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Selima Fourati Ben Mustapha

15

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Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa.

2021 International Journal of Molecular Sciences
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A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.

2021 Human Genetics
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Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player.

2020 Human Genetics
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Tunisian Recommendations for resumption of Reproductive Medicine activity in the Covid-19 pandemic.

2020 La Tunisie médicale
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Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice

2019 American Journal of Human Genetics
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Author response for "Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations"

2019
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Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations

2019 Clinical Genetics
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Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

2018 Nature Communications
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Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella

2018 Human Reproduction
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A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.

2018 American Journal of Human Genetics
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Citations (43)