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Hamza Dallali

Pasteur Institute

16

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38

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Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohort.

2021 Molecular Biology Reports
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A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa.

2021 npj Genomic Medicine
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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment.

2021 PLOS ONE
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Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk

2020
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Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing

2019 Acta Diabetologica
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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 Molecular Biology Reports
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Pharmacogenetic landscape of metabolic syndrome components drug response in Tunisia and comparison with worldwide populations

2018 PLOS ONE
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Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population

2017 Annales D Endocrinologie
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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 Journal of Dermatological Science
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P34- Preliminary results of the association of apolipoprotein A5 gene with metabolic syndrome in Tunisian population

2016
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