A two-stage approach identifies a Q344X mutation in the rhodopsin gene of a Chinese Singaporean family with autosomal dominant retinitis pigmentosa

by Yong, R.Y.Y., Chee, C.K.L., Yap, E.P.H.
Published 2016

A molecular approach for identifying individuals with Li-Fraumeni syndrome who have a limited family history

by Ang, P., Lim, I.H.K., Yong, R.Y.Y., Lee, A.S.G.
Published 2015

Association between an intronic apolipoprotein E polymorphism and bone mineral density in Singaporean Chinese females

by Tong, T.Y.Y., Mok, H.P.P., Yong, E.L., Yong, R.Y.Y., Chong, A.P.L., Yap, E.P.H., Moochhala, S., Goh, V.H.H., Liang, S.
Published 2011

Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

by Khor, C.C., Miyake, M., Chen, L.J., Shi, Y., Barathi, V.A., Qiao, F., Nakata, I., Yamashiro, K., Zhou, X., Tam, P.O.S., Cheng, C.-Y., Tai, E.S., Vithana, E.N., Aung, T., Teo, Y.-Y., Wong, T.-Y., Moriyama, M., Ohno-Matsui, K., Mochizuki, M., Matsuda, F., Yong, R.Y.Y., Yap, E.P.H., Yang, Z., Pang, C.P., Saw, S.-M., Yoshimura, N.
Published 2014

Identification of an I Na-dependent and I to-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient

by Ma D., Liu Z., Loh L.J., Zhao Y., Li G., Liew R., Islam O., Wu J., Chung Y.Y., Teo W.S., Ching C.K., Tan B.Y., Chong D., Ho K.L., Lim P., Yong R.Y.Y., Panama B.K., Kaplan A.D., Bett G.C.L., Ware J., Bezzina C.R., Verkerk A.O., Cook S.A., Rasmusson R.L., Wei H.
Published 2018