Singapore National Eye Centre (SNEC)


Singapore, Singapore

Publications in cooperation with FAU scientists

Deng, S.X., Borderie, V., Chan, C.C., Dana, R., Figueiredo, F.C., Gomes, J.A.P.,... Attico, E. (2019). Global Consensus on Definition, Classification, Diagnosis, and Staging of Limbal Stem Cell Deficiency. Cornea, 38(3), 364-375.
Berner, D., Pasutto, F., Hoja, U., Zenkel, M., Ozaki, M., Williams, S.,... Schlötzer-Schrehardt, U. (2018). Pseudoexfoliation associated protective variant, rs7173049, reveals a novel regulatory region downstream of LOXL1.
Haycock, P.C., Burgess, S., Nounu, A., Zheng, J., Okoli, G.N., Bowden, J.,... Smith, G.D. (2017). Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. JAMA Oncology, 3(5), 636-651.
Pasutto, F., Zenkel, M., Hoja, U., Berner, D., Uebe, S., Ferrazzi, F.,... Schlötzer-Schrehardt, U. (2017). Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1. Nature Communications, 8, 15466.
Liu, J., Loncar, I., Collee, J.M., Bolla, M.K., Dennis, J., Michailidou, K.,... Hollestelle, A. (2016). rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk. Scientific Reports, 6.
Aung, T., Ozaki, M., Mizoguchi, T., Allingham, R.R., Li, Z., Haripriya, A.,... Khor, C.-C. (2015). A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nature Genetics, 47(4), 387-92.
Hauser, M.A., Aboobakar, I.F., Liu, Y., Miura, S., Whigham, B.T., Challa, P.,... Allingham, R.R. (2015). Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus. Human Molecular Genetics, 24(22), 6552-63.

Last updated on 2016-18-05 at 07:47