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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Sadeghi-alavijeh O, Chan MM, Moochhala S, Howles S, Gale DP, Böckenhauer D, Genomics England Research Consortium. Rare variants in SLC34A3 explain missing heritability of urinary stone disease.. [DOI: 10.1101/2022.12.02.22283024] [Reference Citation Analysis]
2 Groen In 't Woud S, Maj C, Renkema KY, Westland R, Galesloot T, van Rooij IALM, Vermeulen SH, Feitz WFJ, Roeleveld N, Schreuder MF, van der Zanden LFM; SOFIA Study Group. A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney. Biomedicines 2022;10. [PMID: 36551779 DOI: 10.3390/biomedicines10123023] [Reference Citation Analysis]
3 Allison SJ. Genetics of posterior urethral valves. Nat Rev Nephrol 2022. [DOI: 10.1038/s41581-022-00649-x] [Reference Citation Analysis]