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Hamza Dallali

Insights From Molecular Characterization of Adult Patients of Families With Multigenerational Diabetes
2017 · Serena Pezzilli, Ornella Ludovico, et al. · Diabetes · 28
Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort
2017 · Zied Landoulsi, Sawssan Benromdhan, et al. · BMC Medical Genetics · 28
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Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing
2019 · Hamza Dallali, Serena Pezzilli, et al. · Acta Diabetologica · 25
Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case Report
2021 · Hamza Dallali, Nadia Kheriji, et al. · Frontiers in Genetics · 20
Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa
2020 · Meriem Hechmi, Hamza Dallali, et al. · Bioscience Reports · 19
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Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis
2017 · Mariem Ben Rekaya, Chokri Naouali, et al. · Journal of Dermatological Science · 18
Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population
2017 · Rym Kefi, Meriem Hechmi, et al. · Annales d Endocrinologie · 16
Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
2021 · Maroua Boujemaa, Yosr Hamdi, et al. · PLoS ONE · 14
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Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations
2018 · Haifa Jmel, Lilia Romdhane, et al. · PLoS ONE · 14
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Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young
2020 · Hager Jaouadi, Yosra Bouyacoub, et al. · Herz · 12
Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 Cases
2020 · Sami Bouchoucha, Asma Chikhaoui, et al. · Frontiers in Pediatrics · 11
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Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins
2019 · Amira Jaballah-Gabteni, Haifa Tounsi, et al. · Journal of Translational Medicine · 11
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Cell line-matched reference enables high-precision functional genomics
2025 · Luca Corda, Emilia Volpe, et al. · Nature Communications · 10
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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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Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis
2022 · Hamza Dallali, Meriem Hechmi, et al. · Diabetology & Metabolic Syndrome · 8
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Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis
2021 · Cherine Charfeddine, Nadia Laroussi, et al. · PLoS ONE · 8
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Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome
2019 · Abir Ben Haj Ali, Ahlem Amouri, et al. · Molecular Genetics & Genomic Medicine · 8
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Decoding the genetic relationship between Alzheimer’s disease and type 2 diabetes: potential risk variants and future direction for North Africa
2023 · Wided Boukhalfa, Haifa Jmel, et al. · Frontiers in Aging Neuroscience · 7
Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
2022 · Meriem Hechmi, Majida Charif, et al. · Bioscience Reports · 7
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
2021 · Rahma Mkaouar, Zied Riahi, et al. · PLoS ONE · 7
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Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family
2019 · Saida Lahbib, Mediha Trabelsi, et al. · Molecular Biology Reports · 6
Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohort
2021 · Imen Hemissi, Sami Boussetta, et al. · Molecular Biology Reports · 5
Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing
2024 · Ismail Gouiza, Meriem Hechmi, et al. · Frontiers in Genetics · 4
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Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family
2020 · Cherine Charfeddine, Hamza Dallali, et al. · Journal of Human Genetics · 4
Pharmacogenetic landscape of pain management variants among Mediterranean populations
2024 · Haifa Jmel, Wided Boukhalfa, et al. · Frontiers in Pharmacology · 3
Works count: 52
Citation count: 313
H-index: 11
I10-index: 12
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