Concepedia
Statistics
Publications
18
Citations
995
H-Index
14
Active since
1999
Affiliations
Hopital Universitaire Habib Bourguiba(Current)
Centre of Biotechnology of Sfax
Linköping University
University of Sfax
Institut Pasteur
Mounira Hmani‐Aifa is an author at Hopital Universitaire Habib Bourguiba specializing in medicine, genetics, and pathology.
Top concepts
MedicineGeneticsPathologyMolecular GeneticsAudiologyHearing LossMolecular BiologyArtsGenomicsAuditory Research
Publications per year
1999–2016
A TLR4 polymorphism is associated with asthma and reduced lipopolysaccharide-induced interleukin-12(p70) responses in Swedish children
Malin Fagerås Böttcher, Mounira Hmani‐Aifa, Anna Lindström et al. · Journal of Allergy and Clinical Immunology · 2004 · 228 citations
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice
K. Saidas Nair, Mounira Hmani‐Aifa, Zain Ali et al. · Nature Genetics · 2011 · 107 citations
Angle-closure Glaucoma, Serine Protease Prss56, Ocular Disease +9
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23–24.2
Mounira Hmani‐Aifa, Abdelmonem Ghorbel, Amel Boulila‐Elgaied et al. · European Journal of Human Genetics · 1999 · 84 citations · Full text
Genetic Disorder, Genetics, Pathology +4
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans
Zubair M. Ahmed, Saber Masmoudi, Ersan Kalay et al. · Nature Genetics · 2008 · 84 citations · Full text
Nonsyndromic Deafness, Mendelian Disorder, Genetic Disorder +9
Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation
Saber Masmoudi, Ilhem Charfedine, Mounira Hmani‐Aifa et al. · American Journal of Medical Genetics · 2000 · 72 citations
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