Replace Sarn Jiralerspong with:
Sarn Jiralerspong Canada
Hiroyuki Ishiura Japan
Johann Böhm France
Jun Mitsui Japan
Norma B. Romero France
A. Nazlı Başak Türkiye
Nigel F. Clarke Australia
Louise Deltour United States
Laetitia Mazelin France
Dietmar Bächner Germany
Delphine Simon relative to Sarn Jiralerspong Canada Sarn Jiralerspong's profile →
Citations per field
00.5×4.2×
Sarn Jiralerspong · 1×
Citations per year

Countries citing papers authored by Delphine Simon

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Delphine Simon Line = papers co-authored together Delphine Simon links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#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 →
2001626
2 2004190
3 2004165
4 201081
5 200733
6 200930
7 201627
8 200925
9 200424
10 201322
11 200919
12 20234
13 20062

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 Mitochondrial Function and Pathology (3 papers), Chromosomal and Genetic Variations (3 papers), Genetic Neurodegenerative Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Ubiquitin and proteasome pathways (2 papers), Congenital limb and hand anomalies (2 papers), Biofuel production and bioconversion (1 paper) and Amyotrophic Lateral Sclerosis Research (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (664 citations), Cell Biology (218 citations), Molecular Biology (906 citations), Clinical Biochemistry (77 citations) and Developmental Biology (25 citations). Delphine Simon has collaborated with scholars based in France, Morocco and United States. Frequent co-authors include Hélène Puccio, Pierre Rustin, Francesco Danilo Tiziano, C. Hindelang, Judith Melki, Mireille Cossée, H. Seznec, Michel Kœnig, Philipp Weber and Anne Gansmüller. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, Molecular & Cellular Proteomics, Nature Genetics and Thrombosis 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.

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