Sonia Nizard
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Dermatological and Skeletal Disorders
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in ⓘ
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- Metabolism and Genetic Disorders 2
- Genetics 8
- Genomic variations and chromosomal abnormalities 4
- Dermatological and Skeletal Disorders 2
- Genomics and Rare Diseases 2
- Genetic and rare skin diseases. 2
- Co-authors
- Emmanuelle Lemyre (4 shared papers)Géraldine Mathonnet (3 shared papers)Grant A. Mitchell (1 shared paper)Isabelle De Bie (1 shared paper)Alain Hovnanian (1 shared paper)Jean‐Louis Bonafé (1 shared paper)Nicolas Chassaing (1 shared paper)Patrick Calvas (1 shared paper)
- Journals
- Clinical Genetics (2 papers)Journal of Medical Genetics (2 papers)Muscle & Nerve (1 paper)JAMA Psychiatry (1 paper)Journal of Investigative Dermatology (1 paper)
- Partner nations
- FranceCanadaUnited Kingdom
In The Last Decade
Sonia Nizard
12 papers receiving 353 citations
Peers
Comparison fields: 5 of 46
- Genetics 227
- Pediatrics, Perinatology and Child Health 87
- Clinical Biochemistry 27
- Cell Biology 62
- Cancer Research 36
Countries citing papers authored by Sonia Nizard
This map shows the geographic impact of Sonia Nizard'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 Sonia Nizard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sonia Nizard more than expected).
Fields of papers citing papers by Sonia Nizard
This network shows the impact of papers produced by Sonia Nizard. 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 Sonia Nizard. The network helps show where Sonia Nizard may publish in the future.
Co-authors
The 25 scholars most cited alongside Sonia Nizard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 66 | |
| 2 | 2011 | 65 | |
| 3 | 2018 | 45 | |
| 4 | Renal lesions and pheochromocytoma in von Hippel-Lindau disease. | 1994 | 40 |
| 5 | 2009 | 32 | |
| 6 | 2018 | 26 | |
| 7 | 1999 | 25 | |
| 8 | 2013 | 22 | |
| 9 | 2014 | 12 | |
| 10 | 1990 | 11 | |
| 11 | [Unilateral atrophoderma following Blaschko's lines: Blaschkolinear morphoea or Moulin's linear atrophoderma?]. | 2002 | 7 |
| 12 | 1991 | 6 |
About Sonia Nizard
Sonia Nizard is a scholar working on Clinical Biochemistry, Genetics, Pediatrics, Perinatology and Child Health, Biochemistry and Surgery, having authored 12 papers that have together received 357 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Metabolism and Genetic Disorders (2 papers), Dermatological and Skeletal Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (2 papers), Genetic and rare skin diseases. (2 papers), Intestinal Malrotation and Obstruction Disorders (1 paper) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Genetics (227 citations), Pediatrics, Perinatology and Child Health (87 citations), Clinical Biochemistry (27 citations), Cell Biology (62 citations) and Cancer Research (36 citations). Sonia Nizard has collaborated with scholars based in France, Canada and United Kingdom. Frequent co-authors include Emmanuelle Lemyre, Géraldine Mathonnet, Grant A. Mitchell, Isabelle De Bie, Alain Hovnanian, Jean‐Louis Bonafé, Nicolas Chassaing, Patrick Calvas, Ludovic Martin and Raouf Fetni. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Muscle & Nerve, JAMA Psychiatry and Journal of Investigative Dermatology.
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.