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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Airik M, Schüler M, McCourt B, Weiss AC, Herdman N, Lüdtke TH, Widmeier E, Stolz DB, Nejak-Bowen KN, Yimlamai D, Wu YL, Kispert A, Airik R, Hildebrandt F. Loss of Anks6 leads to YAP deficiency and liver abnormalities. Hum Mol Genet 2020;29:3064-80. [PMID: 32886109 DOI: 10.1093/hmg/ddaa197] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
2 Airik M, McCourt B, Ozturk TT, Huynh AB, Zhang X, Tometich JT, Topaloglu R, Ozen H, Orhan D, Nejak-Bowen K, Monga SP, Hand TW, Ozaltin F, Airik R. Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion. FASEB J 2022;36:e22157. [PMID: 35032404 DOI: 10.1096/fj.202101387R] [Reference Citation Analysis]
3 Mandato C, Siano MA, Nazzaro L, Gelzo M, Francalanci P, Rizzo F, D'Agostino Y, Morleo M, Brillante S, Weisz A, Franco B, Vajro P. A ZFYVE19 gene mutation associated with neonatal cholestasis and cilia dysfunction: case report with a novel pathogenic variant. Orphanet J Rare Dis 2021;16:179. [PMID: 33853651 DOI: 10.1186/s13023-021-01775-8] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]