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Author Details

Adrian S Woolf
The University of Manchester
1976
241
55
PMIDPaper TitleJournal TitlePublished Year
38056891When should we offer antenatal sequencing for urinary tract malformations? A systematic review, cohort study and meta-analysis.Prenat Diagn2024
37441484Neurogenic Defects Occur in <i>LRIG2</i>-Associated Urinary Bladder Disease.Kidney Int Rep2023
37580336Predicting congenital renal tract malformation genes using machine learning.Sci Rep2023
36977792Modelling human lower urinary tract malformations in zebrafish.Mol Cell Pediatr2023
34838308Building human renal tracts.J Pediatr Surg2022
35772019Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney Malformations.Nephrol Dial Transplant2022
35575937The term CAKUT has outlived its usefulness: the case for the prosecution.Pediatr Nephrol2022
35491304Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophy-epispadias complex.J Pediatr Urol2022
35812751Expanding the <i>HPSE2</i> Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder.Front Genet2022
36275765Monocyte-derived peritoneal macrophages protect C57BL/6 mice against surgery-induced adhesions.Front Immunol2022
36352089A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.Commun Biol2022
36124557Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valves.Elife2022
34919690Haploinsufficiency of the mouse Tshz3 gene leads to kidney defects.Hum Mol Genet2022
33306987The miR-199a/214 Cluster Controls Nephrogenesis and Vascularization in a Human Embryonic Stem Cell Model.Stem Cell Reports2021
33609573Making human collecting ducts and modeling disease in the laboratory.Kidney Int2021
33774632Towards Modelling Genetic Kidney Diseases with Human Pluripotent Stem Cells.Nephron2021
33958779Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney.Nat Genet2021
34312114Envisioning treating genetically-defined urinary tract malformations with viral vector-mediated gene therapy.J Pediatr Urol2021
34330963Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder.Sci Rep2021
32534991Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformations.Eur J Med Genet2020
31701459Formation of Mature Nephrons by Implantation of Human Pluripotent Stem Cell-Derived Progenitors into Mice.Methods Mol Biol2020
33102976Early B-cell Factor 3-Related Genetic Disease Can Mimic Urofacial Syndrome.Kidney Int Rep2020
33206176Hypertension and renin-angiotensin system blockers are not associated with expression of angiotensin-converting enzyme 2 (ACE2) in the kidney.Eur Heart J2020
32609936Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice.Neurourol Urodyn2020
32850778SLC20A1 Is Involved in Urinary Tract and Urorectal Development.Front Cell Dev Biol2020
32756058Aberrant Differentiation of Human Pluripotent Stem Cell-Derived Kidney Precursor Cells inside Mouse Vascularized Bioreactors.Nephron2020
32274739Heparanase 2 and Urofacial Syndrome, a Genetic Neuropathy.Adv Exp Med Biol2020
3062814822q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complex.Am J Med Genet A2019
31808745Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease.Elife2019
31441039A homozygous missense variant in CHRM3 associated with familial urinary bladder disease.Clin Genet2019
31517149HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During Childhood.Kidney Int Rep2019
31400222Overactivity or blockade of transforming growth factor-β each generate a specific ureter malformation.J Pathol2019
31399199Growing a new human kidney.Kidney Int2019
31032239Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies.Front Pediatr2019
30885509Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder.Kidney Int2019
31051115Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction.Am J Hum Genet2019
30784661Uncovering genetic mechanisms of kidney aging through transcriptomics, genomics, and epigenomics.Kidney Int2019
28647851A questionnaire survey of radiological diagnosis and management of renal dysplasia in children.J Nephrol2018
30125361Vangl2, a planar cell polarity molecule, is implicated in irreversible and reversible kidney glomerular injury.J Pathol2018
30148153From human pluripotent stem cells to functional kidney organoids and models of renal disease.Stem Cell Investig2018
30467309Molecular insights into genome-wide association studies of chronic kidney disease-defining traits.Nat Commun2018
28084682Exogenous transforming growth factor-β1 enhances smooth muscle differentiation in embryonic mouse jejunal explants.J Tissue Eng Regen Med2018
29774544Functional molecules in mesothelial-to-mesenchymal transition revealed by transcriptome analyses.J Pathol2018
29429961Generation of Functioning Nephrons by Implanting Human Pluripotent Stem Cell-Derived Kidney Progenitors.Stem Cell Reports2018
29311702Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux.Sci Rep2018
29220674ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder.Am J Hum Genet2017
28176844ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development.Sci Rep2017
28968868International multi-centre study of pregnancy outcomes with interleukin-1 inhibitors.Rheumatology (Oxford)2017
29097723Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux.Sci Rep2017
26038530Vascular Endothelial Growth Factor C for Polycystic Kidney Diseases.J Am Soc Nephrol2016
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Collaborators

Royal Devon University Healthcare NHS Foundation Trust
Co-authored papers 9
Great Ormond Street Hospital for Children, NHS Foundation Trust
Co-authored papers 6
Population Health Sciences Institute, Newcastle University
Co-authored papers 6
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Guys' and St Thomas' NHS Foundation Trust
Co-authored papers 5
University Children's Hospital Heidelberg
Co-authored papers 4
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Co-authored papers 4
Imperial College London
Co-authored papers 4
UCL Great Ormond Street Institute of Child Health, University College London
Co-authored papers 3
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 3
UCL Great Ormond Street Institute of Child Health Library
Co-authored papers 3
Co-authored papers 3
University of Manchester
Co-authored papers 3
Medical Clinic and Policlinic IV, University of Munich
Co-authored papers 2
Manchester University Hospitals NHS Foundation Trust, St Mary's Hospital
Co-authored papers 2
Co-authored papers 2
Boston Children's Hospital
Co-authored papers 2
Co-authored papers 2
Wellcome Sanger Institute
Co-authored papers 2
University of Manchester
Co-authored papers 2
The University of Manchester
Co-authored papers 2
Institute of Human Development, University of Manchester
Co-authored papers 2
Hospital Clinico Universitario de Santiago de Compostela
Co-authored papers 2
University of Michigan ann arbor
Co-authored papers 2
Institute of Human Genetics, University Hospital of Bonn & University of Bonn
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UCL Institute of Child Health and Great Ormond Street NHS Foundation Trust
Co-authored papers 1
The University of Melbourne, The Royal Children's Hospital
Co-authored papers 1