Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 519 Records) |
Query Trace: Congenital heart disease [original query] |
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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 |
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 |
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 |
SMAD5 as a novel gene for familial pulmonary arterial hypertension. Clinical science (London, England : 1979) 2024 12 . Ding Cao, Ekkehard Grünig, Yuriy Sirenko, Ganna Radchenko, Henning Gall, Ayat Ahmed, Susanne Theiß, Mareike Lankeit, Benjamin Meder, Magdalena Laugsch, Christina A Eichstae |
Association of maternal folic acid supplementation and offspring MTRR gene polymorphism with congenital heart disease: a hospital-based case-control study in Han population. Journal of health, population, and nutrition 2024 12 43 (1): 220. Liuxuan Li, Jun Ou, Yige Chen, Qian Chen, Manjun Luo, Tingting Wang, Yingfan Zhang, Jiabi Q |
Determination of Genotype and Phenotypes in Pediatric Patients With Biventricular Noncompaction. Journal of the American Heart Association 2024 11 13 (21): e035614. Keiichi Hirono, Yukiko Hata, Teruhiko Imamura, Kaori Tsuboi, Shinya Takarada, Mako Okabe, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Shojiro Ichimata, Naoki Nishida, Hidenori Iwasaki, Susumu Urata, Seigo Okada, Tomoya Hiratsuji, Heima Sakaguchi, Kiyohiro Takigiku, Makoto Nakazawa, Eiki Nishihara, Masako Harada, Osamu Matsuo, Kenji Yasuda, Yoko Yoshida, Hidemasa Namiki, Kazushi Yasuda, Toshinobu Ifuku, Kotaro Urayama, Hideharu Oka, Kayo Ogino, Akio Kato, Nobuhiko Kan, Shunji Seki, Mitsuru Seki, Yutaka Odanaka, Satoru Iwashima, Shuichiro Yoshida, Toyohisa Miyata, Tomoyuki Miyamoto, Ken Watanabe, Naoki Kuwabara, Ryo Inuzuka, Yoshihiro Takahashi, Hisanori Sakazaki, Jun Muneuchi, Shigetoyo Kogaki, Fujito Numano, Sachiko Kido, Masaki Nii, Shinsuke Hoshino, Hidekazu Ishida, Jun Maeda, Yasunobu Hayabuchi, Yoshikazu Otsubo, Kazuyuki Ikeda, Shinya Tsukano, Makoto Watanabe, Nobuo Momoi, Takanari Fujii, Tao Fujioka, Mitsuhiro Fujino, Hiroki Uchiyama, Shigehito Baba, Hitoshi Horigome, Takashi Honda, Kazutaka Suzuki, Fukiko Ichi |
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 |
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