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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 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]
2 Chan MMY, Sadeghi-Alavijeh O, Lopes FM, Hilger AC, Stanescu HC, Voinescu CD, Beaman GM, Newman WG, Zaniew M, Weber S, Ho YM, Connolly JO, Wood D, Maj C, Stuckey A, Kousathanas A, Kleta R, Woolf AS, Bockenhauer D, Levine AP, Gale DP; Genomics England Research Consortium. Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves. Elife 2022;11:e74777. [PMID: 36124557 DOI: 10.7554/eLife.74777] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [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 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. J Pediatr Urol 2022;18:362.e1-8. [PMID: 35491304 DOI: 10.1016/j.jpurol.2022.04.006] [Reference Citation Analysis]
5 Jordan P, Dorval G, Arrondel C, Morinière V, Tournant C, Audrezet MP, Michel-Calemard L, Putoux A, Lesca G, Labalme A, Whalen S, Loeuillet L, Martinovic J, Attie-Bitach T, Bessières B, Schaefer E, Scheidecker S, Lambert L, Beneteau C, Patat O, Boute-Benejean O, Molin A, Guimiot F, Fontanarosa N, Nizon M, Lefebvre M, Jeanpierre C, Saunier S, Heidet L. Targeted next-generation sequencing in a large series of fetuses with severe renal diseases. Hum Mutat 2022. [PMID: 35005812 DOI: 10.1002/humu.24324] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
6 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]
7 Woolf AS. The term CAKUT has outlived its usefulness: the case for the prosecution. Pediatr Nephrol 2022;37:2785-91. [PMID: 35575937 DOI: 10.1007/s00467-022-05576-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Dinsmore CJ, Soriano P. Differential regulation of cranial and cardiac neural crest by Serum Response Factor.. [DOI: 10.1101/2021.10.28.466305] [Reference Citation Analysis]
9 Chan MM, Sadeghi-alavijeh O, Lopes FM, Hilger AC, Stanescu HC, Voinescu CD, Beaman GM, Newman WG, Zaniew M, Weber S, Connolly JO, Wood D, Stuckey A, Kousathanas A, Kleta R, Woolf AS, Bockenhauer D, Levine AP, Gale DP, Genomics England Research Consortium. Mixed ancestry analysis of whole-genome sequencing identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves.. [DOI: 10.1101/2021.08.09.21261801] [Reference Citation Analysis]
10 Hashmi SK, Ceron RH, Heuckeroth RO. Visceral myopathy: clinical syndromes, genetics, pathophysiology, and fall of the cytoskeleton. Am J Physiol Gastrointest Liver Physiol 2021;320:G919-35. [PMID: 33729000 DOI: 10.1152/ajpgi.00066.2021] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
11 Verberne EA, Faries S, Mannens MMAM, Postma AV, van Haelst MM. Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiency. Am J Med Genet A 2020;182:1952-6. [PMID: 32462814 DOI: 10.1002/ajmg.a.61632] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 3.7] [Reference Citation Analysis]