Genome-wide significant association with seven novel multiple sclerosis risk loci
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A. Alcina | F. Matesanz | X. Montalban | H. Hartung | C. Graetz | L. Bertram | F. Zipp | C. Lill | M. Buttmann | E. Urcelay | K. Vandenbroeck | I. Alloza | T. Dörner | M. Comabella | P. Rieckmann | C. Schmied | A. Chan | R. Hintzen | G. Izquierdo | A. Winkelmann | U. Zettl | H. Binder | M. Filipenko | C. Kubisch | J. Epplen | B. Fontaine | M. Fedetz | E. Reinthaler | I. Astobiza | F. Luessi | O. Favorova | E. Sokolova | I. Cournu-Rebeix | A. Zimprich | E. Popova | O. Aktas | J. Mescheriakova | T. Kümpfel | S. Hoffjan | P. Lohse | L. Leyva | L. Gerdes | Á. García-Martínez | R. Arroyo | D. Korobko | S. Malhotra | L. Guillot-nöel | A. Kroner | N. Malkova | I. Smagina | D. Akkad | Andriy Mashychev | A. Antigüedad | Ó. Fernández | A. N. Boyko | E. Tsareva | P. Blaschke | B. Schjeide | Nerea Ugidos | Inken Wohlers | B. de la Hera | Alexei S Rozhdestvenskii
[1] M. Daly,et al. Genetic and Epigenetic Fine-Mapping of Causal Autoimmune Disease Variants , 2014, Nature.
[2] U. Lindenberger,et al. Assessment of microRNA-related SNP effects in the 3′ untranslated region of the IL22RA2 risk locus in multiple sclerosis , 2014, neurogenetics.
[3] J. Shendure,et al. A general framework for estimating the relative pathogenicity of human genetic variants , 2014, Nature Genetics.
[4] M. Pirinen,et al. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis , 2013, Nature Genetics.
[5] M. Peters,et al. Systematic identification of trans eQTLs as putative drivers of known disease associations , 2013, Nature Genetics.
[6] M. Ban,et al. MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. , 2013, Brain : a journal of neurology.
[7] J. Ioannidis,et al. Meta-analysis methods for genome-wide association studies and beyond , 2013, Nature Reviews Genetics.
[8] Y. Aulchenko,et al. Association of SNPs of CD40 Gene with Multiple Sclerosis in Russians , 2013, PloS one.
[9] Shu-Chen Li,et al. Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk , 2013, Journal of Medical Genetics.
[10] J. Todd,et al. Seven newly identified loci for autoimmune thyroid disease , 2012, Human molecular genetics.
[11] M. Pirinen,et al. Including known covariates can reduce power to detect genetic effects in case-control studies , 2012, Nature Genetics.
[12] C. Gieger,et al. Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients , 2012, neurogenetics.
[13] Chuong B. Do,et al. Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database , 2012, PLoS genetics.
[14] Manolis Kellis,et al. HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants , 2011, Nucleic Acids Res..
[15] John P A Ioannidis,et al. Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma. , 2011, Journal of the National Cancer Institute.
[16] Simon C. Potter,et al. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis , 2011, Nature.
[17] Kasper Lage,et al. Pervasive Sharing of Genetic Effects in Autoimmune Disease , 2011, PLoS genetics.
[18] M. González-Gay,et al. Correlation between endothelial function and carotid atherosclerosis in rheumatoid arthritis patients with long-standing disease , 2011, Arthritis research & therapy.
[19] M. Brown,et al. Promise and pitfalls of the Immunochip , 2011, Arthritis research & therapy.
[20] Atul J. Butte,et al. Autoimmune Disease Classification by Inverse Association with SNP Alleles , 2009, PLoS genetics.
[21] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[22] G. Stewart,et al. Association of common T cell activation gene polymorphisms with multiple sclerosis in Australian patients , 2004, Journal of Neuroimmunology.
[23] Douglas G Altman,et al. Interaction revisited: the difference between two estimates , 2003, BMJ : British Medical Journal.
[24] A. Compston,et al. Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis , 2001, Annals of neurology.
[25] D. Silberberg,et al. New diagnostic criteria for multiple sclerosis: Guidelines for research protocols , 1983, Annals of neurology.
[26] Linda,et al. MANBA , CXCR 5 , SOX 8 , RPS 6 KB 1 and ZBTB 46 are genetic risk loci for multiple sclerosis , 2013 .
[27] K. Mossman. The Wellcome Trust Case Control Consortium, U.K. , 2008 .
[28] Pak Chung Sham,et al. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits , 2003, Bioinform..