Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility

by Tran-Viet, K.-N., St. Germain, E., Soler, V., Powell, C., Lim, S.-H., Klemm, T., Saw, S.M., Young, T.L.
Published 2014

Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystonia

by Calakos, N., Patel, V.D., Gottron, M., Wang, G., Tran-Viet, K.-N., Brewington, D., Beyer, J.L., Steffens, D.C., Krishnan, R.R., Züchner, S.
Published 2014

CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United States

by Lim, S.-H., Tran-Viet, K.-N., Yanovitch, T.L., Freedman, S.F., Klemm, T., Call, W., Powell, C., Ravichandran, A., Metlapally, R., Nading, E.B., Rozen, S., Young, T.L.
Published 2014

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

by 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.
Published 2014

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

by 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.
Published 2013

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

by 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.
Published 2014