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Last Posted: May 28, 2024

• 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

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