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Folia Microbiologica|June 3, 2026
Gut microbiome-blood cholesterol crosstalk: towards personalized strategies for dyslipidemiaWirath Ben Ncir, Fatma Abdelhedi, Leila Ammar KeskesThe European Journal of Neuroscience|August 26, 2025
Gut Microbiota Composition and Modulation in Developmental and Epileptic EncephalopathiesTakwa Ammar, Fatma Abdelhedi, Leila Ammar Keskes, et al.American Journal of Medical Genetics. Part A|April 28, 2016
A de novo 10p11.23-p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disordersFatma Abdelhedi, Laila El Khattabi, Nouha Essid, et al.American Journal of Medical Genetics. Part A|February 4, 2012
First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femurFatma Abdelhedi, Johanna Corcos, Laurence Cuisset, et al.American Journal of Clinical Pathology|July 13, 2014
Neonatal Silver-Russell syndrome with maternal uniparental heterodisomy, trisomy 7 mosaicism, and dysplasia of the cerebellumFatma Abdelhedi, Laila El Khattabi, Laurence Cuisset, et al.Heliyon|December 6, 2024
Angiotensin-converting-enzyme gene insertion-deletion polymorphism and renin angiotensin aldosterone system activity in different phenotypes of polycystic ovary syndromeKhansa Chaabouni, Amana Saadallah-Kallel, Samia Ben Brahim, et al.Journal of Assisted Reproduction and Genetics|October 27, 2018
Altered three-dimensional organization of sperm genome in DPY19L2-deficient globozoospermic patientsFatma Abdelhedi, Céline Chalas, Jean-Maurice Petit, et al.The Journal of Sexual Medicine|May 19, 2012
A novel nonsense mutation in HSD17B3 gene in a Tunisian patient with sexual ambiguityBochra Ben Rhouma, Neila Belguith, Mouna Feki Mnif, et al.Journal of Cellular and Molecular Medicine|January 6, 2026
First LDLRAP1 and Recurrent LDLR Mutations in Tunisian Families With Familial HypercholesterolemiaWirath Ben Ncir, Afif Ben-Mahmoud, Hamdi Frikha, et al.Endocrine Regulations|March 31, 2026
One genotype with a myriad of phenotypes: A family with multiple endocrine neoplasiaOumeyma Trimeche, Fatma Mnif, Fatma Abdelhedi, et al.Pageof 2