Sonia Nizard

664 total citations
12 papers, 357 citations indexed

About

Sonia Nizard is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Sonia Nizard has authored 12 papers receiving a total of 357 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 3 papers in Surgery and 3 papers in Molecular Biology. Recurrent topics in Sonia Nizard's work include Genomic variations and chromosomal abnormalities (4 papers), Dermatological and Skeletal Disorders (2 papers) and Genomics and Rare Diseases (2 papers). Sonia Nizard is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Dermatological and Skeletal Disorders (2 papers) and Genomics and Rare Diseases (2 papers). Sonia Nizard collaborates with scholars based in France, Canada and United Kingdom. Sonia Nizard's co-authors include Emmanuelle Lemyre, Grant A. Mitchell, Géraldine Mathonnet, Isabelle De Bie, Nicolas Chassaing, Jean‐Louis Bonafé, Alain Hovnanian, Raouf Fetni, Patrick Calvas and Ludovic Martin and has published in prestigious journals such as Journal of Investigative Dermatology, JAMA Psychiatry and Journal of Medical Genetics.

In The Last Decade

Sonia Nizard

12 papers receiving 353 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sonia Nizard France 10 227 131 87 62 36 12 357
E. Vámos Belgium 11 205 0.9× 156 1.2× 111 1.3× 27 0.4× 27 0.8× 23 420
Mohammed Zain Seidahmed Saudi Arabia 12 227 1.0× 277 2.1× 65 0.7× 26 0.4× 35 1.0× 21 409
Marjan M. Nezarati Canada 10 198 0.9× 232 1.8× 38 0.4× 23 0.4× 40 1.1× 17 447
Mary Willis United States 10 197 0.9× 200 1.5× 55 0.6× 33 0.5× 22 0.6× 17 361
Jaime Garcia‐Heras United States 14 244 1.1× 208 1.6× 93 1.1× 28 0.5× 20 0.6× 25 440
Deborah Morrogh United Kingdom 9 299 1.3× 247 1.9× 29 0.3× 83 1.3× 14 0.4× 13 542
Eri Imagawa Japan 13 170 0.7× 250 1.9× 29 0.3× 24 0.4× 26 0.7× 30 418
Angela L. Duker United States 10 267 1.2× 284 2.2× 46 0.5× 28 0.5× 58 1.6× 25 471
Luis Rohena United States 12 154 0.7× 192 1.5× 46 0.5× 52 0.8× 13 0.4× 27 383
Mónica Rosello Spain 14 360 1.6× 295 2.3× 95 1.1× 25 0.4× 27 0.8× 41 535

Countries citing papers authored by Sonia Nizard

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Sonia Nizard

This figure shows the co-authorship network connecting the top 25 collaborators of Sonia Nizard. A scholar is included among the top collaborators of Sonia Nizard based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sonia Nizard. Sonia Nizard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Huguet, Guillaume, Catherine Schramm, Élise Douard, et al.. (2018). Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples. JAMA Psychiatry. 75(5). 447–447. 45 indexed citations
2.
Lopes, Fátima, J Gauthier, Virginie Saillour, et al.. (2018). Refining the phenotype associated with biallelic DNAJC21 mutations. Clinical Genetics. 94(2). 252–258. 26 indexed citations
3.
Mathonnet, Géraldine, Raouf Fetni, Sonia Nizard, et al.. (2014). SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay. BMC Medical Genomics. 7(1). 70–70. 12 indexed citations
4.
Meijer, Inge A., Michel Vanasse, Sonia Nizard, Yves Robitaille, & Elsa Rossignol. (2013). An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorder. Muscle & Nerve. 49(1). 134–138. 22 indexed citations
5.
Kibar, Zoha, Géraldine Mathonnet, Raouf Fetni, et al.. (2011). Whole‐genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype. Clinical Genetics. 81(2). 128–141. 65 indexed citations
6.
Bie, Isabelle De, Sonia Nizard, & Grant A. Mitchell. (2009). Fetal dilated cardiomyopathy: an unsuspected presentation of methylmalonic aciduria and hyperhomocystinuria, cblC type. Prenatal Diagnosis. 29(3). 266–270. 32 indexed citations
7.
Chassaing, Nicolas, Ludovic Martin, Sonia Nizard, et al.. (2004). Novel ABCC6 Mutations in Pseudoxanthoma Elasticum. Journal of Investigative Dermatology. 122(3). 608–613. 66 indexed citations
8.
Georgescu, Véra, et al.. (2002). [Unilateral atrophoderma following Blaschko's lines: Blaschkolinear morphoea or Moulin's linear atrophoderma?].. PubMed. 129(4 Pt 1). 431–2. 7 indexed citations
9.
Nizard, Sonia, et al.. (1999). Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q. Journal of Medical Genetics. 36(3). 246–250. 25 indexed citations
10.
Kahnoski, Richard J., Dominique Chauveau, Yves Chrétien, et al.. (1994). Renal lesions and pheochromocytoma in von Hippel-Lindau disease.. PubMed. 23. 1–27. 40 indexed citations
11.
Roux, C., F.A. Rey, Stanislas Lyonnet, et al.. (1991). An animal model for maternal phenylketonuria.. Journal of Medical Genetics. 28(10). 718–719. 6 indexed citations
12.

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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