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Multiple Sclerosis
Multiple sclerosis is one of the most prevalent diseases of the central nervous system, affecting over two million people worldwide. Canada has one of the highest rates of MS in the world with an estimated 75,000 Canadians living with this disease. The economical and personal burden of this disease makes unraveling its causes and the development of knowledge based treatments a high priority.
Familial Genetics
Approximately 10-15% of all patients suffering from multiple sclerosis have a first or second degree relative also diagnosed with the disease. The aggregation of multiple sclerosis within families highlights the existence of a single major genetic component determining the onset of disease in these patients.
Population Analysis
Over 13,000 biological samples from patients and healthy controls have been collected for the identification of genetic risk factors of multiple sclerosis. In contrast to the rare variants of strong effect observed in familial forms, risk variants are common genetic changes that results in a moderate increase to develop disease.
Multiple Sclerosis
Multiple sclerosis is one of the most prevalent diseases of the central nervous system, affecting over two million people worldwide. Canada has one of the highest rates of MS in the world with an estimated 75,000 Canadians living with this disease. The economical and personal burden of this disease makes unraveling its causes and the development of knowledge based treatments a high priority.
Familial Genetics
Approximately 10-15% of all patients suffering from multiple sclerosis have a first or second degree relative also diagnosed with the disease. The aggregation of multiple sclerosis within families highlights the existence of a single major genetic component determining the onset of disease in these patients.
Population Analysis
Over 13,000 biological samples from patients and healthy controls have been collected for the identification of genetic risk factors of multiple sclerosis. In contrast to the rare variants of strong effect observed in familial forms, risk variants are common genetic changes that results in a moderate increase to develop disease.
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论文共 146 篇作者统计合作学者相似作者
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Emil K Gustavsson,Jordan Follett,Joanne Trinh,Sandeep K Barodia,Raquel Real,Zhiyong Liu,Melissa Grant-Peters,Jesse D Fox,Silke Appel-Cresswell,A Jon Stoessl,Alex Rajput,Ali H Rajput,Roland Auer, Russel Tilney,Marc Sturm,Tobias B Haack,Suzanne Lesage,Christelle Tesson,Alexis Brice,Carles Vilariño-Güell,Mina Ryten,Matthew S Goldberg,Andrew B West,Michele T Hu,Huw R Morris,Manu Sharma,Ziv Gan-Or,Bedia Samanci,Pawel Lis, Teresa Tocino,Rim Amouri,Samia Ben Sassi,Faycel Hentati,Global Parkinson’s Genetics Program (GP),Francesca Tonelli,Dario R Alessi,Matthew J Farrer
medRxiv the preprint server for health sciences (2024)
Emil K. Gustavsson,Jordan Follett,Joanne Trinh,Sandeep K. Barodia,Raquel Real,Zhiyong Liu,Melissa Grant-Peters,Jesse D. Fox,Silke Appel-Cresswell,A. Jon Stoessl,Alex Rajput,Ali H. Rajput,Roland Auer, Russel Tilney,Marc Sturm,Tobias B. Haack,Suzanne Lesage,Christelle Tesson,Alexis Brice,Carles Vilarino-Gueell,Mina Ryten,Matthew S. Goldberg,Andrew B. West,Michele T. Hu,Huw R. Morris,Manu Sharma,Ziv Gan-Or,Bedia Samanci,Pawel Lis,Maria Teresa Perinan,Samia Ben Sassi,Faycel Hentati,Francesca Tonelli,Dario R. Alessi,Matthew j Farrer
Alison M Pagalilauan,Elif Everest, Suzanna Rachimi, Daniel Reich,Alex D Waldman,A Dessa Sadovnick,Carles Vilariño-Guell,Michael J Lenardo
medRxiv : the preprint server for health sciences (2024)
Joanne Trinh,Andrew A. Hicks,Inke R. Koenig,Sylvie Delcambre,Theresa Lueth,Susen Schaake,Kobi Wasner,Jenny Ghelfi,Max Borsche,Carles Vilarino-Gueell,Faycel Hentati,Elisabeth L. Germer,Peter Bauer,Masashi Takanashi,Vladimir Kostic,Anthony E. Lang,Norbert Brueggemann,Peter P. Pramstaller,Irene Pichler,Alex Rajput,Nobutaka Hattori,Matthew J. Farrer,Katja Lohmann,Hansi Weissensteiner,Patrick May,Christine Klein,Anne Gruenewald
MULTIPLE SCLEROSIS JOURNAL (2023): 9-9
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Calwing Liao,Charles-Etienne Castonguay,Karl Heilbron,Veikko Vuokila,Miranda Medeiros,Gabrielle Houle,Fulya Akçimen,Jay P. Ross,Hélène Catoire,Mónica Díez-Fairén,Jooeun Kang,Stefanie H. Mueller,Simon Girard,Franziska Hopfner,Delia Lorenz,Lorraine N. Clark,Alexandra I. Soto‐Beasley,Stephan Klebe,Mark Hallett,Zbigniew K. Wszołek,Manuela Pendziwiat,Oswaldo Lorenzo‐Betancor,Klaus Seppi,Daniela Berg,Carles Vilariño‐Güell,Ronald B. Postuma,Geneviève Bernard, Nicolas Dupré,Joseph Jankovic,Claudia Testa,Owen A. Ross,Thomas Arzberger,Sylvain Chouinard,Elan D. Louis,Paola Mandich,Carmine Vitale,Paolo Barone,Elena García‐Martín,Hortensia Alonso‐Navarro,José A. G. Agúndez,Félix Javier Jiménez‐Jiménez,Pau Pástor,Alex Rajput,Günther Deuschl,Gregor Kuhlenbäumer,Inge A. Meijer,Patrick A. Dion,Guy A. Rouleau
JAMA neurologyno. 2 (2022): 185-185
Federica Esposito,Ana Maria Osiceanu,Melissa Sorosina,Linda Ottoboni,Bryan Bollman,Silvia Santoro,Barbara Bettegazzi,Andrea Zauli,Ferdinando Clarelli,Elisabetta Mascia,Andrea Calabria,Daniele Zacchetti,Ruggero Capra,Maurizio Ferrari,Paolo Provero,Dejan Lazarevic,Davide Cittaro,Paola Carrera,Nikolaos Patsopoulos,Daniela Toniolo,A. Dessa Sadovnick,Gianvito Martino,Philip L. De Jager,Giancarlo Comi,Elia Stupka,Carles Vilarino-Guell,Laura Piccio,Filippo Martinelli Boneschi
Genesno. 12 (2022): 2392-2392
Monica Diez-Fairen,Gabrielle Houle,Sara Ortega-Cubero,Sara Bandres-Ciga,Ignacio Alvarez,Maria Carcel,Laura Ibanez,Maria Victoria Fernandez,John P. Budde,Jean-Remi Trotta,Raul Tonda,Jessica X. Chong,Michael J. Bamshad,Deborah A. Nickerson,Miquel Aguilar,Juan P. Tartari,Alexandre Gironell,Elena Garcia-Martin,Jose A. G. Agundez,Hortensia Alonso-Navarro,Felix Javier Jimenez-Jimenez,Manel Fernandez,Francesc Valldeoriola,Maria Jose Marti,Eduard Tolosa,Francisco Coria,Maria A. Pastor,Carles Vilarino-Guell,Alex Rajput,Patrick A. Dion,Carlos Cruchaga,Guy A. Rouleau,Pau Pastor
bioRxiv (Cold Spring Harbor Laboratory) (2021)
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作者统计
#Papers: 147
#Citation: 6107
H-Index: 38
G-Index: 74
Sociability: 7
Diversity: 3
Activity: 16
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