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Cited by in F6Publishing
For: Gaut JP, Jain S, Pfeifer JD, Vigh-Conrad KA, Corliss M, Sharma MK, Heusel JW, Cottrell CE. Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathies. Mod Pathol 2017;30:1739-47. [PMID: 28752844 DOI: 10.1038/modpathol.2017.90] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
Number Citing Articles
1 Park J, Yhim HY, Kang KP, Bae TW, Cho YG. Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report. Hematology 2022;27:603-8. [PMID: 35617302 DOI: 10.1080/16078454.2022.2075121] [Reference Citation Analysis]
2 Lien YH. No More Thrombotic Thrombocytopenic Purpura/Hemolytic Uremic Syndrome Please. Am J Med 2019;132:134-5. [PMID: 30367852 DOI: 10.1016/j.amjmed.2018.10.009] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
3 Wenderfer SE, Gaut JP. Glomerular Diseases in Children. Adv Chronic Kidney Dis 2017;24:364-71. [PMID: 29229167 DOI: 10.1053/j.ackd.2017.09.005] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 4.2] [Reference Citation Analysis]
4 Ren Z, Perkins SJ, Love-Gregory L, Atkinson JP, Java A. Clinicopathologic Implications of Complement Genetic Variants in Kidney Transplantation. Front Med (Lausanne) 2021;8:775280. [PMID: 34912830 DOI: 10.3389/fmed.2021.775280] [Reference Citation Analysis]