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Cited by in F6Publishing
For: Eronen M, Kajantie E, Boldt T, Pitkänen O, Aittomäki K. Right atrial isomerism in four siblings. Pediatr Cardiol 2004;25:141-4. [PMID: 14648004 DOI: 10.1007/s00246-003-0540-1] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 0.6] [Reference Citation Analysis]
Number Citing Articles
1 Kaasinen E, Aittomaki K, Eronen M, Vahteristo P, Karhu A, Mecklin J, Kajantie E, Aaltonen LA, Lehtonen R. Recessively inherited right atrial isomerism caused by mutations in growth/differentiation factor 1 (GDF1). Human Molecular Genetics 2010;19:2747-53. [DOI: 10.1093/hmg/ddq164] [Cited by in Crossref: 37] [Cited by in F6Publishing: 30] [Article Influence: 3.1] [Reference Citation Analysis]
2 Gariballa N, Ali BR. Endoplasmic Reticulum Associated Protein Degradation (ERAD) in the Pathology of Diseases Related to TGFβ Signaling Pathway: Future Therapeutic Perspectives. Front Mol Biosci 2020;7:575608. [PMID: 33195419 DOI: 10.3389/fmolb.2020.575608] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
3 Marek‐yagel D, Bolkier Y, Barel O, Vardi A, Mishali D, Katz U, Salem Y, Abudi S, Nayshool O, Kol N, Raas‐rothschild A, Rechavi G, Anikster Y, Pode‐shakked B. A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds. Am J Med Genet 2020;182:987-93. [DOI: 10.1002/ajmg.a.61509] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
4 Akalın M, Demirci O, Kumru P, Yücel İK. Heterotaxy syndrome: Prenatal diagnosis, concomitant malformations and outcomes. Prenat Diagn 2022. [PMID: 35102577 DOI: 10.1002/pd.6110] [Reference Citation Analysis]
5 Lee MY, Won HS, Shim JY, Lee PR, Lee BS, Kim EA, Kim YH, Park JJ, Yun TJ, Kim A. Prenatal diagnosis of atrial isomerism in the Korean population. Obstet Gynecol Sci 2014;57:193-200. [PMID: 24883290 DOI: 10.5468/ogs.2014.57.3.193] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.1] [Reference Citation Analysis]
6 Eronen MP, Aittomäki KAU, Kajantie EO, Sairanen HI, Pesonen EJ. The Outcome of Patients With Right Atrial Isomerism is Poor. Pediatr Cardiol 2013;34:302-7. [DOI: 10.1007/s00246-012-0445-y] [Cited by in Crossref: 21] [Cited by in F6Publishing: 17] [Article Influence: 2.1] [Reference Citation Analysis]
7 Paulussen AD, Steyls A, Vanoevelen J, van Tienen FH, Krapels IP, Claes GR, Chocron S, Velter C, Tan-Sindhunata GM, Lundin C, Valenzuela I, Nagy B, Bache I, Maroun LL, Avela K, Brunner HG, Smeets HJ, Bakkers J, van den Wijngaard A. Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. Eur J Hum Genet 2016;24:1783-91. [PMID: 27406248 DOI: 10.1038/ejhg.2016.91] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
8 Freedom RM, Jaeggi ET, Lim JS, Anderson RH. Hearts with isomerism of the right atrial appendages – one of the worst forms of disease in 2005. CTY 2005;15:554. [DOI: 10.1017/s1047951105001708] [Cited by in Crossref: 34] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
9 Lim JS, Mccrindle BW, Smallhorn JF, Golding F, Caldarone CA, Taketazu M, Jaeggi ET. Clinical Features, Management, and Outcome of Children With Fetal and Postnatal Diagnoses of Isomerism Syndromes. Circulation 2005;112:2454-61. [DOI: 10.1161/circulationaha.105.552364] [Cited by in Crossref: 72] [Cited by in F6Publishing: 13] [Article Influence: 4.2] [Reference Citation Analysis]