Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
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Records 1 - 30 (of 51 Records) |
| Query Trace: Sudden Cardiac Arrest[original query] |
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Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.
Nature communications 2017 03 8 14694. Heilmann-Heimbach Stefanie, Herold Christine, Hochfeld Lara M, Hillmer Axel M, Nyholt Dale R, Hecker Julian, Javed Asif, Chew Elaine G Y, Pechlivanis Sonali, Drichel Dmitriy, Heng Xiu Ting, Del Rosario Ricardo C-H, Fier Heide L, Paus Ralf, Rueedi Rico, Galesloot Tessel E, Moebus Susanne, Anhalt Thomas, Prabhakar Shyam, Li Rui, Kanoni Stavroula, Papanikolaou George, Kutalik Zoltán, Deloukas Panos, Philpott Michael P, Waeber Gérard, Spector Tim D, Vollenweider Peter, Kiemeney Lambertus A L M, Dedoussis George, Richards J Brent, Nothnagel Michael, Martin Nicholas G, Becker Tim, Hinds David A, Nöthen Markus |
| Identification of pathogenic variants in genes related to channelopathy and cardiomyopathy in Korean sudden cardiac arrest survivors. Journal of human genetics 2017 Jun 62 (6): 615-620. Song Ju Sun, Kang Jong-Sun, Kim Young-Eun, Park Seung-Jung, Park Kyoung-Min, Huh June, Kim June Soo, Cho Hana, Ki Chang-Seok, On Young Ke |
| Determinants of occurrence and survival after sudden cardiac arrest-A European perspective: The ESCAPE-NET project. Resuscitation 2017 12 124 7-13. Empana Jean-Philippe, Blom Marieke T, B?ttiger Bernd W, Dagres Nikolaos, Dekker Jacqueline M, Gislason Gunnar, Jouven Xavier, Meitinger Thomas, Ristagno Giuseppe, Schwartz Peter J, Jonsson Martin, Tfelt-Hansen Jacob, Truhlar Anatolij, Tan Hanno L, |
| Role of angiotensin-converting enzyme insertion/deletion polymorphism in sudden cardiac arrest. Journal of cellular biochemistry 2018 Sep . Liu Aifen, Wang Sai, Zhang Chunxiao, Sun Di, Song Xiaozhe |
| A comprehensive evaluation of the genetic architecture of sudden cardiac arrest.
European heart journal 2018 11 39 (44): 3961-3969. Ashar Foram N, Mitchell Rebecca N, Albert Christine M, Newton-Cheh Christopher, Brody Jennifer A, Müller-Nurasyid Martina, Moes Anna, Meitinger Thomas, Mak Angel, Huikuri Heikki, Junttila M Juhani, Goyette Philippe, Pulit Sara L, Pazoki Raha, Tanck Michael W, Blom Marieke T, Zhao XiaoQing, Havulinna Aki S, Jabbari Reza, Glinge Charlotte, Tragante Vinicius, Escher Stefan A, Chakravarti Aravinda, Ehret Georg, Coresh Josef, Li Man, Prineas Ronald J, Franco Oscar H, Kwok Pui-Yan, Lumley Thomas, Dumas Florence, McKnight Barbara, Rotter Jerome I, Lemaitre Rozenn N, Heckbert Susan R, O'Donnell Christopher J, Hwang Shih-Jen, Tardif Jean-Claude, VanDenburgh Martin, Uitterlinden André G, Hofman Albert, Stricker Bruno H C, de Bakker Paul I W, Franks Paul W, Jansson Jan-Hakan, Asselbergs Folkert W, Halushka Marc K, Maleszewski Joseph J, Tfelt-Hansen Jacob, Engstrøm Thomas, Salomaa Veikko, Virmani Renu, Kolodgie Frank, Wilde Arthur A M, Tan Hanno L, Bezzina Connie R, Eijgelsheim Mark, Rioux John D, Jouven Xavier, Kääb Stefan, Psaty Bruce M, Siscovick David S, Arking Dan E, Sotoodehnia No |
| ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.
Circulation. Genomic and precision medicine 2018 01 11 (1): e001758. Bihlmeyer Nathan A, Brody Jennifer A, Smith Albert Vernon, Warren Helen R, Lin Honghuang, Isaacs Aaron, Liu Ching-Ti, Marten Jonathan, Radmanesh Farid, Hall Leanne M, Grarup Niels, Mei Hao, Müller-Nurasyid Martina, Huffman Jennifer E, Verweij Niek, Guo Xiuqing, Yao Jie, Li-Gao Ruifang, van den Berg Marten, Weiss Stefan, Prins Bram P, van Setten Jessica, Haessler Jeffrey, Lyytikäinen Leo-Pekka, Li Man, Alonso Alvaro, Soliman Elsayed Z, Bis Joshua C, Austin Tom, Chen Yii-Der Ida, Psaty Bruce M, Harrris Tamara B, Launer Lenore J, Padmanabhan Sandosh, Dominiczak Anna, Huang Paul L, Xie Zhijun, Ellinor Patrick T, Kors Jan A, Campbell Archie, Murray Alison D, Nelson Christopher P, Tobin Martin D, Bork-Jensen Jette, Hansen Torben, Pedersen Oluf, Linneberg Allan, Sinner Moritz F, Peters Annette, Waldenberger Melanie, Meitinger Thomas, Perz Siegfried, Kolcic Ivana, Rudan Igor, de Boer Rudolf A, van der Meer Peter, Lin Henry J, Taylor Kent D, de Mutsert Renée, Trompet Stella, Jukema J Wouter, Maan Arie C, Stricker Bruno H C, Rivadeneira Fernando, Uitterlinden André, Völker Uwe, Homuth Georg, Völzke Henry, Felix Stephan B, Mangino Massimo, Spector Timothy D, Bots Michiel L, Perez Marco, Raitakari Olli T, Kähönen Mika, Mononen Nina, Gudnason Vilmundur, Munroe Patricia B, Lubitz Steven A, van Duijn Cornelia M, Newton-Cheh Christopher H, Hayward Caroline, Rosand Jonathan, Samani Nilesh J, Kanters Jørgen K, Wilson James G, Kääb Stefan, Polasek Ozren, van der Harst Pim, Heckbert Susan R, Rotter Jerome I, Mook-Kanamori Dennis O, Eijgelsheim Mark, Dörr Marcus, Jamshidi Yalda, Asselbergs Folkert W, Kooperberg Charles, Lehtimäki Terho, Arking Dan E, Sotoodehnia No |
| Sudden cardiac arrest in patients without overt heart disease: a limited value of next generation sequencing. Polish archives of internal medicine 2018 12 128 (12): 721-730. St?pie?-Wojno Ma?gorzata, Poni?ska Joanna, Rydzanicz Ma?gorzata, Bili?ska Maria, Truszkowska Gra?yna, Baranowski Rafa?, Luty?ska Anna, Biernacka El?bieta K, St?pi?ska Janina, Kowalik Ilona, P?oski Rafa?, Bili?ska Zofia |
| Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy. Molecular genetics & genomic medicine 2018 11 6 (6): 1104-1113. Cui Hao, Wang Jizheng, Zhang Ce, Wu Guixin, Zhu Changsheng, Tang Bing, Zou Yubao, Huang Xiaohong, Hui Rutai, Song Lei, Wang Shuiy |
| Baseline fragmented QRS increases the risk of major arrhythmic events in hypertrophic cardiomyopathy: Systematic review and meta-analysis. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2018 1 23 (4): e12533. Rattanawong Pattara, Riangwiwat Tanawan, Kanitsoraphan Chanavuth, Chongsathidkiet Pakawat, Kanjanahattakij Napatt, Vutthikraivit Wasawat, Chung Eugene |
| Are minor alleles more likely to be risk alleles? BMC medical genomics 2018 1 11 (1): 3. Kido Takashi, Sikora-Wohlfeld Weronika, Kawashima Minae, Kikuchi Shinichi, Kamatani Naoyuki, Patwardhan Anil, Chen Richard, Sirota Marina, Kodama Keiichi, Hadley Dexter, Butte Atul |
| Usefulness of Genetic Testing in Sudden Cardiac Arrest Survivors With or Without Previous Clinical Evidence of Heart Disease. The American journal of cardiology 2019 Mar . Asatryan Babken, Schaller André, Seiler Jens, Servatius Helge, Noti Fabian, Baldinger Samuel H, Tanner Hildegard, Roten Laurent, Dillier Roger, Lam Anna, Haeberlin Andreas, Conte Giulio, Saguner Ardan M, Müller Stephan Andreas, Duru Firat, Auricchio Angelo, Ammann Peter, Sticherling Christian, Burri Haran, Reichlin Tobias, Wilhelm Matthias, Medeiros-Domingo Argel |
| "Concealed cardiomyopathy" as a cause of previously unexplained sudden cardiac arrest. International journal of cardiology 2020 9 324 96-101. Isbister Julia C, Nowak Natalie, Butters Alexandra, Yeates Laura, Gray Belinda, Sy Raymond W, Ingles Jodie, Bagnall Richard D, Semsarian Christoph |
| GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death. EBioMedicine 2020 Jul 57 102843. Juang Jyh-Ming Jimmy, Binda Anna, Lee Shyh-Jye, Hwang Juey-Jen, Chen Wen-Jone, Liu Yen-Bin, Lin Lian-Yu, Yu Chih-Chieh, Ho Li-Ting, Huang Hui-Chun, Chen Ching-Yu Julius, Lu Tzu-Pin, Lai Liang-Chuan, Yeh Shih-Fan Sherri, Lai Ling-Ping, Chuang Eric Y, Rivolta Ilaria, Antzelevitch Charl |
| Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry. Circulation. Genomic and precision medicine 2020 Jun . Jimmy Juang Jyh-Ming, Liu Yen-Bin, Julius Chen Ching-Yu, Yu Qi-You, Chattopadhyay Amrita, Lin Lian-Yu, Chen Wen-Jone, Yu Chih-Chien, Huang Hui-Chun, Ho Li-Ting, Lai Ling-Ping, Hwang Juey-Jen, Lin Ting-Tse, Liao Min-Tsun, Chen Jien-Jiun, Sherri Yeh Shih-Fan, Chuang Jing-Yuan, Yang Dun-Hui, Lin Jiunn-Lee, Lu Tzu-Pin, Chuang Eric Y, Ackerman Michael |
| Prognostic impact of misdiagnosis of cardiac channelopathies as epilepsy. PloS one 2020 4 15 (4): e0231442. Ramos-Maqueda Javier, Bermúdez-Jiménez Francisco, Ruiz Rosa Macías, Ramos Mercedes Cabrera, Lerma Manuel Molina, Millán Pablo Sánchez, López Miguel Álvarez, Sánchez Luis Tercedor, Jiménez-Jáimez Ju |
| 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 |
| 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 |
| Sudden Cardiac Arrest in a Patient With Mitral Valve Prolapse and LMNA and SCN5A Mutations. JACC. Case reports 2021 7 3 (2): 242-246. Mahajan Asha M, Itan Yuval, Cerrone Marina, Horowitz James, Borneman Linda, Chinitz Larry, Jankelson Li |
| Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center's Experience Over 5 Years. Molecular diagnosis & therapy 2021 5 25 (3): 373-385. Janin Alexandre, Januel Louis, Cazeneuve Cécile, Delinière Antoine, Chevalier Philippe, Millat Gill |
| An International Multicenter Cohort Study on ?-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation 2021 12 145 (5): 333-344. Peltenburg Puck J, Kallas Dania, Bos Johan M, Lieve Krystien V V, Franciosi Sonia, Roston Thomas M, Denjoy Isabelle, Sorensen Katrina B, Ohno Seiko, Roses-Noguer Ferran, Aiba Takeshi, Maltret Alice, LaPage Martin J, Atallah Joseph, Giudicessi John R, Clur Sally-Ann B, Blom Nico A, Tanck Michael, Extramiana Fabrice, Kato Koichi, Barc Julien, Borggrefe Martin, Behr Elijah R, Sarquella-Brugada Georgia, Tfelt-Hansen Jacob, Zorio Esther, Swan Heikki, Kammeraad Janneke A E, Krahn Andrew D, Davis Andrew, Sacher Frederic, Schwartz Peter J, Roberts Jason D, Skinner Jonathan R, van den Berg Maarten P, Kannankeril Prince J, Drago Fabrizio, Robyns Tomas, Haugaa Kristina, Tavacova Terezia, Semsarian Christopher, Till Jan, Probst Vincent, Brugada Ramon, Shimizu Wataru, Horie Minoru, Leenhardt Antoine, Ackerman Michael J, Sanatani Shubhayan, van der Werf Christian, Wilde Arthur A |
| Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac Death. Circulation. Genomic and precision medicine 2021 12 15 (1): e003497. Neves Raquel, Tester David J, Simpson Michael A, Behr Elijah R, Ackerman Michael J, Giudicessi John |
| Pregnancy in women with Brugada syndrome: Is there an increased arrhythmia risk? A case-series report. Journal of cardiovascular electrophysiology 2021 10 33 (1): 123-127. van der Crabben Saskia N, Kowsoleea Astra I E, Clur Sally-Ann B, Wilde Arthur A |
| Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics. Circulation. Genomic and precision medicine 2022 9 15 (5): e003675. Nafissi Navid A, Abdulrahim Jawan W, Kwee Lydia Coulter, Coniglio Amanda C, Kraus William E, Piccini Jonathan P, Daubert James P, Sun Albert Y, Shah Svati |
| Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator. European heart journal 2022 6 43 (32): 3053-3067. Protonotarios Alexandros, Bariani Riccardo, Cappelletto Chiara, Pavlou Menelaos, García-García Alba, Cipriani Alberto, Protonotarios Ioannis, Rivas Adrian, Wittenberg Regitze, Graziosi Maddalena, Xylouri Zafeirenia, Larrañaga-Moreira José M, de Luca Antonio, Celeghin Rudy, Pilichou Kalliopi, Bakalakos Athanasios, Lopes Luis Rocha, Savvatis Konstantinos, Stolfo Davide, Dal Ferro Matteo, Merlo Marco, Basso Cristina, Freire Javier Limeres, Rodriguez-Palomares Jose F, Kubo Toru, Ripoll-Vera Tomas, Barriales-Villa Roberto, Antoniades Loizos, Mogensen Jens, Garcia-Pavia Pablo, Wahbi Karim, Biagini Elena, Anastasakis Aris, Tsatsopoulou Adalena, Zorio Esther, Gimeno Juan R, Garcia-Pinilla Jose Manuel, Syrris Petros, Sinagra Gianfranco, Bauce Barbara, Elliott Perry |
| Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant. Circulation. Genomic and precision medicine 2022 12 16 (1): e003672. Hoorntje Edgar T, Burns Charlotte, Marsili Luisa, Corden Ben, Parikh Victoria N, Te Meerman Gerard J, Gray Belinda, Adiyaman Ahmet, Bagnall Richard D, Barge-Schaapveld Daniela Q C M, van den Berg Maarten P, Bootsma Marianne, Bosman Laurens P, Correnti Gemma, Duflou Johan, Eppinga Ruben N, Fatkin Diane, Fietz Michael, Haan Eric, Jongbloed Jan D H, Hauer Arnaud D, Lam Lien, van Lint Freyja H M, Lota Amrit, Marcelis Carlo, McCarthy Hugh J, van Mil Anneke M, Oldenburg Rogier A, Pachter Nicholas, Planken R Nils, Reuter Chloe, Semsarian Christopher, van der Smagt Jasper J, Thompson Tina, Vohra Jitendra, Volders Paul G A, van Waning Jaap I, Whiffin Nicola, van den Wijngaard Arthur, Amin Ahmad S, Wilde Arthur A M, van Woerden Gijs, Yeates Laura, Zentner Dominica, Ashley Euan A, Wheeler Matthew T, Ware James S, van Tintelen J Peter, Ingles Jod |
| Genetic variants in Colombian patients with inherited cardiac conditions. Molecular genetics & genomic medicine 2022 10 10 (11): e2046. Rucinski Cynthia, Yunis Luz Karime, Rosas Fernando, Santacruz David, Camargo Juan Manuel, Yunis Juan Jo |
| Vigorous Exercise in Patients With Hypertrophic Cardiomyopathy. JAMA cardiology 2023 5 . Rachel Lampert, Michael J Ackerman, Bradley S Marino, Matthew Burg, Barbara Ainsworth, Lisa Salberg, Maria Teresa Tome Esteban, Carolyn Y Ho, Roselle Abraham, Seshadri Balaji, Cheryl Barth, Charles I Berul, Martijn Bos, David Cannom, Lubna Choudhury, Maryann Concannon, Robert Cooper, Richard J Czosek, Anne M Dubin, James Dziura, Benjamin Eidem, Michael S Emery, N A Mark Estes, Susan P Etheridge, Jeffrey B Geske, Belinda Gray, Kevin Hall, Kimberly G Harmon, Cynthia A James, Ashwin K Lal, Ian H Law, Fangyong Li, Mark S Link, William J McKenna, Silvana Molossi, Brian Olshansky, Steven R Ommen, Elizabeth V Saarel, Sara Saberi, Laura Simone, Gordon Tomaselli, James S Ware, Douglas P Zipes, Sharlene M Day, |
| 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 |
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- Page last updated:Jun 02, 2023
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