Shzeena Dad

An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients

Crystel Bonnet, Zied Riahi, Sandra Chantot‐Bastaraud et al. · European Journal of Human Genetics · 2016 · 111 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin

Peter Huppke, Cornelia Brendel, Vera M. Kalscheuer et al. · The American Journal of Human Genetics · 2012 · 105 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Usher syndrome in Denmark: mutation spectrum and some clinical observations

Shzeena Dad, Nanna Dahl Rendtorff, Lisbeth Tranebjærg et al. · Molecular Genetics & Genomic Medicine · 2016 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Partial USH2A deletions contribute to Usher syndrome in Denmark

Shzeena Dad, Nanna Dahl Rendtorff, Erik Kann et al. · European Journal of Human Genetics · 2015 · 11 citations · Full text

Life Sciences, Genetics, Molecular Medicine +5