Expression of human endogenous retrovirus HERV-K18 is associated with clinical severity in osteoarthritis patients.

Autor: Garcia-Montojo, M¹ (AUTHOR), Varade, J² (AUTHOR), Villafuertes, E³ (AUTHOR), de La Hera, B² (AUTHOR), Hoyas-Fernandez, J³ (AUTHOR), Domínguez-Mozo, MI¹ (AUTHOR), Rodriguez-Rodriguez, L³ (AUTHOR), Tornero-Esteban, P³ (AUTHOR), Arias-Leal, A¹ (AUTHOR), León, L³ (AUTHOR), Lamas, JR³ (AUTHOR), Alvarez-Lafuente, R¹ (AUTHOR), Urcelay, E² (AUTHOR), Fernandez-Gutierrez, B³ (AUTHOR) bfernandez.hcsc@salud.madrid.org

Publikováno v: Scandinavian Journal of Rheumatology. Nov2013, Vol. 42 Issue 6, p498-504. 7p.

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

Confirmation of Human Endogenous Retrovirus HERV-Fc1 role in multiple sclerosis risk

Autor: Iraide Alloza, De La Hera B, lvarez-Lafuente R, Matesanz F, Varade J, Elena Urcelay, Antonio Alcina, Koen Vandenbroeck

Publikováno v: Frontiers in Immunology. 4

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a007814a768c847773e17904400e138a
https://doi.org/10.3389/conf.fimmu.2013.02.00309

Novel genetic loci associated HLA-B*08:01 positive myasthenia gravis.

Autor: Varade J; Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, SE-14186, Stockholm, Sweden. Electronic address: jezabel.varade@ki.se., Wang N; Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, SE-14186, Stockholm, Sweden., Lim CK; Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, SE-14186, Stockholm, Sweden; Department of Clinical Translational Research, Singapore General Hospital, Academia Discovery Tower Level 9, Research Office 2, 20 College Road, Singapore, 169856, Singapore., Zhang T; BGI-Shenzhen, Shenzhen, China, China National GeneBank-Shenzhen, 518083, Shenzhen, China., Zhang Y; BGI-Shenzhen, Shenzhen, China, China National GeneBank-Shenzhen, 518083, Shenzhen, China., Liu X; BGI-Shenzhen, Shenzhen, China, China National GeneBank-Shenzhen, 518083, Shenzhen, China., Piehl F; Department of Clinical Neuroscience (CNS), Karolinska Institutet at Karolinska University Hospital Solna, SE-17177, Stockholm, Sweden., Matell R; Department of Clinical Neuroscience (CNS), Karolinska Institutet at Karolinska University Hospital Solna, SE-17177, Stockholm, Sweden., Cao H; Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, SE-14186, Stockholm, Sweden; iCarbonX, Shenzhen, 518053, China., Xu X; BGI-Shenzhen, Shenzhen, China, China National GeneBank-Shenzhen, 518083, Shenzhen, China., Hammarström L; Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, SE-14186, Stockholm, Sweden; BGI-Shenzhen, Shenzhen, China, China National GeneBank-Shenzhen, 518083, Shenzhen, China.

Publikováno v: Journal of autoimmunity [J Autoimmun] 2018 Mar; Vol. 88, pp. 43-49. Date of Electronic Publication: 2017 Oct 14.

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