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Mouna Mnif‐Feki

Observed names: M. Mnif-Feki, M. Mnif‐Féki, Mouna Mnif-Feki
Observed institution: Hopital Universitaire Hedi Chaker
ORCID: 0009-0005-5383-9488
Observed ORCID: 0009-0005-5383-9488
OpenAlex ID: A5030173094
Autoimmune thyroid diseases: genetic susceptibility of thyroid‐specific genes and thyroid autoantigens contributions
2009 · H. Hadj‐Kacem, S. Rebuffat, et al. · International Journal of Immunogenetics · 71
Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism
2019 · Mariam Moalla, Faten Hadj Kacem, et al. · Journal of Assisted Reproduction and Genetics · 21
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Affinity kinetics of leptin-reactive immunoglobulins are associated with plasma leptin and markers of obesity and diabetes
2018 · Houda Bouhajja, Noura Bougacha-Elleuch, et al. · Nutrition and Diabetes · 18
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Potential Predictive Role of Lipid Peroxidation Markers for Type 2 Diabetes in the Adult Tunisian Population
2017 · Houda Bouhajja, Faten Hadj Kacem, et al. · Canadian Journal of Diabetes · 13
La tuberculose hypophysaire : à propos d’un cas
2005 · L. Trabelsi, N. Majdoub-Rekik, et al. · Annales d Endocrinologie · 10
Absence of anti-pendrin auto-antibodies in the sera of Tunisian patients with autoimmune thyroid diseases.
2010 · Salima Belguith-Maalej, Hassen Hadj-Kacem, et al. · PubMed · 8
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation
2021 · Mariam Moalla, Wajdi Safi, et al. · Frontiers in Endocrinology · 7
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Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency
2022 · Mariam Moalla, Mouna Mnif-Feki, et al. · Journal of Clinical Medicine · 3
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Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population
2018 · Houda Bouhajja, Rania Abdelhedi, et al. · Canadian Journal of Physiology and Pharmacology · 3
Hashimoto's Disease
2012 · Noura Bougacha-Elleuch, Mouna Mnif-Feki, et al. · InTech eBooks · 3
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A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations
2022 · Marwa Ammar, Wajdi Safi, et al. · International Journal of Developmental Neuroscience · 2
Occurrence of Hypopituitarism in Tunisian Turner Syndrome patients: familial versus sporadic cases
2021 · M. Mnif-Feki, W. Safi, et al. · Gynecological Endocrinology · 2
Screening of MKRN3, DLK1, KISS1, KISS1R, and PROKR2 genes sequences in related girls with central precocious puberty for a personalized management
2025 · Ayah Alhusseni, Mariam Moalla, et al. · Endocrine and Metabolic Science · 1
Exploring New Biomarkers for Autoimmune Thyroid Diseases Through Whole Exome Sequencing and Pathway-Based Enrichment
2024 · Roa M. Younsou, Mariam Moalla, et al. · Advances in Science and Engineering Technology International Conferences (ASET) · 1
Screening of MKRN3, DLK1, KISS1, KISS1R, and PROKR2 genes sequences in related girls with precocious puberty for a personalized management
2024 · A. Alhusseni, M. Moalla, et al. · Annales d Endocrinologie
Congenital hypopituitarism in familial Turner syndrome cases caused by a highly prevalent PROP1 gene mutation in Tunisia
2024 · Hassen Hadj Kacem, Mariam Moalla, et al. · Endocrine and Metabolic Science
Séquençage à haut débit de l’exome entier d’une famille Tunisienne atteinte d’Hypogonadisme Hypogonadotrope Congénital Normosmique
2020 · M. Moalla, W. Safi, et al. · Annales d Endocrinologie
Works count: 17
Citation count: 163
H-index: 7
I10-index: 5
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