المؤلفون: Hunt, KA, Smyth, DJ, Balschun, T, Ban, M, Mistry, V, Ahmad, T, Anand, V, Barrett, JC, Bhaw-Rosun, L, Bockett, NA, Brand, OJ, Brouwer, E, Concannon, P, Cooper, JD, Dias, KRM, van Diemen, CC, Dubois, PC, Edkins, S, Folster-Holst, R, Fransen, K, Glass, DN, Heap, GAR, Hofmann, S, Huizinga, TWJ, Hunt, S, Langford, C, Lee, J, Mansfield, J, Marrosu, MG, Mathew, CG, Mein, CA, Muller-Quernheim, J, Nutland, S, Onengut-Gumuscu, S, Ouwehand, W, Pearce, K, Prescott, NJ, Posthumus, MD, Potter, S, Rosati, G, Sambrook, J, Satsangi, J, Schreiber, S, Shtir, C, Simmonds, MJ, Sudman, M, Thompson, SD, Toes, R, Trynka, G, Vyse, TJ, Walker, NM, Weidinger, S, Zhernakova, A, Zoledziewska, M, Weersma, RK, Gough, SCL, Sawcer, S, Wijmenga, C, Parkes, M, Cucca, F, Franke, A, Deloukas, P, Rich, SS, Todd, JA, van Heel, DA

المصدر: Nature genetics. 44(1):3-5

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:123857374

المؤلفون: O'Riain, C^{Aff1, IDleu2009114_cor1}, O'Shea, D M, Yang, Y, Le Dieu, R, Gribben, J G, Summers, K, Yeboah-Afari, J, Bhaw-Rosun, L, Fleischmann, C, Mein, C A, Crook, T, Smith, P, Kelly, G, Rosenwald, A, Ott, G^{Aff5, Aff6}, Campo, E, Rimsza, L M, Smeland, E B^{Aff9, Aff10}, Chan, W C, Johnson, N, Gascoyne, R D, Reimer, S, Braziel, R M, Wright, G W, Staudt, L M, Lister, T A, Fitzgibbon, J

المصدر: Leukemia. 23(10):1858-1866

المؤلفون: 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

المساهمون: Trynka, G, Hunt, K, Bockett, N, Romanos, J, Mistry, V, Szperl, A, Bakker, S, Bardella, M, Bhaw Rosun, L, Castillejo, G, De la Concha, E, De Almeida, R, Dias, K, Van Diemen, C, Dubois, P, Duerr, R, Edkins, S, Franke, L, Fransen, K, Gutierrez, J, Heap, G, Hrdlickova, B, Hunt, S, Izurieta, L, Izzo, V, Joosten, L, Langford, C, Mazzilli, M, Mein, C, Midah, V, Mitrovic, M, Mora, B, Morelli, M, Nutland, S, Núñez, C, Onengut Gumuscu, S, Pearce, K, Platteel, M, Polanco, I, Potter, S, Ribes Koninckx, C, Ricaño Ponce, I, Rich, S, Rybak, A, Santiago, J, Senapati, S, Sood, A, Szajewska, H, Troncone, R, Varadé, J, Wallace, C, Wolters, V, Zhernakova, A, Spanish Consortium on the Genetics of Coeliac, D, PreventCD Study, G, Wellcome Trust Case Control, C, Thelma, B, Cukrowska, B, Urcelay, E, Bilbao, J, Mearin, M, Barisani, D, Barrett, J, Plagnol, V, Deloukas, P, Wijmenga, C, Van Heel, D, Gastroenterology and hepatology, CCA - Disease profiling, Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Stem Cell Aging Leukemia and Lymphoma (SALL), Translational Immunology Groningen (TRIGR)

المصدر: 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

مصطلحات موضوعية: EXPRESSION, Linkage disequilibrium, Population, LOCI, Genome-wide association study, Locus (genetics), Human leukocyte antigen, Biology, PHENOTYPE, Polymorphism, Single Nucleotide, Linkage Disequilibrium, REGION, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Risk Factors, Genetics, RISK VARIANTS, Humans, 1000 Genomes Project, GENOME-WIDE ASSOCIATION, education, Genotyping, POPULATION, 030304 developmental biology, 0303 health sciences, education.field_of_study, celiac disease, GWAS, LARGE-SCALE, BIO/13 - BIOLOGIA APPLICATA, Chromosome Mapping, Pathogenesis and modulation of inflammation Infection and autoimmunity [N4i 1], GENE, Genetic architecture, Celiac Disease, Haplotypes, Genetic Loci, 030220 oncology & carcinogenesis, Case-Control Studies, MAP, Genome-Wide Association Study

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

المؤلفون: Hunt, K.A., Smyth, D.J., Balschun, T., Ban, M., Mistry, V., Ahmad, T., Anand, V., Barrett, J.C., Bhaw-Rosun, L., Bockett, N.A., Brand, O.J., Brouwer, E., Concannon, P., Cooper, J.D., Dias, K.R.M., Diemen, C.C. van, Dubois, P.C., Edkins, S., Folster-Holst, R., Fransen, K., Glass, D.N., Heap, G.A.R., Hofmann, S., Huizinga, T.W.J., Hunt, S., Langford, C., Lee, J., Mansfield, J., Marrosu, M.G., Mathew, C.G., Mein, C.A., Muller-Quernheim, J., Nutland, S., Onengut-Gumuscu, S., Ouwehand, W., Pearce, K., Prescott, N.J., Posthumus, M.D., Potter, S., Rosati, G., Sambrook, J., Satsangi, J., Schreiber, S., Shtir, C., Simmonds, M.J., Sudman, M., Thompson, S.D., Toes, R., Trynka, G., Vyse, T.J., Walker, N.M., Weidinger, S., Zhernakova, A., Zoledziewska, M., Weersma, R.K., Gough, S.C.L., Sawcer, S., Wijmenga, C., Parkes, M., Cucca, F., Franke, A., Deloukas, P., Rich, S.S., Todd, J.A., Heel, D.A. van, Type 1 Diabet Genetics, UK Inflammatory Bowel Dis IBD, Wellcome Trust Case

المصدر: Nature Genetics, 44(1), 3-5

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4ba8eee19bf77847ccf9259124e6bd6f
https://hdl.handle.net/1887/117960

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