Imen Rejeb

A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric features

Imen Rejeb, Yoann Saillour, L. Castelnau et al. · European Journal of Human Genetics · 2008 · 44 citations

Life Sciences, Genetics, Molecular Genetics +12

Mosaic parental germline mutations causing recurrent forms of malformations of cortical development

Julia Lauer Zillhardt, Karine Poirier, Loïc Broix et al. · European Journal of Human Genetics · 2015 · 36 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly

Manèl Chograni, Imen Rejeb, Lamia Ben Jemâa et al. · European Journal of Human Genetics · 2011 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations

Imen Rejeb, Houweyda Jilani, Yasmina Elaribi et al. · BMC Medical Genetics · 2017 · 22 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardation

Imen Rejeb, Lamia Ben Jemâa, Leila Abaied et al. · European Journal of Medical Genetics · 2011 · 19 citations

Life Sciences, Genetics, Molecular Genetics +6