Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 516 Records) |
| Query Trace: Congenital heart disease [original query] |
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| Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients. Orphanet journal of rare diseases 2023 9 18 (1): 284. Biyun Feng, Xin Li, Qianwen Zhang, Yirou Wang, Shili Gu, Ru-En Yao, Zhiying Li, Shiyang Gao, Guoying Chang, Qun Li, Niu Li, Lijun Fu, Jian Wang, Xiumin Wa |
| Evaluation of maternal-fetal outcomes in pregnancy complicated with severe pulmonary hypertension and its influencing factors: a single-center retrospective study in China. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2023 12 36 (2): 2290923. Qiulan Dai, Manman Shang, Yu Zhou, Qin W |
| 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 |
| Molecular Genetic Study on HAND2 Gene Promoter in Ventricular Septal Defect. International heart journal 2023 11 64 (6): 1140-1147. Meikun Li, Yahui Cai, Shuchao Pang, Bo Y |
| Association of genetic and sulcal traits with executive function in congenital heart disease. Annals of clinical and translational neurology 2023 11 . Lara Maleyeff, Jane W Newburger, David Wypij, Nina H Thomas, Evdokia Anagnoustou, Martina Brueckner, Wendy K Chung, John Cleveland, Sean Cunningham, Bruce D Gelb, Elizabeth Goldmuntz, Donald J Hagler, Hao Huang, Eileen King, Patrick McQuillen, Thomas A Miller, Ami Norris-Brilliant, George A Porter, Amy E Roberts, P Ellen Grant, Kiho Im, Sarah U Mort |
| Rare loss-of-function variants in matrisome genes are enriched in Ebstein's anomaly. HGG advances 2023 11 100258. Zhou Zhou, Xia Tang, Wen Chen, Qianlong Chen, Bo Ye, Angad S Johar, Iftikhar J Kullo, Keyue Di |
| Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot. Translational pediatrics 2023 11 12 (10): 1835-1841. Yu Pan, Manli Liu, Songsong Zhang, Huaxian Mei, Jing |
| Association between NOS3 gene polymorphisms and genetic susceptibility to congenital heart Disease: A systematic review and meta-analysis. Cytokine 2023 11 173 156415. Kang Yi, Wei Wang, Xin Zhang, Xin Dong, Zhengye Fan, Yuhu Ma, Jie Gao, Xinyao Li, Tao Y |
| Single-Cell Reconstruction and Mutation Enrichment Analysis Identifies Dysregulated Cardiomyocyte and Endothelial Cells in Congenital Heart Disease. Physiological genomics 2023 10 . Richa Tambi, Binte Ashraf, Sharon Nandkishore, Shermin Sharafat, Faiza Kader, Nasna Nassir, Nesrin Mohamed, Awab Ahmed, Reem Abdel Hameid, Samah Alasrawi, Martina Brueckner, Wolfgang M Kuebler, Wendy Chung, Alawi Alsheikh-Ali, Roberto M Di Donato, Mohammed Uddin, Bakhrom K Berdi |
| Relationships between Maternal Folic Acid Supplementation and GATA4 Gene Polymorphisms in Patients with Non-Chromosomal Congenital Heart Disease: A Hospital-Based Case-Control Study in China. Nutrients 2023 10 15 (20): . Letao Chen, Tubao Yang, Tingting Wang, Mengting Sun, Jiabi Q |
| Repurposing Normal Chromosomal Microarray Data to Harbor Genetic Insights into Congenital Heart Disease. Biology 2023 10 12 (10): . Nephi A Walton, Hoang H Nguyen, Sara S Procknow, Darren Johnson, Alexander Anzelmi, Patrick Y J |
| Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot. Frontiers in cardiovascular medicine 2023 10 10 1249605. Drayton C Harvey, Riya Verma, Brandon Sedaghat, Brooke E Hjelm, Sarah U Morton, Jon G Seidman, S Ram Kum |
| Rare homozygous cilia gene variants identified in consanguineous congenital heart disease patients. Human genetics 2024 9 . Daniel A Baird, Hira Mubeen, Canan Doganli, Jasmijn B Miltenburg, Oskar Kaaber Thomsen, Zafar Ali, Tahir Naveed, Asif Ur Rehman, Shahid Mahmood Baig, Søren Tvorup Christensen, Muhammad Farooq, Lars Allan Lars |
| 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 |
| Methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms and five related serum molecular levels in 2587 patients: Associated differentially with adverse pregnancy. Molecular biology reports 2024 9 51 (1): 1014. Zhanqi Feng, Yue Gao, Mengting Zhang, Yaoping Wang, Xiuming Liu, Bo Zhang, Junxiang Su, Hongdan Wa |
| FLT4 gene polymorphisms influence isolated ventricular septal defect predisposition in a Southwest China population. BMC medical genomics 2024 8 17 (1): 197. Yunhan Zhang, Xiaoli Dong, Jun Zhang, Miao Zhao, Jiang Wang, Jiayou Chu, Zhaoqing Yang, Shaohui Ma, Keqin Lin, Hao Sun, Zhiling L |
| [Whole exome sequencing analysis of 37 fetuses with cardiac abnormalities]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 8 41 (8): 903-908. Xiayuan Xu, Fenglei Ye, Jun Zhang, Keqin Jin, Qian Shen, Shuangshuang Shen, Fan J |
| Predictive Modeling of Endocardial Fibroelastosis Recurrence in Patients with Congenital Heart Disease. The Journal of thoracic and cardiovascular surgery 2024 8 . Daniel Diaz-Gil, Natalia Silva-Gomez, Sarah U Morton, Jonathan G Seidman, Christine E Seidman, David Zurakowski, Steven J Staffa, Gerald R Marx, Sitaram M Emani, Pedro J Del Nido, Ingeborg Frie |
| ENU-based dominant genetic screen identifies contractile and neuronal gene mutations in congenital heart disease. Genome medicine 2024 8 16 (1): 97. Xiaoxi Luo, Lifeng Liu, Haowei Rong, Xiangyang Liu, Ling Yang, Nan Li, Hongjun S |
| Exploring Genetic Diversity of SOD2 and POU5F1 for Congenital Heart Disease in the Southwest Chinese Population. International heart journal 2024 7 65 (4): 723-729. Ye Jin, Jun Zhang, Qiuzhe Guo, Xiaoli Dong, Jian Li, Jiang Wang, Shuang Li, Yan Shen, Keqin Lin, Zhaoqing Yang, Jiayou Chu, Hao Sun, Zhiling L |
| Congenital Heart Disease and Genetic Changes in Folate/Methionine Cycles. Genes 2024 7 15 (7): . Nataša Karas Kuželi?ki, Bojan Dolj |
| Coronary arteriopathy in a patient with Noonan phenotype: Case report. Annals of pediatric cardiology 2024 6 17 (1): 70-73. Simran Jain, M S Ravindra, Yogesh Chintaman Sathe, Snehal M Kulkarni, Ashish Banpurk |
| Prenatal diagnosis and pregnancy outcomes in fetuses with ventriculomegaly. Frontiers in medicine 2024 5 11 1349171. Fagui Yue, Xiao Yang, Ning Liu, Ruizhi Liu, Hongguo Zha |
| Impact of Genotype-Phenotype Interactions on Cardiovascular Function in Paediatric Loeys-Dietz Syndrome. CJC pediatric and congenital heart disease 2024 5 3 (2): 47-54. Nairy Khodabakhshian, Alison J Howell, Pablo Perez Lopez, Wei Hui, Luc L Mertens, Vitor C Guer |
| Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China. Italian journal of pediatrics 2024 4 50 (1): 62. Ye Jin, Miao Zhao, Qiuzhe Guo, Wanyu Zhao, Min Lei, Yifei Zhang, Yunhan Zhang, Yan Shen, Keqin Lin, Zhaoqing Yang, Jiayou Chu, Hao Sun, Zhiling L |
| NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy. Genome medicine 2024 4 16 (1): 53. Zain Dardas, Jawid M Fatih, Angad Jolly, Moez Dawood, Haowei Du, Christopher M Grochowski, Edward G Jones, Shalini N Jhangiani, Xander H T Wehrens, Pengfei Liu, Weimin Bi, Eric Boerwinkle, Jennifer E Posey, Donna M Muzny, Richard A Gibbs, James R Lupski, Zeynep Coban-Akdemir, Shaine A Morr |
| 22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity. Genes 2024 4 15 (4): . Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno, Chong Ae Kim, Elaine Lustosa Mendes, Erlane Marques Ribeiro, Amanda Oliveira, Têmis Maria Félix, Agnes Cristina Fett-Conte, Luciana Cardoso Bonadia, Gabriela Roldão Correia-Costa, Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes, Társis Paiva Viei |
| 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 |
| Atrial Fibrillation and Clonal Hematopoiesis in TET2 and ASXL1. JAMA cardiology 2024 4 . Seyedmohammad Saadatagah, Mohammadreza Naderian, Mesbah Uddin, Ozan Dikilitas, Abhishek Niroula, Art Schuermans, Elizabeth Selvin, Ron C Hoogeveen, Kunihiro Matsushita, Vijay Nambi, Bing Yu, Lin Yee Chen, Alexander G Bick, Benjamin L Ebert, Michael C Honigberg, Na Li, Amil Shah, Pradeep Natarajan, Iftikhar J Kullo, Christie M Ballanty |
| A Prevalent TMEM260 Deletion Causes Conotruncal Heart Defects, Including Truncus Arteriosus. American journal of medical genetics. Part A 2024 10 e63906. Naoya Saijo, Hisao Yaoita, Jun Takayama, Chiharu Ota, Eiichiro Kawai, Masato Kimura, Akira Ozawa, Gen Tamiya, Shigeo Kure, Atsuo Kikuc |
- Page last reviewed:Feb 1, 2024
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