Mathilde Lefebvre
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
- Genetics 24
- Genomics and Rare Diseases 12
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 7
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- Fetal and Pediatric Neurological Disorders 4
- Prenatal Screening and Diagnostics 4
- Co-authors
- Julien Thévenon (3 shared papers)Patrick Callier (2 shared papers)Judith St‐Onge (2 shared papers)Yannis Duffourd (2 shared papers)Laurence Faivre (2 shared papers)Mondher Chouchane (1 shared paper)Salima El Chehadeh-Djebbar (1 shared paper)Alice Masurel‐Paulet (1 shared paper)
- Journals
- Genetics in Medicine (6 papers)Prenatal Diagnosis (4 papers)Journal of Medical Genetics (4 papers)European Journal of Human Genetics (4 papers)Clinical Genetics (3 papers)
- Partner nations
- FranceUnited StatesItaly
In The Last Decade
Mathilde Lefebvre
49 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 96
- Genetics 637
- Clinical Biochemistry 100
- Molecular Biology 507
- Aging 12
- Pediatrics, Perinatology and Child Health 114
Countries citing papers authored by Mathilde Lefebvre
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
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.
All Works
Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 198 | |
| 2 | 2017 | 140 | |
| 3 | 2018 | 133 | |
| 4 | 2014 | 117 | |
| 5 | 2017 | 113 | |
| 6 | 2010 | 56 | |
| 7 | 2018 | 48 | |
| 8 | 2017 | 47 | |
| 9 | 2016 | 43 | |
| 10 | 2020 | 42 | |
| 11 | 2021 | 29 | |
| 12 | 2020 | 28 | |
| 13 | 2017 | 27 | |
| 14 | 2025 | 22 | |
| 15 | 2016 | 22 | |
| 16 | 2015 | 21 | |
| 17 | 2019 | 19 | |
| 18 | 2022 | 16 | |
| 19 | 2018 | 16 | |
| 20 | 2015 | 13 |
About Mathilde Lefebvre
Mathilde Lefebvre is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Pathology and Forensic Medicine and Developmental Neuroscience, having authored 50 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (7 papers), RNA modifications and cancer (4 papers), Fetal and Pediatric Neurological Disorders (4 papers), Prenatal Screening and Diagnostics (4 papers), Chromatin Remodeling and Cancer (4 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Genetics (637 citations), Clinical Biochemistry (100 citations), Molecular Biology (507 citations), Aging (12 citations) and Pediatrics, Perinatology and Child Health (114 citations). Mathilde Lefebvre has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Julien Thévenon, Patrick Callier, Judith St‐Onge, Yannis Duffourd, Laurence Faivre, Mondher Chouchane, Salima El Chehadeh-Djebbar, Alice Masurel‐Paulet, Christel Thauvin‐Robinet and François Feillet. Their work appears in journals such as Genetics in Medicine, Prenatal Diagnosis, Journal of Medical Genetics, European Journal of Human Genetics and Clinical 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.