Prof Adrian S. WoolfMA MD

Chair in Paediatric Science

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Publications

  1. 2019
  2. Accepted/In press

    Loss-of-function variants in myocardin cause congenital megabladder in humans and mice

    Beaman, G., Lopes, F., Ellingford, J., Newman, W., Woolf, A. S. & et al., 4 Sep 2019, (Accepted/In press) In : Journal of Clinical Investigation.

    Research output: Contribution to journalArticle

  3. Accepted/In press

    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., 6 Aug 2019, (Accepted/In press) In : Journal of Pathology.

    Research output: Contribution to journalArticle

  4. Accepted/In press

    A homozygous missense variant in CHRM3 associated with familial urinary bladder disease

    Newman, W., O'Keefe, R., Thomas, H., Wood, K., Urquhart, J., O'Sullivan, J., Beaman, G., Woolf, A. S. & Stuart, H., 2 Aug 2019, (Accepted/In press) In : Clinical Genetics.

    Research output: Contribution to journalArticle

  5. Accepted/In press

    HNF1B mutations are associated with a Gitelman-like tubulopathy that develops during childhood

    Adalat, S., Hayes, W., Bryant, W. A., Booth, J., Woolf, A. S., Kleta, R., Subtil, S., Clissold, R., Colclough, K., Ellard, S. & Bockenhauer, D., 21 May 2019, (Accepted/In press) In : Kidney International Reports.

    Research output: Contribution to journalArticle

  6. Published

    Uncovering genetic mechanisms of kidney aging through transcriptomics, genomics, and epigenomics

    Rowland, J., Akbarov, A., Eales, J., Xu, X., Dormer, J., Guo, H., Denniff, M., Jiang, X., Ranjzad, P., Nazgiewicz, A., Ribeiro Prestes, P., Antczak, A., Szulinska, M., Wise, I., Zukowska-Szczechowska, E., Bogdanski, P., Woolf, A. S., Samani, N. J., Charchar, F. J. & Tomaszewski, M., Mar 2019, In : Kidney International. 95, 3, p. 624-635 12 p.

    Research output: Contribution to journalArticle

  7. Published

    22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complex

    Newman, W., Woolf, A. S., Beaman, G., Cervellione, R., Stuart, H., Keene, D. & Mushtaq, I., 2019, In : American Journal of Medical Genetics. Part A.

    Research output: Contribution to journalArticle

  8. Published

    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 journalArticle

  9. Published

    Growing a new human kidney

    Woolf, A. S., 2019, In : Kidney International.

    Research output: Contribution to journalArticle

  10. Published

    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., 2019, In : Kidney International.

    Research output: Contribution to journalArticle

  11. Published

    Rare Variants in BNC2 are implicated in autosomal dominant congenital lower urinary tract obstruction

    Kolvenbach, C. M., Dworschak, G. C., Frese, S., Japp, A. S., Schuster, P., Wenzlitschke, N., Yilmaz, O., Lopes, F., Pryalukhin, A., Schierbaum, L., van der Zanden, L. F. M., Kause, F., Schneider, R., Taranta-Janusz, K., Szczepanska, M., Pawlaczyk, K., Newman, W. G., Beaman, G. M., Stuart, H. M., Cervellione, R. & 20 othersFeitz, W. F. J., van Rooij, I. A. L. M., Schreuder, M. F., Steffens, M., Weber, S., Merz, W. M., Feldkotter, M., Hoppe, B., Thiele, H., Altmuller, J., Berg, C., Kristiansen, G., Ludwig, M., Reutter, H., Woolf, A. S., Hilderbrandt, F., Grote, P., Zaniew, M., Odermatt, B. & Hilger, A. C., 2019, In : American Journal of Human Genetics.

    Research output: Contribution to journalArticle

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