HuGE Literature Finder
Records
1
-
30
| Androgen receptor (CAG) repeat polymorphism contributes to risk of sudden cardiac death originated from coronary artery disease with sex discrepancy. Forensic science international 2023 1 343 111563. Zhen Xiaoyuan, Zhao Wenfeng, Wang Jiawen, Li Lijuan, He Yan, Zhang Jianhua, Li Chengtao, Zhang Suhua, Luo Bin, Huang Jiang, Gao Yuzh |
| Estimated glomerular filtration rate in Brazilian adults with sickle cell disease: results from the REDS-III multicenter cohort study. Annals of hematology 2023 3 . Belisário André Rolim, Simões E Silva Ana Cristina, Moura Isabel Cristina Gomes, Carneiro-Proietti Anna Bárbara, Sabino Ester Cerdeira, Loureiro Paula, Máximo Cláudia, Flor-Park Miriam V, Rodrigues Daniela de Oliveira Werneck, Ozahata Mina Cintho, Mota Rosimere Afonso, Dinardo Carla Luana, Kelly Shannon, Custer Brian, |
| Genetic characterization of juvenile sudden cardiac arrest and death in Tuscany: The ToRSADE registry. Frontiers in cardiovascular medicine 2023 1 9 1080608. Girolami Francesca, Spinelli Valentina, Maurizi Niccolò, Focardi Martina, Nesi Gabriella, Maio Vincenza, Grifoni Rossella, Albora Giuseppe, Bertaccini Bruno, Targetti Mattia, Coppini Raffaele, Favilli Silvia, Olivotto Iacopo, Cerbai Elisabet |
| APOL1 G3 Variant Is Associated with Cardiovascular Mortality and Sudden Cardiac Death in Patients Receiving Maintenance Hemodialysis of European Ancestry. Cardiorenal medicine 2022 10 12 (5-6): 229-235. Schwantes-An Tae-Hwi, Robinson-Cohen Cassianne, Liu Sai, Zheng Neil, Stedman Margaret, Wetherill Leah, Edenberg Howard J, Vatta Matteo, Foroud Tatiana M, Chertow Glenn M, Moe Sharon |
| Barlow disease: effect of mitral valve repair on ventricular arrhythmias in 82 patients in a retrospective long-term study. The Journal of cardiovascular surgery 2022 5 63 (4): 514-520. Brunec-Keller Mira, Scharf Christoph, Radulovic Jovana, Berdat Pascal A, Attenhofer Jost Christine H, Vogt Paul, Duru Firat, Caselli Stefa |
| Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome. Frontiers in pharmacology 2022 9 13 984299. Zaklyazminskaya Elena, Shestak Anna, Podolyak Dmitry, Komoliatova Vera, Makarov Leonid, Novitskaya Anna, Revishvili Amir |
| Evaluating Common NOS1AP Variants in Patients with Implantable Cardioverter Defibrillators for Secondary Prevention : Evaluating SNPs in NOS1AP. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2022 3 64 (3): 793-800. Zang Xiaobiao, Zhang Shulong, Li Sisi, Wang Xianqing, Song Weifeng, Chen Ke, Ma Jifang, Tu Xin, Xia Yunlong, Zhao Yonghui, Gao Chuan |
| Genotype-Specific ECG-Based Risk Stratification Approaches in Patients With Long-QT Syndrome. Frontiers in cardiovascular medicine 2022 8 9 916036. Rieder Marina, Kreifels Paul, Stuplich Judith, Ziupa David, Servatius Helge, Nicolai Luisa, Castiglione Alessandro, Zweier Christiane, Asatryan Babken, Odening Katja |
| LRP6 Polymorphisms Is Associated With Sudden Cardiac Death in Patients With Chronic Heart Failure in the Chinese Han Population. Frontiers in cardiovascular medicine 2022 2 8 815595. Guo Qi, Lai Yiwei, Chu Jianmin, Chen Xuhua, Gao Mingyang, Sang Caihua, Dong Jianzeng, Pu Jielin, Ma Changshe |
| Novel Indel Variation of NPC1 Gene Associates With Risk of Sudden Cardiac Death. Frontiers in genetics 2022 4 13 869859. Zhao Wenfeng, Zhang Qing, Wang Jiawen, Yu Huan, Zhen Xiaoyuan, Li Lijuan, Qu Yan, He Yan, Zhang Jianhua, Li Chengtao, Zhang Suhua, Luo Bin, Huang Jiang, Gao Yuzh |
| Post-mortem toxicology analysis in a young sudden cardiac death cohort. Forensic science international. Genetics 2022 5 59 102723. Coll Mònica, Fernàndez-Falgueras Anna, Tiron Coloma, Iglesias Anna, Buxó Maria, Simón Adrià, Nogué-Navarro Laia, Moral Sergio, Pérez-Serra Alexandra, Puigmulé Marta, Del Olmo Bernat, Campuzano Oscar, Castellà Josep, Picó Ferran, Lopez Laura, Neto Nuria, Corona Mònica, Alcalde Mireia, Brugada Ram |
| Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies. Journal of the American College of Cardiology 2022 11 80 (21): 1981-1994. Paldino Alessia, Dal Ferro Matteo, Stolfo Davide, Gandin Ilaria, Medo Kristen, Graw Sharon, Gigli Marta, Gagno Giulia, Zaffalon Denise, Castrichini Matteo, Masè Marco, Cannatà Antonio, Brun Francesca, Storm Garrett, Severini Giovanni Maria, Lenarduzzi Stefania, Girotto Giorgia, Gasparini Paolo, Bortolotti Francesca, Giacca Mauro, Zacchigna Serena, Merlo Marco, Taylor Matthew R G, Mestroni Luisa, Sinagra Gianfran |
| Risk of sudden cardiac death associated with QRS, QTc, and JTc intervals in the general population. Heart rhythm 2022 4 19 (8): 1297-1303. Tikkanen Jani T, Kentta Tuomas, Porthan Kimmo, Anttonen Olli, Eranti Antti, Aro Aapo L, Kerola Tuomas, Rissanen Harri A, Knekt Paul, Heliövaara Markku, Holkeri Arttu, Haukilahti Anette, Niiranen Teemu, Hernesniemi Jussi, Jula Antti, Nieminen Markku S, Myerburg Robert J, Albert Christine M, Salomaa Veikko, Huikuri Heikki V, Junttila M Juha |
| The protective effect of the spleen in sickle cell patients. A comparative study between patients with asplenia/hyposplenism and hypersplenism. Frontiers in physiology 2022 9 13 796837. Peretz Sari, Livshits Leonid, Pretorius Etheresia, Makhro Asya, Bogdanova Anna, Gassmann Max, Koren Ariel, Levin Cari |
| Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples. International journal of molecular sciences 2022 10 23 (20): . Coll Monica, Fernandez-Falgueras Anna, Iglesias Anna, Del Olmo Bernat, Nogue-Navarro Laia, Simon Adria, Perez Serra Alexandra, Puigmule Marta, Lopez Laura, Pico Ferran, Corona Monica, Vallverdu-Prats Marta, Tiron Coloma, Campuzano Oscar, Castella Josep, Brugada Ramon, Alcalde Mire |
| Compound Mutation in Cardiac Sarcomere Proteins Is Associated with Increased Risk for Major Arrhythmic Events in Pediatric Onset Hypertrophic Cardiomyopathy. Journal of clinical medicine 2021 Nov 10 (22): . Pollmann Kathrin, Kaltenecker Emanuel, Schleihauf Julia, Ewert Peter, Görlach Agnes, Wolf Cordula |
| Filamin-C variant-associated cardiomyopathy: A pooled analysis of individual patient data to evaluate the clinical profile and risk of sudden cardiac death. Heart rhythm 2021 Sep . Celeghin Rudy, Cipriani Alberto, Bariani Riccardo, Bueno Marinas Maria, Cason Marco, Bevilacqua Michela, De Gaspari Monica, Rizzo Stefania, Rigato Ilaria, Da Pozzo Stefano, Zorzi Alessandro, Perazzolo Marra Martina, Thiene Gaetano, Iliceto Sabino, Basso Cristina, Corrado Domenico, Pilichou Kalliopi, Bauce Barba |
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
Circulation. Genomic and precision medicine 2021 Jul . Choi Seung Hoan, Jurgens Sean J, Haggerty Christopher M, Hall Amelia W, Halford Jennifer L, Morrill Valerie N, Weng Lu-Chen, Lagerman Braxton, Mirshahi Tooraj, Pettinger Mary, Guo Xiuqing, Lin Henry J, Alonso Alvaro, Soliman Elsayed Z, Kornej Jelena, Lin Honghuang, Moscati Arden, Nadkarni Girish N, Brody Jennifer A, Wiggins Kerri L, Cade Brian E, Lee Jiwon, Austin-Tse Christina, Blackwell Tom, Chaffin Mark D, Lee Christina J-Y, Rehm Heidi L, Roselli Carolina, , Redline Susan, Mitchell Braxton D, Sotoodehnia Nona, Psaty Bruce M, Heckbert Susan R, Loos Ruth J F, Vasan Ramachandran S, Benjamin Emelia J, Correa Adolfo, Boerwinkle Eric, Arking Dan E, Rotter Jerome I, Rich Stephen S, Whitsel Eric A, Perez Marco, Kooperberg Charles, Fornwalt Brandon K, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven A, |
| Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals. JAMA cardiology 2021 Jun . Guo Liang, Torii Sho, Fernandez Raquel, Braumann Ryan E, Fuller Daniela T, Paek Ka-Hyun, Gadhoke Neel V, Maloney Kristin A, Harris Kathryn, Mayhew Christina M, Zarpak Roya, Stevens Laura M, Gaynor Brady J, Jinnouchi Hiroyuki, Sakamoto Atsushi, Sato Yu, Mori Hiroyoshi, Kutyna Matthew D, Lee Parker J, Weinstein Leah M, Collado-Rivera Carlos J, Ali Bakr B, Atmakuri Dheeraj R, Dhingra Roma, Finn Emma L B, Bell Mack W, Lynch Megan, Cornelissen Anne, Kuntz Salome H, Park Joo-Hyung, Kutys Robert, Park Ji-Eun, Wang Libin, Hong Susie N, Gupta Anuj, Hall Jennifer L, Kolodgie Frank D, Romero Maria E, Jeng Linda J B, Mitchell Braxton D, Surve Dipti, Fowler David R, Hong Charles C, Virmani Renu, Finn Aloke |
| Genetic investigations of 100 inherited cardiac disease-related genes in deceased individuals with schizophrenia. International journal of legal medicine 2021 May . Christiansen Sofie Lindgren, Andersen Jeppe Dyrberg, Themudo Gonçalo Espregueira, Hertz Christin Løth, Busch Johannes Rødbro, Christensen Martin Roest, Olsen Kristine Boisen, Banner Jytte, Morling Nie |
| A Functional Indel Polymorphism Within MIR155HG Is Associated With Sudden Cardiac Death Risk in a Chinese Population. Frontiers in cardiovascular medicine 2021 6 8 671168. Zhang Qing, Yu Huan, Yang Zhenzhen, Li Lijuan, He Yan, Zhu Shaohua, Li Chengtao, Zhang Suhua, Luo Bin, Gao Yuzh |
| Differential Methylation in the GSTT1 Regulatory Region in Sudden Unexplained Death and Sudden Unexpected Death in Epilepsy. International journal of molecular sciences 2021 4 22 (6): . Christiansen Steffan Noe, Jacobsen Stine Bøttcher, Andersen Jeppe Dyrberg, Kampmann Marie-Louise, Trudsø Linea Christine, Olsen Kristine Boisen, Tfelt-Hansen Jacob, Banner Jytte, Morling Nie |
| Genetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victims. Scientific reports 2021 5 11 (1): 11171. Holmström Lauri, Pylkäs Katri, Tervasmäki Anna, Vähätalo Juha, Porvari Katja, Pakanen Lasse, Kaikkonen Kari S, Perkiömäki Juha S, Kiviniemi Antti M, Kerkelä Risto, Ukkola Olavi, Myerburg Robert J, Huikuri Heikki V, Junttila Juha |
| Genetic Variants Associated With Sudden Cardiac Death in Victims With Single Vessel Coronary Artery Disease and Left Ventricular Hypertrophy With or Without Fibrosis. Frontiers in cardiovascular medicine 2021 8 755062. Vähätalo Juha H, Holmström Lauri T A, Pylkäs Katri, Skarp Sini, Porvari Katja, Pakanen Lasse, Kaikkonen Kari S, Perkiömäki Juha S, Kerkelä Risto, Huikuri Heikki V, Myerburg Robert J, Junttila M Juha |
| Modulation of STIM1 by a risk insertion/deletion polymorphism underlying genetics susceptibility to sudden cardiac death originated from coronary artery disease. Forensic science international 2021 9 328 111010. Zhang Qing, He Yan, Xu Hongfei, Li Lijuan, Guo Yadong, Zhang Jianhua, Cheng Lei, Yu Huan, Dai Yunda, Yang Qi, Yang Zhenzhen, Li Chengtao, Zhang Suhua, Zhu Shaohua, Luo Bin, Gao Yuzh |
| Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients. Functional & integrative genomics 2021 2 21 (3-4): 331-340. Ghaffari Taraneh, Mirhosseini Motlagh Naser, Daraei Abdolreza, Tafrihi Majid, Saravi Mehrdad, Sabour Davo |
| RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy. The Canadian journal of cardiology 2021 8 37 (11): 1751-1759. Dai Jiaqi, Li Zongzhe, Huang Wei, Chen Peng, Sun Yang, Wang Hong, Wu Dongyang, Chen Yanghui, Li Chenze, Xiao Lei, Liu Hao, Wei Haoran, Li Rui, Duan Quanlu, Peng Liyuan, Song Xiuli, Yu Ting, Wang Yan, Wang Dao W |
| Risk of sudden coronary death based on genetic background in Chinese Han population. Experimental and therapeutic medicine 2021 8 22 (4): 1068. Zhang Nenghua, Lv Xiaochun, Cheng Xiaojuan, Wang Jiaqi, Liu Jinding, Shi Jie, Liu Jie, Hu Bo, Chen Deqing, Zhang Gengqi |
| The Contribution of Known Familial Cardiovascular Disease Genes to Sudden Cardiac Death in Patients Undergoing Hemodialysis. Cardiorenal medicine 2021 11 (4): 174-183. Schwantes-An Tae-Hwi, Vatta Matteo, Abreu Marco, Wetherill Leah, Edenberg Howard J, Foroud Tatiana M, Chertow Glenn M, Moe Sharon |
| Verification of Single Nucleotide Polymorphisms rs34554140, rs6670279, and rs6874185 as Novel Molecular Genetic Markers of Sudden Cardiac Death. Sovremennye tekhnologii v meditsine 2021 9 13 (2): 40-44. Ivanova A A, Gurazheva A A, Melnikova E S, Nesterets A M, Malyutina S K, Rodina I A, Maksimov V |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 28, 2023
- Content source: