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Cited by in F6Publishing
For: Wopperer FJ, Knaup KX, Stanzick KJ, Schneider K, Jobst-schwan T, Ekici AB, Uebe S, Wenzel A, Schliep S, Schürfeld C, Seitz R, Bernhardt W, Gödel M, Wiesener A, Popp B, Stark KJ, Gröne H, Friedrich B, Weiß M, Basic-jukic N, Schiffer M, Schröppel B, Huettel B, Beck BB, Sayer JA, Ziegler C, Büttner-herold M, Amann K, Heid IM, Reis A, Pasutto F, Wiesener MS. Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases. Kidney International 2022. [DOI: 10.1016/j.kint.2022.04.031] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Mallett AJ. Which patients with CKD will benefit from genomic sequencing? Synthesizing progress to illuminate the future. Curr Opin Nephrol Hypertens 2022;31:541-7. [PMID: 36093902 DOI: 10.1097/MNH.0000000000000836] [Reference Citation Analysis]
2 Popp B, Ekici AB, Knaup KX, Schneider K, Uebe S, Park J, Bafna V, Meiselbach H, Eckardt K, Schiffer M, Reis A, Kraus C, Wiesener M. Prevalence of hereditary tubulointerstitial kidney diseases in the German Chronic Kidney Disease study. Eur J Hum Genet. [DOI: 10.1038/s41431-022-01177-9] [Reference Citation Analysis]