Mathilde Lefebvre

1.8k citations
18 papers · 400 indexed · h-index 8

Impact in

    • Metabolism and Genetic Disorders
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

Mathilde Lefebvre

18 papers receiving 396 citations

Peers

Mathilde Lefebvre
Comparison fields: 5 of 73
  • Clinical Biochemistry 67
  • Genetics 136
  • Aging 6
  • Molecular Biology 207
  • Infectious Diseases 43
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Citations per field
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Citations per year

Countries citing papers authored by Mathilde Lefebvre

Since Specialization
Citations

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

Fields of papers citing papers by Mathilde Lefebvre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

18 of 18 papers shown
#Work
1 2016138
2 2017103
3 201053
4 201626
5 20219
6 20218
7 20148
8 20187
9 20237
10 20157
11 20227
12 20227
13 20186
14 20216
15 20195
16 20241
17 20231
18 20161

About Mathilde Lefebvre

Mathilde Lefebvre is a scholar working on Applied Microbiology and Biotechnology, Developmental Neuroscience, Molecular Medicine, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 18 papers that have together received 400 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (2 papers), Chromatin Remodeling and Cancer (2 papers), Congenital heart defects research (2 papers), Mitochondrial Function and Pathology (2 papers), Neurogenesis and neuroplasticity mechanisms (1 paper), Single-cell and spatial transcriptomics (1 paper), Connective tissue disorders research (1 paper) and Genetic and Kidney Cyst Diseases (1 paper). The work is most often cited by research in Clinical Biochemistry (67 citations), Genetics (136 citations), Aging (6 citations), Molecular Biology (207 citations) and Infectious Diseases (43 citations). Mathilde Lefebvre has collaborated with scholars based in France, Italy and Belgium. Frequent co-authors include Frédéric Morel, Patrick Callier, Philippe Lachaume, Judith St‐Onge, Patrick Vernet, Yannis Duffourd, Julien Thévenon, Laurence Faivre, Géraldine Farge and Amandine Moretton. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, FEBS Letters, DNA repair and Science Advances.

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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