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For: Momma K. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. Am J Cardiol 2010;105:1617-24. [PMID: 20494672 DOI: 10.1016/j.amjcard.2010.01.333] [Cited by in Crossref: 153] [Cited by in F6Publishing: 113] [Article Influence: 12.8] [Reference Citation Analysis]
Number Citing Articles
1 Habel A, Herriot R, Kumararatne D, Allgrove J, Baker K, Baxendale H, Bu'Lock F, Firth H, Gennery A, Holland A, Illingworth C, Mercer N, Pannebakker M, Parry A, Roberts A, Tsai-Goodman B. Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times. Eur J Pediatr 2014;173:757-65. [PMID: 24384789 DOI: 10.1007/s00431-013-2240-z] [Cited by in Crossref: 42] [Cited by in F6Publishing: 26] [Article Influence: 5.3] [Reference Citation Analysis]
2 Yang SH, Li XQ, Yang ZJ, Tian XX, Wei HW. Persistent truncus arteriosus with absent semilunar valve in first trimester. J Med Ultrason (2001) 2019;46:273-5. [PMID: 30637595 DOI: 10.1007/s10396-018-00926-y] [Reference Citation Analysis]
3 Jones BA, Conaway MR, Spaeder MC, Dean PN. Hospital Survival After Surgical Repair of Truncus Arteriosus with Interrupted Aortic Arch: Results from a Multi-institutional Database. Pediatr Cardiol 2021;42:1058-63. [PMID: 33786651 DOI: 10.1007/s00246-021-02582-5] [Reference Citation Analysis]
4 Dykes IM, van Bueren KL, Ashmore RJ, Floss T, Wurst W, Szumska D, Bhattacharya S, Scambler PJ. HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region. Circ Res 2014;115:23-31. [PMID: 24748541 DOI: 10.1161/CIRCRESAHA.115.303300] [Cited by in Crossref: 19] [Cited by in F6Publishing: 15] [Article Influence: 2.4] [Reference Citation Analysis]
5 Abduljawad EM, AlHarthi A, AlMatrafi SA, Hussain M, Shawli A, Waggass R. The Prevalence of Congenital Heart Diseases in Syndromic Children at King Khalid National Guard Hospital from 2005 to 2016. Cureus 2020;12:e7891. [PMID: 32489745 DOI: 10.7759/cureus.7891] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Nakajima Y. Mechanism responsible for D-transposition of the great arteries: Is this part of the spectrum of right isomerism? Congenit Anom (Kyoto) 2016;56:196-202. [PMID: 27329052 DOI: 10.1111/cga.12176] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.2] [Reference Citation Analysis]
7 Karatza AA, Gkentzi D, Kostopoulou E, Rammos S. Native aortic coarctation presenting as prolonged pyrexia in a teenager with 22q11.2 deletion. J Paediatr Child Health 2019;55:711-4. [PMID: 30636080 DOI: 10.1111/jpc.14341] [Reference Citation Analysis]
8 Pan H, Guo M, Xiong Y, Ren J, Zhang J, Gao Q, Ke Z, Xu G, Tan Y, Sheng J, Huang H. Differential proteomic analysis of umbilical artery tissue from preeclampsia patients, using iTRAQ isobaric tags and 2D nano LC–MS/MS. Journal of Proteomics 2015;112:262-73. [DOI: 10.1016/j.jprot.2014.09.006] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
9 Wonkam A, Toko R, Chelo D, Tekendo-Ngongang C, Kingue S, Dahoun S. The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon. Glob Heart 2017;12:115-20. [PMID: 28302550 DOI: 10.1016/j.gheart.2017.01.003] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
10 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]
11 Hoshino Y, Machida M, Shimano SI, Taya T. An Adult Case of Chromosome 22q11.2 Deletion Syndrome Associated with a High-positioned Right Aortic Arch. Intern Med 2017;56:865-72. [PMID: 28381757 DOI: 10.2169/internalmedicine.56.7558] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Philipp U, Menzel J, Distl O. A rare form of persistent right aorta arch in linkage disequilibrium with the DiGeorge critical region on CFA26 in German Pinschers. J Hered 2011;102 Suppl 1:S68-73. [PMID: 21846749 DOI: 10.1093/jhered/esr053] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
13 Miyagawa-tomita S, Arima Y, Kurihara H. The “Cardiac Neural Crest” Concept Revisited. In: Nakanishi T, Markwald RR, Baldwin H, Keller BB, Srivastava D, Yamagishi H, editors. Etiology and Morphogenesis of Congenital Heart Disease. Tokyo: Springer Japan; 2016. pp. 227-32. [DOI: 10.1007/978-4-431-54628-3_30] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
14 Valenzuela N, Fan Q, Fa'ak F, Soibam B, Nagandla H, Liu Y, Schwartz RJ, McConnell BK, Stewart MD. Cardiomyocyte-specific conditional knockout of the histone chaperone HIRA in mice results in hypertrophy, sarcolemmal damage and focal replacement fibrosis. Dis Model Mech 2016;9:335-45. [PMID: 26935106 DOI: 10.1242/dmm.022889] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
15 Chang CS, Hong SY, Kim SY, Kim YM, Sung JH, Choi SJ, Oh SY, Roh CR, Song J, Huh J, Kang IS. Prevalence of associated extracardiac anomalies in prenatally diagnosed congenital heart diseases. PLoS One 2021;16:e0248894. [PMID: 33735284 DOI: 10.1371/journal.pone.0248894] [Reference Citation Analysis]
16 He X, Zhang X, Jing H, Zhang X, Gao M, Chen H, Geng J, Zheng Z, Fu Q, Zhu Z, Zheng J. Rare Copy Number Variations Might Not be Involved in the Molecular Pathogenesis of PA-IVS in an Unselected Chinese Cohort. Pediatr Cardiol 2019;40:762-7. [PMID: 30868185 DOI: 10.1007/s00246-019-02062-x] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
17 Deng HY, He ZY, Dong ZC, Zhang YL, Han X, Li HH. MicroRNA-451a attenuates angiotensin II-induced cardiac fibrosis and inflammation by directly targeting T-box1. J Physiol Biochem 2021. [PMID: 34851490 DOI: 10.1007/s13105-021-00861-6] [Reference Citation Analysis]
18 Greulich F, Rudat C, Kispert A. Mechanisms of T-box gene function in the developing heart. Cardiovasc Res 2011;91:212-22. [PMID: 21498422 DOI: 10.1093/cvr/cvr112] [Cited by in Crossref: 166] [Cited by in F6Publishing: 145] [Article Influence: 15.1] [Reference Citation Analysis]
19 Sistino J. Attention deficit/hyperactivity disorder after neonatal surgery: review of the pathophysiology and risk factors. Perfusion 2013;28:484-94. [DOI: 10.1177/0267659113499598] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
20 Long F, Wang X, Fang S, Xu Y, Sun K, Chen S, Xu R. A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects. PLoS One 2013;8:e72515. [PMID: 24009689 DOI: 10.1371/journal.pone.0072515] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
21 Liu D. The adaptor protein Crk in immune response. Immunol Cell Biol 2014;92:80-9. [PMID: 24165979 DOI: 10.1038/icb.2013.64] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 2.2] [Reference Citation Analysis]
22 Karakurt C, Koçak G, Elkiran O. Prenatal diagnosis of a patient with tetralogy of Fallot and an absent pulmonary valve. Pediatr Cardiol 2011;32:241-2. [PMID: 21188373 DOI: 10.1007/s00246-010-9861-z] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
23 Noël AC, Pelluard F, Delezoide AL, Devisme L, Loeuillet L, Leroy B, Martin A, Bouvier R, Laquerriere A, Jeanne-Pasquier C, Bessieres-Grattagliano B, Mechler C, Alanio E, Leroy C, Gaillard D. Fetal phenotype associated with the 22q11 deletion. Am J Med Genet A 2014;164A:2724-31. [PMID: 25111715 DOI: 10.1002/ajmg.a.36720] [Cited by in Crossref: 26] [Cited by in F6Publishing: 22] [Article Influence: 3.3] [Reference Citation Analysis]
24 Escot S, Blavet C, Härtle S, Duband JL, Fournier-Thibault C. Misregulation of SDF1-CXCR4 signaling impairs early cardiac neural crest cell migration leading to conotruncal defects. Circ Res 2013;113:505-16. [PMID: 23838132 DOI: 10.1161/CIRCRESAHA.113.301333] [Cited by in Crossref: 57] [Cited by in F6Publishing: 33] [Article Influence: 6.3] [Reference Citation Analysis]
25 Calcagni G, Pugnaloni F, Digilio MC, Unolt M, Putotto C, Niceta M, Baban A, Piceci Sparascio F, Drago F, De Luca A, Tartaglia M, Marino B, Versacci P. Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights. Genes (Basel) 2021;12:1047. [PMID: 34356063 DOI: 10.3390/genes12071047] [Reference Citation Analysis]
26 Cirillo A, Lioncino M, Maratea A, Passariello A, Fusco A, Fratta F, Monda E, Caiazza M, Signore G, Esposito A, Baban A, Versacci P, Putotto C, Marino B, Pignata C, Cirillo E, Giardino G, Sarubbi B, Limongelli G, Russo MG. Clinical Manifestations of 22q11.2 Deletion Syndrome. Heart Fail Clin 2022;18:155-64. [PMID: 34776076 DOI: 10.1016/j.hfc.2021.07.009] [Reference Citation Analysis]
27 Ju ZR, Wang HJ, Ma XJ, Ma D, Huang GY. HIRA Gene is Lower Expressed in the Myocardium of Patients with Tetralogy of Fallot. Chin Med J (Engl) 2016;129:2403-8. [PMID: 27748330 DOI: 10.4103/0366-6999.191745] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
28 van Mil S, Heung T, Malecki S, Van L, Chang J, Breetvelt E, Wald R, Oechslin E, Silversides C, Bassett AS. Impact of a 22q11.2 Microdeletion on Adult All-Cause Mortality in Tetralogy of Fallot Patients. Can J Cardiol 2020;36:1091-7. [PMID: 32348848 DOI: 10.1016/j.cjca.2020.04.019] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
29 Aggarwal V, Imamura M, Acuna C, Cabrera AG. Chromosome 22q11 deletion in a patient with pulmonary atresia, intact ventricular septum, and confluent branch pulmonary arteries. Cardiol Young 2018;28:467-70. [PMID: 29233233 DOI: 10.1017/S104795111700227X] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
30 Combes N, Waldmann V, Heitz F, Bruguiere E, Quedreux JF, Vahdat O, Chambran P, Narayanan K, Marijon E. Interruption of the Aortic Arch. Am J Med 2017;130:e251-2. [PMID: 28161345 DOI: 10.1016/j.amjmed.2016.12.041] [Cited by in Crossref: 2] [Article Influence: 0.4] [Reference Citation Analysis]
31 Agergaard P, Hebert A, Sørensen KM, Østergaard JR, Olesen C. Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review. Eur J Med Genet 2011;54:3-8. [PMID: 20965293 DOI: 10.1016/j.ejmg.2010.09.016] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
32 Cairello F, Gagliardi M, Magrassi SA, Secco A, Strozzi MC, Felici E. Crossed pulmonary arteries and DiGeorge syndrome: case reports and literature review. Cardiol Young 2022;:1-2. [PMID: 35193728 DOI: 10.1017/S1047951122000221] [Reference Citation Analysis]
33 Sinha T, Li D, Théveniau-Ruissy M, Hutson MR, Kelly RG, Wang J. Loss of Wnt5a disrupts second heart field cell deployment and may contribute to OFT malformations in DiGeorge syndrome. Hum Mol Genet 2015;24:1704-16. [PMID: 25410658 DOI: 10.1093/hmg/ddu584] [Cited by in Crossref: 34] [Cited by in F6Publishing: 26] [Article Influence: 4.3] [Reference Citation Analysis]
34 Murillo H, Lane MJ, Punn R, Fleischmann D, Restrepo CS. Imaging of the Aorta: Embryology and Anatomy. Seminars in Ultrasound, CT and MRI 2012;33:169-90. [DOI: 10.1053/j.sult.2012.01.013] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
35 Singampalli KL, Jui E, Shani K, Ning Y, Connell JP, Birla RK, Bollyky PL, Caldarone CA, Keswani SG, Grande-Allen KJ. Congenital Heart Disease: An Immunological Perspective. Front Cardiovasc Med 2021;8:701375. [PMID: 34434978 DOI: 10.3389/fcvm.2021.701375] [Reference Citation Analysis]
36 Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME. Human gene copy number spectra analysis in congenital heart malformations. Physiol Genomics 2012;44:518-41. [PMID: 22318994 DOI: 10.1152/physiolgenomics.00013.2012] [Cited by in Crossref: 66] [Cited by in F6Publishing: 58] [Article Influence: 6.6] [Reference Citation Analysis]
37 Bansal V, Dorn C, Grunert M, Klaassen S, Hetzer R, Berger F, Sperling SR. Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot. PLoS One 2014;9:e85375. [PMID: 24400131 DOI: 10.1371/journal.pone.0085375] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 2.3] [Reference Citation Analysis]
38 Phillips HM, Stothard CA, Shaikh Qureshi WM, Kousa AI, Briones-Leon JA, Khasawneh RR, O'Loughlin C, Sanders R, Mazzotta S, Dodds R, Seidel K, Bates T, Nakatomi M, Cockell SJ, Schneider JE, Mohun TJ, Maehr R, Kist R, Peters H, Bamforth SD. Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis. Development 2019;146:dev177618. [PMID: 31444215 DOI: 10.1242/dev.177618] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
39 Agergaard P, Olesen C, Østergaard JR, Christiansen M, Sørensen KM. The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study. Am J Med Genet 2012;158A:498-508. [DOI: 10.1002/ajmg.a.34250] [Cited by in Crossref: 28] [Cited by in F6Publishing: 21] [Article Influence: 2.5] [Reference Citation Analysis]
40 Dorn C, Grunert M, Sperling SR. Application of high-throughput sequencing for studying genomic variations in congenital heart disease. Brief Funct Genomics 2014;13:51-65. [PMID: 24095982 DOI: 10.1093/bfgp/elt040] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 1.1] [Reference Citation Analysis]
41 De Bono C, Thellier C, Bertrand N, Sturny R, Jullian E, Cortes C, Stefanovic S, Zaffran S, Théveniau-Ruissy M, Kelly RG. T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field. Hum Mol Genet 2018;27:3747-60. [PMID: 30016433 DOI: 10.1093/hmg/ddy266] [Cited by in Crossref: 27] [Cited by in F6Publishing: 23] [Article Influence: 9.0] [Reference Citation Analysis]
42 Verhagen JM, Diderich KE, Oudesluijs G, Mancini GM, Eggink AJ, Verkleij-hagoort AC, Groenenberg IA, Willems PJ, du Plessis FA, de Man SA, Srebniak MI, van Opstal D, Hulsman LO, van Zutven LJ, Wessels MW. Phenotypic variability of atypical 22q11.2 deletions not including TBX1. Am J Med Genet 2012;158A:2412-20. [DOI: 10.1002/ajmg.a.35517] [Cited by in Crossref: 41] [Cited by in F6Publishing: 35] [Article Influence: 4.1] [Reference Citation Analysis]
43 Friedman MA, Miletta N, Roe C, Wang D, Morrow BE, Kates WR, Higgins AM, Shprintzen RJ. Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study. Int J Pediatr Otorhinolaryngol 2011;75:1167-72. [PMID: 21763005 DOI: 10.1016/j.ijporl.2011.06.013] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 1.5] [Reference Citation Analysis]
44 Prasad R, Chan LF, Hughes CR, Kaski JP, Kowalczyk JC, Savage MO, Peters CJ, Nathwani N, Clark AJ, Storr HL, Metherell LA. Thioredoxin Reductase 2 (TXNRD2) mutation associated with familial glucocorticoid deficiency (FGD). J Clin Endocrinol Metab 2014;99:E1556-63. [PMID: 24601690 DOI: 10.1210/jc.2013-3844] [Cited by in Crossref: 65] [Cited by in F6Publishing: 54] [Article Influence: 8.1] [Reference Citation Analysis]
45 Heusinkveld LE, Majumdar S, Gao JL, McDermott DH, Murphy PM. WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure. J Clin Immunol 2019;39:532-56. [PMID: 31313072 DOI: 10.1007/s10875-019-00665-w] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 7.0] [Reference Citation Analysis]
46 Liu Z, Yin N, Gong L, Tan Z, Yin B, Yang Y, Luo C. Microduplication of 7q36.3 encompassing the SHH longrange regulator (ZRS) in a patient with triphalangeal thumbpolysyndactyly syndrome and congenital heart disease. Mol Med Rep. 2017;15:793-797. [PMID: 28035386 DOI: 10.3892/mmr.2016.6092] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
47 Miranda JO, Callaghan N, Miller O, Simpson J, Sharland G. Right aortic arch diagnosed antenatally: associations and outcome in 98 fetuses. Heart 2014;100:54-9. [PMID: 24192976 DOI: 10.1136/heartjnl-2013-304860] [Cited by in Crossref: 40] [Cited by in F6Publishing: 35] [Article Influence: 4.4] [Reference Citation Analysis]
48 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]
49 Olsen M, Sørensen HT, Hjortdal VE, Christensen TD, Pedersen L. Congenital heart defects and developmental and other psychiatric disorders: a Danish nationwide cohort study. Circulation 2011;124:1706-12. [PMID: 21947292 DOI: 10.1161/CIRCULATIONAHA.110.002832] [Cited by in Crossref: 27] [Cited by in F6Publishing: 13] [Article Influence: 2.5] [Reference Citation Analysis]
50 Krishnamurthy VK, Godby RC, Liu GR, Smith JM, Hiratzka LF, Narmoneva DA, Hinton RB. Review of Molecular and Mechanical Interactions in the Aortic Valve and Aorta: Implications for the Shared Pathogenesis of Aortic Valve Disease and Aortopathy. J of Cardiovasc Trans Res 2014;7:823-46. [DOI: 10.1007/s12265-014-9602-4] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
51 Sánchez-Más J, Lax A, Asensio-López MC, Fernández-Del Palacio MJ, Caballero L, Navarro-Peñalver M, Pérez-Martínez MT, Gimeno-Blanes JR, Pascual-Figal DA. The TBX1 Transcription Factor in Cardiac Remodeling After Myocardial Infarction. Rev Esp Cardiol (Engl Ed) 2016;69:1042-50. [PMID: 27422448 DOI: 10.1016/j.rec.2016.04.033] [Reference Citation Analysis]
52 Parisot P, Mesbah K, Théveniau-Ruissy M, Kelly RG. Tbx1, subpulmonary myocardium and conotruncal congenital heart defects. Birth Defects Res A Clin Mol Teratol 2011;91:477-84. [PMID: 21591244 DOI: 10.1002/bdra.20803] [Cited by in Crossref: 35] [Cited by in F6Publishing: 28] [Article Influence: 3.2] [Reference Citation Analysis]
53 Thorsson T, Russell WW, El-Kashlan N, Soemedi R, Levine J, Geisler SB, Ackley T, Tomita-Mitchell A, Rosenfeld JA, Töpf A, Tayeh M, Goodship J, Innis JW, Keavney B, Russell MW. Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development. Congenit Heart Dis 2015;10:193-208. [PMID: 24720490 DOI: 10.1111/chd.12179] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 1.9] [Reference Citation Analysis]
54 Lincoln J, Yutzey KE. Molecular and developmental mechanisms of congenital heart valve disease. Birth Defects Res A Clin Mol Teratol 2011;91:526-34. [PMID: 21538813 DOI: 10.1002/bdra.20799] [Cited by in Crossref: 41] [Cited by in F6Publishing: 34] [Article Influence: 3.7] [Reference Citation Analysis]
55 Cazavet A, Seguela PE, Acar P, Leobon B. A new type of aortic arch interruption without significant patent ductus arteriosus and with no ventricular septal defect. J Thorac Cardiovasc Surg 2012;143:237-9. [PMID: 21798564 DOI: 10.1016/j.jtcvs.2011.06.031] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
56 Wu Y, Jin X, Zhang Y, Zheng J, Yang R. Genetic and epigenetic mechanisms in the development of congenital heart diseases. World Jnl Ped Surgery 2021;4:e000196. [DOI: 10.1136/wjps-2020-000196] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
57 Veerapandiyan A, Abdul-Rahman OA, Adam MP, Lyons MJ, Manning M, Coleman K, Kobrynski L, Taneja D, Schoch K, Zimmerman HH, Shashi V. Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge. Am J Med Genet A 2011;155A:2186-95. [PMID: 21834039 DOI: 10.1002/ajmg.a.34226] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 1.1] [Reference Citation Analysis]
58 Peyvandi S, Lupo PJ, Garbarini J, Woyciechowski S, Edman S, Emanuel BS, Mitchell LE, Goldmuntz E. 22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases. Pediatr Cardiol 2013;34:1687-94. [PMID: 23604262 DOI: 10.1007/s00246-013-0694-4] [Cited by in Crossref: 61] [Cited by in F6Publishing: 53] [Article Influence: 6.8] [Reference Citation Analysis]
59 Breckpot J, Thienpont B, Bauters M, Tranchevent L, Gewillig M, Allegaert K, Vermeesch JR, Moreau Y, Devriendt K. Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1. Am J Med Genet 2012;158A:574-80. [DOI: 10.1002/ajmg.a.35217] [Cited by in Crossref: 27] [Cited by in F6Publishing: 27] [Article Influence: 2.7] [Reference Citation Analysis]
60 Lahiri S, Gil W, Daria S, Joshua G, Parul J, Redmond B, Elizabeth W. Genetic abnormalities/syndromes significantly impact perioperative outcomes of conotruncal heart defects. Ann Pediatr Cardiol 2020;13:38-45. [PMID: 32030034 DOI: 10.4103/apc.APC_51_19] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
61 Serra-Juhé C, Rodríguez-Santiago B, Cuscó I, Vendrell T, Camats N, Torán N, Pérez-Jurado LA. Contribution of rare copy number variants to isolated human malformations. PLoS One 2012;7:e45530. [PMID: 23056206 DOI: 10.1371/journal.pone.0045530] [Cited by in Crossref: 21] [Cited by in F6Publishing: 18] [Article Influence: 2.1] [Reference Citation Analysis]
62 Worhunsky DJ, Levy BE, Stephens EH, Backer CL. Vascular rings. Semin Pediatr Surg 2021;30:151128. [PMID: 34930596 DOI: 10.1016/j.sempedsurg.2021.151128] [Reference Citation Analysis]
63 Spaeth JM, Kim NH, Boyer TG. Mediator and human disease. Semin Cell Dev Biol 2011;22:776-87. [PMID: 21840410 DOI: 10.1016/j.semcdb.2011.07.024] [Cited by in Crossref: 63] [Cited by in F6Publishing: 64] [Article Influence: 5.7] [Reference Citation Analysis]
64 Hacıhamdioğlu B, Hacıhamdioğlu D, Delil K. 22q11 deletion syndrome: current perspective. Appl Clin Genet 2015;8:123-32. [PMID: 26056486 DOI: 10.2147/TACG.S82105] [Cited by in Crossref: 46] [Cited by in F6Publishing: 16] [Article Influence: 6.6] [Reference Citation Analysis]
65 Fagerberg CR, Graakjaer J, Heinl UD, Ousager LB, Dreyer I, Kirchhoff M, Rasmussen AA, Lautrup CK, Birkebaek N, Sorensen K. Heart defects and other features of the 22q11 distal deletion syndrome. European Journal of Medical Genetics 2013;56:98-107. [DOI: 10.1016/j.ejmg.2012.09.009] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 2.7] [Reference Citation Analysis]
66 Sarac Sivrikoz T, Basaran S, Has R, Karaman B, Kalelioglu IH, Kirgiz M, Altunoglu U, Yuksel A. Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center. Arch Gynecol Obstet 2021. [PMID: 34145474 DOI: 10.1007/s00404-021-06125-4] [Reference Citation Analysis]
67 Chinnadurai S, Goudy S. Understanding velocardiofacial syndrome: how recent discoveries can help you improve your patient outcomes. Curr Opin Otolaryngol Head Neck Surg 2012;20:502-6. [PMID: 23000736 DOI: 10.1097/MOO.0b013e328359b476] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 0.9] [Reference Citation Analysis]
68 Gong X, Wu X, Ma X, Wu D, Zhang T, He L, Qin S, Li X. Microdeletion and microduplication analysis of chinese conotruncal defects patients with targeted array comparative genomic hybridization. PLoS One 2013;8:e76314. [PMID: 24098474 DOI: 10.1371/journal.pone.0076314] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
69 Aresvik DM, Lima K, Øverland T, Mollnes TE, Abrahamsen TG. Increased Levels of Interferon-Inducible Protein 10 (IP-10) in 22q11.2 Deletion Syndrome. Scand J Immunol 2016;83:188-94. [PMID: 26708691 DOI: 10.1111/sji.12406] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
70 Monteiro FP, Vieira TP, Sgardioli IC, Molck MC, Damiano AP, Souza J, Monlleó IL, Fontes MI, Fett-Conte AC, Félix TM, Leal GF, Ribeiro EM, Banzato CE, Dantas Cde R, Lopes-Cendes I, Gil-da-Silva-Lopes VL. Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature. Eur J Pediatr 2013;172:927-45. [PMID: 23440478 DOI: 10.1007/s00431-013-1964-0] [Cited by in Crossref: 34] [Cited by in F6Publishing: 32] [Article Influence: 3.8] [Reference Citation Analysis]
71 Gao W, Higaki T, Eguchi-Ishimae M, Iwabuki H, Wu Z, Yamamoto E, Takata H, Ohta M, Imoto I, Ishii E, Eguchi M. DGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defects. Hum Genome Var 2015;2:15004. [PMID: 27081520 DOI: 10.1038/hgv.2015.4] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 2.3] [Reference Citation Analysis]
72 Oswal N, Christov G, Sridharan S, Khambadkone S, Bull C, Sullivan I. Aberrant subclavian artery origin in tetralogy of Fallot with pulmonary stenosis is associated with chromosomal or genetic abnormality. Cardiol Young 2014;24:478-84. [PMID: 23732114 DOI: 10.1017/S1047951113000644] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
73 Zhang X, Xu Y, Liu D, Geng J, Chen S, Jiang Z, Fu Q, Sun K. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease. BMC Genomics 2015;16:364. [PMID: 25952753 DOI: 10.1186/s12864-015-1590-5] [Cited by in Crossref: 33] [Cited by in F6Publishing: 30] [Article Influence: 4.7] [Reference Citation Analysis]
74 Xu YJ, Wang J, Xu R, Zhao PJ, Wang XK, Sun HJ, Bao LM, Shen J, Fu QH, Li F, Sun K. Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus. BMC Med Genet 2011;12:169. [PMID: 22185286 DOI: 10.1186/1471-2350-12-169] [Cited by in Crossref: 23] [Cited by in F6Publishing: 20] [Article Influence: 2.1] [Reference Citation Analysis]
75 Pan Y, Wang ZG, Liu XY, Zhao H, Zhou N, Zheng GF, Qiu XB, Li RG, Yuan F, Shi HY, Hou XM, Yang YQ. A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease. Pediatr Cardiol 2015;36:1400-10. [PMID: 25860641 DOI: 10.1007/s00246-015-1173-x] [Cited by in Crossref: 23] [Cited by in F6Publishing: 18] [Article Influence: 3.3] [Reference Citation Analysis]
76 Kobayashi D, Sallaam S, Humes RA. Tetralogy of Fallot with complete DiGeorge syndrome: report of a case and a review of the literature. Congenit Heart Dis 2013;8:E119-26. [PMID: 22883347 DOI: 10.1111/j.1747-0803.2012.00694.x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]
77 Hayabuchi Y, Inoue M, Sakata M, Ohnishi T, Kagami S. Subclavian and pulmonary artery steal phenomenon in a patient with isolated left subclavian artery and right aortic arch. J Clin Ultrasound 2013;41:265-8. [DOI: 10.1002/jcu.21874] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
78 Yasuda K, Morihana E, Fusazaki N, Ishikawa S. Cardiovascular Malformations in CHARGE Syndrome with DiGeorge Phenotype: Two Case Reports. Case Rep Pediatr 2016;2016:8013530. [PMID: 27957375 DOI: 10.1155/2016/8013530] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
79 Sojak V, Lugo J, Koolbergen D, Hazekamp M. Surgery for truncus arteriosus. Multimed Man Cardiothorac Surg 2012;2012:mms011. [PMID: 24414715 DOI: 10.1093/mmcts/mms011] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
80 Kloesel B, DiNardo JA, Body SC. Cardiac Embryology and Molecular Mechanisms of Congenital Heart Disease: A Primer for Anesthesiologists. Anesth Analg 2016;123:551-69. [PMID: 27541719 DOI: 10.1213/ANE.0000000000001451] [Cited by in Crossref: 26] [Cited by in F6Publishing: 13] [Article Influence: 5.2] [Reference Citation Analysis]
81 Burchill L, Greenway S, Silversides CK, Mital S. Genetic Counseling in the Adult with Congenital Heart Disease: What is the Role? Curr Cardiol Rep 2011;13:347-55. [DOI: 10.1007/s11886-011-0188-z] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 1.4] [Reference Citation Analysis]
82 Warkala M, Chen D, Ramirez A, Jubran A, Schonning M, Wang X, Zhao H, Astrof S. Cell-Extracellular Matrix Interactions Play Multiple Essential Roles in Aortic Arch Development. Circ Res 2021;128:e27-44. [PMID: 33249995 DOI: 10.1161/CIRCRESAHA.120.318200] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
83 Chin AJ, Saint-Jeannet JP, Lo CW. How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease. Mech Dev 2012;129:75-97. [PMID: 22640994 DOI: 10.1016/j.mod.2012.05.005] [Cited by in Crossref: 22] [Cited by in F6Publishing: 20] [Article Influence: 2.2] [Reference Citation Analysis]
84 Bossi G, Gertosio C, Meazza C, Farello G, Bozzola M. Failure to thrive as presentation in a patient with 22q11.2 microdeletion. Ital J Pediatr 2016;42:14. [PMID: 26864739 DOI: 10.1186/s13052-016-0224-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
85 Poirsier C, Besseau-Ayasse J, Schluth-Bolard C, Toutain J, Missirian C, Le Caignec C, Bazin A, de Blois MC, Kuentz P, Catty M, Choiset A, Plessis G, Basinko A, Letard P, Flori E, Jimenez M, Valduga M, Landais E, Lallaoui H, Cartault F, Lespinasse J, Martin-Coignard D, Callier P, Pebrel-Richard C, Portnoi MF, Busa T, Receveur A, Amblard F, Yardin C, Harbuz R, Prieur F, Le Meur N, Pipiras E, Kleinfinger P, Vialard F, Doco-Fenzy M. A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH. Eur J Hum Genet 2016;24:844-51. [PMID: 26508576 DOI: 10.1038/ejhg.2015.219] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 2.9] [Reference Citation Analysis]
86 Hartwig C, Monis WJ, Chen X, Dickman DK, Pazour GJ, Faundez V. Neurodevelopmental disease mechanisms, primary cilia, and endosomes converge on the BLOC-1 and BORC complexes. Dev Neurobiol 2018;78:311-30. [PMID: 28986965 DOI: 10.1002/dneu.22542] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.2] [Reference Citation Analysis]
87 Márquez-Ávila CS, Vizcaíno-Alarcón A, García-Delgado C, Núñez-Martínez PM, Flores-Ramírez F, Reyes-de la Rosa Adel P, Mendelsberg-Fishbein P, Ibarra-Grajeda D, Medina-Bravo P, Balderrábano-Saucedo N, Esteva-Solsona S, Márquez-Quiróz Ldel C, Flores-Cuevas A, Sánchez-Urbina R, Morales-Jiménez AB, Garibay-Nieto N, Del Bosque-Garza J, Pietropaolo-Cienfuegos D, Gutiérrez-Camacho C, García-Morales L, Morán-Barroso VF. Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease. Int J Pediatr Otorhinolaryngol 2015;79:1886-91. [PMID: 26409294 DOI: 10.1016/j.ijporl.2015.08.038] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
88 Hempel A, Kühl M. A Matter of the Heart: The African Clawed Frog Xenopus as a Model for Studying Vertebrate Cardiogenesis and Congenital Heart Defects. J Cardiovasc Dev Dis 2016;3:E21. [PMID: 29367567 DOI: 10.3390/jcdd3020021] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.5] [Reference Citation Analysis]
89 Nabekura T, Chen Z, Schroeder C, Park T, Vivier E, Lanier LL, Liu D. Crk Adaptor Proteins Regulate NK Cell Expansion and Differentiation during Mouse Cytomegalovirus Infection. J Immunol 2018;200:3420-8. [PMID: 29618525 DOI: 10.4049/jimmunol.1701639] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
90 Rana MS, Théveniau-ruissy M, De Bono C, Mesbah K, Francou A, Rammah M, Domínguez JN, Roux M, Laforest B, Anderson RH, Mohun T, Zaffran S, Christoffels VM, Kelly RG. Tbx1 Coordinates Addition of Posterior Second Heart Field Progenitor Cells to the Arterial and Venous Poles of the Heart. Circ Res 2014;115:790-9. [DOI: 10.1161/circresaha.115.305020] [Cited by in Crossref: 74] [Cited by in F6Publishing: 34] [Article Influence: 9.3] [Reference Citation Analysis]
91 Lee MY, Won HS, Baek JW, Cho JH, Shim JY, Lee PR, Kim A. Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome. Obstet Gynecol Sci 2014;57:11-6. [PMID: 24596813 DOI: 10.5468/ogs.2014.57.1.11] [Cited by in Crossref: 16] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
92 Prasad S, Katina S, Hennessy RJ, Murphy KC, Bowman AW, Waddington JL. Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis. Am J Med Genet A 2015;167A:529-36. [PMID: 25691406 DOI: 10.1002/ajmg.a.36893] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 2.3] [Reference Citation Analysis]
93 Zhang W, Shen L, Deng Z, Ding Y, Mo X, Xu Z, Gao Q, Yi L. Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4. PLoS One 2014;9:e102379. [PMID: 25025186 DOI: 10.1371/journal.pone.0102379] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 1.9] [Reference Citation Analysis]
94 Quinonez ZA, Downey L, Abbasi RK, Kuan C, Asija R, Mcelhinney DB, Hanley FL, Mainwaring RD, Wise-faberowski L. Anesthetic Management During Surgery for Tetralogy of Fallot With Pulmonary Atresia and Major Aortopulmonary Collateral Arteries. World J Pediatr Congenit Heart Surg 2018;9:236-41. [DOI: 10.1177/2150135118754522] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
95 Liu L, Wang HD, Cui CY, Wu D, Li T, Fan TB, Peng BT, Zhang LZ, Wang CZ. Application of array-comparative genomic hybridization in tetralogy of Fallot. Medicine (Baltimore) 2016;95:e5552. [PMID: 27930557 DOI: 10.1097/MD.0000000000005552] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 1.2] [Reference Citation Analysis]
96 Novo A, Woestelandt L, Rousselot-Pailley B, Leitgel M, Eutrope J, Rio M, Lyonnet S, Robel L. [Child psychiatry interventions in patients with 22q11 deletion syndrome: From treatment to prevention]. Encephale 2019;45:175-81. [PMID: 30470499 DOI: 10.1016/j.encep.2018.09.011] [Reference Citation Analysis]
97 Nabeshima T, Fujii T, Nagamatsu T, Hashimoto A, Seyama T, Kubota K, Sayama S, Nakayama T, Kumasawa K, Iriyama T, Osuga Y, Fujii T. Polyhydramnios is associated with postnatal dysphagia determining short-term prognosis of the newborn with 22q11.2 deletion syndrome - A case series analysis. Taiwan J Obstet Gynecol 2020;59:744-7. [PMID: 32917329 DOI: 10.1016/j.tjog.2020.07.021] [Reference Citation Analysis]
98 Grassi MS, Jacob CM, Kulikowski LD, Pastorino AC, Dutra RL, Miura N, Jatene MB, Pegler SP, Kim CA, Carneiro-Sampaio M. Congenital Heart Disease as a Warning Sign for the Diagnosis of the 22q11.2 Deletion. Arq Bras Cardiol 2014;103:382-90. [PMID: 25317860 DOI: 10.5935/abc.20140145] [Cited by in Crossref: 1] [Cited by in F6Publishing: 5] [Article Influence: 0.1] [Reference Citation Analysis]
99 Chikkabyrappa S, Mahadevaiah G, Buddhe S, Alsaied T, Tretter J. Common Arterial Trunk: Physiology, Imaging, and Management. Semin Cardiothorac Vasc Anesth 2019;23:225-36. [PMID: 30596352 DOI: 10.1177/1089253218821382] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
100 Sistino JJ, Atz AM, Ellis C Jr, Simpson KN, Ikonomidis JS, Bradley SM. Association Between Method of Cerebral Protection During Neonatal Aortic Arch Surgery and Attention Deficit/Hyperactivity Disorder. Ann Thorac Surg 2015;100:663-70. [PMID: 26138764 DOI: 10.1016/j.athoracsur.2015.04.119] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
101 Erhardt S, Zheng M, Zhao X, Le TP, Findley TO, Wang J. The Cardiac Neural Crest Cells in Heart Development and Congenital Heart Defects. J Cardiovasc Dev Dis 2021;8:89. [PMID: 34436231 DOI: 10.3390/jcdd8080089] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
102 Kaltenbrun E, Tandon P, Amin NM, Waldron L, Showell C, Conlon FL. Xenopus: An emerging model for studying congenital heart disease. Birth Defects Res A Clin Mol Teratol 2011;91:495-510. [PMID: 21538812 DOI: 10.1002/bdra.20793] [Cited by in Crossref: 33] [Cited by in F6Publishing: 33] [Article Influence: 3.0] [Reference Citation Analysis]
103 Cancrini C, Puliafito P, Digilio MC, Soresina A, Martino S, Rondelli R, Consolini R, Ruga EM, Cardinale F, Finocchi A, Romiti ML, Martire B, Bacchetta R, Albano V, Carotti A, Specchia F, Montin D, Cirillo E, Cocchi G, Trizzino A, Bossi G, Milanesi O, Azzari C, Corsello G, Pignata C, Aiuti A, Pietrogrande MC, Marino B, Ugazio AG, Plebani A, Rossi P. Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. The Journal of Pediatrics 2014;164:1475-1480.e2. [DOI: 10.1016/j.jpeds.2014.01.056] [Cited by in Crossref: 72] [Cited by in F6Publishing: 61] [Article Influence: 9.0] [Reference Citation Analysis]
104 Knudson JD, Lopez KN, Maskatia S, Mckenzie ED, Lantin-hermoso MR, Masand PM, Vick Iii GW. Type B Interrupted Left Aortic Arch with Isolated Right Subclavian Artery: Isolated Subclavian Artery in Type B IAA. Congenital Heart Disease 2012;7:E25-30. [DOI: 10.1111/j.1747-0803.2011.00625.x] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
105 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]
106 Vogels A, Schevenels S, Cayenberghs R, Weyts E, Van Buggenhout G, Swillen A, Van Esch H, de Ravel T, Corveleyn P, Devriendt K. Presenting symptoms in adults with the 22q11 deletion syndrome. Eur J Med Genet 2014;57:157-62. [PMID: 24576609 DOI: 10.1016/j.ejmg.2014.02.008] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
107 Shang J, Chen D, Fang W, Dong F. Isolated subclavian or brachiocephalic arteries with tetralogy of Fallot, left retro-aortic brachiocephalic vein. Cardiovasc Pathol 2021;51:107304. [PMID: 33157206 DOI: 10.1016/j.carpath.2020.107304] [Reference Citation Analysis]
108 Xie H, Hong N, Zhang E, Li F, Sun K, Yu Y. Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect. Front Genet 2019;10:15. [PMID: 30745907 DOI: 10.3389/fgene.2019.00015] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
109 Licari A, Manca E, Rispoli GA, Mannarino S, Pelizzo G, Marseglia GL. Congenital vascular rings: A clinical challenge for the pediatrician: Congenital Vascular Rings: A Clinical Challenge. Pediatr Pulmonol 2015;50:511-24. [DOI: 10.1002/ppul.23152] [Cited by in Crossref: 38] [Cited by in F6Publishing: 21] [Article Influence: 5.4] [Reference Citation Analysis]
110 Jonas RK, Montojo CA, Bearden CE. The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan. Biol Psychiatry 2014;75:351-60. [PMID: 23992925 DOI: 10.1016/j.biopsych.2013.07.019] [Cited by in Crossref: 113] [Cited by in F6Publishing: 96] [Article Influence: 12.6] [Reference Citation Analysis]
111 Gao M, He X, Zheng J. Advances in molecular genetics for pulmonary atresia. Cardiol Young 2017;27:207-16. [PMID: 27655138 DOI: 10.1017/S1047951116001487] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
112 Chatila S, Houyel L, Hily M, Bonnet D. Common Arterial Trunk Associated with Functionally Univentricular Heart: Anatomical Study and Review of the Literature. J Cardiovasc Dev Dis 2021;8:175. [PMID: 34940530 DOI: 10.3390/jcdd8120175] [Reference Citation Analysis]
113 Kotecha MK, Krishnamanohar SR, Kumar RS. Absent pulmonary valve syndrome coexisting with coarctation of aorta in an adult. Congenit Heart Dis 2013;8:E17-9. [PMID: 22010955 DOI: 10.1111/j.1747-0803.2011.00566.x] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
114 Théveniau-Ruissy M, Pérez-Pomares JM, Parisot P, Baldini A, Miquerol L, Kelly RG. Coronary stem development in wild-type and Tbx1 null mouse hearts. Dev Dyn 2016;245:445-59. [PMID: 26708418 DOI: 10.1002/dvdy.24380] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 2.8] [Reference Citation Analysis]
115 Delea M, Espeche LD, Bruque CD, Bidondo MP, Massara LS, Oliveri J, Brun P, Cosentino VR, Martinoli C, Tolaba N, Picon C, Ponce Zaldua ME, Ávila S, Gutnisky V, Perez M, Furforo L, Buzzalino ND, Liascovich R, Groisman B, Rittler M, Rozental S, Barbero P, Dain L. Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects. Genes (Basel) 2018;9:E454. [PMID: 30208644 DOI: 10.3390/genes9090454] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
116 Çivilibal Tang N, Çelik Alaçam N, Bornaun H, Erdem A, Yılmaz Güleç E. Left subclavian artery originating from left pulmonary artery in DiGeorge syndrome. Turk Gogus Kalp Damar Cerrahisi Derg 2020;28:691-4. [PMID: 33403146 DOI: 10.5606/tgkdc.dergisi.2020.19613] [Reference Citation Analysis]
117 Goldmuntz E. 22q11.2 deletion syndrome and congenital heart disease. Am J Med Genet C Semin Med Genet 2020;184:64-72. [PMID: 32049433 DOI: 10.1002/ajmg.c.31774] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
118 Majumdar U, Yasuhara J, Garg V. In Vivo and In Vitro Genetic Models of Congenital Heart Disease. Cold Spring Harb Perspect Biol 2021;13:a036764. [PMID: 31818859 DOI: 10.1101/cshperspect.a036764] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
119 Human A, Murguia-favela L, Benson L, Roifman I, Grunebaum E. Cardiovascular abnormalities in primary immunodeficiency diseases. LymphoSign Journal 2015;2:107-34. [DOI: 10.14785/lpsn-2014-0013] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
120 Epelman M, Kondrachuk O, Restrepo R, Lee EY. Congenital and Acquired Mediastinal Vascular Disorders in Children. In: Garcia-peña P, Guillerman RP, editors. Pediatric Chest Imaging. Berlin: Springer Berlin Heidelberg; 2014. pp. 241-65. [DOI: 10.1007/174_2013_834] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
121 Versacci P, Michielon G, Carotti A, Marino B. Surgical results in patients with cardiac defects and del 22q11.2 syndrome. Am J Cardiol 2011;107:337-8. [PMID: 21211615 DOI: 10.1016/j.amjcard.2010.10.034] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
122 Traisrisilp K, Tongprasert F, Srisupundit K, Luewan S, Tongsong T. Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women. Obstet Gynecol Sci 2020;63:330-6. [PMID: 32489978 DOI: 10.5468/ogs.2020.63.3.330] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
123 Rump P, de Leeuw N, van Essen AJ, Verschuuren-Bemelmans CC, Veenstra-Knol HE, Swinkels ME, Oostdijk W, Ruivenkamp C, Reardon W, de Munnik S, Ruiter M, Frumkin A, Lev D, Evers C, Sikkema-Raddatz B, Dijkhuizen T, van Ravenswaaij-Arts CM. Central 22q11.2 deletions. Am J Med Genet A 2014;164A:2707-23. [PMID: 25123976 DOI: 10.1002/ajmg.a.36711] [Cited by in Crossref: 36] [Cited by in F6Publishing: 32] [Article Influence: 4.5] [Reference Citation Analysis]
124 Rana MS, Sizarov A, Christoffels VM, Moorman AF. Development of the human aortic arch system captured in an interactive three-dimensional reference model. Am J Med Genet A 2014;164A:1372-83. [PMID: 23613216 DOI: 10.1002/ajmg.a.35881] [Cited by in Crossref: 17] [Cited by in F6Publishing: 12] [Article Influence: 1.9] [Reference Citation Analysis]
125 Parikh R, Eisses M, Latham GJ, Joffe DC, Ross FJ. Perioperative and Anesthetic Considerations in Truncus Arteriosus. Semin Cardiothorac Vasc Anesth 2018;22:285-93. [PMID: 29808750 DOI: 10.1177/1089253218778826] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
126 Sistino JJ, Atz AM, Simpson KN, Ellis C, Ikonomidis JS, Bradley SM. The prevalence of attention-deficit/hyperactivity disorder following neonatal aortic arch repair. Cardiol Young 2015;25:663-9. [PMID: 24775274 DOI: 10.1017/S1047951114000547] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 0.9] [Reference Citation Analysis]