Celia Zazo Seco

The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands

Celia Zazo Seco, Mieke Wesdorp, Ilse Feenstra et al. · European Journal of Human Genetics · 2016 · 148 citations · Full text

Medicine, Genetics, Molecular Genetics +14

A Mutation in CABP2 , Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment

Isabelle Schrauwen, Sarah Helfmann, Akira Inagaki et al. · The American Journal of Human Genetics · 2012 · 135 citations · Full text

Health Professions, Genetics, Molecular Genetics +14

Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

Kemal O. Yariz, Duygu Duman, Celia Zazo Seco et al. · The American Journal of Human Genetics · 2012 · 131 citations · Full text

Medicine, Genetics, Molecular Genetics +9

Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

Margit Schraders, Laura Ruiz-Palmero, Ersan Kalay et al. · The American Journal of Human Genetics · 2012 · 93 citations · Full text

Medicine, Genetics, Molecular Genetics +11

Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2

Celia Zazo Seco, Luciana Serrão de Castro, Josephine W. van Nierop et al. · The American Journal of Human Genetics · 2015 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13