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Study of the association between the CAPSL-IL7R locus and type 1 diabetes.
Published in:
Diabetologia, 2008, v. 51, n. 9, p. 1653, doi. 10.1007/s00125-008-1070-4
By:
- Santiago, J.;
- Alizadeh, B.;
- Martínez, A.;
- Espino, L.;
- Calle, H.;
- Fernández-Arquero, M.;
- Figueredo, M.;
- Concha, E.;
- Roep, B.;
- Koeleman, B.;
- Urcelay, E.
Publication type:
Article
Distribution of HERV-LTR elements in HLA-DQB1 alleles: comments on the article by Bieda et al.
Published in:
Diabetologia, 2003, v. 46, n. 6, p. 869, doi. 10.1007/s00125-003-1113-9
By:
- Pascual, M.;
- Koeleman, B. P.;
- Eerligh, P.;
- Roep, B. O.;
- Martin, J.
Publication type:
Article
Epidemiology, pathophysiology and putative genetic basis of carbamazepine- and oxcarbazepine-induced hyponatremia.
Published in:
European Journal of Neurology, 2016, v. 23, n. 9, p. 1393, doi. 10.1111/ene.13069
By:
- Berghuis, B.;
- Haan, G. ‐ J.;
- Broek, M. P. H.;
- Sander, J. W.;
- Lindhout, D.;
- Koeleman, B. P. C.
Publication type:
Article
Poly (ADP-ribose) polymerase-1 haplotypes are associated with coeliac disease.
Published in:
International Journal of Immunogenetics, 2005, v. 32, n. 4, p. 245, doi. 10.1111/j.1744-313X.2005.00521.x
By:
- Rueda, B.;
- Koeleman, B. P. C.;
- López-Nevot, M. A.;
- Ortega, E.;
- Maldonado, J.;
- López, M.;
- Polanco, I.;
- Martín, J.
Publication type:
Article
Post-transcriptional control of candidate risk genes for type 1 diabetes by rare genetic variants.
Published in:
Genes & Immunity, 2013, v. 14, n. 1, p. 58, doi. 10.1038/gene.2012.38
By:
- de Jong, V M;
- Zaldumbide, A;
- van der Slik, A R;
- Persengiev, S P;
- Roep, B O;
- Koeleman, B P C
Publication type:
Article
Functional consequences of HLA-DQ8 homozygosity versus heterozygosity for islet autoimmunity in type 1 diabetes.
Published in:
Genes & Immunity, 2011, v. 12, n. 6, p. 415, doi. 10.1038/gene.2011.24
By:
- Eerligh, P;
- van Lummel, M;
- Zaldumbide, A;
- Moustakas, A K;
- Duinkerken, G;
- Bondinas, G;
- Koeleman, B P C;
- Papadopoulos, G K;
- Roep, B O
Publication type:
Article
Genetic variants of RANTES are associated with serum RANTES level and protection for type 1 diabetes.
Published in:
Genes & Immunity, 2006, v. 7, n. 7, p. 544, doi. 10.1038/sj.gene.6364326
By:
- Zhernakova, A.;
- Alizadeh, B. Z.;
- Eerligh, P.;
- Hanifi-Moghaddam, P.;
- Schloot, N. C.;
- Diosdado, B.;
- Wijmenga, C.;
- Roep, B. O.;
- Koeleman, B. P. C.
Publication type:
Article
Evidence of association of macrophage migration inhibitory factor gene polymorphisms with systemic lupus erythematosus.
Published in:
Genes & Immunity, 2006, v. 7, n. 5, p. 433, doi. 10.1038/sj.gene.6364310
By:
- Sánchez, E;
- Gómez, L M;
- Lopez-Nevot, M A;
- González-Gay, M A;
- Sabio, J M;
- Ortego-Centeno, N;
- de Ramón, E;
- Anaya, J M;
- González-Escribano, M F;
- Koeleman, B P;
- Martín, J
Publication type:
Article
Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population.
Published in:
Genes & Immunity, 2005, v. 6, n. 6, p. 459, doi. 10.1038/sj.gene.6364220
By:
- Zhernakova, A.;
- Eerligh, P.;
- Wijmenga, C.;
- Barrera, P.;
- Roep, B. O.;
- Koeleman, B. P. C.
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
Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients.
Published in:
Genes & Immunity, 2004, v. 5, n. 3, p. 215, doi. 10.1038/sj.gene.6364061
By:
- van Belzen, M. J.;
- Koeleman, B. P. C.;
- Crusius, J. B. A.;
- Meijer, J. W. R.;
- Bardoel, A. F. J.;
- Pearson, P. L.;
- Sandkuijl, L. A.;
- Houwen, R. H. J.;
- Wijmenga, C.
Publication type:
Article
Association between age, IL-10, IFNγ, stimulated C-peptide and disease progression in children with newly diagnosed Type 1 diabetes.
Published in:
2012
By:
- Kaas, A.;
- Pfleger, C.;
- Kharagjitsingh, A. V.;
- Schloot, N. C.;
- Hansen, L.;
- Buschard, K.;
- Koeleman, B. P. C.;
- Roep, B. O.;
- Mortensen, H. B.;
- Alizadeh, B. Z.
Publication type:
Journal Article
Association between age, IL-10, IFNγ, stimulated C-peptide and disease progression in children with newly diagnosed Type 1 diabetes.
Published in:
Diabetic Medicine, 2012, v. 29, n. 6, p. 734, doi. 10.1111/j.1464-5491.2011.03544.x
By:
- Kaas, A.;
- Pfleger, C.;
- Kharagjitsingh, A. V.;
- Schloot, N. C.;
- Hansen, L.;
- Buschard, K.;
- Koeleman, B. P. C.;
- Roep, B. O.;
- Mortensen, H. B.;
- Alizadeh, B. Z.
Publication type:
Article
Association of interferon-γ and interleukin 10 genotypes and serum levels with partial clinical remission in type 1 diabetes.
Published in:
Clinical & Experimental Immunology, 2006, v. 145, n. 3, p. 480, doi. 10.1111/j.1365-2249.2006.03172.x
By:
- Alizadeh, B. Z.;
- Hanifi-Moghaddam, P.;
- Eerligh, P.;
- van der Slik, A. R.;
- Kolb, H.;
- Kharagjitsingh, A. V.;
- Arias, A. M. Pereira;
- Ronkainen, M.;
- Knip, M.;
- Bonfanti, R.;
- Bonifacio, E.;
- Devendra, D.;
- Wilkin, T.;
- Giphart, M. J.;
- Koeleman, B. P. C.;
- Nolsøe, R.;
- Poulsen, T. Mandrup;
- Schloot, N. C.;
- Roep, B. O.
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
Adaptation of the extended transmission/disequilibrium test to distinguish disease associations of multiple loci: the Conditional Extended Transmission/Disequilibrium Test.
Published in:
Annals of Human Genetics, 2000, v. 64, n. 3, p. 207
By:
- KOELEMAN, B. P. C.;
- DUDBRIDGE, F.;
- CORDELL, H. J.;
- TODD, J. A.
Publication type:
Article
Differential inhibition of autoreactive memory- and alloreactive naive T cell responses by soluble cytotoxic T lymphocyte antigen 4 (sCTLA4), CTLA4Ig and LEA29Y.
Published in:
Clinical & Experimental Immunology, 2007, v. 150, n. 3, p. 487, doi. 10.1111/j.1365-2249.2007.03513.x
By:
- Huurman, V. A. L.;
- Unger, W. W. J.;
- Koeleman, B. P. C.;
- Oaks, M. K.;
- Chandraker, A. K.;
- Terpstra, O. T.;
- Roep, B. O.
Publication type:
Article
Refractory juvenile myoclonic epilepsy: a meta‐analysis of prevalence and risk factors.
Published in:
European Journal of Neurology, 2019, v. 26, n. 6, p. 856, doi. 10.1111/ene.13811
By:
- Jansen, F. E.;
- Braun, K. P. J.;
- Stevelink, R.;
- Koeleman, B. P. C.;
- Sander, J. W.
Publication type:
Article
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
Identification of novel genetic markers associated with the clinical phenotypes of systemic sclerosis through a genome wide association strategy.
Published in:
2010
By:
- Gorlova, O.;
- Martin, J. M.;
- Rueda, B.;
- Koeleman, B. P. C.;
- Ying, J.;
- Teruel, M.;
- Diaz-Gallo, L. M.;
- Broen, J. C.;
- Vonk, M. C.;
- Simeon, C. P.;
- Alizadeh, B. Z.;
- Coenen, M. J. H.;
- Voskuyl, A. E.;
- Schuerwegh, A. J.;
- van Riel, P. L. C. M.;
- Vanthuyne, M.;
- van't Slot, R.;
- Italiaander, A.;
- Ophoff, R. A.;
- Hunzelmann, N.
Publication type:
Abstract
Increased prime edit rates in KCNQ2 and SCN1A via single nicking all-in-one plasmids.
Published in:
BMC Biology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12915-023-01646-7
By:
- Dirkx, N.;
- Weuring, Wout J.;
- De Vriendt, E.;
- Smal, N.;
- van de Vondervoort, J.;
- van 't Slot, Ruben;
- Koetsier, M.;
- Zonnekein, N.;
- De Pooter, Tim;
- Weckhuysen, S.;
- Koeleman, B. P. C.
Publication type:
Article
Male patients affected by mosaic PCDH19 mutations: five new cases.
Published in:
Neurogenetics, 2017, v. 18, n. 3, p. 147, doi. 10.1007/s10048-017-0517-5
By:
- Lange, I.;
- Rump, P.;
- Neuteboom, R.;
- Augustijn, P.;
- Hodges, K.;
- Kistemaker, A.;
- Brouwer, O.;
- Mancini, G.;
- Newman, H.;
- Vos, Y.;
- Helbig, K.;
- Peeters-Scholte, C.;
- Kriek, M.;
- Knoers, N.;
- Lindhout, D.;
- Koeleman, B.;
- Kempen, M.;
- Brilstra, E.
Publication type:
Article
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.
Published in:
Neurogenetics, 2013, v. 14, n. 1, p. 23, doi. 10.1007/s10048-013-0353-1
By:
- Harssel, J.;
- Weckhuysen, S.;
- Kempen, M.;
- Hardies, K.;
- Verbeek, N.;
- Kovel, C.;
- Gunning, W.;
- Daalen, E.;
- Jonge, M.;
- Jansen, A.;
- Vermeulen, R.;
- Arts, W.;
- Verhelst, H.;
- Fogarasi, A.;
- Rijk-van Andel, J.;
- Kelemen, A.;
- Lindhout, D.;
- Jonghe, P.;
- Koeleman, B.;
- Suls, A.
Publication type:
Article
Revisiting infant growth prior to childhood onset type 1 diabetes.
Published in:
Clinical Endocrinology, 2010, v. 72, n. 5, p. 620, doi. 10.1111/j.1365-2265.2009.03691.x
By:
- Kharagjitsingh, A. V.;
- de Ridder, M. A. J.;
- Roep, B. O.;
- Koeleman, B. P. C.;
- Bruining, G. J.;
- Veeze, H. J.
Publication type:
Article
A specific allele of the histidine-rich glycoprotein (HRG) locus is linked with elevated plasma levels of HRG in a Dutch family with thrombosis.
Published in:
British Journal of Haematology, 1995, v. 89, n. 4, p. 845, doi. 10.1111/j.1365-2141.1995.tb08423.x
By:
- Hennis, B. C.;
- Van Boheemen, P. A.;
- Koeleman, B. P. C.;
- Boomsma, D. I.;
- Engbsser, L.;
- Van Wees, A. G. M.;
- Novakova, I.;
- Brommer, E. J. P.;
- Klufft, C.
Publication type:
Article

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