Inès Ouertani

472 total citations
15 papers, 252 citations indexed

About

Inès Ouertani is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Inès Ouertani has authored 15 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Inès Ouertani's work include Genetic Syndromes and Imprinting (5 papers), Hedgehog Signaling Pathway Studies (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Inès Ouertani is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Hedgehog Signaling Pathway Studies (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Inès Ouertani collaborates with scholars based in Tunisia, France and Italy. Inès Ouertani's co-authors include Faouzi Mâazoul, Habiba Chaâbouni, Jean Muller, Hélène Dollfus, Claire Redin, Corinne Stoetzel, Jean‐Louis Mandel, Ridha Mrad, Florence Petit and Pietro Chiurazzi and has published in prestigious journals such as Journal of Medical Genetics, Pediatric Nephrology and Clinical Genetics.

In The Last Decade

Inès Ouertani

15 papers receiving 248 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Inès Ouertani Tunisia	7	208	193	16	15	15	15	252
Kirsley Chennen France	6	161 0.8×	193 1.0×	10 0.6×	11 0.7×	22 1.5×	14	244
Christian Decker Germany	5	88 0.4×	138 0.7×	18 1.1×	7 0.5×	8 0.5×	5	187
Katie Weihbrecht United States	4	219 1.1×	212 1.1×	24 1.5×	24 1.6×	80 5.3×	4	268
Yoko Hiraki Japan	10	131 0.6×	97 0.5×	22 1.4×	13 0.9×	10 0.7×	17	219
A. Tessitore United Kingdom	2	86 0.4×	89 0.5×	8 0.5×	40 2.7×	15 1.0×	2	151
Rachel V. Bowie Ireland	5	236 1.1×	220 1.1×	20 1.3×	13 0.9×	91 6.1×	6	289
Claudia Soler‐Alfonso United States	12	135 0.6×	197 1.0×	33 2.1×	10 0.7×	5 0.3×	21	333
Huanzheng Li China	8	63 0.3×	158 0.8×	30 1.9×	7 0.5×	9 0.6×	29	248
Ilse M. van der Werf Belgium	7	111 0.5×	79 0.4×	32 2.0×	14 0.9×	6 0.4×	8	155
Emanuela Ponzi Italy	7	93 0.4×	87 0.5×	22 1.4×	6 0.4×	9 0.6×	14	182

Countries citing papers authored by Inès Ouertani

Since Specialization

Citations

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

Fields of papers citing papers by Inès Ouertani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inès Ouertani

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

All Works

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15 of 15 papers shown

Ouertani, Inès, et al.. (2022). 3M syndrome: A Tunisian seven-cases series. European Journal of Medical Genetics. 65(3). 104448–104448. 5 indexed citations

Ouertani, Inès, et al.. (2022). Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis. Pediatric Nephrology. 38(1). 119–129. 1 indexed citations

Kraoua, Lilia, Inès Ouertani, Faouzi Mâazoul, et al.. (2018). WDR73-related galloway mowat syndrome with collapsing glomerulopathy. European Journal of Medical Genetics. 62(9). 103550–103550. 6 indexed citations

Mâazoul, Faouzi, Lilia Kraoua, Inès Ouertani, et al.. (2017). Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients. International Journal of Pediatric Otorhinolaryngology. 103. 14–19. 3 indexed citations

Ouertani, Inès, et al.. (2016). Complete Trisomy 9 with unusual phenotypic associations.. PubMed. 94(12). 895–895. 2 indexed citations

Ouertani, Inès, Myriam Châabouni, Lilia Kraoua, et al.. (2014). Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients. 4(5). 385–391. 2 indexed citations

Messaoud, Olfa, Mariem Ben Rekaya, Inès Ouertani, et al.. (2013). The Experience of a Tunisian Referral Centre in Prenatal Diagnosis of <b><i>Xeroderma pigmentosum</i></b>. Public Health Genomics. 16(5). 251–254. 6 indexed citations

Ouertani, Inès, et al.. (2013). Update on the Genetics of Bardet-Biedl Syndrome. Molecular Syndromology. 5(2). 51–56. 80 indexed citations

Redin, Claire, Corinne Stoetzel, Inès Ouertani, et al.. (2013). Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis. Clinical Genetics. 85(2). 172–177. 25 indexed citations

10.

Mâazoul, Faouzi, Myriam Châabouni, Inès Ouertani, et al.. (2012). Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy. European Journal of Medical Genetics. 56(1). 13–19. 1 indexed citations

11.

Redin, Claire, Stéphanie Le Gras, Véronique Geoffroy, et al.. (2012). Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes. Journal of Medical Genetics. 49(8). 502–512. 81 indexed citations

12.

Kraoua, Lilia, Myriam Châabouni, Elisabeth Ewers, et al.. (2011). Hexasomy of the Prader–Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: Case report. European Journal of Medical Genetics. 54(4). e446–e450. 8 indexed citations

13.

Ouertani, Inès, et al.. (2011). Prevalence of Bardet–Biedl syndrome in Tunisia. Journal of Community Genetics. 2(2). 97–99. 22 indexed citations

14.

Ouertani, Inès, Myriam Châabouni, Ilhem Turki, et al.. (2009). A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasia. European Journal of Medical Genetics. 52(4). 256–259. 1 indexed citations

15.

Chaâbouni, M, Mohamed Trabelsi, Inès Ouertani, et al.. (2008). Analyse génétique du syndrome de Turner : étude tunisienne de 89 cas. Annales d Endocrinologie. 69(5). 440–445. 9 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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