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Nature
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May 24, 2013
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
Karen 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 mechanisms
Daniel 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 sclerosis
Loukas 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 ancestry
Karen 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 Risk
Maristella 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.
Page
of 7
Search research articles
Search
Showing results (51-60 of 61) with videos related to
Sort By:
Page
of 7
Nature
|
May 24, 2013
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
Karen 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 mechanisms
Daniel 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 sclerosis
Loukas 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 ancestry
Karen 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 Risk
Maristella 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.
Page
of 7