Analysis of the IL28RA locus as genetic risk factor for multiple sclerosis

Autor: Lopez de Lapuente, A., Alloza, I., Goertsches, R., Zettl, U.K., Urcelay, E., Arroyo, R., Comabella, M., Montalban, X., Antigüedad, A., Vandenbroeck, K.

Publikováno v: In Journal of Neuroimmunology April 2012 245(1-2):98-101

Differential association of two PTPN22 coding variants with Crohn’s disease and ulcerative colitis

Autor: Weersma R K, Roberts R L, Gearry R B, Ponsioen C Y, Wijmenga C, van Bodegraven A A, Crusius J B, Barclay M L, Bottini N, López-Nevot M A, Cueto I, Nieto A, Alcain G, Taxonera C, Mendoza J L, Rodrigo L, Cardeña C, van Sommeren S, Gómez-García M, Fransen K, Espino-Paisán L, Diaz-Gallo L M, Urcelay E, Merriman T R, Alizadeh B Z, Martin J

Publikováno v: Journal of Translational Medicine, Vol 8, Iss Suppl 1, p P2 (2010)

Externí odkaz: https://doaj.org/article/dcbc9900d3f9460d8d888e93cd40b78a

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MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

Autor: Lill, C., Schjeide, B., Graetz, C., Ban, M., Alcina, A., Ortiz, M., Perez, J., Damotte, V., Booth, D., de Lapuente, A., Broer, L., Schilling, M., Akkad, D., Aktas, O., Alloza, I., Antiguedad, A., Arroyo, R., Blaschke, P., Buttmann, M., Chan, A., Compston, A., Cournu-Rebeix, I., Dorner, T., Epplen, J., Fernandez, O., Gerdes, L., Guillot-Noel, L., Hartung, H., Hoffjan, S., Izquierdo, G., Kemppinen, A., Kroner, A., Kubisch, C., Kumpfel, T., Li, S., Lindenberger, U., Lohse, P., Lubetzki, C., Luessi, F., Malhotra, S., Mescheriakova, J., Montalban, X., Papeix, C., Paredes, L., Rieckmann, P., Steinhagen-Thiessen, E., Winkelmann, A., Zettl, U., Hintzen, R., Vandenbroeck, K., Stewart, G., Fontaine, B., Comabella, M., Urcelay, E., Matesanz, F., Sawcer, S., Bertram, L., Zipp, F., Genetics, I.

Publikováno v: Brain, 136, 1778-1782. Oxford University Press
Brain

A recent genome-wide association study reported five loci for which there was strong, but sub-genome-wide significant evidence for association with multiple sclerosis risk. The aim of this study was to evaluate the role of these potential risk loci i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c049e307391aade3d9d24183c6a196f
https://pure.eur.nl/en/publications/ee32921a-ca37-4da5-8b40-f987496bedfb

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Autor: Trynka, G., Hunt, K.A., Bockett, N.A., Romanos, J., Mistry, V., Szperl, A., Bakker, S.F., Bardella, M.T., Bhaw-Rosun, L., Castillejo, G., Concha, E.G. de la, Almeida, R.C. de, Dias, K.R.M., Diemen, C.C. van, Dubois, P.C.A., Duerr, R.H., Edkins, S., Franke, L., Fransen, K., Gutierrez, J., Heap, G.A.R., Hrdlickova, B., Hunt, S., Izurieta, L.P., Izzo, V., Joosten, L.A.B., Langford, C., Mazzilli, M.C., Mein, C.A., Midah, V., Mitrovic, M., Mora, B., Morelli, M., Nutland, S., Nunez, C., Onengut-Gumuscu, S., Pearce, K., Platteel, M., Polanco, I., Potter, S., Ribes-Koninckx, C., Ricano-Ponce, I., Rich, S.S., Rybak, A., Santiago, J.L., Senapati, S., Sood, A., Szajewska, H., Troncone, R., Varade, J., Wallace, C., Wolters, V.M., Zhernakova, A., Thelma, B.K., Cukrowska, B., Urcelay, E., Bilbao, J.R., Mearin, M.L., Barisani, D., Barrett, J.C., Plagnol, V., Deloukas, P., Wijmenga, C., Heel, D.A. van, Spanish Consortium Genetics Coelia, PreventCD Study Grp, WTCCC

Publikováno v: Nature Genetics, 43(12), 1193-U45
Nature Genetics, 43(12), 1193-1201. Nature Publishing Group
NATURE GENETICS
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Trynka, G, Hunt, K A, Bockett, N A, Romanos, J, Mistry, V, Szperl, A, Bakker, S F, Bardella, M T, Bhaw-Rosun, L, Castillejo, G, de la Concha, E G, de Almeida, R C, Dias, K R M, van Diemen, C C, Dubois, P C A, Duerr, R H, Edkins, S, Franke, L, Fransen, K, Gutierrez, J, Heap, G A R, Hrdlickova, B, Hunt, S, Izurieta, L P, Izzo, V, Joosten, L A B, Langford, C, Mazzilli, M C, Mein, C A, Midah, V, Mitrovic, M, Mora, B, Morelli, M, Nutland, S, Nunez, C, Onengut-Gumuscu, S, Pearce, K, Platteel, M, Polanco, I, Potter, S, Ribes-Koninckx, C, Ricano-Ponce, I, Rich, S S, Rybak, A, Santiago, J L, Senapati, S, Sood, A, Szajewska, H, Troncone, R, Varade, J, Wallace, C, Wolters, V M, Zhernakova, A, Thelma, B K, Cukrowska, B, Urcelay, E, Bilbao, J R, Mearin, M L, Barisani, D, Barrett, J C, Plagnol, V, Deloukas, P, Wijmenga, C & van Heel, D A 2011, ' Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease ', Nature Genetics, vol. 43, no. 12, pp. 1193-1201 . https://doi.org/10.1038/ng.998
Nature Genetics, 43, 12, pp. 1193-201
Nature Genetics, 43(12), 1193-U45. Nature Publishing Group
Nature Genetics, 43, 1193-201

Using variants from the 1000 Genomes Project pilot European CEU dataset and data from additional resequencing studies, we densely genotyped 183 non-HLA risk loci previously associated with immune-mediated diseases in 12,041 individuals with celiac di

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5c16dae5ef8183111d0ff16a82086e8
http://hdl.handle.net/11573/431911