Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene
Nele Hilgert(University of Antwerp), Karianne Hostmark(Bispebjerg Hospital), Helena Caria(University of Lisbon), Arti Pandya(Virginia Commonwealth University), Petr Janoušek(Charles University), Agata Skórka(Medical University of Warsaw), Anne‐Françoise Roux(Université de Montpellier), Graça Fialho(University of Lisbon), Elena Mennucci(University of Ferrara), Pierangela Castorina, Paul Govaerts, Erik Fransén(University of Antwerp), Paul Van de Heyning(University of Antwerp), Vasiliki Iliadou(Aristotle University of Thessaloniki), Doris Nekahm-Heis, Guenaëlle Lancelot(Hôpital Pellegrin), Sandrine Marlin(Hôpital Necker-Enfants Malades), Jerzy Bal, Matthew J. Huentelman(Translational Genomics Research Institute), Rafał Płoski(Medical University of Warsaw), Ewa Nowakowska(Institute of Physiology and Pathology of Hearing), Alessandro Martini(University of Padua), Ashley Q. Thorburn(Translational Genomics Research Institute), Eva Orzan(IRCCS Materno Infantile Burlo Garofolo), Tímea Tóth, Cyril Goizet(Centre National de la Recherche Scientifique), Armağan İncesulu, Andreas Janecke(Innsbruck Medical University), Karen Grønskov(University of Copenhagen), Ignacio del Castillo, Agnieszka Pollak(Institute of Physiology and Pathology of Hearing), Mustafa Tekin(University of Miami), Kathleen S. Arnos(Gallaudet University), Alessandra Murgia, Paola Primignani(Ospedale Maggiore), Françoise Denoyelle(Hôpital Necker-Enfants Malades), Catherine Blanchet, Umberto Ambrosetti, Xue Zhong Liu(University of Miami), Pavel Seeman, Delphine Feldmann(Hôpital Armand-Trousseau), Felipe Moreno, Carla Nishimura(University of Iowa), Virginia W. Norris(Gallaudet University), J Waligora, Małgorzata Mueller‐Malesińska, Michael B. Petersen(Aalborg University Hospital), István Sziklai(Semmelweis University), Nele Dieltjens(University of Antwerp)
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