Increased prime edit rates in KCNQ2 and SCN1A via single nicking all-in-one plasmids von 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

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Male patients affected by mosaic PCDH19 mutations: five new cases von de Lange, I. M., Rump, P., Neuteboom, R. F., Augustijn, P. B., Hodges, K., Kistemaker, A. I., Brouwer, O. F., Mancini, G. M. S., Newman, H. A., Vos, Y. J., Helbig, K. L., Peeters-Scholte, C., Kriek, M., Knoers, N. V., Lindhout, D., Koeleman, B. P. C., van Kempen, M. J. A., Brilstra, E. H.

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Variation in the CTLA4 3′UTR has phenotypic consequences for autoreactive T cells and associates with genetic risk for type 1 diabetes von de Jong, V M, Zaldumbide, A, van der Slik, A R, Laban, S, Koeleman, B P C, Roep, B O

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Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain von Kremer, P H C, Koeleman, B P C, Pawlikowska, L, Weinsheimer, S, Bendjilali, N, Sidney, S, Zaroff, J G, Rinkel, G J E, van den Berg, L H, Ruigrok, Y M, de Kort, G A P, Veldink, J H, Kim, H, Klijn, C J M

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Epidemiology, pathophysiology and putative genetic basis of carbamazepine- and oxcarbazepine-induced hyponatremia von Berghuis, B., de Haan, G.-J., van den Broek, M. P. H., Sander, J. W., Lindhout, D., Koeleman, B. P. C.

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Study of the association between the CAPSL-IL7R locus and type 1 diabetes von Santiago, J. L, Alizadeh, B. Z, Martínez, A, Espino, L, de la Calle, H, Fernández-Arquero, M, Figueredo, M. A, de la Concha, E. G, Roep, B. O, Koeleman, B. P. C, Urcelay, E

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Survival of autoreactive T lymphocytes by microRNA-mediated regulation of apoptosis through TRAIL and Fas in type 1 diabetes von de Jong, V M, van der Slik, A R, Laban, S, van ‘t Slot, R, Koeleman, B P C, Zaldumbide, A, Roep, B O

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Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders von van Harssel, J. J. T., Weckhuysen, S., van Kempen, M. J. A., Hardies, K., Verbeek, N. E., de Kovel, C. G. F., Gunning, W. B., van Daalen, E., de Jonge, M. V., Jansen, A. C., Vermeulen, R. J., Arts, W. F. M., Verhelst, H., Fogarasi, A., de Rijk-van Andel, J. F., Kelemen, A., Lindhout, D., De Jonghe, P., Koeleman, B. P. C., Suls, A., Brilstra, E. H.

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Functional consequences of HLA-DQ8 homozygosity versus heterozygosity for islet autoimmunity in type 1 diabetes von Eerligh, P, van Lummel, M, Zaldumbide, A, Moustakas, A K, Duinkerken, G, Bondinas, G, Koeleman, B P C, Papadopoulos, G K, Roep, B O

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Refractory juvenile myoclonic epilepsy: a meta‐analysis of prevalence and risk factors von Stevelink, R., Koeleman, B. P. C., Sander, J. W., Jansen, F. E., Braun, K. P. J.

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Post-transcriptional control of candidate risk genes for type 1 diabetes by rare genetic variants von de Jong, V M, Zaldumbide, A, van der Slik, A R, Persengiev, S P, Roep, B O, Koeleman, B P C

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Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis von de Kovel, C.G.F, Pinto, D, Tauer, U, Lorenz, S, Muhle, H, Leu, C, Neubauer, B.A, Hempelmann, A, Callenbach, P.M.C, Scheffer, I.E, Berkovic, S.F, Rudolf, G, Striano, P, Siren, A, Baykan, B, Sander, T, Lindhout, D, Trenité, D.G. Kasteleijn-Nolst, Stephani, U, Koeleman, B.P.C

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Genetic variants of RANTES are associated with serum RANTES level and protection for type 1 diabetes von Zhernakova, A, Alizadeh, B Z, Eerligh, P, Hanifi-Moghaddam, P, Schloot, N C, Diosdado, B, Wijmenga, C, Roep, B O, Koeleman, B P C

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Epistatic interaction between FCRL3 and NFκB1 genes in Spanish patients with rheumatoid arthritis von Martínez, A, Sánchez, E, Valdivia, A, Orozco, G, López-Nevot, M A, Pascual-Salcedo, D, Balsa, A, Fernández-Gutiérrez, B, de la Concha, E G, García-Sánchez, A, Koeleman, B P C, Urcelay, E, Martín, J

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A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides von Bossini-Castillo, L, de Kovel, C, Kallberg, H, van ‘t Slot, R, Italiaander, A, Coenen, M, Tak, P P, Posthumus, M D, Wijmenga, C, Huizinga, T, van der Helm-van Mil, A H M, Stoeken-Rijsbergen, G, Rodriguez-Rodriguez, Luis, Balsa, Alejandro, González-Álvaro, Isidoro, González-Gay, Miguel Ángel, Gómez-Vaquero, Carmen, Franke, B, Vermeulen, S, van der Horst-Bruinsma, IE, Dijkmans, B A C, Wolbink, G J, Ophoff, R A, Maehlen, M T, van Riel, P, Merriman, M, Klareskog, L, Lie, B A, Merriman, T, Crusius, J B A, Brouwer, E, Martin, J, de Vries, N, Toes, R, Padyukov, L, Koeleman, B P C

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Susceptibility loci for sporadic brain arteriovenous malformation; a replication study and meta-analysis von Kremer, P H C, Koeleman, B P C, Rinkel, G JE, Diekstra, F P, van den Berg, L H, Veldink, J H, Klijn, C J M

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Revisiting infant growth prior to childhood onset type 1 diabetes von Kharagjitsingh, A. V., De Ridder, M. A. J., Roep, B. O., Koeleman, B. P. C., Bruining, G. J., Veeze, H. J.

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Association of interferon‐γ and interleukin 10 genotypes and serum levels with partial clinical remission in type 1 diabetes von 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.

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Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population von Zhernakova, A, Eerligh, P, Wijmenga, C, Barrera, P, Roep, B O, Koeleman, B P C

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Association between age, IL-10, IFNγ, stimulated C-peptide and disease progression in children with newly diagnosed Type 1 diabetes von 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.

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