Author Correction: EMPReSS: standardized phenotype screens for functional annotation of the mouse genome
Year: 2022
Type: erratum
Source: Nature Genetics
Authors: Marc Janier, Mohammed Almadjub, Olivier Beuf, Claire Billotey, Radu Bolbos, Laurence Canaple, Emmanuel Chereul, Denis Grenier, Bassem Hiba, Christophe Odet, Jean-Baptiste Langlois, Carole Lartizien, Luc Magnier, Wilfried Ma, Tarik Zouagui, Mark Lathrop, Ivo Gut, Anne Puech, Yann Hérault, Véronique Blanquet, Veronique Brault, Jacques Samarut, Denise Aubert, Michela Plateroti, Nadia Rosenthal, Mumna Al Banchaabouchi, Janice Carter, Olga Ermakova, Karin Gale, Jose Gonzalez, Emerald Perlas, Jeanette Rientjes, Annett Spanner, Anne-Cecile Trillat, Glauco Tocchini-Valentini, Silvia Mandillo, Elisabetta Golini, Daniela Marazziti, Giancarlo Deidda, Nicoletta Rossi, Rafaele Matteoni, Marcello Raspa, Ferdinando Scavizzi, Mariano Barbacid, Marivi Victoria Campuzano, Pierre Dubus, Lucía Perez Gallego, Carmen Guerra González, Rudi Balling, Ursula Frischmann, Hansjörg Hauser, Andreas Lengeling, Werner Müller, Bastian Pasche, Martin Hrabé de Angelis, Wolfgang Wurst, Koichiro Abe, Johannes Beckers, Dirk H. Busch, Claudia Dalke, Valerie Gailus Durner, Ralf Elvert, Tobias J. Franz, Helmut Fuchs, Jochen Graw, Sabine M. Hölter, Thilo Jakob, Svetoslav Kalaydjiev, Magdalena Kallnik, Martina Klempt, Martin Klingenspor, Thomas Klopstock, Christoph Lengger, Leticia Quintanilla Martinez, Vera Pedersen, Oliver Puk, Ilka Schneider, Daniela Vogt Weisenhorn, Sabine Wagner, Eckhard Wolf, Pierre Chambon, Johan Auwerx, Dalila Ali-Hadji, Marie-France Champy, Nelly Frossard, Jean-Jacques Helwig, Manuel Mark, Laurent Monassier, Maria Cristina Antal, Mariette Barthelmebs, Agnes Bloch-Zupan, Andre Constantinesco, Pascal Doll, Lahcen El Fertak, Françoise Gofflot, Laurent Juillard, Wojciech Krezel, Hamid Meziane, Abdel-Mouttalib Ouagazzal, Françoise Pons, Raymond Romand, Mohammed Selloum, Tania Sorg, Marius Teletin, Laurent Vasseur, Olivia Wendling, Philip Avner, Sophie Chantalat, Urban Lendahl, Johannes Wilbertz, Kay Davies, Peter Oliver, Michael Cheeseman, Emma Coghill, Roger Cox, Liz Bentley, Simon Ferguson, Hilary Gates, Georgios Gkoutos, Eain Green, John Hancock, Tertius Hough, Robert Johnson, Heena Lad, Ann-Marie Mallon, Pat Nolan, Andy Parker, Julie Quarterman, Adrian Smith, Mandy Studley, Aadya Shukla, Hilda Tateossian, Valter Tucci, Joseph Weekes, Ian Jackson, Sally Cross, Duncan Davidson, Alan Hart, Angus Murray, Anton Berns, Marco Breuer, Evert van Garderen, Jos Jonkers, Ji Ying Song, Martin van der Valk, Ludwig Neyses, Elizabeth Cartwright, Delvac Oceandy, Michael Emerson, Walter Wahli, Maria Belen Delgado, Batrice Desvergne, Liliane Michalik, Elodie Bedu, Denis Duboule, Marie Kmita, Jozsef Zakany, Francois Spitz, Allan Bradley, Madhuri Warren
Institutions: Centre d'Exploration et de Recherche Médicale par Emission de Positons, Centre National de Recherche en Génomique Humaine, Centre National de la Recherche Scientifique, École Normale Supérieure de Lyon, European Molecular Biology Laboratory, University of Cambridge, Addenbrooke's Hospital, Spanish National Cancer Research Centre, Université de Bordeaux, Helmholtz Centre for Infection Research, Technical University of Munich, Philipps University of Marburg, Ludwig-Maximilians-Universität München, LMU Klinikum, Helmholtz Munich, Phénotypage et ingénierie précliniques des systèmes d’organismes modèles, Inserm, Hôpital Edouard Herriot, Institut Pasteur, Karolinska Institutet, University of Oxford, Medical Research Council, Mary Lyon Centre at MRC Harwell, Western General Hospital, MRC Human Genetics Unit, The Netherlands Cancer Institute, De Gezondheidsdienst voor Dieren, Manchester Royal Infirmary, University of Manchester, Imperial College London, University of Lausanne, University of Geneva, Wellcome Sanger Institute
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4213138709