Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2

بواسطة Limviphuvadh, V, Chua, L.L, Rahim, R.A.B, Eisenhaber, F, Maurer-Stroh, S, Adhikari, S.
منشور في 2020

Discovering novel SNPs that are correlated with patient outcome in a Singaporean cancer patient cohort treated with gemcitabine-based chemotherapy

بواسطة Limviphuvadh, V, Tan, C.S, Konishi, F, Jenjaroenpun, P, Xiang, J.S, Kremenska, Y, Mu, Y.S, Syn, N, Lee, S.C, Soo, R.A, Eisenhaber, F, Maurer-Stroh, S, Yong, W.P
منشور في 2020

Novel SNP improves differential survivability and mortality in non-small cell lung cancer patients

بواسطة Mah, T.L, Yap, X.N.A, Limviphuvadh, V, Li, N, Sridharan, S, Kuralmani, V, Feng, M, Liem, N, Adhikari, S, Yong, W.P, Soo, R.A, Maurer-Stroh, S, Eisenhaber, F, Tong, J.C
منشور في 2020

Mutations in SCO2 are associated with autosomal-dominant high-grade myopia

بواسطة Tran-Viet, K.-N., Powell, C., Barathi, V.A., Klemm, T., Maurer-Stroh, S., Limviphuvadh, V., Soler, V., Ho, C., Yanovitch, T., Schneider, G., Li, Y.-J., Nading, E., Metlapally, R., Saw, S.-M., Goh, L., Rozen, S., Young, T.L.
منشور في 2014

Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

بواسطة Maurer-Stroh, Sebastian, Soler, V. J., Tran-Viet, K.-N., Galiacy, S. D., Limviphuvadh, V., Klemm, T. P., St Germain, E., Fournie, P. R., Guillaud, C., Hawthorne, F., Suarez, C., Kantelip, B., Afshari, N. A., Creveaux, I., Luo, X., Meng, W., Calvas, P., Cassagne, M., Arne, J.-L., Malecaze, F., Young, T. L., Rozen, Steve G.
منشور في 2013

Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

بواسطة Soler, V.J., Tran-Viet, K.-N., Galiacy, S.D., Limviphuvadh, V., Klemm, T.P., St Germain, E., Fournié, P.R., Guillaud, C., Maurer-Stroh, S., Hawthorne, F., Suarez, C., Kantelip, B., Afshari, N.A., Creveaux, I., Luo, X., Meng, W., Calvas, P., Cassagne, M., Arné, J.-L., Rozen, S.G., Malecaze, F., Young, T.L.
منشور في 2014