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

Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: A pooled analysis from the international lung cancer consortium

by Truong, T., Hung, R.J., Amos, C.I., Wu, X., Bickeböller, H., Rosenberger, A., Sauter, W., Illig, T., Wichmann, H.-E., Risch, A., Dienemann, H., Kaaks, R., Yang, P., Jiang, R., Wiencke, J.K., Wrensch, M., Hansen, H., Kelsey, K.T., Matsuo, K., Tajima, K., Schwartz, A.G., Wenzlaff, A., Seow, A., Ying, C., Staratschek-Jox, A., Nürnberg, P., Stoelben, E., Wolf, J., Lazarus, P., Muscat, J.E., Gallagher, C.J., Zienolddiny, S., Haugen, A., Van Der Heijden, H.F.M., Kiemeney, L.A., Isla, D., Mayordomo, J.I., Rafnar, T., Stefansson, K., Zhang, Z.-F., Chang, S.-C., Kim, J.H., Hong, Y.-C., Duell, E.J., Andrew, A.S., Lejbkowicz, F., Rennert, G., Müller, H., Brenner, H., Le Marchand, L., Benhamou, S., Bouchardy, C., Teare, M.D., Xue, X., McLaughlin, J., Liu, G., McKay, J.D., Brennan, P., Spitz, M.R.
Published 2016