Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Elia Gil‐Varea"'
Autor:
Elia Gil-Varea, Elena Urcelay, Carles Vilariño-Güell, Carme Costa, Luciana Midaglia, Fuencisla Matesanz, Alfredo Rodríguez-Antigüedad, Jorge Oksenberg, Laura Espino-Paisan, A. Dessa Sadovnick, Albert Saiz, Luisa M. Villar, Juan Antonio García-Merino, Lluís Ramió-Torrentà, Juan Carlos Triviño, Ester Quintana, René Robles, Antonio Sánchez-López, Rafael Arroyo, Jose C. Alvarez-Cermeño, Angela Vidal-Jordana, Sunny Malhotra, Nicolas Fissolo, Xavier Montalban, Manuel Comabella
Publikováno v:
Journal of Neuroinflammation, Vol 15, Iss 1, Pp 1-10 (2018)
Abstract Background It remains unclear whether disease course in multiple sclerosis (MS) is influenced by genetic polymorphisms. Here, we aimed to identify genetic variants associated with benign and aggressive disease courses in MS patients. Methods
Externí odkaz:
https://doaj.org/article/833c0146c0374957a77d4180572e95c7
Autor:
Elia Gil-Varea, Maria Fedetz, Herena Eixarch, Nino Spataro, Luisa María Villar, Elena Urcelay, Albert Saiz, Óscar Fernández, Laura Leyva, Lluís Ramió-Torrentà, Koen Vandenbroeck, David Otaegui, Tamara Castillo-Triviño, Guillermo Izquierdo, Sunny Malhotra, Elena Bosch, Arcadi Navarro, Antonio Alcina, Xavier Montalban, Fuencisla Matesanz, Manuel Comabella
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 3, p 625 (2020)
Genome-wide association studies and meta-analysis have contributed to the identification of more than 200 loci associated with multiple sclerosis (MS). However, a proportion of MS heritability remains unknown. We aimed to uncover new genetic variants
Externí odkaz:
https://doaj.org/article/b64cf5b47fc64c8dbf7f8e97e9bf526e
Autor:
Sunny Malhotra, Luciana Midaglia, Omar Chuquisana, Nikolaos A. Patsopoulos, Roser Ferrer, Marina Giralt, Nicolas Fissolo, Elia Gil‐Varea, Juan Carlos Triviño, Jan D. Lünemann, Xavier Montalban, Manuel Comabella
Publikováno v:
European Journal of Neurology.
Autor:
Sunny Malhotra, Luciana Midaglia, Omar Chuquisana, Nikolaos A Patsopoulos, Roser Ferrer, Marina Giralt, Nicolas Fissolo, Elia Gil-Varea, Jan D Lünemann, Xavier Montalban, Manuel Comabella
Background: Vitamin D is considered to play a role in multiple sclerosis (MS) etiopathogenesis. We recently identified a polymorphism located in the cytochrome P450 family 24 subfamily A member 1 (CYP24A1) gene, rs2762943, that was found to be associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c23feca856d20530abc110ea3b06a550
https://doi.org/10.21203/rs.3.rs-1158231/v1
https://doi.org/10.21203/rs.3.rs-1158231/v1
Autor:
Antonio Alcina, Maria Fedetz, Isabel Vidal-Cobo, Eduardo Andrés-León, Maria-Isabel García-Sánchez, Alicia Barroso-del-Jesus, Sara Eichau, Elia Gil-Varea, null Luisa-Maria Villar, Albert Saiz, Laura Leyva, Koen Vandenbroeck, David Otaegui, Guillermo Izquierdo, Manuel Comabella, Elena Urcelay, Fuencisla Matesanz
Publikováno v:
Human molecular genetics. 31(13)
Multiple sclerosis (MS) is a complex and demyelinating disease of the central nervous system. One of the challenges of the post-genome-wide association studies (GWAS) era is to understand the molecular basis of statistical associations to reveal gene
Autor:
Herena Eixarch, Elena Bosch, David Otaegui, Luisa M. Villar, Laura Leyva, Guillermo Izquierdo, Oscar Fernández, Fuencisla Matesanz, Elena Urcelay, Nino Spataro, María Fedetz, Elia Gil-Varea, Albert Saiz, Manuel Comabella, Sunny Malhotra, Antonio Alcina, Lluís Ramió-Torrentà, Tamara Castillo-Triviño, Xavier Montalban, Arcadi Navarro, Koen Vandenbroeck
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 3
Dipòsit Digital de la UB
Universidad de Barcelona
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of Clinical Medicine, Vol 9, Iss 3, p 625 (2020)
Volume 9
Issue 3
Dipòsit Digital de la UB
Universidad de Barcelona
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of Clinical Medicine, Vol 9, Iss 3, p 625 (2020)
Genome-wide association studies and meta-analysis have contributed to the identification of more than 200 loci associated with multiple sclerosis (MS). However, a proportion of MS heritability remains unknown. We aimed to uncover new genetic variants
Autor:
Luciana Midaglia, Manuel Comabella, Sunny Malhotra, Antonio Alcina, Nikolaos A. Patsopoulos, Lluís Ramió-Torrentà, Begoña Oliver-Martos, Oscar Fernandez, Guillermo Izquierdo, Elena Bosch, Albert Saiz, Xavier Montalban, Nino Spataro, Herena Eixarch, Ester Quintana, Luisa M. Villar, Arcadi Navarro, Amalia Tejeda-Velarde, Sara Llufriu, Elia Gil-Varea, Fuencisla Matesanz
Publikováno v:
HUMAN MUTATION
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Digital.CSIC. Repositorio Institucional del CSIC
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Digital.CSIC. Repositorio Institucional del CSIC
Although genome-wide association studies have identified a number of common variants associated with multiple sclerosis (MS) susceptibility, little is known about the relevance of rare variants. Here, we aimed to explore the role of rare variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81e07c458b88eda753187c45aa13d805
http://hdl.handle.net/10261/216748
http://hdl.handle.net/10261/216748