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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 9, 2009
No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch populationIsabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, et al.
Annals of Human Genetics|July 23, 2011
Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian populationAyda Khalfallah, Isabelle Schrauwen, Malek Mnejja, et al.
Molecular Genetics & Genomic Medicine|June 14, 2022
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian familyAbdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, et al.
Human Mutation|April 25, 2019
Heterozygosity mapping for human dominant trait variantsAtsuko Imai-Okazaki, Yi Li, Sukanya Horpaopan, et al.
Genes|October 14, 2020
Splicing Characteristics of Dystrophin Pseudoexons and Identification of a Novel Pathogenic Intronic Variant in the <i>DMD</i> GeneZhiying Xie, Liuqin Tang, Zhihao Xie, et al.
European Journal of Human Genetics : EJHG|February 14, 2023
Rare-variant association analysis reveals known and new age-related hearing loss genesDiana M Cornejo-Sanchez, Guangyou Li, Tabassum Fabiha, et al.
Annals of Human Genetics|July 21, 2010
Genetic variants in RELN are associated with otosclerosis in a non-European population from TunisiaAyda Khalfallah, Isabelle Schrauwen, Malek Mnaja, et al.
Molecular Genetics and Genomics : MGG|April 11, 2019
Insufficient evidence for a role of SERPINF1 in otosclerosisHanne Valgaeren, Manou Sommen, Matthias Beyens, et al.
Human Molecular Genetics|November 10, 2022
Syntaxin 4 is essential for hearing in human and zebrafishIsabelle Schrauwen, Amama Ghaffar, Thashi Bharadwaj, et al.
European Journal of Human Genetics : EJHG|June 19, 2014
Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairmentErik Fransen, Sarah Bonneux, Jason J Corneveaux, et al.
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