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For: Digilio MC, Marino B, Capolino R, Angioni A, Sarkozy A, Roberti MC, Conti E, de Zorzi A, Dallapiccola B. Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2. Am J Med Genet A 2005;134A:158-64. [PMID: 15669097 DOI: 10.1002/ajmg.a.30587] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 0.7] [Reference Citation Analysis]
Number Citing Articles
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5 Cirillo E, Giardino G, Gallo V, Puliafito P, Azzari C, Bacchetta R, Cardinale F, Cicalese MP, Consolini R, Martino S, Martire B, Molinatto C, Plebani A, Scarano G, Soresina A, Cancrini C, Rossi P, Digilio MC, Pignata C. Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects. BMC Med Genet 2014;15:1. [PMID: 24383682 DOI: 10.1186/1471-2350-15-1] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 1.5] [Reference Citation Analysis]
6 Unolt M, Versacci P, Anaclerio S, Lambiase C, Calcagni G, Trezzi M, Carotti A, Crowley TB, Zackai EH, Goldmuntz E, Gaynor JW, Digilio MC, McDonald-McGinn DM, Marino B. Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers. Am J Med Genet A 2018;176:2087-98. [PMID: 29663641 DOI: 10.1002/ajmg.a.38662] [Cited by in Crossref: 21] [Cited by in F6Publishing: 15] [Article Influence: 5.3] [Reference Citation Analysis]
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8 Chin-yee NJ, Costain G, Swaby J, Silversides CK, Bassett AS. Reproductive Fitness and Genetic Transmission of Tetralogy of Fallot in the Molecular Age. Circ Cardiovasc Genet 2014;7:102-9. [DOI: 10.1161/circgenetics.113.000328] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 1.4] [Reference Citation Analysis]
9 Swaby JA, Silversides CK, Bekeschus SC, Piran S, Oechslin EN, Chow EW, Bassett AS. Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome. Am J Cardiol 2011;107:466-71. [PMID: 21257016 DOI: 10.1016/j.amjcard.2010.09.045] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 1.4] [Reference Citation Analysis]
10 Calcagni G, Unolt M, Digilio MC, Baban A, Versacci P, Tartaglia M, Baldini A, Marino B. Congenital heart disease and genetic syndromes: new insights into molecular mechanisms. Expert Rev Mol Diagn 2017;17:861-70. [PMID: 28745539 DOI: 10.1080/14737159.2017.1360766] [Cited by in Crossref: 19] [Cited by in F6Publishing: 15] [Article Influence: 3.8] [Reference Citation Analysis]
11 Contro E, Stefani L, Berto S, Lapucci C, Arcelli D, Prandstraller D, Perolo A, Rizzo N, Farina A. Circulating mRNA in Maternal Plasma at the Second Trimester of Pregnancy: A Possible Screening Tool for Cardiac Conotruncal and Left Ventricular Outflow Tract Abnormalities. Mol Diagn Ther 2017;21:653-61. [PMID: 28744745 DOI: 10.1007/s40291-017-0295-7] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
12 Calcagni G, Digilio MC, Sarkozy A, Dallapiccola B, Marino B. Familial recurrence of congenital heart disease: an overview and review of the literature. Eur J Pediatr. 2007;166:111-116. [PMID: 17091259 DOI: 10.1007/s00431-006-0295-9] [Cited by in Crossref: 58] [Cited by in F6Publishing: 43] [Article Influence: 3.6] [Reference Citation Analysis]