Table of contents

New loci

• Original article: Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways (14 April, 2011) Free

  Giorgia Girotto, Nicola Pirastu, Rossella Sorice, Ginevra Biino, Harry Campbell, Adamo P d'Adamo, Nicholas D Hastie, Teresa Nutile, Ozren Polasek, Laura Portas, Igor Rudan, Sheila Ulivi, Tatijana Zemunik, Alan F Wright, Marina Ciullo, Caroline Hayward, Mario Pirastu, Paolo Gasparini
• Original article:

  Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1

  (20 April, 2011)

  Anne M Slavotinek, Sergio E Baranzini, Denny Schanze, Cassandre Labelle-Dumais, Kieran M Short, Ryan Chao, Mani Yahyavi, Emilia K Bijlsma, Catherine Chu, Stacey Musone, Ashleigh Wheatley, Pui-Yan Kwok, Sandra Marles, Jean-Pierre Fryns, A Murat Maga, Mohamed G Hassan, Douglas B Gould, Lohith Madireddy, Chumei Li, Timothy C Cox, Ian Smyth, Albert E Chudley, Martin Zenker
• Original article:

  Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN

  (14 April, 2011)

  Gal Maydan, Iris Noyman, Adi Har-Zahav, Ziva Ben Neriah, Metsada Pasmanik-Chor, Adva Yeheskel, Adi Albin-Kaplanski, Idit Maya, Nurit Magal, Efrat Birk, Amos J Simon, Ayelet Halevy, Gideon Rechavi, Mordechai Shohat, Rachel Straussberg, Lina Basel-Vanagaite
• Communications:

  C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome

  (4 March, 2011)

  Heleen H Arts, Ernie M H F Bongers, Dorus A Mans, Sylvia E C van Beersum, Machteld M Oud, Emine Bolat, Liesbeth Spruijt, Elisabeth A M Cornelissen, Janneke H M Schuurs-Hoeijmakers, Nicole de Leeuw, Valérie Cormier-Daire, Han G Brunner, Nine V A M Knoers, Ronald Roepman