Rita Menassa

589 total citations
14 papers, 234 citations indexed

About

Rita Menassa is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Rita Menassa has authored 14 papers receiving a total of 234 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Endocrinology, Diabetes and Metabolism and 2 papers in Genetics. Recurrent topics in Rita Menassa's work include Sexual Differentiation and Disorders (7 papers), Hormonal and reproductive studies (4 papers) and Muscle Physiology and Disorders (3 papers). Rita Menassa is often cited by papers focused on Sexual Differentiation and Disorders (7 papers), Hormonal and reproductive studies (4 papers) and Muscle Physiology and Disorders (3 papers). Rita Menassa collaborates with scholars based in France, Tunisia and Italy. Rita Menassa's co-authors include Yves Morel, M David, Véronique Tardy, C Lecointre, Anne Lienhardt-Roussie, V. Sulmont, Raja Brauner, Florence Roucher‐Boulez, F. Lorenzini and Jean‐Marc Costa and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Clinica Chimica Acta and Frontiers in Endocrinology.

In The Last Decade

Rita Menassa

14 papers receiving 231 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rita Menassa France	8	181	112	71	35	32	14	234
Matthias Viemann Germany	7	217 1.2×	160 1.4×	80 1.1×	16 0.5×	12 0.4×	10	269
Pablo Ramírez Argentina	11	260 1.4×	185 1.7×	206 2.9×	56 1.6×	18 0.6×	25	381
Raúl Sánchón Spain	6	102 0.6×	134 1.2×	39 0.5×	21 0.6×	11 0.3×	6	352
Susanne Fricke‐Otto Germany	10	194 1.1×	115 1.0×	174 2.5×	12 0.3×	83 2.6×	15	299
Miki Nishitani United States	4	257 1.4×	212 1.9×	71 1.0×	32 0.9×	12 0.4×	12	289
Soara Menabò Italy	9	188 1.0×	161 1.4×	81 1.1×	33 0.9×	15 0.5×	19	248
Athanasia Stoupa France	9	161 0.9×	197 1.8×	92 1.3×	6 0.2×	32 1.0×	23	261
Valeria Brunelli Italy	6	250 1.4×	130 1.2×	185 2.6×	17 0.5×	8 0.3×	7	314
F Kurtz France	4	92 0.5×	71 0.6×	52 0.7×	22 0.6×	7 0.2×	6	155
Christian Pina United States	3	108 0.6×	31 0.3×	65 0.9×	32 0.9×	118 3.7×	9	194

Countries citing papers authored by Rita Menassa

Since Specialization

Citations

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

Fields of papers citing papers by Rita Menassa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rita Menassa

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

All Works

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14 of 14 papers shown

Rendu, John, Laurence Michel‐Calemard, Rita Menassa, et al.. (2023). Muscular phenotype description of abnormal THOC2 splicing. Neuromuscular Disorders. 33(12). 978–982. 2 indexed citations

Menassa, Rita, et al.. (2023). Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation.. PubMed. 42(4). 106–112. 1 indexed citations

Pégat, Antoine, Nathalie Streichenberger, Nicolas Lacoste, et al.. (2022). Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report. Genes. 13(12). 2245–2245. 5 indexed citations

Svahn, Juliette, Pascal Laforêt, Christophe Vial, et al.. (2019). Dilated cardiomyopathy and limb-girdle muscular dystrophy-dystroglycanopathy due to novel pathogenic variants in the DPM3 gene. Neuromuscular Disorders. 29(7). 497–502. 7 indexed citations

Mallet, Delphine, Alexandre Janin, Rita Menassa, et al.. (2018). Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene. Frontiers in Endocrinology. 9. 491–491. 15 indexed citations

Roucher‐Boulez, Florence, et al.. (2018). News about the genetics of congenital primary adrenal insufficiency. Annales d Endocrinologie. 79(3). 174–181. 12 indexed citations

Roucher‐Boulez, Florence, Rita Menassa, Nathalie Streichenberger, et al.. (2015). A splicing mutation in the DMD gene detected by next-generation sequencing and confirmed by mRNA and protein analysis. Clinica Chimica Acta. 448. 146–149. 5 indexed citations

Svahn, Juliette, Nathalie Streichenberger, Olivier Benvéniste, et al.. (2015). Significant response to immune therapies in a case of subacute necrotizing myopathy and FKRP mutations. Neuromuscular Disorders. 25(11). 865–868. 4 indexed citations

Menassa, Rita, et al.. (2015). Place actuelle du diagnostic anténatal des anomalies de la différenciation sexuelle. Mise au point sur la prise en charge prénatale des hyperplasies congénitales des surrénales et les dilemmes soulevés par leur traitement prénatal. Revue de médecine périnatale. 7(3). 147–155. 1 indexed citations

10.

Menassa, Rita, Jean‐Marc Costa, M David, et al.. (2014). New Management Strategy of Pregnancies at Risk of Congenital Adrenal Hyperplasia Using Fetal Sex Determination in Maternal Serum: French Cohort of 258 Cases (2002–2011). The Journal of Clinical Endocrinology & Metabolism. 99(4). 1180–1188. 49 indexed citations

11.

Farra, Chantal, Rita Menassa, Johnny Awwad, et al.. (2010). Mutational spectrum of cystic fibrosis in the Lebanese population. Journal of Cystic Fibrosis. 9(6). 406–410. 36 indexed citations

12.

Menassa, Rita, et al.. (2010). Three Novel <i>CYP11B1</i> Mutations in Congenital Adrenal Hyperplasia due to Steroid 11Beta-Hydroxylase Deficiency in a Moroccan Population. Hormone Research in Paediatrics. 74(3). 182–189. 16 indexed citations

13.

Tardy, Véronique, Rita Menassa, V. Sulmont, et al.. (2010). Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier. The Journal of Clinical Endocrinology & Metabolism. 95(3). 1288–1300. 52 indexed citations

14.

Menassa, Rita, et al.. (2008). p.H62L, a Rare Mutation of the CYP21 Gene Identified in Two Forms of 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 93(5). 1901–1908. 29 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.

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