Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy

Por Votruba, M, Thiselton, D, Bhattacharya, S S
Publicado em 2003

Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa

Por Flaxel, C., Jay, M., Thiselton, D., Nayudu, M., Hardcastle, A., Wright, A., Bird, A.
Publicado em 1999

Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study o...

Por Thiselton, D.L., Maher, B.S., Webb, B.T., Bigdeli, T.B., O’Neill, F.A., Walsh, D., Kendler, K.S., Riley, B.P.
Publicado em 2010

Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study.

Por Hardcastle, A J, Thiselton, D L, Van Maldergem, L, Saha, B K, Jay, M, Plant, C, Taylor, R, Bird, A C, Bhattacharya, S
Publicado em 1999

Association Study of SNAP25 and Schizophrenia in Irish Family and Case–Control Samples

Por Fanous, A.H., Zhao, Z., van den Oord, E.J.C.G., Maher, B.S., Thiselton, D.L., Bergen, S.E., Wormley, B., Bigdeli, T., Amdur, R.L., O'Neill, F.A., Walsh, D., Kendler, K.S., Riley, B.P.
Publicado em 2010