Publications by authors named "Manou Sommen"

11Publications

Insufficient evidence for a role of SERPINF1 in otosclerosis.

Mol Genet Genomics 2019 Aug 9;294(4):1001-1006. Epub 2019 Apr 9.

Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Universiteitsplein 1, Wilrijk, 2610, Antwerp, Belgium.

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August 2019

Unique autosomal recessive variant of palmoplantar keratoderma associated with hearing loss not caused by known mutations.

An Bras Dermatol 2017 ;92(5 Suppl 1):154-158

Department of Medical Genetics, University of Antwerp, Universiteitsplein - Antwerp, Belgium.

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March 2018

Molecular diagnostics for hereditary hearing loss in children.

Expert Rev Mol Diagn 2017 08 19;17(8):751-760. Epub 2017 Jun 19.

a Center of Medical Genetics , University of Antwerp & Antwerp University Hospital , Antwerp , Belgium.

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August 2017

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.

Otol Neurotol 2014 Jul;35(6):1058-64

*University of Antwerp, Department of Medical Genetics, Antwerp, Belgium; †Bajcsy-Zsilinszky Hospital, ENT Department, Budapest; and ‡University of Debrecen, Medical and Health Science Center, Department of Otolaryngology and Head and Neck Surgery, Debrecen, Hungary.

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July 2014