Cécile Rittore

813 total citations
21 papers, 450 citations indexed

About

Cécile Rittore is a scholar working on Molecular Biology, Immunology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Cécile Rittore has authored 21 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Immunology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Cécile Rittore's work include Inflammasome and immune disorders (8 papers), Prenatal Screening and Diagnostics (7 papers) and Gestational Trophoblastic Disease Studies (6 papers). Cécile Rittore is often cited by papers focused on Inflammasome and immune disorders (8 papers), Prenatal Screening and Diagnostics (7 papers) and Gestational Trophoblastic Disease Studies (6 papers). Cécile Rittore collaborates with scholars based in France, Tunisia and Canada. Cécile Rittore's co-authors include Isabelle Touitou, Laurent Philibert, Hanène Landolsi, Rosemary A. Fisher, Bruce E. Hayward, Ian Carr, John Huntriss, Clare V. Logan, Michael Shires and Christine P. Diggle and has published in prestigious journals such as PLoS ONE, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Cécile Rittore

21 papers receiving 447 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cécile Rittore France 12 233 230 185 130 89 21 450
Hagit Daum Israel 12 172 0.7× 70 0.3× 87 0.5× 141 1.1× 34 0.4× 39 420
Heidi M. Hermes United States 6 184 0.8× 37 0.2× 94 0.5× 84 0.6× 113 1.3× 9 376
Varpu Jokimaa Finland 12 127 0.5× 185 0.8× 115 0.6× 65 0.5× 128 1.4× 18 509
Sjerp M. Weima Netherlands 13 116 0.5× 207 0.9× 185 1.0× 88 0.7× 27 0.3× 20 442
Ronald F. Feinberg United States 13 217 0.9× 199 0.9× 59 0.3× 90 0.7× 176 2.0× 21 646
Sami B. Kanaan United States 12 140 0.6× 38 0.2× 49 0.3× 55 0.4× 142 1.6× 35 338
Lorenza Romitti Italy 13 205 0.9× 67 0.3× 137 0.7× 136 1.0× 38 0.4× 31 531
Csaba Papp United States 13 77 0.3× 87 0.4× 64 0.3× 81 0.6× 236 2.7× 27 495
Sarah Keating Canada 9 111 0.5× 94 0.4× 87 0.5× 36 0.3× 142 1.6× 17 369
Ania Kowalik United States 15 136 0.6× 220 1.0× 48 0.3× 82 0.6× 255 2.9× 17 821

Countries citing papers authored by Cécile Rittore

Since Specialization
Citations

This map shows the geographic impact of Cécile Rittore'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 Cécile Rittore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cécile Rittore more than expected).

Fields of papers citing papers by Cécile Rittore

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cécile Rittore. 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 Cécile Rittore. The network helps show where Cécile Rittore may publish in the future.

Co-authorship network of co-authors of Cécile Rittore

This figure shows the co-authorship network connecting the top 25 collaborators of Cécile Rittore. A scholar is included among the top collaborators of Cécile Rittore 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 Cécile Rittore. Cécile Rittore is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Slim, Rima, Rosemary A. Fisher, Florian Milhavet, et al.. (2022). Biallelic NLRP7 variants in patients with recurrent hydatidiform mole: A review and expert consensus. Human Mutation. 43(12). 1732–1744. 14 indexed citations
3.
Rittore, Cécile, Elodie Sanchez, Aude Mallavialle, et al.. (2021). TNFR1-d2 carrying the p.(Thr79Met) pathogenic variant is a potential novel actor of TNFα/TNFR1 signalling regulation in the pathophysiology of TRAPS. Scientific Reports. 11(1). 4172–4172. 3 indexed citations
4.
Boursier, Guilaine, Cécile Rittore, Florian Milhavet, Laurence Cuisset, & Isabelle Touitou. (2021). Mevalonate Kinase-Associated Diseases: Hunting for Phenotype–Genotype Correlation. Journal of Clinical Medicine. 10(8). 1552–1552. 15 indexed citations
5.
Boursier, Guilaine, Maryam Piram, Cécile Rittore, Guillaume Sarrabay, & Isabelle Touitou. (2020). Phenotypic Associations of PSTPIP1 Sequence Variants in PSTPIP1-Associated Autoinflammatory Diseases. Journal of Investigative Dermatology. 141(5). 1141–1147. 16 indexed citations
6.
Massardier, Jérôme, Pierre‐Adrien Bolze, Touria Hajri, et al.. (2020). Pregnancy after oocyte donation in a patient with NLRP7 gene mutations and recurrent molar hydatidiform pregnancies. Journal of Assisted Reproduction and Genetics. 37(9). 2273–2277. 11 indexed citations
7.
Boursier, Guilaine, Cécile Rittore, Sophie Georgin‐Lavialle, et al.. (2019). Positive Impact of Expert Reference Center Validation on Performance of Next-Generation Sequencing for Genetic Diagnosis of Autoinflammatory Diseases. Journal of Clinical Medicine. 8(10). 1729–1729. 9 indexed citations
8.
Ruyssen‐Witrand, Adeline, Cécile Rittore, Yannick Degboé, et al.. (2019). A single nucleotide polymorphism of IL6-receptor is associated with response to tocilizumab in rheumatoid arthritis patients. The Pharmacogenomics Journal. 19(4). 368–374. 22 indexed citations
9.
Grandemange, Sylvie, Guillaume Sarrabay, Jérôme Pène, et al.. (2017). Clinical dose effect and functional consequences of R92Q in two families presenting with a TRAPS/PFAPA‐like phenotype. Molecular Genetics & Genomic Medicine. 5(2). 110–116. 8 indexed citations
10.
Pers, Yves‐Marie, Cécile Rittore, Gautier Téjédor, et al.. (2016). Association of TRAF1-C5 with risk of uveitis in juvenile idiopathic arthritis. Joint Bone Spine. 84(3). 305–308. 11 indexed citations
11.
Grandemange, Sylvie, Elodie Sanchez, Pascale Louis‐Plence, et al.. (2015). NLRP1 mutations cause autoinflammatory diseases in human. Pediatric Rheumatology. 13(S1). 5 indexed citations
12.
Rittore, Cécile, Elodie Sanchez, Mouna Barat‐Houari, et al.. (2013). Identification of a new exon 2-skipped TNFR1 transcript: regulation by three functional polymorphisms of the TNFR-associated periodic syndrome (TRAPS) gene. Annals of the Rheumatic Diseases. 73(1). 290–297. 11 indexed citations
13.
Landolsi, Hanène, Cécile Rittore, Laurent Philibert, et al.. (2011). Screening for NLRP7 Mutations in Familial and Sporadic Recurrent Hydatidiform Moles. International Journal of Gynecological Pathology. 30(4). 348–353. 15 indexed citations
14.
Daïen, C., Sylvie Fabre, Cécile Rittore, et al.. (2011). TGF beta1 polymorphisms are candidate predictors of the clinical response to rituximab in rheumatoid arthritis. Joint Bone Spine. 79(5). 471–475. 25 indexed citations
15.
Parry, David, Clare V. Logan, Bruce E. Hayward, et al.. (2011). Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte. The American Journal of Human Genetics. 89(3). 451–458. 174 indexed citations
16.
Golfier, François, Cécile Rittore, Touria Hajri, et al.. (2011). The spectrum of NLRP7 mutations in French patients with recurrent hydatidiform mole. European Journal of Obstetrics & Gynecology and Reproductive Biology. 157(2). 197–199. 19 indexed citations
17.
Roberto, Raphaël B. Di, Cécile Rittore, Any Cheung, et al.. (2011). NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage. Journal of Medical Genetics. 48(8). 540–548. 65 indexed citations
18.
Pallarès-Ruiz, Nathalie, Laurent Philibert, Bruno Dumont, et al.. (2010). Combined Mutation And Rearrangement Screening by Quantitative PCR High-Resolution Melting: Is It Relevant for Hereditary Recurrent Fever Genes?. PLoS ONE. 5(11). e14096–e14096. 2 indexed citations
19.
20.
Touitou, Isabelle, Cécile Rittore, Laurent Philibert, et al.. (2009). An international external quality assessment for molecular diagnosis of hereditary recurrent fevers: a 3-year scheme demonstrates the need for improvement. European Journal of Human Genetics. 17(7). 890–896. 8 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Hagit Daum Breakdown of academic impact, for papers by Heidi M. Hermes Breakdown of academic impact, for papers by Varpu Jokimaa Breakdown of academic impact, for papers by Sjerp M. Weima Breakdown of academic impact, for papers by Ronald F. Feinberg Breakdown of academic impact, for papers by Sami B. Kanaan Breakdown of academic impact, for papers by Lorenza Romitti Breakdown of academic impact, for papers by Csaba Papp Breakdown of academic impact, for papers by Sarah Keating Breakdown of academic impact, for papers by Ania Kowalik
Rankless by CCL
2026