Moien Kanaan

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott et al. · The American Journal of Human Genetics · 2019 · 303 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82

Tom Walsh, Hashem Shahin, T. Elkan Miller et al. · The American Journal of Human Genetics · 2010 · 288 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

Tom Walsh, Vanessa Walsh, Sarah Vreugde et al. · Proceedings of the National Academy of Sciences · 2002 · 262 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

Zippora Brownstein, Lilach M. Friedman, Hashem Shahin et al. · Genome biology · 2011 · 201 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici et al. · Proceedings of the National Academy of Sciences · 2002 · 182 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +12