François Lecoquierre

1.4k citations
18 papers · 114 indexed · h-index 7
    • Genomics and Rare Diseases 7
    • Genetics and Neurodevelopmental Disorders 7
    • Genomic variations and chromosomal abnormalities 6
    • Genetic Syndromes and Imprinting 2
    • Genomics and Rare Diseases 7
    • Genetics and Neurodevelopmental Disorders 7
    • Genomic variations and chromosomal abnormalities 6
    • Genetic Syndromes and Imprinting 2
    • RNA modifications and cancer 2
    • RNA Research and Splicing 2
    • Viral gastroenteritis research and epidemiology 1
    • SARS-CoV-2 and COVID-19 Research 1

François Lecoquierre

17 papers receiving 113 citations

Peers

François Lecoquierre
Comparison fields: 5 of 41
  • Genetics 57
  • Genetics 10
  • Cell Biology 15
  • Molecular Biology 63
  • Cellular and Molecular Neuroscience 15
Replace Bekir Ergüner with:
Bekir Ergüner Türkiye
Dominik S. Westphal Germany
Nuria García Segarra Switzerland
Samantha Penney United States
Benjamin M. Nash Australia
Mary Koziura United States
Theresa Brunet Germany
Norine Voisin Switzerland
Anne‐Marie Guerrot France
Sebastian Röner Germany
François Lecoquierre relative to Bekir Ergüner Türkiye Bekir Ergüner's profile →
Citations per field
00.5×3.8×
Bekir Ergüner · 1×
Citations per year

Countries citing papers authored by François Lecoquierre

Since Specialization
Citations

This map shows the geographic impact of François Lecoquierre'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 François Lecoquierre with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites François Lecoquierre more than expected).

Fields of papers citing papers by François Lecoquierre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by François Lecoquierre. 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 François Lecoquierre. The network helps show where François Lecoquierre may publish in the future.

Co-authorship network

The 25 scholars most cited alongside François Lecoquierre, 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 François Lecoquierre Line = papers co-authored together François Lecoquierre links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 20250
2 20242
3 20234
4 20233
5 20223
6 20224
7 20221
8 20222
9 20229
10 202114
11 20217
12 20211
13 20209
14 201920
15 20193
16 20197
17 201723
18 20172

About François Lecoquierre

François Lecoquierre is a scholar working on Genetics, Physiology and Gastroenterology, having authored 18 papers that have together received 114 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetic Syndromes and Imprinting (2 papers), RNA modifications and cancer (2 papers), RNA Research and Splicing (2 papers), Viral gastroenteritis research and epidemiology (1 paper) and SARS-CoV-2 and COVID-19 Research (1 paper). The work is most often cited by research in Genetics (57 citations), Genetics (10 citations) and Cell Biology (15 citations). François Lecoquierre has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Pascale Saugier-Véber, Thierry Frébourg, Gaël Nicolas, Alice Goldenberg, Sophie Coutant, Olivier Quenez, Sophie Patrier, Annie Laquerrière, Florent Marguet and Homa Adle‐Biassette. Their work appears in journals such as Scientific Reports, International Journal of Molecular Sciences and PLoS Genetics.

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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