Dr Neil Roberts PhD

Expanding the HPSE2 genotypic spectrum in urofacial syndrome, a disease featuring a peripheral neuropathy of the urinary bladder

Beaman, G., Lopes, F., Hofmann, A., Roesch, W., Promm, M., Bijlsma, E. K., Patel, C., Akinci, A., Burgu, B., Knijnenburg, J., Ho, G., Aufschlaeger, C., Dathe, S., Voelckel, M. A., Cohen, M., Yue, W. W., Stuart, H., Mckenzie, E., Elvin, M., Roberts, N. & 2 others, Woolf, A. S. & Newman, W., 23 May 2022, (Accepted/In press) In: Frontiers in Genetics.

Research output: Contribution to journal › Article › peer-review

Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder

Hindi, E., Williams, C., Zeef, L., Lopes, F., Newman, K., Davey, M. M. M., Hodson, N., Hilton, E., Huang, J. L., Price, K. L., Roberts, N., Long, D. A., Woolf, A. S. & Gardiner, N., 30 Jul 2021, In: Scientific Reports.

Research output: Contribution to journal › Article › peer-review

Envisioning treating genetically-defined urinary tract malformations with viral vector-mediated gene therapy

Lopes, F., Woolf, A. S. & Roberts, N., 5 Jul 2021, (Accepted/In press) In: Journal of Pediatric Urology.

Research output: Contribution to journal › Article › peer-review

Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice

Manak, I., Gurney, A., McCloskey, K. D., Woolf, A. S. & Roberts, N., 1 Jul 2020, In: Neurourology and Urodynamics . 39, 7, p. 1930-1938

Research output: Contribution to journal › Article › peer-review

Heparanase 2 and urofacial syndrome, a genetic neuropathy.

Woolf, A. S. & Roberts, N., 2020, In: Adv Exp Med Biol. 1221, p. 807-819

Research output: Contribution to journal › Review article › peer-review

Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder.

Roberts, N., Hilton, E., Lopes, F., Randles, M., Singh, S., Gardiner, N., Chopra, K., Bajwa, Z., Coletta, R., Hall, R., Yue, W., Schaefer, F., Weber, S., Henriksson, R., Stuart, H., hedman, H., Newman, W. & Woolf, A. S., May 2019, In: Kidney International. 95, 5, p. 1138-1152 15 p.

Research output: Contribution to journal › Article › peer-review

Congenital disorders of the human urinary tract: recent insights from genetic and molecular studies.

Woolf, A. S., Lopes, F., Ranjzad, P. & Roberts, N., 2019, In: Frontiers in pediatrics.

Research output: Contribution to journal › Article › peer-review

Overactivity or blockade of transforming growth factor-β each generate a specific ureter malformation

Lopes, F., Roberts, N., Zeef, L., Gardiner, N. & Woolf, A. S., 2019, In: Journal of Pathology.

Research output: Contribution to journal › Article › peer-review

ACTB loss-of-function mutations result in a pleiotropic developmental disorder

Cuvertino, S., Stuart, H., Chandler, K. E., Roberts, N., Armstrong, R., Bernardini, L., Bhaskar, S., Callewaert, B., Clayton-Smith, J., Hernando Davalillo, C., Deshpande, C., Devriendt, K., Digilio, M. C., Dixit, A., Edwards, M., Friedman, J. M., Gonzalez-Meneses, A., Joss, S., Kerr, B., Lampe, A. K. & 21 others, Langlois, S., Lennon, R., Loget, P., Ma, D. Y. T., Ruth, M., Des Medt, M., O'Sullivan, J., Odent, S., Parker, M. J., Pebrel-Richard, C., Petit, F., Stark, Z., Stockler-Ipsiroglu, S., Tinschert, S., Vasudevan, P., Villa, O., White, S. M., Zahir, F. R., study, T. DDD., Woolf, A. S. & Banka, S., 7 Dec 2017, In: American Journal of Human Genetics. 101, 6, p. 1021-1033 13 p.

Research output: Contribution to journal › Article › peer-review

Exogenous transforming growth factor-beta 1 enhances smooth muscle differentiation in embryonic mouse jejunal explants.

Coletta, R., Roberts, N., Randles, M., Morabito, A. & Woolf, A. S., 2017, In: Journal of Tissue Engineering and Regenerative Medicine.

Research output: Contribution to journal › Article › peer-review