Zobrazeno 1 - 10
of 295
pro vyhledávání: '"BARISANI, D."'
Genetica formale Metodo e prove sperimentali di Mendel Caratteri singoli e segregazione, Caratteri e assortimento indipendente, Esperienze mendeliane "ieri ed oggi", I Leggi di Mendel, I Caratteri mendeliani e reincrocio IGenetica "oltre" Mendel Domi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::9bf8ed65a89d38e6362b2d6ab19d7230
http://hdl.handle.net/10447/427509
http://hdl.handle.net/10447/427509
Autor:
De Leo, G, Fasano, S, Ginelli, E, Alessandro, R, Antognelli, C, Barisani, D, Brancolini, C, Di Bella MA, Fontana, S, Meneveri, R, Mezzasoma, L, Minucci, S, Modesti, A, Olivieri, A, Pelleri, Mc, Pierantoni, R, Purrello, M, Robledo, R, Sidoti, A, Talesa, Vn, Tognon, M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3982::0d83a55b81c57c7b455128daacfde10d
http://hdl.handle.net/11391/1496825
http://hdl.handle.net/11391/1496825
Akademický článek
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Autor:
Romanos, J., Rosén, A., Kumar, V., Trynka, G., Franke, L., Szperl, A., Gutierrez-Achury, J., van Diemen, C.C., Kanninga, R., Jankipersadsing, S.A., Steck, A., Eisenbarth, G., van Heel, D.A., Cukrowska, B., Bruno, V., Mazzilli, M.C., Núñez, C., Bilbao, J.R., Mearin, M.L., Barisani, D., Rewers, M., Norris, J.M., Ivarsson, A., Boezen. H.M., Liu, E., Wijmenga, C., Prevent, C.D., Kolaček, Sanja, Steck, A, Mearin, M, L, Barisani, D, Rewers, M, Boezen, H.M.
Publikováno v:
Gut
Gut, 63(3), 415-422
Europe PubMed Central
Gut, 63(3), 415-422. BMJ PUBLISHING GROUP
Gut, 63(3), 415-422
Europe PubMed Central
Gut, 63(3), 415-422. BMJ PUBLISHING GROUP
Background The majority of coeliac disease (CD) patients are not being properly diagnosed and therefore remain untreated, leading to a greater risk of developing CD-associated complications. The major genetic risk heterodimer, HLA-DQ2 and DQ8, is alr
Autor:
Ginelli, E, Malcovati, M, Asselta, Rosanna, Badaracco, G, Barbon, Alessandro, Barisani, D, Bonaldo, P, Braghetta, P, Brancolini, C, Cecconi, S, Ciafrè, S, Defelippi, P, DE PETRO, Giuseppina, Duga, S, Gallone, A, Limonta, Patrizia, Marini, M, Messi, E, Modesti, A, Moretti, Rm, Mottes, M, Nigro, Matteo, Piomboni, P, Poletti, A, Principato, G, Romanelli, Mg, Salvetti, Angelo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3662::75ebb0ac02c4bb81adda875d57665ab9
http://hdl.handle.net/11379/491134
http://hdl.handle.net/11379/491134
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
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
http://hdl.handle.net/11573/431911
Autor:
Dubois PC, Trynka G, Francke L, Hunt KA, Rpmanos J, Curtotti A, Zhernakova A, Heap GA, Adàny R, Aromaa A, Bardella MT, Van Den Berg LH, Bockett NA, De La Concha EG, DEma B, Fehrmann RS, Fernandez Aquero M, Fiatal S, Grandone E, Green PM, Groen HJ, Gwilliam R, Houwn RH, Hunt SE, Kaukinen K, Kelleher D, Korponay Szabo I, Kurppa K, Mac Mathuna P, Maki M, Mazzilli MC, McCann OT, Mearin ML, Mein CA, Mirza MM, Mistry V, Mora B, Morley KI, Mulder CJ, Murray JA, Nunez C, Oosterom E, Ophoff RA, Polanco I, Peltonen L, Platteel M, Rybak A, Salomaa V, Schweizer JJ, Sperandeo MP, Tack GJ, Turner G, Veldink JH, Verbeek WH, Weersma RK, Wolters WM, Urcelay E, Cukrowska B, Neuhausen SL, McManus R, Barisani D, Deloukas P, Barrett JC, Saavalainen P, Wijmenga C, Van Heel DA, GRECO, LUIGI
We performed a second-generation genome-wide association study of 4,533 individuals with celiac disease (cases) and 10,750 control subjects. We genotyped 113 selected SNPs with P(GWAS) < 10(-4) and 18 SNPs from 14 known loci in a further 4,918 cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::a9f83733ed613dd5b9f22f2c58da1f02
http://hdl.handle.net/11588/365958
http://hdl.handle.net/11588/365958
Autor:
Picarelli, A., Di Tola, M., Sabbatella, L., Anania, M., Calabrò, A., Renzi, D., Bai, J., Sugai, E., CARROCCIO, Antonio, DI PRIMA, Lidia, Bardella, M., Barisani, D., Ribes Koninckx, C., Aliaga, E., Gasparin, M., Bravi, E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c2d9caa9193af78c0f5817ff2c73ff82
http://hdl.handle.net/10447/230669
http://hdl.handle.net/10447/230669