Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 190 Records) |
| Query Trace: Death and SCD[original query] |
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| Evaluation of a prophylactic transfusion program on obstetric outcomes in pregnant women with sickle cell disease: A single centre retrospective cohort study. European journal of obstetrics, gynecology, and reproductive biology 2023 9 290 103-108. O Sobczyk, E Gottardi, M Lefebvre, F Canouï-Poitrine, A Jebali, G De Luna, F Pirenne, D Redel, F Galacteros, E Boutin, P Bartolucci, B Haddad, A Habibi, E Lecarpenti |
| Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease. Gene 2023 9 890 147824. Mengna Zhang, William B Hillegass, Xue Yu, Suvankar Majumdar, J Daryl Pollard, Erin Jackson, Jarrod Knudson, Douglas Wolfe, Gregory J Kato, Joseph F Maher, Hao M |
| Left cardiac sympathetic denervation in children with Jervell Lange-Nielsen syndrome and drug refractory torsades - A case series. Pacing and clinical electrophysiology : PACE 2023 9 . Deepanjan Bhattacharya, Narayanan Namboodiri, Madhusoodanan Pillai Sreelekshmi, Mukund A Prabhu, Abhilash Sreevilasam Pushpangadhan, Sabarinath Menon, Baiju S Dharan, Ajitkumar Valaparamb |
| In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome. Molecular genetics & genomic medicine 2023 8 e2263. Hung Manh Pham, Duy Phuong Nguyen, Thanh Dat Ta, Thi Phuong Le, Phong Hai Phan, Hoai An Trinh, Tuan Viet Tran, Thi Lan Anh Luong, Ha Minh Nguyen, The-Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van-Khanh Tr |
| Genetic Variations Within METTL16 and Susceptibility to Sudden Cardiac Death in Chinese Populations With Coronary Artery Disease. The American journal of cardiology 2023 7 202 90-99. Xiaoyuan Zhen, Wenfeng Zhao, Jiawen Wang, Lijuan Li, Yan He, Jianhua Zhang, Chengtao Li, Suhua Zhang, Jiang Huang, Bin Luo, Yuzhen G |
| MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2023 7 . Luisa Marsili, Freyja H M van Lint, Francesco Russo, Karin Y van Spaendonck-Zwarts, Flavie Ader, Marie-Line Bichon, Laurence Faivre, Arjan C Houweling, Bertrand Isidor, Ronald H Lekanne Deprez, Moniek G P J Cox, Arthur A M Wilde, Benoit Mazel, Sandra Mercier, Dennis Dooijes, Gilles Millat, Karine Nguyen, Jan G Post, Pascale Richard, Irma van de Beek, Alexa M C Vermeer, Ludolf Boven, Jan D H Jongbloed, J Peter van Tintelen, |
| Deep learning-derived 12-lead electrocardiogram-based genotype prediction for hypertrophic cardiomyopathy: a pilot study. Annals of medicine 2023 7 55 (1): 2235564. LaiTe Chen, GuoSheng Fu, ChenYang Jia |
| A Genome-Wide Analysis of a Sudden Cardiac Death Cohort: Identifying Novel Target Variants in the Era of Molecular Autopsy. Genes 2023 6 14 (6): . Livia Beccacece, Paolo Abondio, Arianna Giorgetti, Carla Bini, Guido Pelletti, Donata Luiselli, Susi Pelot |
| Non?synonymous polymorphisms in the HRC and ADRB1 genes may be associated with all?cause death in patients with non?ischemic heart failure. Experimental and therapeutic medicine 2023 12 27 (1): 48. Tanise Machado Telles, Bruna Miers May, Mauricio Pimentel, Bruna Letícia Da Silva Pereira, Michael Andrades, Luis Eduardo Rohde, Kátia Gonçalves Dos Sant |
| Genetic QT Score and Sleep Apnea as Predictors of Sudden Cardiac Death in the UK Biobank. medRxiv : the preprint server for health sciences 2023 11 . Amit Arora, Wojciech Zareba, Raymond L Woosley, Yann C Klimentidis, Imran Y Patel, Stuart F Quan, Christopher Wendel, Fadi Shamoun, Stefano Guerra, Sairam Parthasarathy, Salma I Pat |
| Improving sudden cardiac death risk stratification in hypertrophic cardiomyopathy using established clinical variables and genetic information. Clinical research in cardiology : official journal of the German Cardiac Society 2023 10 . Ali Amr, Jan Koelemen, Christoph Reich, Farbod Sedaghat-Hamedani, Elham Kayvanpour, Jan Haas, Karen Frese, David Lehmann, Hugo A Katus, Norbert Frey, Benjamin Med |
| RAF1 mutation leading to hypertrophic cardiomyopathy in a Chinese family with a history of sudden cardiac death: A diagnostic insight into Noonan syndrome. Molecular genetics & genomic medicine 2023 10 e2290. Jingjing Zheng, Longyun Peng, Ruofei Cheng, Zhiyan Li, Jianjie Xie, Erwen Huang, Jianding Cheng, Qianhao Zh |
| Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review. The Indian journal of medical research 2023 10 158 (2): 119-135. Linda Koshy, Sanjay Ganapathi, Panniyammakal Jeemon, M Madhuma, Y Vysakh, L R Lakshmikanth, Sivadasanpillai Harikrishn |
| THE ROLE OF LEFT VENTRICULAR HYPERTROPHY, RS1801253 AND RS1801252 ALLELIC POLYMORPHISMS OF ADRB1 IN ASSESSING THE RISK OF SUDDEN CARDIAC DEATH IN PATIENTS WITH ARTERIAL HYPERTENSION. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2023 10 76 (9): 2054-2060. Olexandr N Grytsay, Boris M Todurov, Yaroslav V Skybchyk, Dina V Shorikova, Eugene I Shorik |
| Patients With Hypertrophic Cardiomyopathy and Normal Genetic Investigations Have Few Affected Relatives. Journal of the American College of Cardiology 2023 10 82 (18): 1751-1761. Søren K Nielsen, Frederikke G Hansen, Torsten B Rasmussen, Thomas Fischer, Jens F Lassen, Trine Madsen, Dorthe S Møller, Ib C Klausen, John B Brodersen, Morten S K Jensen, Jens Mogens |
| Case report: Additional variants induced sudden cardiac death among pediatric ACM with DSG2 homozygous mutant genotype: a report of three cases. Frontiers in genetics 2024 9 15 1428796. Meng Wei, Yifei Li, Xiaoliang Liu, Kaiyu Zhou, Yu Qiu, Lei Liu, Lili Huang, Zhongqiang L |
| Novel Genetic Variants Associated with Primary Myocardial Fibrosis in Sudden Cardiac Death Victims. Journal of cardiovascular translational research 2024 6 . Sini Skarp, Anne Doedens, Lauri Holmström, Valerio Izzi, Samu Saarimäki, Eeva Sliz, Johannes Kettunen, Lasse Pakanen, Risto Kerkelä, Katri Pylkäs, Heikki V Huikuri, Robert J Myerburg, Juhani Juntti |
| Investigating cardiac genetic background in sudden infant death syndrome (SIDS). International journal of legal medicine 2024 6 . Francesca Cazzato, Mònica Coll, Simone Grassi, Anna Fernàndez-Falgueras, Laia Nogué-Navarro, Anna Iglesias, Josep Castellà, Antonio Oliva, Ramon Bruga |
| LV-predominant arrhythmogenic cardiomyopathy related to pathogenic DSP-variant. Clinical case reports 2024 6 12 (6): e9003. Soban Ahmad, Husam El Sharu, Robin Fernandes, Mark Kolasa, Constantin Bogdan Mar |
| Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience. Biomedicines 2024 6 12 (6): . Cinzia Forleo, Maria Cristina Carella, Paolo Basile, Eugenio Carulli, Michele Luca Dadamo, Francesca Amati, Francesco Loizzi, Sandro Sorrentino, Ilaria Dentamaro, Marco Maria Dicorato, Stefano Ricci, Rosanna Bagnulo, Matteo Iacoviello, Vincenzo Ezio Santobuono, Carlo Caiati, Martino Pepe, Jean-Francois Desaphy, Marco Matteo Ciccone, Nicoletta Resta, Andrea Igoren Guaric |
| A method of identifying the high-risk mutations of sudden cardiac death at KCNQ1 and KCNH2 genes. Journal of forensic and legal medicine 2024 6 105 102707. Jiaqi Wang, Zidong Liu, Yuxin Zhang, Mingming Zhang, Deqing Chen, Gengqian Zha |
| The NOS1AP gene rs10494366 common genetic variant does not modify the risk of sudden cardiac death in users of digoxin. British journal of clinical pharmacology 2024 6 . Negin Soroush, Albert-Jan Aarnoudse, Maryam Kavousi, Jan A Kors, M Arfan Ikram, Bruno H Stricker, Fariba Ahmadiz |
| Targeted genetic analysis in a cohort of sporadic death from spontaneous rupture of thoracic aortic dissection in Han Chinese population. Forensic science international. Genetics 2024 4 71 103051. Qianhao Zhao, Nan Zhou, Qiuping Wu, Kai Zhang, Jiacheng Yue, Da Zheng, Yunyi Wang, Yuxi Xiao, Rui Li, Ruofei Cheng, Li Quan, Erwen Huang, Bingjie Hu, Jiangding Che |
| Novel Gain-of-Function Mutation in the Kv11.1 Channel Found in the Patient with Brugada Syndrome and Mild QTc Shortening. Biochemistry. Biokhimiia 2024 4 89 (3): 543-552. Denis Abramochkin, Bowen Li, Han Zhang, Ekaterina Kravchuk, Tatiana Nesterova, Grigory Glukhov, Anna Shestak, Elena Zaklyazminskaya, Olga S Sokolo |
| Maternal and infant outcomes in women with sickle cell disease: a matched cohort study. Archives of disease in childhood. Fetal and neonatal edition 2024 4 . Oishi Sikdar, Hemant Ambulkar, Allan Jenkinson, Catherine Hedley, Jemma Johns, Ravindra Bhat, Theodore Dassios, Christopher Harris, Anne Greenou |
| Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic Diagnostics. Biomolecules 2024 11 14 (11): . Maria Gnazzo, Giovanni Parlapiano, Francesca Di Lorenzo, Daniele Perrino, Silvia Genovese, Valentina Lanari, Daniela Righi, Federica Calì, Massimo Stefano Silvetti, Elena Falcone, Alessia Bauleo, Fabrizio Drago, Antonio Novelli, Anwar Bab |
| Arrhythmic risk stratification in patients with left ventricular ring-like scar. European journal of preventive cardiology 2024 11 . Vanda Parisi, Maddalena Graziosi, Luis R Lopes, Antonio De Luca, Ferdinando Pasquale, Giacomo Tini, Mattia Targetti, Maria R Cueto, Ana R Moura, Raffaello Ditaranto, Camilla Torlasco, Nevio Taglieri, Elena Nardi, Luigi Lovato, João B Augusto, Nazzareno Galiè, Lia Crotti, Alessio Gasperetti, Mauro Biffi, Camillo Autore, Marco Merlo, Iacopo Olivotto, Gianfranco Sinagra, Perry M Elliott, Elena Biagi |
| Genetic variants associated with cardiac hypertrophy-related sudden cardiac death and cardiovascular outcomes in a Finnish population. Heart (British Cardiac Society) 2024 10 . Anne Doedens, Sini Skarp, Lauri Holmström, Lasse Pakanen, Samu Saarimäki, Risto Kerkelä, Katri Pylkäs, Heikki V Huikuri, Juhani Juntti |
| Characterization of cardiac involvement in patients with LMNA splice-site mutation-related dilated cardiomyopathy and sudden cardiac death. Frontiers in genetics 2024 1 14 1291411. Xuebin Ling, Yanjun Hou, Xingyu Jia, Youling Lan, Xiaoping Wu, Julan Wu, Wei Jie, Hui Liu, Shan Huang, Zhenling Wan, Tianfa Li, Junli Guo, Tiebiao Lia |
| Natural history and outcomes in paediatric RASopathy-associated hypertrophic cardiomyopathy. ESC heart failure 2024 1 . Olga Boleti, Gabrielle Norrish, Ella Field, Kathleen Dady, Kim Summers, Gauri Nepali, Vinay Bhole, Orhan Uzun, Amos Wong, Piers E F Daubeney, Graham Stuart, Precylia Fernandes, Karen McLeod, Maria Ilina, Muhammad Najih Liaqath Ali, Tara Bharucha, Grazia Delle Donne, Elspeth Brown, Katie Linter, Caroline B Jones, Jonathan Searle, William Regan, Sujeev Mathur, Nicola Boyd, Zdenka Reinhardt, Sophie Duignan, Terence Prendiville, Satish Adwani, Juan Pablo Kas |
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