Author

Inès Ouertani

Observed names: I. OUERTANI, I. Ouertani, Ines Ouertani, Ines Ourtani

Observed institutions: Tunis University, Hôpital Charles-Nicolle, Faculté de médecine de Tunis, Tunis El Manar University

ORCID: 0000-0001-6015-582X

Observed ORCID: 0000-0001-6015-582X

OpenAlex ID: A5087425699

Update on the Genetics of Bardet-Biedl Syndrome

2013 · O. M'hamdi, I. Ouertani, et al. · Molecular Syndromology · 129

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

2012 · Claire Redin, Stéphanie Le Gras, et al. · Journal of Medical Genetics · 116

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Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

2015 · Marie-Pierre Audrézet, Christine Corbiere, et al. · Journal of the American Society of Nephrology · 88

Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis

2013 · O. M'hamdi, C. Redin, et al. · Clinical Genetics · 32

Prevalence of Bardet–Biedl syndrome in Tunisia

2011 · Oussama M’hamdi, Ines Ouertani, et al. · Journal of Community Genetics · 25

Analyse génétique du syndrome de Turner : étude tunisienne de 89 cas

2008 · I. Kammoun, M. Chaabouni, et al. · Annales d Endocrinologie · 16

2018 · Mariem El Younsi, Lilia Kraoua, et al. · European Journal of Medical Genetics · 13

Genome Tunisia Project: paving the way for precision medicine in North Africa

2024 · Yosr Hamdi, Mediha Trabelsi, et al. · Genome Medicine · 12

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The Experience of a Tunisian Referral Centre in Prenatal Diagnosis of Xeroderma pigmentosum

2013 · O. Messaoud, M. Ben Rekaya, et al. · Public Health Genomics · 11

3M syndrome: A Tunisian seven-cases series

2022 · Khaoula Khachnaoui-Zaafrane, Ines Ouertani, et al. · European Journal of Medical Genetics · 9

Hexasomy of the Prader–Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: Case report

2011 · Lilia Kraoua, Myriam Chaabouni, et al. · European Journal of Medical Genetics · 9

Perinatal-lethal Gaucher disease presenting as hydrops fetalis

2015 · Emira Ben Hamida, Imene Ayadi, et al. · Pan African Medical Journal · 8

Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients

2017 · Mediha Trabelsi, Malek Nouira, et al. · International Journal of Pediatric Otorhinolaryngology · 5

Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy

2012 · Mediha Trabelsi, Imen Chelly, et al. · European Journal of Medical Genetics · 5

Partial Trisomy 4p Syndrome Diagnosed Prenatally

2023 · Kaouther Nasri, Nadia Ben Jamaa, et al. · Fetal and Pediatric Pathology · 3

Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis

2022 · Mariem El Younsi, Médiha Trabelsi, et al. · Pediatric Nephrology · 3

RE(ACT)2014Rare Diseases. 2nd International Congress on Research of Rare and Orphan Diseases. 5th to 8th March 2014, Gehry Building, Novartis Campus, Basel: Abstracts

2014 · B.D. Solomon, F. Hadziselimovic, et al. · Molecular Syndromology · 3

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Complete Trisomy 9 with unusual phenotypic associations.

2016 · Sana Ben Slama, Ines Ouertani, et al. · PubMed · 2

Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients

2014 · Ines Ouertani, Myriam Chaabouni, et al. · Open Journal of Genetics · 2

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A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasia

2009 · Ines Ouertani, Myriam Chaabouni, et al. · European Journal of Medical Genetics · 2

Broad Clinical Spectrum of Mosaic Trisomy 2: Report of Two New Cases in Tunisia

2025 · Kaouther Nasri, Nadia Ben Jamaa, et al. · Fetal and Pediatric Pathology

Le syndrome de Kabuki : étude clinique d’une série de 23 patients tunisiens

2021 · Hana Fredj, Ines Ouertani, et al. · Morphologie

Le syndrome Wolf–Hirschhorn : à propos de 9 cas

2021 · Hana Fredj, Lilia Kraoua, et al. · Morphologie

Pos-010 the Heart-kidney Cross Talk in Cardiac Intensive Care Unit

2021 · I. OUERTANI, E. Allouche, et al. · Kidney International Reports

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Pos-192 Transplant Renal Artery Stenosis: Epidemiologic Profile and Therapeutic Particularities