Mathilde Nizon
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 6
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- Congenital heart defects research 3
- RNA regulation and disease 3
- Ubiquitin and proteasome pathways 2
- Hedgehog Signaling Pathway Studies 2
- Co-authors
- Florence Habarou (2 shared papers)Chris Ottolenghi (2 shared papers)Nathalie Boddaert (2 shared papers)Valérie Malan (3 shared papers)Jean‐Paul Bonnefont (2 shared papers)Bertrand Isidor (10 shared papers)Marie Vincent (5 shared papers)Éric Arnaud (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Journal of Medical Genetics (2 papers)Clinical Genetics (2 papers)Orphanet Journal of Rare Diseases (2 papers)European Journal of Medical Genetics (2 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Mathilde Nizon
27 papers receiving 398 citations
Peers
Comparison fields: 5 of 60
- Clinical Biochemistry 79
- Genetics 148
- Developmental Biology 8
- Molecular Biology 224
- Cellular and Molecular Neuroscience 46
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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 70 | |
| 2 | 2014 | 36 | |
| 3 | 2015 | 33 | |
| 4 | 2021 | 32 | |
| 5 | 2012 | 23 | |
| 6 | 2020 | 23 | |
| 7 | 2015 | 22 | |
| 8 | 2012 | 21 | |
| 9 | 2017 | 19 | |
| 10 | 2020 | 19 | |
| 11 | 2016 | 17 | |
| 12 | 2021 | 17 | |
| 13 | 2013 | 14 | |
| 14 | 2019 | 12 | |
| 15 | 2018 | 11 | |
| 16 | 2021 | 8 | |
| 17 | 2018 | 7 | |
| 18 | 2018 | 6 | |
| 19 | 2021 | 6 | |
| 20 | 2018 | 6 |
About Mathilde Nizon
Mathilde Nizon is a scholar working on Genetics, Molecular Biology, Genetics, Cellular and Molecular Neuroscience and Pulmonary and Respiratory Medicine, having authored 27 papers that have together received 418 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (6 papers), Congenital heart defects research (3 papers), RNA regulation and disease (3 papers), Ubiquitin and proteasome pathways (2 papers), Metabolism and Genetic Disorders (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). The work is most often cited by research in Clinical Biochemistry (79 citations), Genetics (148 citations), Developmental Biology (8 citations), Molecular Biology (224 citations) and Cellular and Molecular Neuroscience (46 citations). Mathilde Nizon has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Florence Habarou, Chris Ottolenghi, Nathalie Boddaert, Valérie Malan, Jean‐Paul Bonnefont, Bertrand Isidor, Marie Vincent, Éric Arnaud, Pascale de Lonlay and Guy Touati. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics, Orphanet Journal of Rare Diseases and European 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.