Mohamed Ali Mosrati

<i>TERT</i> promoter mutations and polymorphisms as prognostic factors in primary glioblastoma

Mohamed Ali Mosrati, Annika Malmström, A. Krysztofiak et al. · Oncotarget · 2015 · 123 citations · Full text

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

Association between TERT promoter polymorphisms and acute myeloid leukemia risk and prognosis

Mohamed Ali Mosrati, Kerstin Willander, Ingrid Jakobsen Falk et al. · Oncotarget · 2015 · 52 citations · Full text

Screening of the <i>DFNB3</i> Locus: Identification of Three Novel Mutations of <i>MYO15A</i> Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus

Hanen Belguith, Mounira Hmani‐Aifa, Houria Dhouib et al. · Genetic Testing and Molecular Biomarkers · 2009 · 40 citations

Genetics, Pathology, Molecular Genetics +19

A novel dominant mutation in SIX1, affecting a highly conserved residue, result in only auditory defects in humans

Mohamed Ali Mosrati, B. Hammami, Imen Ben Rebeh et al. · European Journal of Medical Genetics · 2011 · 32 citations

Biology, Developmental Anomaly, Genetic Disorder +14