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Author

Nessrine Mezzi

Observed name: Mezzi Nesrine
ORCID: 0000-0002-0520-5078
Observed ORCID: 0000-0002-0520-5078
OpenAlex ID: A5007901502
Consanguinity and Inbreeding in Health and Disease in North African Populations
2019 · Lilia Romdhane, Nessrine Mezzi, et al. · Annual Review of Genomics and Human Genetics · 86
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Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved
2021 · Nessrine Mezzi, Olfa Messaoud, et al. · Genes · 15
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A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa
2021 · Lilia Romdhane, Nessrine Mezzi, et al. · npj Genomic Medicine · 9
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Consanguinité et son impact sur la santé et la dynamique du génome : Un exemple de la Tunisie
2024 · Nessrine Mezzi, Najla Abassi, et al. · La Tunisie Médicale · 6
Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticity
2024 · Lilia Romdhane, Sameh Kefi, et al. · Scientific Reports · 4
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African Genomic Medicine Portal: A Web Portal for Biomedical Applications
2022 · Houcemeddine Othman, Lyndon Zass, et al. · Journal of Personalized Medicine · 4
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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
2024 · Rahma Mkaouar, Zied Riahi, et al. · Frontiers in Genetics · 2
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Pharmacogenomics of treatment toxicities in pediatric B-Cell ALL: toward safer precision therapy
2026 · Meriem Lameri, Tarek Kamergi, et al. · Frontiers in Pharmacology · 1
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Precision Medicine of Rare Genetic Diseases in Africa
2025 · Lilia Romdhane, Nessrine Mezzi, et al. · Springer eBooks · 1
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Genetic study of Alport syndrome in Tunisia
2024 · Mariem El Younsi, Ahlem Achour, et al. · Pediatric Nephrology · 1
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
2024 · Rahma Mkaouar, Zied Riahi, et al. · Frontiers in Genetics · 1
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Uncovering COVID-19 dynamics in Tunisian patients: a meta-transcriptomic approach
2026 · Dorra Rjaibi, Marwa Khedhiri, et al. · Scientific Reports
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Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome Sequencing
2024 · Nessrine Mezzi, Anissa Zaouak, et al. · Gene
Works count: 13
Citation count: 130
H-index: 4
I10-index: 2
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