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For: Berauer JP, Mezina AI, Okou DT, Sabo A, Muzny DM, Gibbs RA, Hegde MR, Chopra P, Cutler DJ, Perlmutter DH, Bull LN, Thompson RJ, Loomes KM, Spinner NB, Rajagopalan R, Guthery SL, Moore B, Yandell M, Harpavat S, Magee JC, Kamath BM, Molleston JP, Bezerra JA, Murray KF, Alonso EM, Rosenthal P, Squires RH, Wang KS, Finegold MJ, Russo P, Sherker AH, Sokol RJ, Karpen SJ; Childhood Liver Disease Research Network (ChiLDReN). Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome. Hepatology 2019;70:899-910. [PMID: 30664273 DOI: 10.1002/hep.30515] [Cited by in Crossref: 35] [Cited by in F6Publishing: 29] [Article Influence: 11.7] [Reference Citation Analysis]
Number Citing Articles
1 Gonzales E, Davit-Spraul A, Jacquemin E. A Novel CFC1 Mutation in a Family With Heterotaxy and Biliary Atresia Splenic Malformation Syndromes. J Pediatr Gastroenterol Nutr 2020;70:e24-5. [PMID: 31633655 DOI: 10.1097/MPG.0000000000002531] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Kelly C, Nayagam JS, Vogli S, Samyn M, Joshi D. Paediatric cholestatic liver disorders for the adult gastroenterologist: a practical guide. Frontline Gastroenterol 2021;12:404-13. [DOI: 10.1136/flgastro-2020-101554] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Islek A, Tumgor G. Biliary atresia and congenital disorders of the extrahepatic bile ducts. World J Gastrointest Pharmacol Ther 2022; 13(4): 33-46 [DOI: 10.4292/wjgpt.v13.i4.33] [Reference Citation Analysis]
4 Gu H, Yuan ZZ, Xie XH, Yang YF, Tan ZP. A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient. J Hum Genet 2022. [PMID: 35691949 DOI: 10.1038/s10038-022-01053-w] [Reference Citation Analysis]
5 Mysore KR, Shneider BL, Harpavat S. Biliary Atresia as a Disease Starting In Utero: Implications for Treatment, Diagnosis, and Pathogenesis. J Pediatr Gastroenterol Nutr 2019;69:396-403. [PMID: 31335837 DOI: 10.1097/MPG.0000000000002450] [Cited by in Crossref: 10] [Cited by in F6Publishing: 1] [Article Influence: 5.0] [Reference Citation Analysis]
6 Yerina SE, Ekong UD. Biliary Atresia/Neonatal Cholestasis: What is in the Horizon? Pediatr Clin North Am 2021;68:1333-41. [PMID: 34736593 DOI: 10.1016/j.pcl.2021.08.002] [Reference Citation Analysis]
7 Tran KT, Le VS, Dao LTM, Nguyen HK, Mai AK, Nguyen HT, Ngo MD, Tran QA, Nguyen LT. Novel findings from family-based exome sequencing for children with biliary atresia. Sci Rep 2021;11:21815. [PMID: 34750413 DOI: 10.1038/s41598-021-01148-y] [Reference Citation Analysis]
8 Babu RO, Lui VCH, Chen Y, Yiu RSW, Ye Y, Niu B, Wu Z, Zhang R, Yu MON, Chung PHY, Wong KKY, Xia H, Zhang MQ, Wang B, Lendahl U, Tam PKH. Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia. J Hepatol 2020;73:1391-403. [PMID: 32553668 DOI: 10.1016/j.jhep.2020.06.012] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
9 Cho SJ, Kim GE. A practical approach to the pathology of neonatal cholestatic liver disease. Semin Diagn Pathol 2019;36:375-88. [PMID: 31455583 DOI: 10.1053/j.semdp.2019.07.004] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
10 Nomden M, Beljaars L, Verkade HJ, Hulscher JBF, Olinga P. Current Concepts of Biliary Atresia and Matrix Metalloproteinase-7: A Review of Literature. Front Med (Lausanne) 2020;7:617261. [PMID: 33409288 DOI: 10.3389/fmed.2020.617261] [Reference Citation Analysis]
11 Zhao X, Lorent K, Escobar-Zarate D, Rajagopalan R, Loomes KM, Gillespie K, Mesaros C, Estrada MA, Blair IA, Winkler JD, Spinner NB, Devoto M, Pack M. Impaired Redox and Protein Homeostasis as Risk Factors and Therapeutic Targets in Toxin-Induced Biliary Atresia. Gastroenterology 2020;159:1068-1084.e2. [PMID: 32505743 DOI: 10.1053/j.gastro.2020.05.080] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Malik A, Thanekar U, Mourya R, Shivakumar P. Recent developments in etiology and disease modeling of biliary atresia: a narrative review. Dig Med Res 2020;3:59. [PMID: 33615212 DOI: 10.21037/dmr-20-97] [Reference Citation Analysis]
13 Lendahl U, Lui VCH, Chung PHY, Tam PKH. Biliary Atresia - emerging diagnostic and therapy opportunities. EBioMedicine 2021;74:103689. [PMID: 34781099 DOI: 10.1016/j.ebiom.2021.103689] [Reference Citation Analysis]
14 Feldman AG, Sokol RJ. Neonatal cholestasis: emerging molecular diagnostics and potential novel therapeutics. Nat Rev Gastroenterol Hepatol 2019;16:346-60. [PMID: 30903105 DOI: 10.1038/s41575-019-0132-z] [Cited by in Crossref: 32] [Cited by in F6Publishing: 26] [Article Influence: 10.7] [Reference Citation Analysis]
15 Hukkinen M, Pihlajoki M, Pakarinen MP. Predicting native liver injury and survival in biliary atresia. Seminars in Pediatric Surgery 2020;29:150943. [DOI: 10.1016/j.sempedsurg.2020.150943] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
16 Chung-Davidson YW, Ren J, Yeh CY, Bussy U, Huerta B, Davidson PJ, Whyard S, Li W. TGF-β Signaling Plays a Pivotal Role During Developmental Biliary Atresia in Sea Lamprey (Petromyzon marinus). Hepatol Commun 2020;4:219-34. [PMID: 32025607 DOI: 10.1002/hep4.1461] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
17 Ibrahim SH, Kamath BM, Loomes KM, Karpen SJ. Cholestatic liver diseases of genetic etiology: Advances and controversies. Hepatology 2022;75:1627-46. [PMID: 35229330 DOI: 10.1002/hep.32437] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Luan W, Hao CZ, Li JQ, Wei Q, Gong JY, Qiu YL, Lu Y, Shen CH, Xia Q, Xie XB, Zhang MH, Abuduxikuer K, Li ZD, Wang L, Xing QH, Knisely AS, Wang JS. Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis. J Med Genet 2021;58:514-25. [PMID: 32737136 DOI: 10.1136/jmedgenet-2019-106706] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
19 Correa ARE, Endrakanti M, Naini K, Kabra M, Gupta N. Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum. Ann Hum Genet 2021;85:138-45. [PMID: 33655537 DOI: 10.1111/ahg.12417] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Davenport M, Muntean A, Hadzic N. Biliary Atresia: Clinical Phenotypes and Aetiological Heterogeneity. J Clin Med 2021;10:5675. [PMID: 34884377 DOI: 10.3390/jcm10235675] [Reference Citation Analysis]
21 Zhou JL, Zhao YZ, Wang SS, Chen MX, Zhou S, Chen C. RNA Splicing: A Versatile Regulatory Mechanism in Pediatric Liver Diseases. Front Mol Biosci 2021;8:725308. [PMID: 34651015 DOI: 10.3389/fmolb.2021.725308] [Reference Citation Analysis]
22 Antony D, Gulec Yilmaz E, Gezdirici A, Slagter L, Bakey Z, Bornaun H, Tanidir IC, Van Dinh T, Brunner HG, Walentek P, Arnold SJ, Backofen R, Schmidts M. Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases. Front Genet 2022;13:861236. [DOI: 10.3389/fgene.2022.861236] [Reference Citation Analysis]
23 Karpen SJ. Pediatric Cholestasis: Epidemiology, Genetics, Diagnosis, and Current Management. Clin Liver Dis (Hoboken) 2020;15:115-9. [PMID: 32685137 DOI: 10.1002/cld.895] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Tanimizu N. The neonatal liver: Normal development and response to injury and disease. Semin Fetal Neonatal Med 2021;:101229. [PMID: 33745829 DOI: 10.1016/j.siny.2021.101229] [Reference Citation Analysis]
25 Xu X, Dou R, Zhao S, Zhao J, Gou Q, Wang L, Zhan J. Outcomes of biliary atresia splenic malformation (BASM) syndrome following Kasai operation: a systematic review and meta-analysis. World Jnl Ped Surgery 2022;5:e000346. [DOI: 10.1136/wjps-2021-000346] [Reference Citation Analysis]
26 Lam WY, Tang CS, So MT, Yue H, Hsu JS, Chung PH, Nicholls JM, Yeung F, Lee CD, Ngo DN, Nguyen PAH, Mitchison HM, Jenkins D, O'Callaghan C, Garcia-Barceló MM, Lee SL, Sham PC, Lui VC, Tam PK. Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism. EBioMedicine 2021;71:103530. [PMID: 34455394 DOI: 10.1016/j.ebiom.2021.103530] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Scottoni F, Davenport M. Biliary atresia: Potential for a new decade. Semin Pediatr Surg 2020;29:150940. [PMID: 32861444 DOI: 10.1016/j.sempedsurg.2020.150940] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
28 Kocaaga A, Yimenicioglu S, Alıcı CA. Case report: a de-novo 7p12.3 microduplication detected in an infant with perineal hamartoma and imperforate anus. Egypt J Med Hum Genet 2021;22. [DOI: 10.1186/s43042-021-00205-5] [Reference Citation Analysis]
29 Shaughnessy MP, Spencer-Manzon M, Cowles RA. Antenatally detected liver and biliary pathology. Semin Pediatr Surg 2020;29:150939. [PMID: 32861443 DOI: 10.1016/j.sempedsurg.2020.150939] [Reference Citation Analysis]
30 Aldeiri B, Giamouris V, Pushparajah K, Miller O, Baker A, Davenport M. Cardiac-associated biliary atresia (CABA): a prognostic subgroup. Arch Dis Child 2021;106:68-72. [PMID: 32690577 DOI: 10.1136/archdischild-2020-319122] [Reference Citation Analysis]
31 Nomden M, van Wessel DBE, Ioannou S, Verkade HJ, de Kleine RH, Alizadeh BZ, Bruggink JLM, Hulscher JBF. A Higher Incidence of Isolated Biliary Atresia in Rural Areas: Results From an Epidemiological Study in The Netherlands. J Pediatr Gastroenterol Nutr 2021;72:202-9. [PMID: 32833894 DOI: 10.1097/MPG.0000000000002916] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]