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Olfa Messaoud

Pasteur Institute

39

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252

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Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism.

2021 Frontiers in Genetics
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Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved.

2021 Genes
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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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Second cohomology space of $\mathfrak{sl}(2)$ acting on the space of bilinear bidifferential operators

2020 Revista De La Union Matematica Argentina
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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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The Genetic Epidemiology of Orphan Diseases in North Africa

2019
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Congenital lamellar ichthyosis in Tunisia associated with vitamin D rickets caused by a founder nonsense mutation in the TGM 1 gene

2019 International Journal of Dermatology
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Epidemiological trends and clinicopathological features of cutaneous melanoma in sporadic and xeroderma pigmentosum Tunisian patients

2017 International Journal of Dermatology
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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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