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Author/Creator Landers, John E

1. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories. Issue 6 (4th April 2014)

Authors:
Akimoto, Chizuru; Volk, Alexander E; van Blitterswijk, Marka; Van den Broeck, Marleen; Leblond, Claire S; Lumbroso, Serge; Camu, William; Neitzel, Birgit; Onodera, Osamu; van Rheenen, Wouter; Pinto, Susana; Weber, Markus; Smith, Bradley; Proven, Melanie; Talbot, Kevin; Keagle, Pamela; Chesi, Ales...
Journal:
Journal of medical genetics
Issue:
Volume 51:Issue 6(2014)
Page Start:
419
Record Type:
Journal Article
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2. ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization. Issue 2 (19th May 2020)

Authors:
Tazelaar, Gijs H P; Boeynaems, Steven; De Decker, Mathias; van Vugt, Joke J F A; Kool, Lindy; Goedee, H Stephan; McLaughlin, Russell L; Sproviero, William; Iacoangeli, Alfredo; Moisse, Matthieu; Jacquemyn, Maarten; Daelemans, Dirk; Dekker, Annelot M; van der Spek, Rick A; Westeneng, Henk-Jan; Ken...
Journal:
Brain communications
Issue:
Volume 2:Issue 2(2020)
Page Start:
Record Type:
Journal Article
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3. Quantitative proteomics identifies proteins that resist translational repression and become dysregulated in ALS-FUS. (26th February 2019)

Authors:
Baron, Desiree M; Matheny, Tyler; Lin, Yen-Chen; Leszyk, John D; Kenna, Kevin; Gall, Katherine V; Santos, David P; Tischbein, Maeve; Funes, Salome; Hayward, Lawrence J; Kiskinis, Evangelos; Landers, John E; Parker, Roy; Shaffer, Scott A; Bosco, Daryl A
Journal:
Human molecular genetics
Issue:
Volume 28:Number 13(2019)
Page Start:
2143
Record Type:
Journal Article
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4. Rare variants in MYH15 modify amyotrophic lateral sclerosis risk. (1st April 2019)

Authors:
Kim, Hyerim; Lim, Junghwa; Bao, Han; Jiao, Bin; Canon, Se Min; Epstein, Michael P; Xu, Keqin; Jiang, Jie; Parameswaran, Janani; Li, Yingjie; Moberg, Kenneth H; Landers, John E; Fournier, Christina; Allen, Emily G; Glass, Jonathan D; Wingo, Thomas S; Jin, Peng
Journal:
Human molecular genetics
Issue:
Volume 28:Number 14(2019)
Page Start:
2309
Record Type:
Journal Article
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