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Cited by in F6Publishing
For: Penchev V, Boueva A, Kamenarova K, Roussinov D, Tzveova R, Ivanova M, Dimitrova V, Kremensky I, Mitev V, Kaneva R, Beltcheva O. A familial case of severe infantile nephronophthisis explained by oligogenic inheritance. Eur J Med Genet 2017;60:321-5. [PMID: 28392475 DOI: 10.1016/j.ejmg.2017.04.002] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
Number Citing Articles
1 Luo F, Tao YH. Nephronophthisis: A review of genotype-phenotype correlation. Nephrology (Carlton). 2018;23:904-911. [PMID: 29717526 DOI: 10.1111/nep.13393] [Cited by in Crossref: 22] [Cited by in F6Publishing: 18] [Article Influence: 5.5] [Reference Citation Analysis]
2 Watanabe S, Ino J, Fujimaru T, Taneda S, Akihisa T, Makabe S, Kataoka H, Mori T, Sohara E, Uchida S, Nitta K, Mochizuki T. PKD1 mutation may epistatically ameliorate nephronophthisis progression in patients with NPHP1 deletion. Clin Case Rep 2019;7:336-9. [PMID: 30847201 DOI: 10.1002/ccr3.1947] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
3 Alsemari A, Alsuhaibani M, Alhathlool R, Ali BM. Potential oligogenic disease of mental retardation, short stature, spastic paraparesis, and osteopetrosis. Appl Clin Genet 2018;11:129-34. [PMID: 30510438 DOI: 10.2147/TACG.S172176] [Reference Citation Analysis]
4 Strong A, Muneeruddin S, Parrish R, Lui D, Conley SB. Isosorbide dinitrate in nephronophthisis treatment. Am J Med Genet A 2018;176:1023-6. [PMID: 29575630 DOI: 10.1002/ajmg.a.38650] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]