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Identified 4

TITLE: Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)
AUTHORS: Wouter van Rheenen; Rick A A van der Spek; Mark K Bakker; Joke J F A van Vugt; Paul J Hop; Ramona A J Zwamborn; Niek de Klein; Harm Jan Westra; Olivier B Bakker; Patrick Deelen; Gemma Shireby; Eilis Hannon; Matthieu Moisse; Denis Baird; Restuadi Restuadi; Egor Dolzhenko; Annelot M Dekker; Klara Gawor; Henk Jan Westeneng; Gijs H P Tazelaar; Kristel R van Eijk; Maarten Kooyman; Ross P Byrne; Mark Doherty; Mark Heverin; Ahmad Al Khleifat; Alfredo Iacoangeli; Aleksey Shatunov; Nicola Ticozzi; Johnathan Cooper Knock; Bradley N Smith; Marta Gromicho; Siddharthan Chandran; Suvankar Pal; Karen E Morrison; Pamela J Shaw; John Hardy; Richard W Orrell; Michael Sendtner; Thomas Meyer; Nazli Başak; Anneke J van der Kooi; Antonia Ratti; Isabella Fogh; Cinzia Gellera; Giuseppe Lauria; Stefania Corti; Cristina Cereda; Daisy Sproviero; Sandra D’Alfonso; Gianni Sorarù; Gabriele Siciliano; Massimiliano Filosto; Alessandro Padovani; Adriano Chiò; Andrea Calvo; Cristina Moglia; Maura Brunetti; Antonio Canosa; Maurizio Grassano; Ettore Beghi; Elisabetta Pupillo; Giancarlo Logroscino; Beatrice Nefussy; Alma Osmanovic; Angelica Nordin; Yossef Lerner; Michal Zabari; Marc Gotkine; Robert H Baloh; Shaughn Bell; Patrick Vourc’h; Philippe Corcia; Philippe Couratier; Stéphanie Millecamps; Vincent Meininger; François Salachas; Jesus S Mora Pardina; Abdelilah Assialioui; Ricardo Rojas García; Patrick A Dion; Jay P Ross; Albert C Ludolph; Jochen H Weishaupt; David Brenner; Axel Freischmidt; Gilbert Bensimon; Alexis Brice; Alexandra Durr; Christine A M Payan; Safa Saker Delye; Nicholas W Wood; Simon Topp; Rosa Rademakers; Lukas Tittmann; Wolfgang Lieb; Andre Franke; Stephan Ripke; Alice Braun; Julia Kraft; ...More
PUBLISHED: 2022, SOURCE: Nature Genetics

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TITLE: Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis Full Text
AUTHORS: Tazelaar, Gijs H. P.; Hop, Paul J.; Seelen, Meinie; van Vugt, Joke J. F. A.; van Rheenen, Wouter; Kool, Lindy; van Eijk, Kristel R.; Gijzen, Marleen; Dooijes, Dennis; Moisse, Matthieu; Calvo, Andrea; Moglia, Cristina; Brunetti, Maura; Canosa, Antonio; Nordin, Angelica; Pardina, Jesus S. Mora; Ravits, John; Al Chalabi, Ammar; Chio, Adriano; McLaughlin, Russell L.; Hardiman, Orla; Van Damme, Philip; de Carvalho, Mamede; Neuwirth, Christoph; Weber, Markus; Andersen, Peter M.; van den Berg, Leonard H.; Veldink, Jan H.; van Es, Michael A.; ...More
PUBLISHED: 2022, SOURCE: NEUROBIOLOGY OF AGING, VOLUME: 122

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