Mounira Hmani‐Aifa

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

Life Sciences, Immunology, Immunogenetics +15

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 · 111 citations

Medicine, Molecular Biology, Ophthalmology +9

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 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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 · 85 citations

Life Sciences, Genetics, Molecular Genetics +10

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

Medicine, Genetics, Molecular Genetics +17