Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
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Records 1 - 30 (of 63 Records) |
| Query Trace: Patent Ductus Arteriosus[original query] |
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| Genetic variants associated with patent ductus arteriosus in extremely preterm infants. Journal of perinatology : official journal of the California Perinatal Association 2019 Mar 39 (3): 401-408. Dagle John M, Ryckman Kelli K, Spracklen Cassandra N, Momany Allison M, Cotten C Michael, Levy Joshua, Page Grier P, Bell Edward F, Carlo Waldemar A, Shankaran Seetha, Goldberg Ronald N, Ehrenkranz Richard A, Tyson Jon E, Stoll Barbara J, Murray Jeffrey C, |
| Can Functional Polymorphisms in VEGF and MMP Predict Intraventricular Hemorrhage in Extremely Preterm Newborns? Developmental neuroscience 2018 40 (4): 337-343. Prasun Pankaj, Madan Raghav, Puthuraya Subhash, Subramanian Divya, Datta Ishita, Kalra Vaneet, Thomas Ronald, Stockton David W, Sundaram Senthil, Callaghan Joseph, Callaghan Michael, Chouthai Nit |
| Association between 5,10-methylenetetrahydrofolate, gene polymorphism and congenital heart disease. Journal of biological regulators and homeostatic agents 0 32 (5): 1255-1260. Wang H L, Sun L, Zhou S, Wang |
| Vascular endothelial growth factor polymorphism rs2010963 status does not affect patent ductus arteriosus incidence or cyclooxygenase inhibitor treatment success in preterm infants. Cardiology in the young 2019 Jun 1-5. Sallmon Hannes, Aydin Tünay, Hort Stefanie, Kubinski Anja, Bode Christina, Klippstein Tamara, Endesfelder Stefanie, Bührer Christoph, Koehne Pet |
| [Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 5 36 (6): 620-623. Shen Nan, Gou Rui, Yu Han, Gao Xin, Pang Huanping, Liu Yi, Gai Zhongt |
| Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children. Molecular genetics & genomic medicine 2019 Mar e612. Behiry Eman G, Al-Azzouny Mahmoud A, Sabry Dina, Behairy Ola G, Salem Nessrine |
| Cardiac manifestations and gene mutations of patients with RASopathies in Taiwan. American journal of medical genetics. Part A 2019 12 182 (2): 357-364. Lee Chung-Lin, Tan Louis Tan Hock-Cheong, Lin Hsiang-Yu, Hwu Wuh-Liang, Lee Ni-Chung, Chien Yin-Hsiu, Chuang Chih-Kuang, Wu Mei-Hwan, Wang Jou-Kou, Chu Shao-Yin, Lin Ju-Li, Lo Fu-Sung, Su Pen-Hua, Hsu Chia-Chi, Ko Yu-Yuan, Chen Ming-Ren, Chiu Hui-Ching, Lin Shuan-P |
| Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry. American journal of medical genetics. Part C, Seminars in medical genetics 2019 12 181 (4): 658-681. Grange Dorothy K, Roessler Helen I, McClenaghan Conor, Duran Karen, Shields Kathleen, Remedi Maria S, Knoers Nine V A M, Lee Jin-Moo, Kirk Edwin P, Scurr Ingrid, Smithson Sarah F, Singh Gautam K, van Haelst Mieke M, Nichols Colin G, van Haaften Gi |
| 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. Advances in therapy 2020 Nov . He Xin, Qiu Jin-Chun, Lu Ke-Yu, Guo Hong-Li, Li Ling, Jia Wei-Wei, Ni Ming-Ming, Liu Yun, Xu Jing, Chen Feng, Cheng R |
| 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. Xenobiotica; the fate of foreign compounds in biological systems 2021 Sep 1-32. Sridharan Kannan, Al Jufairi Muna, Al Ansari Eman, Jasim Anfal, Eltayeb Diab Diab, Al Marzooq Reem, Al Madhoob Abdulrao |
| Association analysis of maternal MTHFR gene polymorphisms and the occurrence of congenital heart disease in offspring. BMC cardiovascular disorders 2021 Jun 21 (1): 298. Sun Mengting, Wang Tingting, Huang Peng, Diao Jingyi, Zhang Senmao, Li Jinqi, Luo Liu, Li Yihuan, Chen Letao, Liu Yiping, Wei Jianhui, Song Xinli, Sheng Xiaoqi, Qin Jia |
| Interactions between PDA-associated polymorphisms and genetic ancestry alter ductus arteriosus gene expression. Pediatric research 2021 4 91 (4): 903-911. Clyman Ronald I, Hills Nancy K, Dagle John M, Murray Jeffrey C, Kelsey Keeg |
| The effects of ductal size on the severity of pulmonary hypertension in children with patent ductus arteriosus (PDA): a multi-center study. BMC pulmonary medicine 2021 3 21 (1): 79. Chinawa Josephat M, Chukwu Bartholomew F, Chinawa Awoere T, Duru Chika |
| Association of Maternal Betaine-Homocysteine Methyltransferase (BHMT) and BHMT2 Genes Polymorphisms with Congenital Heart Disease in Offspring. Reproductive sciences (Thousand Oaks, Calif.) 2022 Jul . Luo Manjun, Wang Tingting, Huang Peng, Zhang Senmao, Song Xinli, Sun Mengting, Liu Yiping, Wei Jianhui, Shu Jing, Zhong Taowei, Chen Qian, Zhu Ping, Qin Jia |
| A novel KLF13 mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve. Experimental and therapeutic medicine 2022 4 23 (4): 311. Abhinav Pradhan, Zhang Gao-Feng, Zhao Cui-Mei, Xu Ying-Jia, Wang Juan, Yang Yi-Qi |
| Randomized Trial on Echocardiography-Guided Ductus Arteriosus Treatment to Reduce Necrotizing Enterocolitis. Frontiers in pediatrics 2022 2 9 807712. Bravo María Carmen, Sánchez-Salmador Rebeca, Moral-Pumarega María Teresa, López-Azorín Manuela, Mosqueda-Peña Rocío, Dorronsoro Izaskun, Cabañas Fernando, Pellicer Adeli |
| 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. Frontiers in cardiovascular medicine 2022 12 9 1048795. Peng Yongxuan, Ye Jiajun, Xu Yuejuan, Huang Jihong, Wu Yurong, Liu Wei, Bai Kai, Chen Sun, Lu Yan |
| Etiology and prognosis of nephrocalcinosis according to gestational age in Korean children. BMC pediatrics 2023 9 23 (1): 451. Jinwoon Joung, Heeyeon C |
| Association of the EPAS1 rs7557402 Polymorphism with Hemodynamically Significant Patent Ductus Arteriosus Closure Failure in Premature Newborns under Pharmacological Treatment with Ibuprofen. Diagnostics (Basel, Switzerland) 2023 8 13 (15): . Diana G Rogel-Ayala, José Esteban Muñoz-Medina, Valeria Dejanira Vicente-Juárez, Patricia Grether-González, Deneb Algedi Morales-Barquet, Alfonso de Jesús Martínez-García, María Olga Leticia Echaniz-Aviles, Rosalba Sevilla-Montoya, Alejandro Martínez-Juárez, Jazmin Artega-Vázquez, Javier Angeles-Martínez, Gilberto Vargas-Alarcón, Alberto Hidalgo-Bravo, Irma Eloisa Monroy-Muñ |
| Early neurodevelopmental outcomes of extreme preterm infants exposed to paracetamol: a retrospective cohort study. Pediatric research 2023 5 1-6. Bella Zhong, Kenneth Tan, Abdul Razak, Vathana Sackett, Catherine Machipisa, Lindsay Zhou, Samira Samiee-Zafarghandy, Arvind Sehgal, Rod W Hunt, Pramod Pharande, Atul Malhot |
| Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome. Frontiers in genetics 2023 4 14 1085210. Lin Yunting, Chen Xiaohong, Xie Bobo, Guan Zhihong, Chen Xiaodan, Li Xiuzhen, Yi Peng, Du Rong, Mei Huifen, Liu Li, Zhang Wen, Zeng Chunh |
| The risk of pediatric cardiovascular diseases in offspring born to mothers with systemic lupus erythematosus: a nationwide study. Frontiers in pediatrics 2023 12 11 1294823. Jong Ho Cha, Jae Kyoon Hwang, Young-Jin Choi, Jae Yoon |
| Whole-exome sequencing analysis of patent ductus arteriosus in a Japanese macaque (Macaca fuscata). Journal of medical primatology 2023 11 . Young-Jin Jang, Byung-Yong Park, Hyun-Jin Tae, Jeoungha Sim, Dongchoon A |
| Missense mutations in the CITED2 gene may contribute to congenital heart disease. BMC cardiovascular disorders 2024 9 24 (1): 516. Hira Yaqoob, Hussain Ahmad, Syed Irtiza Ali, Najma Patel, Afsheen Ar |
| Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki Syndrome. Diagnostics (Basel, Switzerland) 2024 4 14 (8): . Chung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, Ju-Li Lin, Huei-Ching Chiu, Ya-Hui Chang, Yuan-Rong Tu, Yun-Ting Lo, Hsiang-Yu Lin, Shuan-Pei L |
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