Mathilde Nizon
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Developmental Biology top 5%
Papers in
- Genetics 102
- Genetics and Neurodevelopmental Disorders 59
- Genomics and Rare Diseases 41
- Genomic variations and chromosomal abnormalities 14
- Genetic and Kidney Cyst Diseases 6
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- Fetal and Pediatric Neurological Disorders 6
- Prenatal Screening and Diagnostics 5
- Co-authors
- Jean‐Paul Bonnefont (3 shared papers)Bertrand Isidor (11 shared papers)Chris Ottolenghi (2 shared papers)Pascale de Lonlay (2 shared papers)Florence Habarou (2 shared papers)Nathalie Boddaert (2 shared papers)Valérie Malan (3 shared papers)Marie Vincent (6 shared papers)
- Journals
- The American Journal of Human Genetics (19 papers)European Journal of Human Genetics (17 papers)Genetics in Medicine (14 papers)Clinical Genetics (6 papers)Journal of Medical Genetics (6 papers)
- Partner nations
- FranceUnited StatesNetherlands
In The Last Decade
Mathilde Nizon
118 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 97
- Genetics 1.3k
- Developmental Biology 57
- Developmental Neuroscience 80
- Clinical Biochemistry 105
- Pediatrics, Perinatology and Child Health 190
Countries citing papers authored by Mathilde Nizon
This map shows the geographic impact of Mathilde Nizon'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 Nizon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mathilde Nizon more than expected).
Fields of papers citing papers by Mathilde Nizon
This network shows the impact of papers produced by Mathilde Nizon. 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 Nizon. The network helps show where Mathilde Nizon may publish in the future.
Co-authors
The 25 scholars most cited alongside Mathilde Nizon, 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 129 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 142 | |
| 2 | 2017 | 140 | |
| 3 | 2018 | 135 | |
| 4 | 2021 | 95 | |
| 5 | 2017 | 90 | |
| 6 | 2013 | 75 | |
| 7 | 2017 | 74 | |
| 8 | 2015 | 73 | |
| 9 | 2018 | 65 | |
| 10 | 2017 | 56 | |
| 11 | 2018 | 54 | |
| 12 | 2018 | 49 | |
| 13 | 2021 | 48 | |
| 14 | 2012 | 47 | |
| 15 | 2014 | 42 | |
| 16 | 2020 | 42 | |
| 17 | 2021 | 42 | |
| 18 | 2022 | 36 | |
| 19 | 2014 | 35 | |
| 20 | 2015 | 34 |
About Mathilde Nizon
Mathilde Nizon is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Clinical Biochemistry, Developmental Biology and Molecular Biology, having authored 129 papers that have together received 2.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (59 papers), Genomics and Rare Diseases (41 papers), Genomic variations and chromosomal abnormalities (14 papers), Fetal and Pediatric Neurological Disorders (6 papers), Genetic and Kidney Cyst Diseases (6 papers), RNA Research and Splicing (5 papers), Prenatal Screening and Diagnostics (5 papers) and Hereditary Neurological Disorders (4 papers). The work is most often cited by research in Genetics (1.3k citations), Developmental Biology (57 citations), Developmental Neuroscience (80 citations), Clinical Biochemistry (105 citations) and Pediatrics, Perinatology and Child Health (190 citations). Mathilde Nizon has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Jean‐Paul Bonnefont, Bertrand Isidor, Chris Ottolenghi, Pascale de Lonlay, Florence Habarou, Nathalie Boddaert, Valérie Malan, Marie Vincent, Arnold Münnich and Cécile Acquaviva. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Genetics in Medicine, Clinical Genetics and Journal of Medical 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.