检索结果 - Raymond D. Schellevis
- Showing 1 - 6 results of 6
-
1
-
2
<scp>C</scp>9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits 由 Max Koppers, Anna M. Blokhuis, Henk‐Jan Westeneng, Margo L. Terpstra, Caroline A. C. Zundel, Renata Vieira de Sá, Raymond D. Schellevis, Adrian J. Waite, Derek J. Blake, Jan H. Veldink, Leonard H. van den Berg, R. Jeroen Pasterkamp
出版 2015Artigo -
3
Detection of long repeat expansions from PCR-free whole-genome sequence data 由 Egor Dolzhenko, Joke J.F.A. van Vugt, Richard J. Shaw, Mitchell A. Bekritsky, Marka van Blitterswijk, Giuseppe Narzisi, Subramanian S. Ajay, Vani Rajan, Bryan R. Lajoie, Nathan Johnson, Zoya Kingsbury, Sean Humphray, Raymond D. Schellevis, William J. Brands, Matt Baker, Rosa Rademakers, Maarten Kooyman, Gijs H.P. Tazelaar, Michael A. van Es, Russell L. McLaughlin, William Sproviero, Aleksey Shatunov, Ashley Jones, Ahmad Al Khleifat, Alan Pittman, Sarah Morgan, Orla Hardiman, Ammar Al‐Chalabi, Christopher E. Shaw, Bradley Smith, Edmund Jin Rui Neo, Karen Morrison, Pamela J. Shaw, Catherine Reeves, Lara Winterkorn, Nancy S. Wexler, David E. Housman, Christopher Ng, Alina L. Li, Ryan J. Taft, Leonard H. van den Berg, David Bentley, Jan H. Veldink, Michael A. Eberle
出版 2017Artigo -
4
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis 由 Wouter van Rheenen, Aleksey Shatunov, Annelot M. Dekker, Russell L. McLaughlin, Frank P. Diekstra, Sara L. Pulit, Rick A. A. van der Spek, Urmo Võsa, Simone de Jong, Matthew R. Robinson, Jian Yang, Isabella Fogh, Perry Tc van Doormaal, Gijs Tazelaar, Max Koppers, Anna M. Blokhuis, William Sproviero, Ashley 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‐Glavač, Blaž Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesús S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen 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, A. Nazlı Başak, Ceren Tunca, Hamid Hamzeiy, Yeşim Parman, Thomas Meitinger, Peter Lichtner, Milena Radivojkov‐Blagojevic, Christian Andrés, Cindy Maurel, Gilbert Bensimon, G. Bernhard Landwehrmeyer, Alexis Brice, Christine Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas Wood, Lukas Tittmann, Wolfgang Lieb, André Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Philippe Amouyel, Christophe Tzourio, Jean‐François Dartigues, André G. Uitterlinden, Fernando Rivadeneira, Karol Estrada, Albert Hofman, Charles Curtis, Hylke M. Blauw, Anneke J. van der Kooi
出版 2016Artigo -
5
Unexpected frequency of the pathogenic <i>AR</i> CAG repeat expansion in the general population 由 Matteo Zanovello, Kristina Ibáñez, Anna‐Leigh Brown, Prasanth Sivakumar, Alessandro Bombaci, Liana Santos, Joke J.F.A. van Vugt, Giuseppe Narzisi, Ramita Karra, Sonja W. Scholz, Jinhui Ding, J. Raphael Gibbs, Adriano Chiò, Clifton L. Dalgard, Ben Weisburd, John C. Ambrose, Prabhu Arumugam, R. Bevers, Marta Bleda, F. Boardman-Pretty, C. R. Boustred, Helen Brittain, Mark J. Caulfield, Georgia C Chan, Greg Elgar, Tom Fowler, Adam Giess, Angela Hamblin, Shirley Henderson, Tim Hubbard, Robert B. Jackson, J. Louise Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, Sarah E A Leigh, Ivonne U S Leong, Javier F Lopez, F. Maleady-Crowe, Meriel McEntagart, Federico Minneci, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Chris A Odhams, Christine Patch, Mariana Buongermino Pereira, D. Perez-Gil, J. Pullinger, T. Rahim, Augusto Rendon, Tim Rogers, K. Savage, Kushmita Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, Samuel C. Smith, Alona Sosinsky, Alexander Stuckey, M. Tanguy, Ana Lisa Taylor Tavares, Ellen Thomas, Simon R. Thompson, Arianna Tucci, Matthew J Welland, Eleanor Williams, Katarzyna Witkowska, Suzanne M Wood, Wouter van Rheenen, Sara L. Pulit, Annelot M. Dekker, Ahmad Al Khleifat, William J Brands, Alfredo Iacoangeli, Kevin P. Kenna, Erşen Kavak, Maarten Kooyman, Russell L. McLaughlin, Bas Middelkoop, Matthieu Moisse, Raymond D. Schellevis, Aleksey Shatunov, William Sproviero, Gijs H.P. Tazelaar, Rick A A Van der Spek, Perry T C Van Doormaal, Kristel R. van Eijk, Joke J.F.A. van Vugt, A Nazli Basak, Ian P. Blair, Jonathan D. Glass, Orla Hardiman, Yoshihide Hayashizaki, John E. Landers, Jesús S. Mora, Karen Morrison
出版 2023Artigo -
6
<i>ATXN1</i> repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization 由 Gijs H P Tazelaar, Steven Boeynaems, Mathias De Decker, Joke J.F.A. van Vugt, Lindy Kool, H. Stephan Goedee, Russell L. McLaughlin, William Sproviero, Alfredo Iacoangeli, Matthieu Moisse, Maarten Jacquemyn, Dirk Daelemans, Annelot M Dekker, Rick A van der Spek, Henk‐Jan Westeneng, Kevin P. Kenna, Abdelilah Assialioui, Nica Da Silva, Fulya Akçimen, Ahmad Al Khleifat, Ammar Al‐Chalabi, Peter Andersen, A Nazli Basak, Denis C. Bauer, Ian P. Blair, William J Brands, Ross P. Byrne, Andrea Calvo, Yolanda Campos, Adriano Chiò, Jonothan Cooper-Knock, Philippe Corcia, Philippe Couratier, Mamede de Carvalho, Annelot M Dekker, Vivian E. Drory, Chen Eitan, Alberto García‐Redondo, Cinzia Gellera, Jonathan D. Glass, Marc Gotkine, Orla Hardiman, Eran Hornstein, Alfredo Iacoangeli, Kevin P. Kenna, Brandon Kenna, Matthew C Kiernan, Cemile Kocoglu, Maarten Kooyman, John E Landers, Victoria López-Alonso, Russell L. McLaughlin, Bas Middelkoop, Jonathan Mill, Miguel Mitne‐Neto, Matthieu Moisse, Jesus S Mora Pardina, Karen Morrison, Susana Pinto, Marta Gromicho, Mónica Povedano Panadés, Sara L. Pulit, Antonia Ratti, Wim Robberecht, Raymond D. Schellevis, Aleksey Shatunov, Christopher E. Shaw, Pamela J. Shaw, Vincenzo Silani, William Sproviero, Christine Staiger, Gijs H P Tazelaar, Nicola Ticozzi, Ceren Tunca, Nathalie A Twine, Philip Van Damme, Leonard H van den Berg, Rick A van der Spek, Perry T.C. van Doormaal, Kristel R. van Eijk, Michael A van Es, Wouter van Rheenen, Joke J.F.A. van Vugt, Jan H. Veldink, Peter M. Visscher, Patrick Vourc’h, Markus Weber, Kelly L. Williams, Naomi R. Wray, Jian Yang, Mayana Zatz, Katharine Zhang, Mónica Povedano, Jesus S Mora Pardina, Orla Hardiman, François Salachas, Stéphanie Millecamps, Patrick Vourc’h, Philippe Corcia, Philippe Couratier
出版 2020Artigo
相关主题
Biology
Gene
Genetics
Medicine
Disease
Internal medicine
Amyotrophic lateral sclerosis
Neuroscience
Allele
Locus (genetics)
Phenotype
Trinucleotide repeat expansion
Allele frequency
Bacterial circadian rhythms
C9orf72
Cell biology
Circadian clock
Circadian rhythm
Computational biology
Computer science
Conditional gene knockout
Confidence interval
Dementia
Environmental health
Expression quantitative trait loci
FOXO3
Fragile X syndrome
Frontotemporal dementia
Genetic architecture
Genetic association