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Authors:
van Rheenen, Wouter
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Shatunov, Aleksey
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Yang, Jian
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de Visser, Marianne
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Goris, An
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Weber, Markus
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Shaw, Christopher E
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Smith, Bradley N
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Pansarasa, Orietta
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Cereda, Cristina
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Del Bo, Roberto
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Comi, Giacomo P
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D'Alfonso, Sandra
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Fogh, Isabella
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Bertolin, Cinzia
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Sorarù, Gianni
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Mazzini, Letizia
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Pensato, Viviana
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Gellera, Cinzia
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Tiloca, Cinzia
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Ratti, Antonia
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Calvo, Andrea
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Moglia, Cristina
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Brunetti, Maura
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van Doormaal, Perry T. C
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Arcuti, Simona
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Capozzo, Rosa
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Zecca, Chiara
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Lunetta, Christian
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Penco, Silvana
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Riva, Nilo
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Padovani, Alessandro
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Filosto, Massimiliano
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Muller, Bernard
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Stuit, Robbert Jan
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Tazelaar, Gijs H. P
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Blair, Ian
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Zhang, Katharine
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McCann, Emily P
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Fifita, Jennifer A
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Nicholson, Garth A
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Rowe, Dominic B
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Pamphlett, Roger
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Kiernan, Matthew C
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Grosskreutz, Julian
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Witte, Otto W
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Koppers, Max
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Ringer, Thomas
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Prell, Tino
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Stubendorff, Beatrice
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Kurth, Ingo
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Hübner, Christian A
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Leigh, P. Nigel
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Casale, Federico
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Chio, Adrian
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Beghi, Ettore
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Pupillo, Elisabetta
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Blokhuis, Anna M
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Tortelli, Rosanna
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Logroscino, Giancarlo
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Powell, John
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Ludolph, Albert C
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Weishaupt, Jochen H
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Robberecht, Wim
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Van Damme, Philip
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Franke, Lude
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Pers, Tune H
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Brown, Robert H
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Sproviero, William
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Glass, Jonathan D
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Landers, John E
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Hardiman, Orla
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Andersen, Peter M
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Corcia, Philippe
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Vourc'h, Patrick
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Silani, Vincenzo
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Wray, Naomi R
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Visscher, Peter M
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de Bakker, Paul I. W
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Jones, Ashley R
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van Es, Michael A
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Pasterkamp, R. Jeroen
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Lewis, Cathryn M
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Breen, Gerome
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Al-Chalabi, Ammar
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van den Berg, Leonard H
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Veldink, Jan H
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Kenna, Kevin P
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van Eijk, Kristel R
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Dekker, Annelot M
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Harschnitz, Oliver
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Schellevis, Raymond D
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Brands, William J
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Medic, Jelena
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Menelaou, Androniki
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Vajda, Alice
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Ticozzi, Nicola
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Lin, Kuang
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Rogelj, Boris
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Vrabec, Katarina
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McLaughlin, Russell L
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Ravnik-Glavač, Metka
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Koritnik, Blaž
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Zidar, Janez
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Leonardis, Lea
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Grošelj, Leja Dolenc
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Millecamps, Stéphanie
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Salachas, François
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Meininger, Vincent
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de Carvalho, Mamede
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Pinto, Susana
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Diekstra, Frank P
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Mora, Jesus S
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Rojas-García, Ricardo
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Polak, Meraida
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Chandran, Siddharthan
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Colville, Shuna
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Swingler, Robert
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Morrison, Karen E
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Shaw, Pamela J
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Hardy, John
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Orrell, Richard W
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Pulit, Sara L
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Pittman, Alan
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Sidle, Katie
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Fratta, Pietro
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Malaspina, Andrea
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Topp, Simon
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Petri, Susanne
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Abdulla, Susanne
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Drepper, Carsten
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Sendtner, Michael
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Meyer, Thomas
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van der Spek, Rick A. A
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Ophoff, Roel A
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Staats, Kim A
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Wiedau-Pazos, Martina
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Lomen-Hoerth, Catherine
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Van Deerlin, Vivianna M
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Trojanowski, John Q
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Elman, Lauren
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McCluskey, Leo
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Basak, A. Nazli
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Tunca, Ceren
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Võsa, Urmo
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Hamzeiy, Hamid
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Parman, Yesim
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Meitinger, Thomas
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Lichtner, Peter
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Radivojkov-Blagojevic, Milena
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Andres, Christian R
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Maurel, Cindy
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Bensimon, Gilbert
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Landwehrmeyer, Bernhard
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Brice, Alexis
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de Jong, Simone
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Payan, Christine A. M
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Saker-Delye, Safaa
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Dürr, Alexandra
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Wood, Nicholas W
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Tittmann, Lukas
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Lieb, Wolfgang
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Franke, Andre
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Rietschel, Marcella
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Cichon, Sven
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Nöthen, Markus M
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Robinson, Matthew R
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Amouyel, Philippe
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Tzourio, Christophe
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Dartigues, Jean-François
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Uitterlinden, Andre G
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Rivadeneira, Fernando
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Estrada, Karol
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Hofman, Albert
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Curtis, Charles
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Blauw, Hylke M
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van der Kooi, Anneke J
Date: 2016
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1208872
Description:
To elucidate the genetic architecture of amyotrophic lateral sclerosis (ALS) and find associated loci, we assembled a custom imputation reference panel from whole-genome-sequenced patients with ALS an
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Reviewed:
Authors:
Smith, Bradley N
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Ticozzi, Nicola
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Calini, Daniela
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Vance, Caroline
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Danielson, Eric W
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Troakes, Claire
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Tiloca, Cinzia
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Al-Sarraj, Safa
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Lewis, Elizabeth A
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King, Andrew
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Colombrita, Claudia
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Pensato, Viviana
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Fallini, Claudia
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Castellotti, Barbara
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de Belleroche, Jacqueline
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Baas, Frank
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ten Asbroek, Anneloor L. M. A
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Sapp, Peter C
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McKenna-Yasek, Diane
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McLaughlin, Russell L
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Polak, Meraida
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Asress, Seneshaw
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Esteban-Peréz, Jesús
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Gkazi, Athina Soragia
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Munoz-Blanco, Jose Luis
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Simpson, Michael
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van Rheenen, Wouter
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Diekstra, Frank P
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Lauria, Giuseppe
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Duga, Stefano
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Corti, Stefania
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Cereda, Cristina
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Corrado, Lucia
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Sorarù, Gianni
|
Topp, Simon
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Morrison, Karen E
|
Williams, Kelly L
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Nicholson, Garth A
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Blair, Ian P
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Dion, Patrick A
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Leblond, Claire S
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Rouleau, Guy A
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Hardiman, Orla
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Veldink, Jan H
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van den Berg, Leonard H
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Kenna, Kevin P
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Al-Chalabi, Ammar
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Pall, Hardev
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Shaw, Pamela J
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Turner, Martin R
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Talbot, Kevin
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Taroni, Franco
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Garcia-Redondo, Alberto
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Wu, Zheyang
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Glass, Jonathan D
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Gellera, Cinzia
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Scotter, Emma L
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Ratti, Antonia
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Brown Jr., Robert H
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Silani, Vincenzo
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Shaw, Christopher E
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Landers, John E
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D'Alfonso, Sandra
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Mazzini, Letizia
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Comi, Giacomo P
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Del Bo, Roberto
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Ceroni, Mauro
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Kost, Jason
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Gagliardi, Stella
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Querin, Giorgia
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Bertolin, Cinzia
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Keagle, Pamela
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Miller, Jack W
Date: 2014
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/343716
Description:
Exome sequencing is an effective strategy for identifying human disease genes. However, this methodology is difficult in late-onset diseases where limited availability of DNA from informative family m
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