Search research articles
Contact Us
Filters
Showing results (21-30 of 86) with videos related to
Page
of 9
Sort By:
The Lancet. Neurology
|
August 13, 2022
Genetics of multiple sclerosis: lessons from polygenicity
An Goris, Marijne Vandebergh, Jacob L McCauley, et al.
Journal of Neurology
|
March 9, 2007
Polymorphisms in the neuromyelitis optica auto-antigen AQP4 and susceptibility to multiple sclerosis
Maria Ban, Amie Walton, An Goris, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
January 6, 2018
Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation
Kelly Hilven, Marijne Vandebergh, Ide Smets, et al.
Scientific Reports
|
January 16, 2021
Quantitative MRI phenotypes capture biological heterogeneity in multiple sclerosis patients
Ide Smets, An Goris, Marijne Vandebergh, et al.
European Journal of Human Genetics : EJHG
|
March 26, 2009
Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke
Robin Lemmens, Shérine Abboud, Wim Robberecht, et al.
Journal of Neurology
|
March 10, 2009
No evidence for association between an MAOA functional polymorphism and susceptibility to Parkinson's disease
Caroline Williams-Gray, An Goris, Thomas Foltynie, et al.
Life Science Alliance
|
September 11, 2023
A targeted sequencing extension for transcript genotyping in single-cell transcriptomics
Lies Van Horebeek, Margaux David, Nina Dedoncker, et al.
Journal of Neuroimmunology
|
October 25, 2003
New candidate loci for multiple sclerosis susceptibility revealed by a whole genome association screen in a Belgian population
An Goris, Stephen Sawcer, Koen Vandenbroeck, et al.
AIDS Research and Human Retroviruses
|
March 11, 2008
HERV-K113 is not associated with multiple sclerosis in a large family-based study
David L Moyes, An Goris, Maria Ban, et al.
European Journal of Human Genetics : EJHG
|
June 1, 2006
No evidence for association of a European-specific chromosome 17 inversion with multiple sclerosis
An Goris, Melanie Maranian, Amie Walton, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 86) with videos related to
Sort By:
Page
of 9
The Lancet. Neurology
|
August 13, 2022
Genetics of multiple sclerosis: lessons from polygenicity
An Goris, Marijne Vandebergh, Jacob L McCauley, et al.
Journal of Neurology
|
March 9, 2007
Polymorphisms in the neuromyelitis optica auto-antigen AQP4 and susceptibility to multiple sclerosis
Maria Ban, Amie Walton, An Goris, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
January 6, 2018
Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation
Kelly Hilven, Marijne Vandebergh, Ide Smets, et al.
Scientific Reports
|
January 16, 2021
Quantitative MRI phenotypes capture biological heterogeneity in multiple sclerosis patients
Ide Smets, An Goris, Marijne Vandebergh, et al.
European Journal of Human Genetics : EJHG
|
March 26, 2009
Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke
Robin Lemmens, Shérine Abboud, Wim Robberecht, et al.
Journal of Neurology
|
March 10, 2009
No evidence for association between an MAOA functional polymorphism and susceptibility to Parkinson's disease
Caroline Williams-Gray, An Goris, Thomas Foltynie, et al.
Life Science Alliance
|
September 11, 2023
A targeted sequencing extension for transcript genotyping in single-cell transcriptomics
Lies Van Horebeek, Margaux David, Nina Dedoncker, et al.
Journal of Neuroimmunology
|
October 25, 2003
New candidate loci for multiple sclerosis susceptibility revealed by a whole genome association screen in a Belgian population
An Goris, Stephen Sawcer, Koen Vandenbroeck, et al.
AIDS Research and Human Retroviruses
|
March 11, 2008
HERV-K113 is not associated with multiple sclerosis in a large family-based study
David L Moyes, An Goris, Maria Ban, et al.
European Journal of Human Genetics : EJHG
|
June 1, 2006
No evidence for association of a European-specific chromosome 17 inversion with multiple sclerosis
An Goris, Melanie Maranian, Amie Walton, et al.
Page
of 9