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Cited by in F6Publishing
For: Jayasinghe K, Stark Z, Kerr PG, Gaff C, Martyn M, Whitlam J, Creighton B, Donaldson E, Hunter M, Jarmolowicz A, Johnstone L, Krzesinski E, Lunke S, Lynch E, Nicholls K, Patel C, Prawer Y, Ryan J, See EJ, Talbot A, Trainer A, Tytherleigh R, Valente G, Wallis M, Wardrop L, West KH, White SM, Wilkins E, Mallett AJ, Quinlan C. Clinical impact of genomic testing in patients with suspected monogenic kidney disease. Genet Med 2021;23:183-91. [PMID: 32939031 DOI: 10.1038/s41436-020-00963-4] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Devarajan P, Chertow GM, Susztak K, Levin A, Agarwal R, Stenvinkel P, Chapman AB, Warady BA. Emerging Role of Clinical Genetics in CKD. Kidney Medicine 2022. [DOI: 10.1016/j.xkme.2022.100435] [Reference Citation Analysis]
2 Pinto E Vairo F, Prochnow C, Kemppainen JL, Lisi EC, Steyermark JM, Kruisselbrink TM, Pichurin PN, Dhamija R, Hager MM, Albadri S, Cornell LD, Lazaridis KN, Klee EW, Senum SR, El Ters M, Amer H, Baudhuin LM, Moyer AM, Keddis MT, Zand L, Sas DJ, Erickson SB, Fervenza FC, Lieske JC, Harris PC, Hogan MC. Genomics Integration Into Nephrology Practice. Kidney Med 2021;3:785-98. [PMID: 34746741 DOI: 10.1016/j.xkme.2021.04.014] [Reference Citation Analysis]
3 Becherucci F, Landini S, Cirillo L, Mazzinghi B, Romagnani P. Look Alike, Sound Alike: Phenocopies in Steroid-Resistant Nephrotic Syndrome. Int J Environ Res Public Health 2020;17:E8363. [PMID: 33198123 DOI: 10.3390/ijerph17228363] [Reference Citation Analysis]
4 Pinto E Vairo F, Kemppainen JL, Lieske JC, Harris PC, Hogan MC. Establishing a nephrology genetic clinic. Kidney Int 2021;100:254-9. [PMID: 34294204 DOI: 10.1016/j.kint.2021.05.008] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Xiao H, Hildebrandt F. Whole exome sequencing identifies monogenic forms of nephritis in a previously unsolved cohort of children with steroid-resistant nephrotic syndrome and hematuria. Pediatr Nephrol 2021. [PMID: 34762194 DOI: 10.1007/s00467-021-05312-4] [Reference Citation Analysis]
6 Chen J, Lin F, Zhai Y, Wang C, Wu B, Ma D, Rao J, Liu J, Liu J, Yu M, Shen Q, Xu H. Diagnostic and clinical utility of genetic testing in children with kidney failure. Pediatr Nephrol 2021. [PMID: 34031707 DOI: 10.1007/s00467-021-05141-5] [Reference Citation Analysis]
7 Zacchia M, Blanco FDV, Trepiccione F, Blasio G, Torella A, Melluso A, Capolongo G, Pollastro RM, Piluso G, Di Iorio V, Simonelli F, Viggiano D, Perna A, Nigro V, Capasso G. Nephroplex: a kidney-focused NGS panel highlights the challenges of PKD1 sequencing and identifies a founder BBS4 mutation. J Nephrol 2021. [PMID: 33964006 DOI: 10.1007/s40620-021-01048-4] [Reference Citation Analysis]
8 Jayasinghe K, Quinlan C, Mallett AJ, Kerr PG, McClaren B, Nisselle A, Mallawaarachchi A, Polkinghorne KR, Patel C, Best S, Stark Z. Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics. Kidney Int Rep 2021;6:272-83. [PMID: 33615052 DOI: 10.1016/j.ekir.2020.10.030] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
9 Mrug M, Bloom MS, Seto C, Malhotra M, Tabriziani H, Gauthier P, Sidlow V, McKanna T, Billings PR. Genetic Testing for Chronic Kidney Diseases: Clinical Utility and Barriers Perceived by Nephrologists. Kidney Med 2021;3:1050-6. [PMID: 34939014 DOI: 10.1016/j.xkme.2021.08.006] [Reference Citation Analysis]
10 Jayasinghe K, Wu Y, Stark Z, Kerr PG, Mallett AJ, Gaff C, Martyn M, Goranitis I, Quinlan C. Cost-Effectiveness of Targeted Exome Analysis as a Diagnostic Test in Glomerular Diseases. Kidney Int Rep 2021;6:2850-61. [PMID: 34805637 DOI: 10.1016/j.ekir.2021.08.028] [Reference Citation Analysis]
11 Thomas CP, Gupta S, Freese ME, Chouhan KK, Dantuma MI, Holanda DG, Katz DA, Darbro BW, Mansilla MA, Smith RJ. Sequential genetic testing of living-related donors for inherited renal disease to promote informed choice and enhance safety of living donation. Transpl Int 2021. [PMID: 34632641 DOI: 10.1111/tri.14133] [Reference Citation Analysis]