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Maria Ban

Showing results (51-60 of 61) with videos related to

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Nature|May 24, 2013
Negligible impact of rare autoimmune-locus coding-region variants on missing heritabilityKaren A Hunt, Vanisha Mistry, Nicholas A Bockett, et al.
Nature Genetics|May 27, 2010
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis, David R Booth, Robert N Heard, et al.
Brain : a Journal of Neurology|June 7, 2013
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis, Christina M Lill, Brit-Maren M Schjeide, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Federated single-cell QTL meta-analysis reveals novel disease mechanismsDaniel Kaptijn, Lieke Michielsen, Drew Neavin, et al.
Journal of Neuroimmunology|August 29, 2006
Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans, Maria Ban, David Booth, et al.
Nature Genetics|September 8, 2015
Class II HLA interactions modulate genetic risk for multiple sclerosisLoukas Moutsianas, Luke Jostins, Ashley H Beecham, et al.
Nature Genetics|December 28, 2011
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestryKaren A Hunt, Deborah J Smyth, Tobias Balschun, et al.
The New England Journal of Medicine|April 27, 2017
Overexpression of the Cytokine BAFF and Autoimmunity RiskMaristella Steri, Valeria Orrù, M Laura Idda, et al.
Nature Genetics|October 1, 2013
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis, Ashley H Beecham, Nikolaos A Patsopoulos, et al.
Nature Genetics|October 24, 2007
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants, , Paul R Burton, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Nature|May 24, 2013
Negligible impact of rare autoimmune-locus coding-region variants on missing heritabilityKaren A Hunt, Vanisha Mistry, Nicholas A Bockett, et al.
Nature Genetics|May 27, 2010
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis, David R Booth, Robert N Heard, et al.
Brain : a Journal of Neurology|June 7, 2013
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis, Christina M Lill, Brit-Maren M Schjeide, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
Federated single-cell QTL meta-analysis reveals novel disease mechanismsDaniel Kaptijn, Lieke Michielsen, Drew Neavin, et al.
Journal of Neuroimmunology|August 29, 2006
Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans, Maria Ban, David Booth, et al.
Nature Genetics|September 8, 2015
Class II HLA interactions modulate genetic risk for multiple sclerosisLoukas Moutsianas, Luke Jostins, Ashley H Beecham, et al.
Nature Genetics|December 28, 2011
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestryKaren A Hunt, Deborah J Smyth, Tobias Balschun, et al.
The New England Journal of Medicine|April 27, 2017
Overexpression of the Cytokine BAFF and Autoimmunity RiskMaristella Steri, Valeria Orrù, M Laura Idda, et al.
Nature Genetics|October 1, 2013
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis, Ashley H Beecham, Nikolaos A Patsopoulos, et al.
Nature Genetics|October 24, 2007
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants, , Paul R Burton, et al.
Pageof 7