Jacques Loiselet
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Inflammasome and immune disorders, Immune Cell Function and Interaction, interferon and immune responses, Neonatal Health and Biochemistry
Most-Cited Works
- → Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene(1997)636 cited
- → Haplotype Diversity and Linkage Disequilibrium at Human G6PD : Recent Origin of Alleles That Confer Malarial Resistance(2001)629 cited
- → A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness(1999)579 cited
- → Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A(1999)275 cited
- → Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22(2002)182 cited
- → Evidence for Balancing Selection from Nucleotide Sequence Analyses of Human G6PD(2002)160 cited
- → Diabetes Mellitus and Optic Atrophy: A Study of Wolfram Syndrome in the Lebanese Population(2004)138 cited
- Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.(1997)
- → X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3(2000)115 cited
- → Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to 19q13.1-13.3 in a Large Consanguineous Lebanese Family: Exclusion of MAG as a Candidate Gene(2000)87 cited