Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1

by Pasutto, F, Zenkel, M, Hoja, U, Berner, D, Uebe, S, Ferrazzi, F, Schödel, J, Liravi, P, Ozaki, M, Paoli, D, Frezzotti, P, Mizoguchi, T, Nakano, S, Kubota, T, Manabe, S, Salvi, E, Manunta, P, Cusi, D, Gieger, C, Wichmann, H.-E, Aung, T, Khor, C.C, Kruse, F.E, Reis, A, Schlötzer-Schrehardt, U
Published 2020

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

by Aung T., Ozaki M., Lee M., Schlötzer-Schrehardt U., Thorleifsson G., Mizoguchi T., Igo R., Haripriya A., Williams S., Astakhov Y., Orr A., Burdon K., Nakano S., Mori K., Abu-Amero K., Hauser M., Li Z., Prakadeeswari G., Bailey J., Cherecheanu A., Kang J., Nelson S., Hayashi K., Manabe S., Kazama S., Zarnowski T., Inoue K., Irkec M., Coca-Prados M., Sugiyama K., Järvelä I., Schlottmann P., Lerner S., Lamari H., Nilgün Y., Bikbov M., Park K., Cha S., Yamashiro K., Zenteno J., Jonas J., Kumar R., Perera S., Chan A., Kobakhidze N., George R., Vijaya L., Do T., Edward D., De Juan Marcos L., Pakravan M., Moghimi S., Ideta R., Bach-Holm D., Kappelgaard P., Wirostko B., Thomas S., Gaston D., Bedard K., Greer W., Yang Z., Chen X., Huang L., Sang J., Jia H., Jia L., Qiao C., Zhang H., Liu X., Zhao B., Wang Y., Xu L., Leruez S., Reynier P., Chichua G., Tabagari S.
Published 2017