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Ze-Qun Liu, Mi Cheng, Fang Fu, Ru Li, Jin Han, Xin Yang, Qiong Deng, Lu-Shan Li, Ting-Ying Lei, Dong-Zhi Li & Can Liao. (2022) Identification of differential microRNAs and messenger RNAs resulting from ASXL transcriptional regulator 3 knockdown during during heart development. Bioengineered 13:4, pages 9948-9961.
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Hailong Huang, Meiying Cai, Yan Wang, Bin Liang, Na Lin & Liangpu Xu. (2021) SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis. Risk Management and Healthcare Policy 14, pages 345-355.
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Articles from other publishers (32)
Lindsay M. Thomson, Christopher A. Mancuso, Kelly R. Wolfe, Ludmila Khailova, Sierra Niemiec, Eiman Ali, Michael DiMaria, Max Mitchell, Mark Twite, Gareth Morgan, Benjamin S. Frank & Jesse A. Davidson. (2023) The proteomic fingerprint in infants with single ventricle heart disease in the interstage period: evidence of chronic inflammation and widespread activation of biological networks. Frontiers in Pediatrics 11.
Crossref
Crossref
Katayoun Heshmatzad, Niloofar Naderi, Majid Maleki, Shiva Abbasi, Serwa Ghasemi, Nooshin Ashrafi, Amir Farjam Fazelifar, Mohammad Mahdavi & Samira Kalayinia. (2023) Role of non‐coding variants in cardiovascular disease. Journal of Cellular and Molecular Medicine 27:12, pages 1621-1636.
Crossref
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Divya Kumari, Deepti Chaudhary, Inusha Panigrahi & Manoj K. Rohit. (2020) Genetic Defects in Children with Cardiac Anomalies/Malformations: Noonan and CFC Syndromes. Journal of Pediatric Genetics 12:01, pages 086-089.
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Fahad A. Alghaith, Heleen H. Arts, Francois J. Plourde, Andrew Boswall, Partima Gulati, P. Daniel McNeely, Philip D. Acott, Kenny K. Wong & Sarah Dyack. (2022) Increased intracranial pressure in a patient with Congenital Heart Defect and Ectodermal Dysplasia (CHDED): Extension of phenotype and review of literature. American Journal of Medical Genetics Part A 191:2, pages 554-558.
Crossref
Crossref
Hashir Ali Awan & Irfan Ullah. 2023. Clinical and Surgical Aspects of Congenital Heart Diseases. Clinical and Surgical Aspects of Congenital Heart Diseases
1
8
.
Yaotse Elikplim Nordjoe, Suzanne Rita Aubin Igombe & Latifa Chat. (2022) Non-cardiovascular findings on chest CT angiography in children with congenital heart disease: How important are they?. BMC Medical Imaging 22:1.
Crossref
Crossref
Yiting Gui, Yawen Zhang, Qi Zhang, Xudong Chen, Feng Wang, Fang Wu, Yonghao Gui & Qiang Li. (2022) The functional verification and analysis of Fugu promoter of cardiac gene tnni1a in zebrafish. Cells & Development 171, pages 203801.
Crossref
Crossref
Laura M. Wienecke, Sarah Cohen, Johann Bauersachs, Alexandre Mebazaa & Benjamin G. Chousterman. (2021) Immunity and inflammation: the neglected key players in congenital heart disease?. Heart Failure Reviews 27:5, pages 1957-1971.
Crossref
Crossref
Gioia Mastromoro, Giulio Calcagni, Walter Vignaroli, Silvia Anaclerio, Flaminia Pugnaloni, Gabriele Rinelli, Aurelio Secinaro, Veronica Bordonaro, Carolina Putotto, Marta Unolt, Maria Cristina Digilio, Bruno Marino & Paolo Versacci. (2022) Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes—A report of 74 cases with systematic review of the literature. American Journal of Medical Genetics Part A.
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Giulio Calcagni, Camilla Calvieri, Anwar Baban, Francesco Bianco, Rosaria Barracano, Massimo Caputo, Andrea Madrigali, Stefani Silva Kikina, Marco Alfonso Perrone, Maria Cristina Digilio, Marco Pozzi, Aurelio Secinaro, Berardo Sarubbi, Lorenzo Galletti, Maria Giulia Gagliardi, Andrea de Zorzi, Fabrizio Drago & Benedetta Leonardi. (2022) Syndromic and Non-Syndromic Patients with Repaired Tetralogy of Fallot: Does It Affect the Long-Term Outcome?. Journal of Clinical Medicine 11:3, pages 850.
Crossref
Crossref
Leslye Venegas-Zamora, Francisco Bravo-Acuña, Francisco Sigcho, Wileidy Gomez, José Bustamante-Salazar, Zully Pedrozo & Valentina Parra. (2022) New Molecular and Organelle Alterations Linked to Down Syndrome Heart Disease. Frontiers in Genetics 12.
Crossref
Crossref
Iván Romero-Rivera, Angélica Grullón & Demián Herrera. (2022) Tamizaje de las cardiopatías congénitas. Cardiovascular and Metabolic Science 33:S5, pages s426-428.
Crossref
Crossref
Anwar Baban, Valentina Lodato, Giovanni Parlapiano & Fabrizio Drago. (2022) Genetics in Congenital Heart Diseases. Heart Failure Clinics 18:1, pages 139-153.
Crossref
Crossref
Ryan Jones, Kristen Sandoz & Kelvin Lee. 2022. Handbook of Treatment Planning for Children with Autism and Other Neurodevelopmental Disorders. Handbook of Treatment Planning for Children with Autism and Other Neurodevelopmental Disorders
129
146
.
Giulio Calcagni, Flaminia Pugnaloni, Maria Cristina Digilio, Marta Unolt, Carolina Putotto, Marcello Niceta, Anwar Baban, Francesca Piceci Sparascio, Fabrizio Drago, Alessandro De Luca, Marco Tartaglia, Bruno Marino & Paolo Versacci. (2021) Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights. Genes 12:7, pages 1047.
Crossref
Crossref
Veronica Romano, Carlo Maria Gallinoro, Rosita Mottola, Alessandro Serio, Franca Di Meglio, Clotilde Castaldo, Felice Sirico & Daria Nurzynska. (2021) Patent Foramen Ovale—A Not So Innocuous Septal Atrial Defect in Adults. Journal of Cardiovascular Development and Disease 8:6, pages 60.
Crossref
Crossref
Emmanuel Suluba, Liu Shuwei, Qing Xia & Ally Mwanga. (2020) Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways. Egyptian Journal of Medical Human Genetics 21:1.
Crossref
Crossref
Qing-Qing Song, Li-Hui Zhu, Ou-Ying Chen, Zhi-Rong Xiao, Zhi Chen, Yun-Bin Xiao, Jian-Chao Meng, Chao Zuo & Jos M. Latour. (2020) Compliance with aspirin in paediatric CHD post-percutaneous transcatheter occlusion: a cross-sectional study. Cardiology in the Young 30:10, pages 1462-1468.
Crossref
Crossref
Liangping Cheng, Yanlai Tang, Yuese Lin, Hongjun Ba, Yiqian Ding, Dubo Chen, Min Liu, Peizhen Pan, Youzhen Qin & Zhan-Peng Huang. (2020) A Chromosomal Inversion of 46XX, inv (6) (p21.3p23) Connects to Congenital Heart Defects. Frontiers in Cardiovascular Medicine 7.
Crossref
Crossref
Giulio Calcagni, Giulia Gagliostro, Giuseppe Limongelli, Marta Unolt, Enrica De Luca, Maria C. Digilio, Anwar Baban, Sonia B. Albanese, Giovanni B. Ferrero, Giuseppina Baldassarre, Gabriella Agnoletti, Elena Banaudi, Jan Marek, Juan P. Kaski, Giulia Tuo, Maurizio Marasini, Francesca Cairello, Andrea Madrigali, Giuseppe Pacileo, Maria G. Russo, Ornella Milanesi, Roberto Formigari, Maurizio Brighenti, Luca Ragni, Andrea Donti, Fabrizio Drago, Bruno Dallapiccola, Marco Tartaglia, Bruno Marino & Paolo Versacci. (2020) Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study. Birth Defects Research 112:10, pages 725-731.
Crossref
Crossref
Anwar Baban, Nicole Olivini, Nicoletta Cantarutti, Federica Calì, Carmen Vitello, Diletta Valentini, Rachele Adorisio, Giulio Calcagni, Viola Alesi, Corrado Di Mambro, Alberto Villani, Bruno Dallapiccola, Maria Cristina Digilio, Bruno Marino, Adriano Carotti & Fabrizio Drago. (2020) Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defect. American Journal of Medical Genetics Part A 182:6, pages 1342-1350.
Crossref
Crossref
Aline Saliba, Ana Carolina Vaqueiro Figueiredo, José Eduardo Baroneza, Jorge Yuseff Afiune, Aline Pic‐Taylor, Silviene Fabiana de Oliveira & Juliana Forte Mazzeu. (2020) Genetic and genomics in congenital heart disease: a clinical review. Jornal de Pediatria (Versão em Português) 96:3, pages 279-288.
Crossref
Crossref
Aline Saliba, Ana Carolina Vaqueiro Figueiredo, José Eduardo Baroneza, Jorge Yuseff Afiune, Aline Pic-Taylor, Silviene Fabiana de Oliveira & Juliana Forte Mazzeu. (2020) Genetic and genomics in congenital heart disease: a clinical review. Jornal de Pediatria 96:3, pages 279-288.
Crossref
Crossref
Wei Wei, Bojian Li, Fen Li, Kun Sun, Xuechao Jiang & Rang Xu. (2020) Identification of FOXH1 mutations in patients with sporadic conotruncal heart defect. Clinical Genetics 97:4, pages 576-585.
Crossref
Crossref
Angela E. Lin, Stephanie Santoro, Frances A. High, Paula Goldenberg & Iris Gutmark‐Little. (2019) Congenital heart defects associated with aneuploidy syndromes: New insights into familiar associations. American Journal of Medical Genetics Part C: Seminars in Medical Genetics 184:1, pages 53-63.
Crossref
Crossref
Arodi Farrera, María Villanueva, Alfredo Vizcaíno, Patricia Medina-Bravo, Norma Balderrábano-Saucedo, Mariana Rives, David Cruz, Elizabeth Hernández-Carbajal, Javier Granados-Riveron & Rocío Sánchez-Urbina. (2019) Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome. Head & Face Medicine 15:1.
Crossref
Crossref
Anwar Baban, Nicole Olivini, Francesca Romana Lepri, Federica Calì, Mafalda Mucciolo, Maria C. Digilio, Giulio Calcagni, Corrado di Mambro, Bruno Dallapiccola, Rachele Adorisio, Antonio Novelli & Fabrizio Drago. (2019)
SOS1
mutations in Noonan syndrome: Cardiomyopathies and not only congenital heart defects! Report of six patients including two novel variants and literature review
. American Journal of Medical Genetics Part A 179:10, pages 2083-2090.
Crossref
Crossref
Florencia Petracchi, Silvina Sisterna, Laura Igarzabal & Louise Wilkins‐Haug. (2019) Fetal cardiac abnormalities: Genetic etiologies to be considered. Prenatal Diagnosis 39:9, pages 758-780.
Crossref
Crossref
Ankush Borlepawar, Norbert Frey & Derk Frank. (2019) Editorial commentary: Epithelial-to-Mesenchymal transition and G protein-coupled receptors: A novel possibility for cardiac regeneration?. Trends in Cardiovascular Medicine 29:4, pages 205-206.
Crossref
Crossref
Tatiana Alicandro, Carolina Putotto, Giulio Calcagni, Marta Unolt, Gioia Mastromoro, Maria Cristina Digilio, Paolo Versacci & Bruno Marino. (2018) Impact of genetic studies on comprehension and treatment of congenital heart disease. Progress in Pediatric Cardiology 51, pages 31-36.
Crossref
Crossref
Sunjidatul Islam, Padma Kaul, Dat T. Tran & Andrew S. Mackie. (2018) Health Care Resource Utilization Among Children With Congenital Heart Disease: A Population-Based Study. Canadian Journal of Cardiology 34:10, pages 1289-1297.
Crossref
Crossref
Abdel-Hady El-Gilany, Sohier Yahia & Yahya Wahba. (2017) Prevalence of congenital heart diseases in children with Down syndrome in Mansoura, Egypt: a retrospective descriptive study. Annals of Saudi Medicine 37:5, pages 386-392.
Crossref
Crossref