Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 30 (of 518 Records) |
Query Trace: Arrhythmia[original query] |
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No association effect of genetic polymorphism was observed between polycystic ovary syndrome and cardiovascular diseases risk: a mendelian randomization study. Endocrine 2023 9 . Xiao Zhang, Zhao Huangfu, Shaowei Wa |
Mitral annular disjunction and Pickelhaube sign in children with mitral valve prolapse: A prospective cohort study. Archives of cardiovascular diseases 2023 9 . Guy Vaksmann, Ivan Bouzguenda, Marie-Paule Guillaume, Pauline Gras, Valentina Silvestri, Adélaïde Richa |
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 |
Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in UK Biobank. JACC. Heart failure 2023 9 . Babken Asatryan, Ravi A Shah, Ghaith Sharaf Dabbagh, Andrew P Landstrom, Dawood Darbar, Mohammed Y Khanji, Luis R Lopes, Stefan van Duijvenboden, Daniele Muser, Aaron Mark Lee, Christopher M Haggerty, Pankaj Arora, Christopher Semsarian, Tobias Reichlin, Virend K Somers, Anjali T Owens, Steffen E Petersen, Rajat Deo, Patricia B Munroe, Nay Aung, C Anwar A Chahal, |
Development and Validation of a Novel Nomogram to Predict the Impact of the Polymorphisms of the Variants of ICAM-1 Gene on the Prognosis of Ischemic Cardiomyopathy. International journal of general medicine 2023 9 16 4051-4066. Tuersunjiang Naman, Refukaiti Abuduhalike, Aihaidan Abudouwayiti, Juan Sun, Ailiman Mahemu |
Clinical and Genetic Features of Korean Inherited Arrhythmia Probands. Korean circulation journal 2023 9 . Joo Hee Jeong, Suk-Kyu Oh, Yun Gi Kim, Yun Young Choi, Hyoung Seok Lee, Jaemin Shim, Yae Min Park, Jun-Hyung Kim, Yong-Seog Oh, Nam-Ho Kim, Hui-Nam Pak, Young Keun On, Hyung Wook Park, Gyo-Seung Hwang, Dae-Kyeong Kim, Young-Ah Park, Hyoung-Seob Park, Yongkeun Cho, Seil Oh, Jong-Il Choi, Young-Hoon K |
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 |
The role of genetic testing in the prevention, diagnosis, and prognosis of sudden cardiac arrest in children. Journal of arrhythmia 2023 8 39 (4): 607-612. Miry Blich, Hodaya Oron, Wisam Darawsha, Mahmoud Suleiman, Lior Gepstein, Monther Boulos, Avraham Lorber, Asaad Kchou |
The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2023 7 31 (7-8): 315-323. Thomas A Bos, Sebastiaan R D Piers, Marja W Wessels, Arjan C Houweling, Regina Bökenkamp, Marianne Bootsma, Laurens P Bosman, Reinder Evertz, Debby M E I Hellebrekers, Yvonne M Hoedemaekers, Jeroen Knijnenburg, Ronald Lekanne Deprez, Anneke M van Mil, Anneline S J M Te Riele, Marjon A van Slegtenhorst, Arthur A M Wilde, Sing-Chien Yap, Dennis Dooijes, Tamara T Koopmann, J Peter van Tintelen, Daniela Q C M Barge-Schaapveld, |
Pulmonary Vein Myocardial Sleeve Length and its Association With Sex and 4q25/PITX2 Genotype. JACC. Clinical electrophysiology 2023 7 9 (7 Pt 2): 1147-1157. Majd A El-Harasis, Zachary T Yoneda, Giovanni E Davogustto, Diane M Crawford, James L Laws, Bradley Frye, Tarrah Herrmann, Bindiya Patel, Steven A Touchton, Dan M Roden, Travis D Richardson, Pablo Saavedra, Sharon T Shen, Juan C Estrada, Arvindh N Kanagasundram, Jay A Montgomery, Gregory F Michaud, George H Crossley, Christopher R Ellis, M Benjamin Shoemak |
Association between polymorphisms in Connexin40 Gene (Cx40) and risk of atrial fibrillation: a meta-analysis based on 3, 452 subjects. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2023 6 1-12. Zheng Lian, Zheng Ma, Zhi-Li Zhang, Pei-Lin Liu, Guo-Yong Zhang, Cai-Xia G |
Antioxidant Genetic Variants Modify Echocardiography Indices in Long COVID. International journal of molecular sciences 2023 6 24 (12): . Milika Asanin, Marko Ercegovac, Gordana Krljanac, Tatjana Djukic, Vesna Coric, Djurdja Jerotic, Marija Pljesa-Ercegovac, Marija Matic, Ivana Milosevic, Mihajlo Viduljevic, Goran Stevanovic, Jovan Ranin, Tatjana Simic, Zoran Bukumiric, Ana Savic-Radojev |
Sudden cardiac death, arrhythmias and abnormal electrocardiography in systemic sclerosis: A systematic review and meta-analysis. Seminars in arthritis and rheumatism 2023 6 62 152229. Jessica L Fairley, Laura Ross, Alannah Quinlivan, Dylan Hansen, Elizabeth Paratz, Wendy Stevens, Peter M Kistler, Alex McLellan, Andre La Gerche, Mandana Nikpo |
The efficacy of detecting arrhythmia is higher with 7-day continuous electrocardiographic patch monitoring than with 24-h Holter monitoring. Journal of arrhythmia 2023 6 39 (3): 422-429. Ju Young Kim, Il-Young Oh, Hyejin Lee, Ji Hyun Lee, Youngjin Cho, Yeongjoon Gil, Sunghoon Jung, Dae In Kim, Myung Geun Shin, Joo Yeon Yoo, Jeong Yeon Kw |
The association between tyrosine kinase inhibitors and fatal arrhythmia in patients with non-small cell lung cancer in Taiwan. Frontiers in oncology 2023 5 13 1172036. Wei-Ting Chang, Hui-Wen Lin, Ting-Chia Chang, Sheng-Hsiang Lin, Yi-Heng |
Associations between high-altitude adaptation and risk of cardiovascular diseases: a bidirectional Mendelian randomization study. Molecular genetics and genomics : MGG 2023 5 . Yuqing Jiang, Jie Ping, Hao Lu, Haoxiang Zhang, Mengyu Liu, Yuanfeng Li, Gangqiao Zh |
Prevalence of arrhythmia in COVID-19 patients with mild/moderate and severe illness: a prospective cohort study. Expert review of cardiovascular therapy 2023 5 1-9. Praveen Gupta, Sandeep Bansal, Anunay Gupta, Kapil Gupta, Sumita Saluja, Sudheesh Kumar Kattumann |
Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome. medRxiv : the preprint server for health sciences 2023 5 . Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, Matthew R Fleming, James T Baker, Hannah G Polikowsky, David C Samuels, Chad D Huff, Dan M Roden, Jennifer E Bel |
Type of syncope and outcome in Brugada syndrome: A systematic review and meta-analysis. Journal of arrhythmia 2023 4 39 (2): 111-120. Rattanawong Pattara, Kewcharoen Jakrin, Yinadsawaphan Thanaboon, Fatunde Olubadewa A, Kanitsoraphan Chanavuth, Vutthikraivit Wasawat, Prasitlumkum Narut, Chung Eugene H, Shen Win-Kua |
Relationship between rheumatoid arthritis and cardiovascular comorbidity, causation or co-occurrence: A Mendelian randomization study. Frontiers in cardiovascular medicine 2023 4 10 1099861. Wang Min, Chao Ce, Mei Kun, Di Dongmei, Qian Yongxiang, Wang Bin, Zhang Xiaoyi |
Effect of ?1-adrenergic receptor gene polymorphism on ventricular arrhythmia and prognosis after myocardial infarction. Coronary artery disease 2023 4 . Tao Ran, Zong Xiaojuan, Yang Pang, Chen Qingxing, Xu Ye, Han Lu, Su Yanling, Hu Wei, Zhu Wenqi |
Association between circulating leukocytes and arrhythmias: Mendelian randomization analysis in immuno-cardiac electrophysiology. Frontiers in immunology 2023 4 14 1041591. Yuxiao Chen, Lian Lou, Xuan Zhang, Luyang Jin, Yao Chen, Lele Chen, Zhihang Li, Fen Zhang, Ting Fu, Shenjiang Hu, Jian Ya |
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young. medRxiv : the preprint server for health sciences 2023 4 . Puckelwartz Megan J, Pesce Lorenzo L, Hernandez Edgar J, Webster Gregory, Dellefave-Castillo Lisa M, Russell Mark W, Geisler Sarah S, Kearns Samuel D, Etheridge Felix K, Etheridge Susan P, Monroe Tanner O, Pottinger Tess D, Kannankeril Prince J, Shoemaker M Benjamin, Fountain Darlene, Roden Dan M, MacLeod Heather, Burns Kristin M, Yandell Mark, Tristani-Firouzi Martin, George Alfred L, McNally Elizabeth |
Genetic Basis of Early Onset Atrial Fibrillation in Patients without Risk Factors. Journal of cardiovascular development and disease 2023 3 10 (3): . Rudaka Irina, Vilne Baiba, Isakova Jekaterina, Kalejs Oskars, Gailite Linda, Rots Dmitri |
Neuromodulation for the Treatment of Refractory Ventricular Arrhythmias. JACC. Clinical electrophysiology 2023 3 9 (2): 161-169. Markman Timothy M, Gugger Douglas, Arkles Jeffrey, Riley Michael P, Dixit Sanjay, Guandalini Gustavo S, Frankel David S, Epstein Andrew E, Callans David J, Singhal Sunil, Marchlinski Francis E, Nazarian Sam |
Inflammation on Endomyocardial Biopsy Predicts Risk of MACE in Undefined Left Ventricular Arrhythmogenic Cardiomyopathy. JACC. Clinical electrophysiology 2023 2 . Peretto Giovanni, Casella Michela, Merlo Marco, Benedetti Sara, Rizzo Stefania, Cappelletto Chiara, Di Resta Chiara, Compagnucci Paolo, De Gaspari Monica, Dello Russo Antonio, Casari Giorgio, Basso Cristina, Sala Simone, Sinagra Gianfranco, Della Bella Paolo, Cooper Leslie |
Pulmonary vein dose and risk of atrial fibrillation in patients with non-small cell lung cancer following definitive radiotherapy: an NI-HEART analysis. Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 2024 1 110085. Gerard M Walls, Conor McCann, John O'Connor, Anna O'Sullivan, David I Johnston, Jonathan McAleese, Conor K McGarry, Aidan J Cole, Suneil Jain, Karl T Butterworth, Gerard G Han |
Dissecting the associations of KCNH2 genetic polymorphisms with various types of cardiac arrhythmias. Gene 2024 1 899 148132. Sen Li, Zhang Zhang, Yining Ding, Tingting Yu, Zongshi Qin, Shuzhen G |
A missense variant in MYOF is associated with ARVC and sudden cardiac death. Gene 2024 1 902 148193. Jiao Xiao, Yi Dong, Jieyuan Jin, Zhuangzhuang Yuan, Chenyu Wang, Rong Xiang, Yadong G |
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young. Genome medicine 2024 1 16 (1): 13. Megan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, Gregory Webster, Lisa M Dellefave-Castillo, Mark W Russell, Sarah S Geisler, Samuel D Kearns, Felix Karthik, Susan P Etheridge, Tanner O Monroe, Tess D Pottinger, Prince J Kannankeril, M Benjamin Shoemaker, Darlene Fountain, Dan M Roden, Meghan Faulkner, Heather M MacLeod, Kristin M Burns, Mark Yandell, Martin Tristani-Firouzi, Alfred L George, Elizabeth M McNal |
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- Page last updated:Apr 22, 2024
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