Manou Sommen
University of Antwerp(BE)Antwerp University Hospital(BE)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Ear Surgery and Otitis Media, Hearing Loss and Rehabilitation, Vestibular and auditory disorders, Connexins and lens biology
Most-Cited Works
- → A Mutation in CABP2 , Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment(2012)134 cited
- → Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6(2015)126 cited
- → DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System(2016)108 cited
- → A sensitive and specific diagnostic test for hearing loss using a microdroplet PCR‐based approach and next generation sequencing(2012)72 cited
- → Osmotic stress inhibits leaf growth of Arabidopsis thaliana by enhancing ARF‐mediated auxin responses(2020)65 cited
- → Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome(2013)51 cited
- → Molecular diagnostics for hereditary hearing loss in children(2017)27 cited
- → Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis(2018)23 cited
- → Genetic Association Analysis in a Clinically and Histologically Confirmed Otosclerosis Population Confirms Association With the TGFB1 Gene but Suggests an Association of the RELN Gene With a Clinically Indistinguishable Otosclerosis-Like Phenotype(2014)22 cited
- → Resequencing of candidate genes for Keratoconus reveals a role for Ehlers–Danlos Syndrome genes(2021)20 cited