Gernetic Basis of Congenital Bladder and Lower Urinary Tract Disorders.

Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves
Genomics England Research Consortium, Chan, M. M. Y., Sadeghi-Alavijeh, O., Lopes, F. M., Hilger, A. C., Stanescu, H. C., Voinescu, C. D., Beaman, G., Newman, W. G., Zaniew, M., Weber, S., Ho, Y. M., Connolly, J. O., Wood, D., Maj, C., Stuckey, A., Kousathanas, A., Kleta, R., Woolf, A. S. & Bockenhauer , D. & 2 others, Levine, A. P. & Gale, D. P., 15 Aug 2022, (Accepted/In press) In: eLife.
Research output: Contribution to journal › Article › peer-review
The genomic architecture of bladder exstrophy epispadias complex
Newman, W., Beaman, G., Keene, D., Cervellione, R. & Reutter, H., 28 Jul 2021, In: Genes.
Research output: Contribution to journal › Review article › peer-review

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Early B-cell factor 3-related genetic disease can mimic urofacial syndrome
Newman, W., Harkness, R., Beaman, G., Thomas, H., Wood, K., Stuart, H. & Woolf, A. S., 1 Jul 2020, (Accepted/In press) In: Kidney International Reports.
Research output: Contribution to journal › Article › peer-review

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