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Mounira Hmani‐Aifa

Observed names: Hmani-Aifa, Mounira, M Hmani-Aifa, M Hmani-aifa, Mounira Aifa-Hmani, Mounira Hmani, Mounira Hmani Aifa, Mounira Hmani- Aifa, Mounira Hmani-Aifa
Observed institutions: Linköping University, University of Sfax, Karolinska Institutet, Linköping University Hospital, Centre of Biotechnology of Sfax, Faculty of Medicine of Sfax, Faculty of Sciences of Sfax
ORCID: 0000-0003-2422-1775
Observed ORCID: 0000-0003-2422-1775
OpenAlex ID: A5002656111
A TLR4 polymorphism is associated with asthma and reduced lipopolysaccharide-induced interleukin-12(p70) responses in Swedish children
2004 · Malin Fagerås Böttcher, Mounira Hmani-Aifa, et al. · Journal of Allergy and Clinical Immunology · 229
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice
2011 · K Saidas Nair, Mounira Hmani-Aifa, et al. · Nature Genetics · 109
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans
2008 · Zubair M Ahmed, Saber Masmoudi, et al. · Nature Genetics · 86
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23–24.2
1999 · Mounira Hmani, Abdelmonem Ghorbel, et al. · European Journal of Human Genetics · 85
Pendred syndrome: Phenotypic variability in two families carrying the same PDS missense mutation
2000 · Saber Masmoudi, Ilhem Charfedine, et al. · American Journal of Medical Genetics · 76
Molecular identification of Helicobacter DNA present in human colorectal adenocarcinomas by 16S rDNA PCR amplification and pyrosequencing analysis
2005 · Niclas Grahn, Mounira Hmani-Aifa, et al. · Journal of Medical Microbiology · 70
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family
2008 · Mounira Hmani-Aifa, Zeineb Benzina, et al. · European Journal of Human Genetics · 62
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High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects
2010 · Mariem Ben Saïd, Mounira Hmani-Aifa, et al. · Genetic Testing and Molecular Biomarkers · 46
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
2016 · Mariem Ben Said, M’hamed Grati, et al. · Human Genetics · 40
Screening of the DFNB3 Locus: Identification of Three Novel Mutations of MYO15A Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus
2009 · Hanen Belguith, Mounira Aifa-Hmani, et al. · Genetic Testing and Molecular Biomarkers · 39
A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family
2011 · Mariem Ben Saïd, Leila Ayedi, et al. · European Journal of Medical Genetics · 26
Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene
2013 · Mariem Ben Said, Ebtissem Chouchène, et al. · Gene · 24
Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome
2002 · M Hmani-Aifa, S Ben Arab, et al. · Journal of Medical Genetics · 23
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A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1
2009 · Mounira Hmani-Aifa, Salma Ben Salem, et al. · Human Genetics · 22
Mutations ofGJB2in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates
2000 · Saïda Ben Arab, Mounira Hmani, et al. · Clinical Genetics · 19
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome
2012 · Mariem Ben Said, Houria Dhouib, et al. · International Journal of Pediatric Otorhinolaryngology · 15
Single-isomer R-salbutamol is not superior to racemate regarding protection for bronchial hyperresponsiveness
2004 · Kerstin Naidu Sjöswärd, Mounira Hmani, et al. · Respiratory Medicine · 12
DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss
2011 · Mariem Bensaïd, Mounira Hmani-Aifa, et al. · European Journal of Medical Genetics · 9
Autosomal recessive congenital hereditary corneal dystrophy associated with a novel SLC4A11 mutation in two consanguineous Tunisian families
2021 · Zohra Chibani, Imen Zone Abid, et al. · British Journal of Ophthalmology · 5
Novel BEST1 gene mutations associated with two different forms of macular dystrophy in Tunisian families
2019 · Zohra Chibani, Imen Zone Abid, et al. · Clinical and Experimental Ophthalmology · 5
Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21
2012 · Mohamed Ali Mosrati, Isabelle Schrauwen, et al. · Journal of Human Genetics · 5
Mutations of GJB2 in three geographic isolates from northern Tunisia
2000 · Hammadi Ayadi, Amel Gaied, et al.
Works count: 24
Citation count: 1,007
H-index: 15
I10-index: 17
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