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For: Woolf AS, Lopes FM, Ranjzad P, Roberts NA. Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies. Front Pediatr 2019;7:136. [PMID: 31032239 DOI: 10.3389/fped.2019.00136] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Adamu-Biu F, Han EY, Miakhil SI, Makhija R. A Rare and Late Complication of Subureteric Teflon Injection With Non-Animal Stabilized Hyaluronic Acid/Dextranomer Gel. Cureus 2023;15:e33238. [PMID: 36601359 DOI: 10.7759/cureus.33238] [Reference Citation Analysis]
2 Grenier C, Lopes FM, Cueto-gonzález AM, Rovira-moreno E, Gander R, Jarvis BW, Mccloskey KD, Gurney AM, Beaman GM, Newman WG, Woolf AS, Roberts NA. Neurogenic defects underlie functional bladder outflow tract obstruction associated with biallelic variants inLRIG2.. [DOI: 10.1101/2022.12.06.22283097] [Reference Citation Analysis]
3 Beaman GM, Lopes FM, Hofmann A, Roesch W, Promm M, Bijlsma EK, Patel C, Akinci A, Burgu B, Knijnenburg J, Ho G, Aufschlaeger C, Dathe S, Voelckel MA, Cohen M, Yue WW, Stuart HM, Mckenzie EA, Elvin M, Roberts NA, Woolf AS, Newman WG. Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder. Front Genet 2022;13:896125. [DOI: 10.3389/fgene.2022.896125] [Reference Citation Analysis]
4 Woolf AS. The term CAKUT has outlived its usefulness: the case for the prosecution. Pediatr Nephrol 2022. [PMID: 35575937 DOI: 10.1007/s00467-022-05576-4] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Beaman GM, Woolf AS, Lopes FM, Guo SA, Harkness JR, Cervellione RM, Keene D, Mushtaq I, Clatworthy MR, Newman WG. Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophy-epispadias complex. Journal of Pediatric Urology 2022. [DOI: 10.1016/j.jpurol.2022.04.006] [Reference Citation Analysis]
6 Kurz J, Weiss A, Thiesler H, Qasrawi F, Deuper L, Kaur J, Rudat C, Lüdtke TH, Wojahn I, Hildebrandt H, Trowe M, Kispert A. Notch signaling is a novel regulator of visceral smooth muscle cell differentiation in the murine ureter. Development 2022;149. [DOI: 10.1242/dev.199735] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Lange-sperandio B, Rosenblum ND. Pediatric Obstructive Uropathy. Pediatric Nephrology 2022. [DOI: 10.1007/978-3-030-52719-8_51] [Reference Citation Analysis]
8 Woolf AS, Ashley SL. Nephrogenesis in health and disease. Regenerative Nephrology 2022. [DOI: 10.1016/b978-0-12-823318-4.00002-0] [Reference Citation Analysis]
9 Sceberras V, Maria Magrelli F, Adamo D, Maurizi E, Attico E, Giuseppe Genna V, Lazzeri M, Barbagli G, Pellegrini G. The cell as a tool to understand and repair urethra. Scientific Advances in Reconstructive Urology and Tissue Engineering 2022. [DOI: 10.1016/b978-0-323-91199-3.00001-3] [Reference Citation Analysis]
10 Anand S, Bajpai M, Kumar A, Kapahtia S. Early Evidence on Genetic Polymorphisms in Conferring A "Two-Hit" Propensity to Renal Injury in Asian Indian Children. J Indian Assoc Pediatr Surg 2022;27:741-6. [PMID: 36714477 DOI: 10.4103/jiaps.jiaps_84_22] [Reference Citation Analysis]
11 Woolf AS. Building human renal tracts. J Pediatr Surg 2021:S0022-3468(21)00735-1. [PMID: 34838308 DOI: 10.1016/j.jpedsurg.2021.10.022] [Reference Citation Analysis]
12 Lopes FM, Woolf AS, Roberts NA. Envisioning treating genetically-defined urinary tract malformations with viral vector-mediated gene therapy. J Pediatr Urol 2021:S1477-5131(21)00339-9. [PMID: 34312114 DOI: 10.1016/j.jpurol.2021.07.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
13 Fédou C, Camus M, Lescat O, Feuillet G, Mueller I, Ross B, Buléon M, Neau E, Alves M, Goudounéche D, Breuil B, Boizard F, Bardou Q, Casemayou A, Tack I, Dreux S, Batut J, Blader P, Burlet-Schiltz O, Decramer S, Wirth B, Klein J, Saulnier-Blache JS, Buffin-Meyer B, Schanstra JP. Mapping of the amniotic fluid proteome of fetuses with congenital anomalies of the kidney and urinary tract identifies plastin 3 as a protein involved in glomerular integrity. J Pathol 2021;254:575-88. [PMID: 33987838 DOI: 10.1002/path.5703] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
14 Lange-sperandio B, Rosenblum ND. Pediatric Obstructive Uropathy. Pediatric Nephrology 2021. [DOI: 10.1007/978-3-642-27843-3_51-2] [Reference Citation Analysis]
15 Kubik MJ, Wyczanska M, Gasparitsch M, Keller U, Weber S, Schaefer F, Lange-Sperandio B. Renal developmental genes are differentially regulated after unilateral ureteral obstruction in neonatal and adult mice. Sci Rep 2020;10:19302. [PMID: 33168884 DOI: 10.1038/s41598-020-76328-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
16 Manak I, Gurney AM, Mccloskey KD, Woolf AS, Roberts NA. Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice. Neurourology and Urodynamics 2020;39:1930-8. [DOI: 10.1002/nau.24450] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
17 Houweling AC, Beaman GM, Postma AV, Gainous TB, Lichtenbelt KD, Brancati F, Lopes FM, van der Made I, Polstra AM, Robinson ML, Wright KD, Ellingford JM, Jackson AR, Overwater E, Genesio R, Romano S, Camerota L, D'Angelo E, Meijers-Heijboer EJ, Christoffels VM, McHugh KM, Black BL, Newman WG, Woolf AS, Creemers EE. Loss-of-function variants in myocardin cause congenital megabladder in humans and mice. J Clin Invest 2019;129:5374-80. [PMID: 31513549 DOI: 10.1172/JCI128545] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 6.0] [Reference Citation Analysis]
18 Barteri F, Esteve-altava B. The Role of Transposable Elements in Congenital Malformations with Notes on Their Potential Implications for Morphological Evolution in Mammals. Curr Mol Bio Rep 2020;6:71-78. [DOI: 10.1007/s40610-020-00134-z] [Reference Citation Analysis]
19 Ikeda Y. Neurophysiological control of urinary bladder storage and voiding-functional changes through development and pathology. Pediatr Nephrol 2021;36:1041-52. [PMID: 32415328 DOI: 10.1007/s00467-020-04594-4] [Reference Citation Analysis]
20 Sukalo AV, Kilchevsky AV, Mazur OC, Sheuchuk IV, Mikhalenkо AP, Baiko SV. Genetic aspects of congenital anomalies of the kidney and urinary tract. Nefrologiâ (St -Peterbg ) 2020;24:9-14. [DOI: 10.36485/1561-6274-2020-24-3-9-14] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
21 Nassau DE, Chu KY, Blachman-braun R, Castellan M, Ramasamy R. The pediatric patient and future fertility: optimizing long-term male reproductive health outcomes. Fertility and Sterility 2020;113:489-99. [DOI: 10.1016/j.fertnstert.2020.01.003] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
22 Prada-rico M, González-chaparro LE, Gastelbondo-amaya R, Malo-rodríguez G, Vergara-méndez D, Gelvez-nieto JC, Hernández-sarmiento R. Síndrome de Prune Belly en una paciente adolescente. Revista Mexicana de Pediatría 2020;87:227-231. [DOI: 10.35366/97685] [Reference Citation Analysis]