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Patent Ductus Arteriosus
What's New
Last Posted: Oct 06, 2024
- Missense mutations in the CITED2 gene may contribute to congenital heart disease.
Hira Yaqoob, et al. BMC cardiovascular disorders 2024 0 (1) 516 - High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.
Gloria K E Zodanu et al. Int J Mol Sci 2024 25(10) - Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki Syndrome.
Chung-Lin Lee, et al. Diagnostics (Basel, Switzerland) 2024 0 (8) - The risk of pediatric cardiovascular diseases in offspring born to mothers with systemic lupus erythematosus: a nationwide study.
Jong Ho Cha, et al. Frontiers in pediatrics 2023 0 1294823 - Whole-exome sequencing analysis of patent ductus arteriosus in a Japanese macaque (Macaca fuscata).
Young-Jin Jang, et al. Journal of medical primatology 2023 0 - Etiology and prognosis of nephrocalcinosis according to gestational age in Korean children.
Jinwoon Joung, et al. BMC pediatrics 2023 0 (1) 451 - Association of the EPAS1 rs7557402 Polymorphism with Hemodynamically Significant Patent Ductus Arteriosus Closure Failure in Premature Newborns under Pharmacological Treatment with Ibuprofen.
Diana G Rogel-Ayala, et al. Diagnostics (Basel, Switzerland) 2023 0 (15) - Early neurodevelopmental outcomes of extreme preterm infants exposed to paracetamol: a retrospective cohort study.
Bella Zhong, et al. Pediatric research 2023 0 1-6 - Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome.
Lin Yunting, et al. Frontiers in genetics 2023 0 1085210 - Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry.
Grange Dorothy K, et al. American journal of medical genetics. Part C, Seminars in medical genetics 2019 0 (4) 658-681 - Cardiac manifestations and gene mutations of patients with RASopathies in Taiwan.
Lee Chung-Lin, et al. American journal of medical genetics. Part A 2019 0 (2) 357-364 - [Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease].
Shen Nan, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 0 (6) 620-623 - Interactions between PDA-associated polymorphisms and genetic ancestry alter ductus arteriosus gene expression.
Clyman Ronald I, et al. Pediatric research 2021 0 (4) 903-911 - The effects of ductal size on the severity of pulmonary hypertension in children with patent ductus arteriosus (PDA): a multi-center study.
Chinawa Josephat M, et al. BMC pulmonary medicine 2021 0 (1) 79 - Two genetic variants in NEXN and ABCC6 genes found in a patient with right coronary artery to right ventricle fistula combined with giant coronary aneurysm and patent ductus arteriosus.
Peng Yongxuan, et al. Frontiers in cardiovascular medicine 2022 0 1048795 - A novel KLF13 mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve.
Abhinav Pradhan, et al. Experimental and therapeutic medicine 2022 0 (4) 311 - Genetic polymorphisms and risk for acute renal failure in preterm neonates.
Vásárhelyi Barna, et al. Pediatric nephrology (Berlin, Germany) 2005 0 (2) 132-5 - Randomized Trial on Echocardiography-Guided Ductus Arteriosus Treatment to Reduce Necrotizing Enterocolitis.
Bravo María Carmen, et al. Frontiers in pediatrics 2022 0 807712 - Bedside tracking of functional autonomic age in preterm infants.
Iyer Kartik K et al. Pediatric research 2022 - Association of Maternal Betaine-Homocysteine Methyltransferase (BHMT) and BHMT2 Genes Polymorphisms with Congenital Heart Disease in Offspring.
Luo Manjun, et al. Reproductive sciences (Thousand Oaks, Calif.) 2022 7 - Evaluation of urinary acetaminophen metabolites and its association with the genetic polymorphisms of the metabolising enzymes, and serum acetaminophen concentrations in preterm neonates with patent ductus arteriosus.
Sridharan Kannan, et al. Xenobiotica; the fate of foreign compounds in biological systems 2021 9 1-32 - Association analysis of maternal MTHFR gene polymorphisms and the occurrence of congenital heart disease in offspring.
Sun Mengting, et al. BMC cardiovascular disorders 2021 6 (1) 298 - Therapy for Apnoea of Prematurity: A Retrospective Study on Effects of Standard Dose and Genetic Variability on Clinical Response to Caffeine Citrate in Chinese Preterm Infants.
He Xin, et al. Advances in therapy 2020 11 - Association between 5,10-methylenetetrahydrofolate, gene polymorphism and congenital heart disease.
Wang H L, et al. Journal of biological regulators and homeostatic agents 0 0 (5) 1255-1260 - Can Functional Polymorphisms in VEGF and MMP Predict Intraventricular Hemorrhage in Extremely Preterm Newborns?
Prasun Pankaj, et al. Developmental neuroscience 2018 0 (4) 337-343 - Genetic variants associated with patent ductus arteriosus in extremely preterm infants.
Dagle John M, et al. Journal of perinatology : official journal of the California Perinatal Association 2019 3 (3) 401-408 - Vascular endothelial growth factor polymorphism rs2010963 status does not affect patent ductus arteriosus incidence or cyclooxygenase inhibitor treatment success in preterm infants.
Sallmon Hannes, et al. Cardiology in the young 2019 6 1-5 - Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.
Behiry Eman G, et al. Molecular genetics & genomic medicine 2019 3 e612 - Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations.
Regalado Ellen S et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 20(10) 1206-1215 - Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa.
Thomford Nicholas Ekow et al. Omics : a journal of integrative biology 2018 May 22(5) 301-321
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About HLBS-PopOmics
HLBS-PopOmics is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to Heart and Vascular Diseases(H), Lung Diseases(L), Blood Diseases(B), and Sleep Disorders(S)...more
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Site Citation:
Mensah GA, Yu W, Barfield WL, Clyne M, Engelgau MM, Khoury MJ. HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders. Genet Med. 2018 Sep 10. doi: 10.1038/s41436-018-0118-1
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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