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Zeineb Benzina

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Tunisia

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Publications

TOP 3
Mariem Ben Said; Saber Masmoudi; Felipe Moreno; Hammadi Ayadi; Zeineb Benzina; Houria Dhouib; Abdelmoneem Ghorbel; Mounira Hmani-Aifa
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.
Mariem Ben Saïd; Zeineb Benzina; Ignacio Del Castillo; Ilhem Charfeddine; Abdelmonem Ghorbel; Bochra Hakim; Ayda Khalfallah; Chamseddine Khifagi; Saber Masmoudi; Melek Mnejja; Khalil Turki; Hammadi Ayadi; Leila Ayedi; Mounira Hmani- Aifa
A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family.
K Saidas Nair; Mounira Hmani-Aifa; Zain Ali; Alison L Kearney; Danilo G Macalinao; Ioan M Cosma; Walid Bouassida; Bochra Hakim; Zeineb Benzina; Ileana Soto; Peter Söderkvist; Gareth R Howell; Richard S Smith; Hammadi Ayadi; Salma Ben Salem; Simon W M John
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice.

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All Publications

2012: Mariem Ben Said; Saber Masmoudi; Felipe Moreno; Hammadi Ayadi; Zeineb Benzina; Houria Dhouib; Abdelmoneem Ghorbel; Mounira Hmani-Aifa
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.
International journal of pediatric otorhinolaryngology 2012;76(6):832-6.
2011: Mariem Ben Saïd; Zeineb Benzina; Ignacio Del Castillo; Ilhem Charfeddine; Abdelmonem Ghorbel; Bochra Hakim; Ayda Khalfallah; Chamseddine Khifagi; Saber Masmoudi; Melek Mnejja; Khalil Turki; Hammadi Ayadi; Leila Ayedi; Mounira Hmani- Aifa
A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family.
European journal of medical genetics 2011;54(6):e535-41.
2011: K Saidas Nair; Mounira Hmani-Aifa; Zain Ali; Alison L Kearney; Danilo G Macalinao; Ioan M Cosma; Walid Bouassida; Bochra Hakim; Zeineb Benzina; Ileana Soto; Peter Söderkvist; Gareth R Howell; Richard S Smith; Hammadi Ayadi; Salma Ben Salem; Simon W M John
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice.
Nature genetics 2011;43(6):579-84.
2010: Imen Ben Rebeh; Madeleine Morinière; Leila Ayadi; Zeineb Benzina; Ilhem Charfedine; Jamel Feki; Hammadi Ayadi; Abdelmonem Ghorbel; Faouzi Baklouti; Saber Masmoudi
Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.
Molecular vision 2010;16():1898-906.
2009: Mounira Hmani-Aifa; Salma Ben Salem; Zeineb Benzina; Walid Bouassida; Riadh Messaoud; Khalil Turki; Moncef Khairallah; Ahmed Rebaï; Faïza Fakhfekh; Peter Söderkvist; Hammadi Ayadi
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.
Human genetics 2009;126(4):575-87.
2009: Mounira Hmani-Aifa; Zeineb Benzina; Fareeha Zulfiqar; Houria Dhouib; Amber Shahzadi; Ali Ghorbel; Ahmed Rebaï; Peter Söderkvist; Sheikh Amer Riazuddin; William J Kimberling; Hammadi Ayadi
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
European journal of human genetics : EJHG 2009;17(4):474-82.
2008: Imen Ben Rebeh; Zeineb Benzina; Houria Dhouib; Imen Hadjamor; Mustapha Amyere; Leila Ayadi; Khalil Turki; Bouthaina Hammami; Noureddine Kmiha; Hassen Kammoun; Bochra Hakim; Ilhem Charfedine; Miikka Vikkula; Abdelmonem Ghorbel; Hammadi Ayadi; Saber Masmoudi
Identification of candidate regions for a novel Usher syndrome type II locus.
Molecular vision 2008;14():1719-26.
2008: Abdelaziz Tlili; Imen Ben Rebeh; Mounira Aifa-Hmani; Houria Dhouib; Jihen Moalla; Jihen Tlili-Chouchène; Mariem Ben Said; Imed Lahmar; Zeineb Benzina; Ilhem Charfedine; Nabil Driss; Ali Ghorbel; Hammadi Ayadi; Saber Masmoudi
TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian families.
Audiology & neuro-otology 2008;13(4):213-8.
2007: Abdelaziz Tlili; Saber Masmoudi; H Dhouib; S Bouaziz; I Ben Rebeh; J Chouchen; K Turki; Zeineb Benzina; Ilhem Charfedine; Mohamed Drira; Hammadi Ayadi
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.
Annals of human genetics 2007;71(Pt 2):271-5.
2005: Abdelaziz Tlili; Ilhem Charfedine; Imed Lahmar; Zeineb Benzina; Ben Amor Mohamed; Dominique Weil; Nabil Idriss; Mohamed Drira; Saber Masmoudi; Hammadi Ayadi
Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss.
Human mutation 2005;25(5):503.
2005: Abdelaziz Tlili; Minna Männikkö; Ilhem Charfedine; Imed Lahmar; Zeineb Benzina; Mohamed Ben Amor; Nabil Driss; Leena Ala-Kokko; Mohamed Drira; Saber Masmoudi; Hammadi Ayadi
A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family.
Human heredity 2005;60(3):123-8.