Carles Vilariño-Güell - Dissemin

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All papers authored by Carles Vilariño-Güell

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2019 Yan Yun, Yun Zhang, Chen Zhang, Liyan Huang, Shichuan Tan, Pin Wang, Carles Vilariño-Gúell

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, Xiulian Sun

Regulator of calcineurin 1 is a novel RNA-binding protein to regulate neuronal apoptosis

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2017 Cecily Q. Bernales, Mary Encarnacion, Maria G. Criscuoli, Irene M. Yee, Anthony L. Traboulsee, A. Dessa Sadovnick, Carles Vilariño-Güell

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Analysis of NOD-like receptor NLRP1 in multiple sclerosis families

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A. Dessa Sadovnick, Anthony L. Traboulsee, Yinshan Zhao, Cecily Q. Bernales, Mary Encarnacion, Jay P. Ross, Irene M. Yee, Maria G. Criscuoli, Carles Vilariño-Güell

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Genetic modifiers of multiple sclerosis progression, severity and onset

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Andreas Puschmann, Fabienne C. Fiesel, Thomas R. Caulfield, Roman Hudec, Maya Ando, Dominika Truban, Xu Hou, Kotaro Ogaki, Michael G. Heckman, Elle D. James, Maria Swanberg, Itzia Jimenez-Ferrer, Oskar Hansson, Grzegorz Opala, Joanna Siuda and 18 other authors

Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder

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Anthony L. Traboulsee, A. Dessa Sadovnick, Mary Encarnacion, Cecily Q. Bernales, Irene M. Yee, Maria G. Criscuoli, Carles Vilariño-Güell

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Common genetic etiology between “multiple sclerosis-like” single-gene disorders and familial multiple sclerosis

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Gabrielle Houle, Jean-François Schmouth, Claire S. Leblond, Amirthagowri Ambalavanan, Dan Spiegelman, Sandra B. Laurent, Cynthia V. Bourassa, Michel Panisset, Sylvain Chouinard, Nicolas Dupré, Carles Vilariño-Güell

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, Alex Rajput, Patrick A. Dion, Guy A. Rouleau

Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population: TENM4and Essential Tremor

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2016 Andreas Puschmann, Fabienne C. Fiesel, Thomas R. Caulfield, Roman Hudec, Maya Ando, Dominika Truban, Xu Hou, Kotaro Ogaki, Michael G. Heckman, Elle D. James, Maria Swanberg, Itzia Jimenez-Ferrer, Oskar Hansson, Grzegorz Opala, Joanna Siuda and 17 other authors

Heterozygous PINK1 p.G411S increases risk of Parkinson’s disease via a dominant-negative mechanism

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Joanne Trinh, Emil K. Gustavsson, Carles Vilariño-Güell

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, Stephanie Bortnick, Jeanne Latourelle, Marna B. McKenzie, Chelsea Szu Tu, Ekaterina Nosova, Jaskaran Khinda, Austen Milnerwood, Suzanne Lesage, Alexis Brice, Meriem Tazir, Jan O. Aasly, Laura Parkkinen and 10 other authors

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study

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Zhe Wang, A. Dessa Sadovnick, Anthony L. Traboulsee, Jay P. Ross, Cecily Q. Bernales, Mary Encarnacion, Irene M. Yee, Madonna de Lemos, Talitha Greenwood, Joshua D. Lee, Galen Wright, Colin J. Ross, Si Zhang, Weihong Song

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, Carles Vilariño-Güell

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Case-Control Studies Are Not Familial Studies

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Zhe Wang, A. Dessa Sadovnick, Anthony L. Traboulsee, Jay P. Ross, Cecily Q. Bernales, Mary Encarnacion, Irene M. Yee, Madonna de Lemos, Talitha Greenwood, Joshua D. Lee, Galen Wright, Colin J. Ross, Si Zhang, Weihong Song

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, Carles Vilariño-Güell

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Nuclear receptor NR1H3 in familial multiple sclerosis

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Amanda L. Forwell, Cecily Q. Bernales, Jay P. Ross, Irene M. Yee, Mary Encarnacion, Joshua D. Lee, A. Dessa Sadovnick, Anthony L. Traboulsee, Carles Vilariño-Güell

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Analysis of CH25H in multiple sclerosis and neuromyelitis optica

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2015 O. Lorenzo Betancor, K. Ogaki, A. I. Soto Ortolaza, C. Labbe, R. L. Walton, A. J. Strongosky, J. A. van Gerpen, R. J. Uitti, P. J. McLean, W. Springer, J. Siuda, G. Opala, A. Krygowska Wajs, M. Barcikowska, K. Czyzewski and 15 other authors

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients

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Joanne Trinh, Carles Vilarino-Guell

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, Owen A. Ross

A commentary on fine mapping and resequencing of the PARK16 locus in Parkinson’s disease

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Joshua D. Lee, Colleen Guimond, Irene M. Yee, Carles Vilariño-Güell

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, Zhi-Ying Wu, Anthony L. Traboulsee, A. Dessa Sadovnick

Incidence of Multiple Sclerosis and Related Disorders in Asian Populations of British Columbia

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2014 Emil K. Gustavsson, Joanne Trinh, Ilaria Guella, Carles Vilariño-Güell

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, Silke Appel-Cresswell, A. Jon Stoessl, Joseph K. Tsui, Martin McKeown, Alex Rajput, Ali H. Rajput, Jan O. Aasly, Matthew J. Farrer

DNAJC13genetic variants in parkinsonism: DNAJC13Genetic Variants in Parkinsonism

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Oswaldo Lorenzo-Betancor, Kotaro Ogaki, Alexandra Soto-Ortolaza, Catherine Labbé, Carles Vilariño-Güell

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, Alex Rajput, Ali H. Rajput, Pau Pastor, Sara Ortega, Elena Lorenzo, Audrey J. Strongosky, Jay A. van Gerpen, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross

Analysis of Nuclear Export Sequence Regions of FUS-Related RNA-Binding Proteins in Essential Tremor

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J. Trinh, E. K. Gustavsson, I. Guella, C. Vilariño-Güell

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, D. Evans, M. Encarnacion, H. Sherman, F. Hentati, M. J. Farrer

The role ofSNCAandMAPTin Parkinson disease andLRRK2parkinsonism in the Tunisian Arab-Berber population

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Silke Appel-Cresswell, Ali H. Rajput, Vesna Sossi, Christina Thompson, Vanessa Silva, Jessamyn McKenzie, Katherine Dinelle, Siobhan E. McCormick, Carles Vilariño-Güell

ORCID

, A. Jon Stoessl, Dennis W. Dickson, Chris A. Robinson, Matthew J. Farrer, Alex Rajput

Clinical, positron emission tomography, and pathological studies of DNAJC13 p.N855S Parkinsonism: Studies of DNAJC13 p.N855S Parkinsonism

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Alex Rajput, Jay P. Ross, Cecily Q. Bernales, Sruti Rayaprolu, Alexandra I. Soto-Ortolaza, Owen A. Ross, Jay van Gerpen, Ryan J. Uitti, Zbigniew K. Wszolek, Ali H. Rajput, Carles Vilariño-Güell

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VPS35 and DNAJC13 disease-causing variants in essential tremor

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Kenya Nishioka, Manabu Funayama, Carles Vilariño-Güell

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, Kotaro Ogaki, Yuanzhe Li, Ryogen Sasaki, Yasumasa Kokubo, Shigeki Kuzuhara, Jennifer M. Kachergus, Stephanie A. Cobb, Hirohide Takahashi, Yoshikuni Mizuno, Matthew J. Farrer, Owen A. Ross, Nobutaka Hattori

EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population

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