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Low frequency of HLA DRB1*03 – DQB1*02 and DQB1*0302 haplotypes in Romania is consistent with the country's low incidence of Type I diabetes.
Published in:
Diabetologia, 2001, v. 44, p. B60, doi. 10.1007/PL00002956
By:
- Ionescu-Tîrgoviste, C.;
- Guja, C.;
- Herr, M.;
- Cucca, F.;
- Welsh, K.;
- Bunce, M.;
- Marshall, S.;
- Todd, J. A.
Publication type:
Article
Genetic testing improves the diagnosis of adult type hypolactasia in the Mediterranean population of Sardinia.
Published in:
European Journal of Clinical Nutrition, 2007, v. 61, n. 10, p. 1220, doi. 10.1038/sj.ejcn.1602638
By:
- Schirru, E.;
- Corona, V.;
- Usai-Satta, P.;
- Scarpa, M.;
- Oppia, F.;
- Loriga, F.;
- Cucca, F.;
- De Virgiliis, S.;
- Rossino, R.;
- Doloretta Macis, M.;
- Jores, R.-D.;
- Congia, M.
Publication type:
Article
Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease.
Published in:
Genes & Immunity, 2004, v. 5, n. 5, p. 381, doi. 10.1038/sj.gene.6364106
By:
- Koeleman, B. P. C.;
- Lie, B. A.;
- Undlien, D. E.;
- Dudbridge, F.;
- Thorsby, E.;
- de Vries, R. R. P.;
- Cucca, F.;
- Roep, B. O.;
- Giphart, M. J.;
- Todd, J. A.
Publication type:
Article
A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis.
Published in:
Molecular Biology & Evolution, 2012, v. 29, n. 6, p. 1599, doi. 10.1093/molbev/mss002
By:
- Cagliani, R.;
- Guerini, F. R.;
- Fumagalli, M.;
- Riva, S.;
- Agliardi, C.;
- Galimberti, D.;
- Pozzoli, U.;
- Goris, A.;
- Dubois, B.;
- Fenoglio, C.;
- Forni, D.;
- Sanna, S.;
- Zara, I.;
- Pitzalis, M.;
- Zoledziewska, M.;
- Cucca, F.;
- Marini, F.;
- Comi, G. P.;
- Scarpini, E.;
- Bresolin, N.
Publication type:
Article
Conditional ETDT analysis of the Human Leukocyte Antigen region in type 1 diabetes.
Published in:
Annals of Human Genetics, 2000, v. 64, n. 3, p. 215
By:
- KOELEMAN, B. P. C.;
- HERR, M. H.;
- ZAVATTARI, P.;
- DUDBRIDGE, F.;
- MARCH, R.;
- CAMPBELL, D.;
- BARNETT, A. H.;
- BAIN, S. C.;
- MULARGIA, A. P.;
- LODDO, M.;
- AMOS, W.;
- CUCCA, F.;
- TODD, J. A.
Publication type:
Article
Genome‐wide search for genes affecting the age at diagnosis of type 1 diabetes.
Published in:
Journal of Internal Medicine, 2021, v. 289, n. 5, p. 662, doi. 10.1111/joim.13187
By:
- Syreeni, A.;
- Sandholm, N.;
- Sidore, C.;
- Cucca, F.;
- Haukka, J.;
- Harjutsalo, V.;
- Groop, P.‐H.
Publication type:
Article
Novel <italic>NALCN</italic> biallelic truncating mutations in siblings with IHPRF1 syndrome.
Published in:
2018
By:
- Angius, A.;
- Cossu, S.;
- Uva, P.;
- Oppo, M.;
- Onano, S.;
- Persico, I.;
- Fotia, G.;
- Atzeni, R.;
- Cuccuru, G.;
- Asunis, M.;
- Cucca, F.;
- Pruna, D.;
- Crisponi, L.
Publication type:
Letter to the Editor
The HLA-DPB1--associated component of the IDDM1 and its relationship to the major loci HLA-DQB1, -DQA1, and -DRB1.
Published in:
2001
By:
- Cucca, F;
- Dudbridge, F;
- Loddo, M;
- Mulargia, A P;
- Lampis, R;
- Angius, E;
- De Virgiliis, S;
- Koeleman, B P;
- Bain, S C;
- Barnett, A H;
- Gilchrist, F;
- Cordell, H;
- Welsh, K;
- Todd, J A
Publication type:
journal article
Investigation of linkage of chromosome 8 to type 1 diabetes: multipoint analysis and exclusion mapping of human chromosome 8 in 593 affected sib-pair families from the U.K. and U.S.
Published in:
1998
By:
- Cucca, Francesco;
- Esposito, Laura;
- Goy, Juliet V.;
- Merriman, Marilyn E.;
- Wilson, Amanda J.;
- Reed, Peter W.;
- Bain, Stephen C.;
- Todd, John A.;
- Cucca, F;
- Esposito, L;
- Goy, J V;
- Merriman, M E;
- Wilson, A J;
- Reed, P W;
- Bain, S C;
- Todd, J A
Publication type:
journal article
Nucleus accumbens shell and core dopamine responsiveness to sucrose in rats: role of response contingency and discriminative/conditioned cues.
Published in:
European Journal of Neuroscience, 2015, v. 41, n. 6, p. 802, doi. 10.1111/ejn.12839
By:
- Bassareo, V.;
- Cucca, F.;
- Musio, P.;
- Lecca, D.;
- Frau, R.;
- Di Chiara, G.
Publication type:
Article
Arterial stiffness and the “phenotype” metabolic syndrome: A cross-country study. The MARE consortium.
Published in:
Artery Research, 2014, v. 8, n. 4, p. 157, doi. 10.1016/j.artres.2014.09.204
By:
- Scuteri, A.;
- Cunha, P.;
- Cockroft, J.;
- Cucca, F.;
- Laurent, S.;
- Raso, F.;
- Muiesan, M.;
- Rietzschel, E.;
- Ryliskyte, L.;
- Vlachopoulos, C.;
- Nilsson, P.;
- Lakatta, E.
Publication type:
Article

Found: 11

Low frequency of HLA DRB103 – DQB102 and DQB1*0302 haplotypes in Romania is consistent with the country's low incidence of Type I diabetes.

Genetic testing improves the diagnosis of adult type hypolactasia in the Mediterranean population of Sardinia.

Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease.

A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis.

Conditional ETDT analysis of the Human Leukocyte Antigen region in type 1 diabetes.

Genome‐wide search for genes affecting the age at diagnosis of type 1 diabetes.

Novel <italic>NALCN</italic> biallelic truncating mutations in siblings with IHPRF1 syndrome.

The HLA-DPB1--associated component of the IDDM1 and its relationship to the major loci HLA-DQB1, -DQA1, and -DRB1.

Investigation of linkage of chromosome 8 to type 1 diabetes: multipoint analysis and exclusion mapping of human chromosome 8 in 593 affected sib-pair families from the U.K. and U.S.

Nucleus accumbens shell and core dopamine responsiveness to sucrose in rats: role of response contingency and discriminative/conditioned cues.

Arterial stiffness and the “phenotype” metabolic syndrome: A cross-country study. The MARE consortium.