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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Bentley-Ford MR, LaBonty M, Thomas HR, Haycraft CJ, Scott M, LaFayette C, Croyle MJ, Andersen RS, Parant JM, Yoder BK. Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypes. Genetics 2021:iyab209. [PMID: 34850872 DOI: 10.1093/genetics/iyab209] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Mansour F, Boivin FJ, Shaheed IB, Schueler M, Schmidt-Ott KM. The Role of Centrosome Distal Appendage Proteins (DAPs) in Nephronophthisis and Ciliogenesis. Int J Mol Sci 2021;22:12253. [PMID: 34830133 DOI: 10.3390/ijms222212253] [Reference Citation Analysis]
3 Stokman MF, Saunier S, Benmerah A. Renal Ciliopathies: Sorting Out Therapeutic Approaches for Nephronophthisis. Front Cell Dev Biol 2021;9:653138. [PMID: 34055783 DOI: 10.3389/fcell.2021.653138] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Al-Hamed MH, Alzaidan H, Hussein M, Albaik L, Qari A, Sayer JA, Imtiaz F. Novel pathogenic MAPKBP1 variant in a family with nephronophthisis. Clin Kidney J 2021;14:728-30. [PMID: 33623699 DOI: 10.1093/ckj/sfaa090] [Reference Citation Analysis]
5 Murray SL, Fennelly NK, Doyle B, Lynch SA, Conlon PJ. Integration of genetic and histopathology data in interpretation of kidney disease. Nephrol Dial Transplant 2020;35:1113-32. [PMID: 32777081 DOI: 10.1093/ndt/gfaa176] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Amano K, Toyoda H, Nishikawa K, Murata T, Hirayama M. Case Report: Effects of Secondary Hyperparathyroidism Treatment on Improvement of Juvenile Nephronophthisis-Induced Pancytopenia and Myelofibrosis. Front Pediatr 2021;9:550158. [PMID: 34046371 DOI: 10.3389/fped.2021.550158] [Reference Citation Analysis]
7 Kulkarni S, Abro B, Duque Lasio ML, Stoll J, Grange DK, He M. Clinical and Pathological Features of a Newborn With Compound Heterozygous ANKS6 Variants. Pediatr Dev Pathol 2020;23:235-9. [PMID: 31635528 DOI: 10.1177/1093526619881541] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
8 Gupta S, Ozimek-Kulik JE, Phillips JK. Nephronophthisis-Pathobiology and Molecular Pathogenesis of a Rare Kidney Genetic Disease. Genes (Basel) 2021;12:1762. [PMID: 34828368 DOI: 10.3390/genes12111762] [Reference Citation Analysis]
9 Zhang J, Zhang C, Gao E, Zhou Q. Next-Generation Sequencing-Based Genetic Diagnostic Strategies of Inherited Kidney Diseases. Kidney Dis (Basel) 2021;7:425-37. [PMID: 34901190 DOI: 10.1159/000519095] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Zhong Z, Yan X, Fang Z, Dong Y, Tan J, Xie J, Hu L, Zhang S, Qin W. Case Report: Adolescent-Onset Isolated Nephronophthisis Caused by a Novel Homozygous Inversin Mutation. Front Genet 2022;13:847397. [PMID: 35664325 DOI: 10.3389/fgene.2022.847397] [Reference Citation Analysis]
11 Yue Z, Lin H, Li M, Wang H, Liu T, Hu M, Chen H, Tong H, Sun L. Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisis. Clin Chim Acta 2020;506:136-44. [PMID: 32173348 DOI: 10.1016/j.cca.2020.03.015] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Sánchez-Bellver L, Toulis V, Marfany G. On the Wrong Track: Alterations of Ciliary Transport in Inherited Retinal Dystrophies. Front Cell Dev Biol 2021;9:623734. [PMID: 33748110 DOI: 10.3389/fcell.2021.623734] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Larrue R, Chamley P, Bardyn T, Lionet A, Gnemmi V, Cauffiez C, Glowacki F, Pottier N, Broly F. Diagnostic utility of whole-genome sequencing for nephronophthisis. NPJ Genom Med 2020;5:38. [PMID: 33024573 DOI: 10.1038/s41525-020-00147-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
14 Santoni M, Piva F, Cimadamore A, Giulietti M, Battelli N, Montironi R, Cosmai L, Porta C. Exploring the Spectrum of Kidney Ciliopathies. Diagnostics (Basel) 2020;10:E1099. [PMID: 33339422 DOI: 10.3390/diagnostics10121099] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Knotek M, Novak R, Jaklin-Kelez A, Mrzljak A. Combined liver-kidney transplantation for rare diseases. World J Hepatol 2020; 12(10): 722-737 [PMID: 33200012 DOI: 10.4254/wjh.v12.i10.722] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
16 Mikoda N, Sonoda H, Oshikawa S, Hoshino Y, Matsuzaki T, Ikeda M. A bell-shaped pattern of urinary aquaporin-2-bearing extracellular vesicle release in an experimental model of nephronophthisis. Physiol Rep 2019;7:e14092. [PMID: 31074077 DOI: 10.14814/phy2.14092] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Hale ZE, Sadoshima J. Primary Cilia and Their Role in Acquired Heart Disease. Cells 2022;11:960. [DOI: 10.3390/cells11060960] [Reference Citation Analysis]
18 Fujimaru T, Kawanishi K, Mori T, Mishima E, Sekine A, Chiga M, Mizui M, Sato N, Yanagita M, Ooki Y, Nagahama K, Ohnuki Y, Hamano N, Watanabe S, Mochizuki T, Nagatsuji K, Tanaka K, Tsukamoto T, Tsushima H, Shimamoto M, Tsuji T, Kuyama T, Kawamoto S, Maki K, Katsuma A, Oishi M, Yamamoto K, Mandai S, Kikuchi H, Ando F, Mori Y, Susa K, Iimori S, Naito S, Rai T, Hoshino J, Ubara Y, Miyazaki M, Nagata M, Uchida S, Sohara E. Genetic Background and Clinicopathologic Features of Adult-onset Nephronophthisis. Kidney Int Rep 2021;6:1346-54. [PMID: 34013113 DOI: 10.1016/j.ekir.2021.02.005] [Reference Citation Analysis]
19 Tsutsumi R, Chaya T, Tsujii T, Furukawa T. The carboxyl-terminal region of SDCCAG8 comprises a functional module essential for cilia formation as well as organ development and homeostasis. Journal of Biological Chemistry 2022. [DOI: 10.1016/j.jbc.2022.101686] [Reference Citation Analysis]
20 Al Alawi I, Powell L, Rice SJ, Al Riyami MS, Al-riyami M, Al Salmi I, Sayer JA. Case Report: A Novel In-Frame Deletion of GLIS2 Leading to Nephronophthisis and Early Onset Kidney Failure. Front Genet 2021;12:791495. [DOI: 10.3389/fgene.2021.791495] [Reference Citation Analysis]
21 Heidenreich LS, Bendel-stenzel EM, Harris PC, Hanna C. Genetic Etiologies, Diagnosis, and Management of Neonatal Cystic Kidney Disease. NeoReviews 2022;23:e175-88. [DOI: 10.1542/neo.23-3-e175] [Reference Citation Analysis]
22 McConnachie DJ, Stow JL, Mallett AJ. Ciliopathies and the Kidney: A Review. Am J Kidney Dis 2021;77:410-9. [PMID: 33039432 DOI: 10.1053/j.ajkd.2020.08.012] [Cited by in Crossref: 11] [Cited by in F6Publishing: 14] [Article Influence: 5.5] [Reference Citation Analysis]
23 Adamiok-Ostrowska A, Piekiełko-Witkowska A. Ciliary Genes in Renal Cystic Diseases. Cells 2020;9:E907. [PMID: 32276433 DOI: 10.3390/cells9040907] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 4.5] [Reference Citation Analysis]
24 König JC, Karsay R, Gerß J, Schlingmann K, Dahmer-heath M, Telgmann A, Kollmann S, Ariceta G, Gillion V, Bockenhauer D, Bertholet-thomas A, Mastrangelo A, Boyer O, Lilien M, Decramer S, Schanstra J, Pohl M, Schild R, Weber S, Hoefele J, Drube J, Cetiner M, Hansen M, Thumfart J, Tönshoff B, Habbig S, Liebau MC, Bald M, Bergmann C, Pennekamp P, Konrad M. Refining Kidney Survival in 383 Genetically Characterized Patients With Nephronophthisis. Kidney International Reports 2022. [DOI: 10.1016/j.ekir.2022.05.035] [Reference Citation Analysis]
25 Nakamura M, Kanda S, Kajiho Y, Morisada N, Iijima K, Harita Y. A case of 17q12 deletion syndrome that presented antenatally with markedly enlarged kidneys and clinically mimicked autosomal recessive polycystic kidney disease. CEN Case Rep 2021;10:543-8. [PMID: 33942272 DOI: 10.1007/s13730-021-00604-y] [Reference Citation Analysis]
26 Jin H, Zhang Y, Liu D, Wang SS, Ding Q, Rastogi P, Purvis M, Wang A, Elhadi S, Ren C, Cao C, Chai Y, Igarashi P, Jetten AM, Lu D, Attanasio M. Innate Immune Signaling Contributes to Tubular Cell Senescence in the Glis2 Knockout Mouse Model of Nephronophthisis. Am J Pathol 2020;190:176-89. [PMID: 31676329 DOI: 10.1016/j.ajpath.2019.09.013] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
27 Alizadeh R, Jamshidi S, Keramatipour M, Moeinian P, Hosseini R, Otukesh H, Talebi S. Whole Exome Sequencing Reveals a XPNPEP3 Novel Mutation Causing Nephronophthisis in a Pediatric Patient. Iran Biomed J 2020;24:405-8. [PMID: 32660933 DOI: 10.29252/ibj.24.6.400] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
28 Monirujjaman M, Aukema HM. Cyclooxygenase 2 inhibition slows disease progression and improves the altered renal lipid mediator profile in the Pkd2WS25/− mouse model of autosomal dominant polycystic kidney disease. J Nephrol 2019;32:401-9. [DOI: 10.1007/s40620-018-00578-8] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
29 Bentley-Ford MR, Andersen RS, Croyle MJ, Haycraft CJ, Clearman KR, Foote JB, Reiter JF, Yoder BK. ATXN10 Is Required for Embryonic Heart Development and Maintenance of Epithelial Cell Phenotypes in the Adult Kidney and Pancreas. Front Cell Dev Biol 2021;9:705182. [PMID: 34970537 DOI: 10.3389/fcell.2021.705182] [Reference Citation Analysis]