ProfileOfResearchers

Identificadas 26

TÃTULO: Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
AUTORES: Wouter van Rheenen; Aleksey Shatunov; Annelot M Dekker; Russell L McLaughlin; Frank P Diekstra; Sara L Pulit; Rick A A van der Spek; Urmo Vosa; Simone de Jong; Matthew R Robinson; Jian Yang; Isabella Fogh; Perry T C van Doormaal; Gijs H P Tazelaar; Max Koppers; Anna M Blokhuis; William Sproviero; Ashley R Jones; Kevin P Kenna; Kristel R van Eijk; Oliver Harschnitz; Raymond D Schellevis; William J Brands; Jelena Medic; Androniki Menelaou; Alice Vajda; Nicola Ticozzi; Kuang Lin; Boris Rogelj; Katarina Vrabec; Metka Ravnik Glavac; Blazi Koritnik; Janez Zidar; Lea Leonardis; Leja Dolenc Groselj; Stephanie Millecamps; Francois Salachas; Vincent Meininger; Mamede de Carvalho; Susana Pinto; Jesus S Mora; Ricardo Rojas Garcia; Meraida Polak; Siddharthan Chandran; Shuna Colville; Robert Swingler; Karen E Morrison; Pamela J Shaw; John Hardy; Richard W Orrell; Alan Pittman; Katie Sidle; Pietro Fratta; Andrea Malaspina; Simon Topp; Susanne Petri; Susanne Abdulla; Carsten Drepper; Michael Sendtner; Thomas Meyer; Roel A Ophoff; Kim A Staats; Martina Wiedau Pazos; Catherine Lomen Hoerth; Vivianna M Van Deerlin; John Q Trojanowski; Lauren Elman; Leo McCluskey; Nazli N Basak; Ceren Tunca; Hamid Hamzeiy; Yesim Parman; Thomas Meitinger; Peter Lichtner; Milena Radivojkov Blagojevic; Christian R Andres; Cindy Maurel; Gilbert Bensimon; Bernhard Landwehrmeyer; Alexis Brice; Christine A M Payan; Safaa Saker Delye; Alexandra Duerr; Nicholas W Wood; Lukas Tittmann; Wolfgang Lieb; Andre Franke; Marcella Rietschel; Sven Cichon; Markus M Noethen; Philippe Amouyel; Christophe Tzourio; Jean Francois Dartigues; Andre G Uitterlinden; Fernando Rivadeneira; Karol Estrada; Albert Hofman; Charles Curtis; Hylke M Blauw; Anneke J van der Kooi; Marianne de Visser; An Goris; Markus Weber; Christopher E Shaw; Bradley N Smith; Orietta Pansarasa; Cristina Cereda; Roberto Del Bo; Giacomo P Comi; Sandra D'Alfonso; Cinzia Bertolin; Gianni Soraru; Letizia Mazzini; Viviana Pensato; Cinzia Gellera; Cinzia Tiloca; Antonia Ratti; Andrea Calvo; Cristina Moglia; Maura Brunetti; Simona Arcuti; Rosa Capozzo; Chiara Zecca; Christian Lunetta; Silvana Penco; Nilo Riva; Alessandro Padovani; Massimiliano Filosto; Bernard Muller; Robbert Jan Stuit; Ian Blair; Katharine Zhang; Emily P McCann; Jennifer A Fifita; Garth A Nicholson; Dominic B Rowe; Roger Pamphlett; Matthew C Kiernan; Julian Grosskreutz; Otto W Witte; Thomas Ringer; Tino Prell; Beatrice Stubendorff; Ingo Kurth; Christian A Huebner; Nigel N Leigh; Federico Casale; Adrian Chio; Ettore Beghi; Elisabetta Pupillo; Rosanna Tortelli; Giancarlo Logroscino; John Powell; Albert C Ludolph; Jochen H Weishaupt; Wim Robberecht; Philip Van Damme; Lude Franke; Tune H Pers; Robert H Brown; Jonathan D Glass; John E Landers; Orla Hardiman; Peter M Andersen; Philippe Corcia; Patrick Vourc'h; Vincenzo Silani; Naomi R Wray; Peter M Visscher; Paul I W de Bakker; Michael A van Es; Jeroen J Pasterkamp; Cathryn M Lewis; Gerome Breen; Ammar Al Chalabi; Leonard H van den Berg; Jan H Veldink; ...Mais
PUBLICAÇÃO: 2016, FONTE: NATURE GENETICS, VOLUME: 48, NÚMERO: 9

INDEXADO EM:

WOS

CrossRef

NO MEU:

ORCID

TÃTULO: Sequence variations in C9orf72 downstream of the hexanucleotide repeat region and its effect on repeat-primed PCR interpretation: a large multinational screening study
AUTORES: Angelica Nordin; Chizuru Akimoto; Anna Wuolikainen; Helena Alstermark; Karin Forsberg; Peter Baumann; Susana Pinto; Mamede de Carvalho; Annemarie Hübers; Frida Nordin; Albert C Ludolph; Jochen H Weishaupt; Thomas Meyer; Torsten Grehl; Kathi Schweikert; Markus Weber; Christian Burkhardt; Christoph Neuwirth; Trygve Holmøy; Mitsuya Morita; Ole-Bjørn Tysnes; Michael Benatar; Joanne Wuu; Dale J Lange; Carsten Bisgård; Nasrin Asgari; Ilkka Tarvainen; Thomas Brännström; Peter M Andersen; ...Mais
PUBLICAÇÃO: 2016, FONTE: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, VOLUME: 18, NÚMERO: 3-4

INDEXADO EM:

CrossRef: 17

NO MEU:

ORCID