Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: A meta-analysis

by Thomson, G., Valdes, A.M., Noble, J.A., Kockum, I., Grote, M.N., Najman, J., Erlich, H.A., Cucca, F., Pugliese, A., Steenkiste, A., Dorman, J.S., Caillat-Zucman, S., Hermann, R., Ilonen, J., Lambert, A.P., Bingley, P.J., Gillespie, K.M., Lernmark, Å., Sanjeevi, C.B., Rønningen, K.S., Undlien, D.E., Thorsby, E., Petrone, A., Buzzetti, R., Koeleman, B.P.C., Roep, B.O., Saruhan-Direskeneli, G., Uyar, F.A., Günoz, H., Gorodezky, C., Alaez, C., Boehm, B.O., Mlynarski, W., Ikegami, H., Berrino, M., Fasano, M.E., Dametto, E., Israel, S., Brautbar, C., Santiago-Cortes, A., Frazer De Llado, T., She, J.-X., Bugawan, T.L., Rotter, J.I., Raffel, L., Zeidler, A., Leyva-Cobian, F., Hawkins, B.R., Chan, S.H., Castano, L., Pociot, F., Nerup, J.
Published 2014

Evaluation of presumably disease causing SCN1A variants in a cohort of common epilepsy syndromes

by Lal D., Reinthaler E.M., Dejanovic B., May P., Thiele H., Lehesjoki A.-E., Schwarz G., Riesch E., Ikram M.A., Van Duijn C.M., Uitterlinden A.G., Hofman A., Steinböck H., Gruber-Sedlmayr U., Neophytou B., Zara F., Hahn A., Gormley P., Becker F., Weber Y.G., Cilio M.R., Kunz W.S., Krause R., Zimprich F., Lemke J.R., Nürnberg P., Sander T., Lerche H., Neubauer B.A., Palotie A., Ruppert A.-K., Suls A., Siren A., Koeleman B., Haberlandt E., Ronen G.M., Caglayan H., Hjalgrim H., Muhle H., Schulz H., Helbig I., Altmüller J., Geldner J., Schubert J., Jabbari K., Everett K., Feucht M., Balestri M., Nothnagel M., Striano P., Møller R.S., Nabbout R., Balling R., Baulac S., Bianchi A., La Neve A., Minetti C., Giuseppe C.
Published 2019