Mondher Chouchane

1.7k total citations
14 papers, 426 citations indexed

About

Mondher Chouchane is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Mondher Chouchane has authored 14 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 6 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Mondher Chouchane's work include Genomic variations and chromosomal abnormalities (3 papers), Viral gastroenteritis research and epidemiology (2 papers) and Genetic Syndromes and Imprinting (2 papers). Mondher Chouchane is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Viral gastroenteritis research and epidemiology (2 papers) and Genetic Syndromes and Imprinting (2 papers). Mondher Chouchane collaborates with scholars based in France and Denmark. Mondher Chouchane's co-authors include Frédéric Huet, Patrick Callier, Alice Masurel‐Paulet, Véronique Darmency‐Stamboul, Salima El Chehadeh-Djebbar, Judith St‐Onge, Yannis Duffourd, Mathilde Lefebvre, François Feillet and A. Steinmetz and has published in prestigious journals such as Neurology, Epilepsia and Clinical Genetics.

In The Last Decade

Mondher Chouchane

13 papers receiving 409 citations

Peers

Mondher Chouchane

GENET

SURGE

PPCH

Sharan Goobie Canada

Rebecca McClellan United States

Aziza Sbiti Morocco

Yingjun Xie China

Mónica Rosello Spain

Simona Cavani Italy

Mauro Pierluigi Italy

Jan-Maarten Cobben Netherlands

Tracy Brandt United States

Mahmoud F. Elsaid Qatar

Sharan Goobie Canada

Mondher Chouchane

281 ×1.3

GENET

162 ×0.9

88 ×0.9

GENET

37 ×0.5

SURGE

52 ×0.9

PPCH

Citations per year, relative to Mondher Chouchane Mondher Chouchane (= 1×) peers Sharan Goobie

Countries citing papers authored by Mondher Chouchane

Since Specialization

Citations

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

Fields of papers citing papers by Mondher Chouchane

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mondher Chouchane

This figure shows the co-authorship network connecting the top 25 collaborators of Mondher Chouchane. A scholar is included among the top collaborators of Mondher Chouchane 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 Mondher Chouchane. Mondher Chouchane 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

Barth, Magalie, Jérémie Lefranc, Karine Mention, et al.. (2021). West Syndrome Is an Exceptional Presentation of Pyridoxine- and Pyridoxal Phosphate-Dependent Epilepsy: Data From a French Cohort and Review of the Literature. Frontiers in Pediatrics. 9. 621200–621200. 7 indexed citations

Daron, Aurore, Carole Vuillerot, Claude Cancés, et al.. (2018). Nusinersen in patients older than 7 months with spinal muscular atrophy type 1. Neurology. 91(14). e1312–e1318. 86 indexed citations

Thévenon, Julien, Yannis Duffourd, Alice Masurel‐Paulet, et al.. (2016). Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole‐exome sequencing as a first‐line diagnostic test. Clinical Genetics. 89(6). 700–707. 138 indexed citations

Giroud, M, Benoît Daubail, Mondher Chouchane, et al.. (2014). Angelman Syndrome: A Case Series Assessing Neurological Issues in Adulthood. European Neurology. 73(1-2). 119–125. 10 indexed citations

Kirchhoff, Maria, Nathalie Marle, Mondher Chouchane, et al.. (2013). Delineation of a new chromosome 20q11.2 duplication syndrome including the ASXL1 gene. American Journal of Medical Genetics Part A. 161(7). 1594–1598. 24 indexed citations

Milh, Mathieu, Nathalie Villeneuve, Mondher Chouchane, et al.. (2011). Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations. Epilepsia. 52(10). 1828–1834. 94 indexed citations

Masurel‐Paulet, Alice, Patrick Callier, Christel Thauvin‐Robinet, et al.. (2009). Multiple cysts of the corpus callosum and psychomotor delay in a patient with a 3.1 Mb 15q24.1q24.2 interstitial deletion identified by array‐CGH. American Journal of Medical Genetics Part A. 149A(7). 1504–1510. 20 indexed citations

Béjot, Yannick, Guy‐Victor Osseby, Mondher Chouchane, et al.. (2009). Les accidents vasculaires cérébraux du nouveau-né et de l’enfant. Revue Neurologique. 165(11). 889–900. 9 indexed citations

Huet, Frédéric, Mondher Chouchane, M Aubert, et al.. (2008). Étude épidémiologique prospective de la gastroentérite à rotavirus en Europe (étude REVEAL). Résultats de la zone d’étude française. Archives de Pédiatrie. 15(4). 362–374. 12 indexed citations

10.

Huet, Frédéric, Mondher Chouchane, M Aubert, et al.. (2008). Iconographies supplémentaires de l'article : Étude épidémiologique prospective de la gastroentérite à rotavirus en Europe (étude REVEAL). Résultats de la zone d’étude française.

11.

Colombani, Marina, Mondher Chouchane, G. Pitelet, et al.. (2006). A new case of megalencephaly and perisylvian polymicrogyria with post-axial polydactyly and hydrocephalus: MPPH syndrome. European Journal of Medical Genetics. 49(6). 466–471. 15 indexed citations

12.

Chouchane, Mondher, et al.. (1999). Les agénésies du corps calleux: aspects étiologiques, cliniques, moyens de diagnostic et pronostic. Archives de Pédiatrie. 6(12). 1306–1311. 6 indexed citations

13.

Gouyon, Jean‐Bernard, et al.. (1994). [Renal effects of prolonged indomethacin therapy in premature infants].. PubMed. 1(10). 894–7. 4 indexed citations

14.

Chouchane, Mondher, et al.. (1993). [Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies].. PubMed. 40(7). 421–5. 1 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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