Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 55 Records) |
Query Trace: MYH6[original query] |
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Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Nature genetics 2018 Jul . Nielsen Jonas B, Thorolfsdottir Rosa B, Fritsche Lars G, Zhou Wei, Skov Morten W, Graham Sarah E, Herron Todd J, McCarthy Shane, Schmidt Ellen M, Sveinbjornsson Gardar, Surakka Ida, Mathis Michael R, Yamazaki Masatoshi, Crawford Ryan D, Gabrielsen Maiken E, Skogholt Anne Heidi, Holmen Oddgeir L, Lin Maoxuan, Wolford Brooke N, Dey Rounak, Dalen Håvard, Sulem Patrick, Chung Jonathan H, Backman Joshua D, Arnar David O, Thorsteinsdottir Unnur, Baras Aris, O'Dushlaine Colm, Holst Anders G, Wen Xiaoquan, Hornsby Whitney, Dewey Frederick E, Boehnke Michael, Kheterpal Sachin, Mukherjee Bhramar, Lee Seunggeun, Kang Hyun M, Holm Hilma, Kitzman Jacob, Shavit Jordan A, Jalife José, Brummett Chad M, Teslovich Tanya M, Carey David J, Gudbjartsson Daniel F, Stefansson Kari, Abecasis Gonçalo R, Hveem Kristian, Willer Cristen |
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval. Circulation. Genomic and precision medicine 2018 May 11 (5): e002037. Lin Honghuang, van Setten Jessica, Smith Albert V, Bihlmeyer Nathan A, Warren Helen R, Brody Jennifer A, Radmanesh Farid, Hall Leanne, Grarup Niels, Müller-Nurasyid Martina, Boutin Thibaud, Verweij Niek, Lin Henry J, Li-Gao Ruifang, van den Berg Marten E, Marten Jonathan, Weiss Stefan, Prins Bram P, Haessler Jeffrey, Lyytikäinen Leo-Pekka, Mei Hao, Harris Tamara B, Launer Lenore J, Li Man, Alonso Alvaro, Soliman Elsayed Z, Connell John M, Huang Paul L, Weng Lu-Chen, Jameson Heather S, Hucker William, Hanley Alan, Tucker Nathan R, Chen Yii-Der Ida, Bis Joshua C, Rice Kenneth M, Sitlani Colleen M, Kors Jan A, Xie Zhijun, Wen Chengping, Magnani Jared W, Nelson Christopher P, Kanters Jørgen K, Sinner Moritz F, Strauch Konstantin, Peters Annette, Waldenberger Melanie, Meitinger Thomas, Bork-Jensen Jette, Pedersen Oluf, Linneberg Allan, Rudan Igor, de Boer Rudolf A, van der Meer Peter, Yao Jie, Guo Xiuqing, Taylor Kent D, Sotoodehnia Nona, Rotter Jerome I, Mook-Kanamori Dennis O, Trompet Stella, Rivadeneira Fernando, Uitterlinden André, Eijgelsheim Mark, Padmanabhan Sandosh, Smith Blair H, Völzke Henry, Felix Stephan B, Homuth Georg, Völker Uwe, Mangino Massimo, Spector Timothy D, Bots Michiel L, Perez Marco, Kähönen Mika, Raitakari Olli T, Gudnason Vilmundur, Arking Dan E, Munroe Patricia B, Psaty Bruce M, van Duijn Cornelia M, Benjamin Emelia J, Rosand Jonathan, Samani Nilesh J, Hansen Torben, Kääb Stefan, Polasek Ozren, van der Harst Pim, Heckbert Susan R, Jukema J Wouter, Stricker Bruno H, Hayward Caroline, Dörr Marcus, Jamshidi Yalda, Asselbergs Folkert W, Kooperberg Charles, Lehtimäki Terho, Wilson James G, Ellinor Patrick T, Lubitz Steven A, Isaacs Aar |
Whole-exome sequencing reveals microsatellite DNA markers for response to dofetilide initiation in patients with persistent atrial fibrillation: A pilot study. Clinical cardiology 2018 Apr . Kinney Nick, Larsen Timothy R, Kim David M, Varghese Robin T, Poelzing Steven, Garner Harold R, AlMahameed Soufian |
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.
European heart journal 2018 Mar . Bjornsson Thorsteinn, Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Sulem Patrick, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Magnusdottir Audur, Danielsen Ragnar, Sigurdsson Emil L, Adalsteinsdottir Berglind, Gunnarsson Sverrir I, Jonsdottir Ingileif, Arnar David O, Helgason Hrodmar, Gudbjartsson Tomas, Gudbjartsson Daniel F, Thorsteinsdottir Unnur, Holm Hilma, Stefansson Ka |
Sarcomere variants in arrhythmogenic cardiomyopathy: Pathogenic factor or bystander? Gene 2019 Mar 687 82-89. Chen Kai, Rao Man, Guo Guangran, Chen Xiao, Chen Liang, Song Jiangpi |
Identification of key pathways and genes in PTEN mutation prostate cancer by bioinformatics analysis. BMC medical genetics 2019 12 20 (1): 191. Sun Jian, Li Shugen, Wang Fei, Fan Caibin, Wang Jianqi |
Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death. Genetics in medicine : official journal of the American College of Medical Genetics 2020 9 23 (1): 86-93. Singer Emma S, Ross Samantha B, Skinner Jon R, Weintraub Robert G, Ingles Jodie, Semsarian Christopher, Bagnall Richard |
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation. Circulation. Genomic and precision medicine 2020 8 13 (5): 387-395. Weng Lu-Chen, Hall Amelia Weber, Choi Seung Hoan, Jurgens Sean J, Haessler Jeffrey, Bihlmeyer Nathan A, Grarup Niels, Lin Honghuang, Teumer Alexander, Li-Gao Ruifang, Yao Jie, Guo Xiuqing, Brody Jennifer A, Müller-Nurasyid Martina, Schramm Katharina, Verweij Niek, van den Berg Marten E, van Setten Jessica, Isaacs Aaron, Ramírez Julia, Warren Helen R, Padmanabhan Sandosh, Kors Jan A, de Boer Rudolf A, van der Meer Peter, Sinner Moritz F, Waldenberger Melanie, Psaty Bruce M, Taylor Kent D, Völker Uwe, Kanters Jørgen K, Li Man, Alonso Alvaro, Perez Marco V, Vaartjes Ilonca, Bots Michiel L, Huang Paul L, Heckbert Susan R, Lin Henry J, Kornej Jelena, Munroe Patricia B, van Duijn Cornelia M, Asselbergs Folkert W, Stricker Bruno H, van der Harst Pim, Kääb Stefan, Peters Annette, Sotoodehnia Nona, Rotter Jerome I, Mook-Kanamori Dennis O, Dörr Marcus, Felix Stephan B, Linneberg Allan, Hansen Torben, Arking Dan E, Kooperberg Charles, Benjamin Emelia J, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven |
A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block. International heart journal 2020 7 61 (4): 761-768. Zhang Yan, Sun Yu-Min, Xu Ying-Jia, Zhao Cui-Mei, Yuan Fang, Guo Xiao-Juan, Guo Yu-Han, Yang Chen-Xi, Gu Jia-Ning, Qiao Qi, Wang Jun, Yang Yi-Qi |
Genetic Association Between Hypoplastic Left Heart Syndrome and Cardiomyopathies. Circulation. Genomic and precision medicine 2020 12 14 (1): e003126. Theis Jeanne L, Hu Jessie J, Sundsbak Rhianna S, Evans Jared M, Bamlet William R, Qureshi M Yasir, O'Leary Patrick W, Olson Timothy |
A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve. Genetics and molecular biology 2020 12 43 (4): e20200142. Jiang Wei-Feng, Xu Ying-Jia, Zhao Cui-Mei, Wang Xin-Hua, Qiu Xing-Biao, Liu Xu, Wu Shao-Hui, Yang Yi-Qi |
Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases. Cardiovascular research 2020 1 116 (13): 2116-2130. Hayashi Kenshi, Teramoto Ryota, Nomura Akihiro, Asano Yoshihiro, Beerens Manu, Kurata Yasutaka, Kobayashi Isao, Fujino Noboru, Furusho Hiroshi, Sakata Kenji, Onoue Kenji, Chiang David Y, Kiviniemi Tuomas O, Buys Eva, Sips Patrick, Burch Micah L, Zhao Yanbin, Kelly Amy E, Namura Masanobu, Kita Yoshihito, Tsuchiya Taketsugu, Kaku Bunji, Oe Kotaro, Takeda Yuko, Konno Tetsuo, Inoue Masaru, Fujita Takashi, Kato Takeshi, Funada Akira, Tada Hayato, Hodatsu Akihiko, Nakanishi Chiaki, Sakamoto Yuichiro, Tsuda Toyonobu, Nagata Yoji, Tanaka Yoshihiro, Okada Hirofumi, Usuda Keisuke, Cui Shihe, Saito Yoshihiko, MacRae Calum A, Takashima Seiji, Yamagishi Masakazu, Kawashiri Masa-Aki, Takamura Masayu |
Association of the MYH6 Gene Polymorphism with the Risk of Atrial Fibrillation and Warfarin Anticoagulation Therapy. Genetic testing and molecular biomarkers 2021 9 25 (9): 590-599. Fu Ting, Chen Mengyan, Xu Lei, Gong Jianping, Zheng Juanqing, Zhang Fen, Ji Ningni |
Genetic predictors of sick sinus syndrome. Molecular biology reports 2021 7 48 (6): 5355-5362. Timasheva Yanina, Badykov Marat, Akhmadishina Leysan, Nasibullin Timur, Badykova Elena, Pushkareva Alfiya, Plechev Vladimir, Sagitov Ildus, Zagidullin Nauf |
Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals. JAMA cardiology 2021 5 6 (7): 811-819. Chalazan Brandon, Mol Denise, Darbar Faisal A, Ornelas-Loredo Aylin, Al-Azzam Bahaa, Chen Yining, Tofovic David, Sridhar Arvind, Alzahrani Zain, Ellinor Patrick, Darbar Dawo |
Genetic Determinants and Genotype-Phenotype Correlations in Vietnamese Patients With Dilated Cardiomyopathy. Circulation journal : official journal of the Japanese Circulation Society 2021 5 85 (9): 1469-1478. Nguyen Thuy Vy, Tran Vu Minh Thu, Do Thi Nam Phuong, Tran Thi Huynh Nga, Do Thi Hao, Nguyen Thi My Hanh, Tran Huynh Bao Nam, Le Lan Anh, Nguyen Pham Ngoc Thieu, Nguyen Thi Dieu Ai, Nguyen Thi My Nuong, Le Ngoc Hong Phuong, Pham Nguyen Vinh, Ho Huynh Thuy Duo |
Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy. Clinical chemistry and laboratory medicine 2021 2 59 (5): 955-963. Qiao Qi, Zhao Cui-Mei, Yang Chen-Xi, Gu Jia-Ning, Guo Yu-Han, Zhang Min, Li Ruo-Gu, Qiu Xing-Biao, Xu Ying-Jia, Yang Yi-Qi |
Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes. PeerJ 2021 2 9 e10711. Guelly Christian, Abilova Zhannur, Nuralinov Omirbek, Panzitt Katrin, Akhmetova Ainur, Rakhimova Saule, Kozhamkulov Ulan, Kairov Ulykbek, Molkenov Askhat, Seisenova Ainur, Trajanoski Slave, Abildinova Rashbayeva Gulzhaina, Kaussova Galina, Windpassinger Christian, Lee Joseph H, Zhumadilov Zhaxybay, Bekbossynova Makhabbat, Akilzhanova Ain |
Genetic insight into sick sinus syndrome.
European heart journal 2021 Feb . Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy-Associated Genes. Journal of the American Heart Association 2022 Sep e025257. Yang Qixin, Berkman Amy M, Ezekian Jordan E, Rosamilia Michael, Rosenfeld Jill A, Liu Pengfei, Landstrom Andrew |
Whole exome analysis reveals the genomic profiling related to chemo-resistance in Chinese population with limited-disease small cell lung cancer. Cancer medicine 2022 Jun . Yu Jiangyong, Zhao Shuangtao, Su Zhe, Song Chengli, Wu Lihong, Wang Jingbo, Bi Nan, Wang Lvh |
Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta. Genes 2022 4 13 (4): . Zhu Wenjuan, Williams Kylia, Young Cullen, Lin Jiaunn-Huey, Teekakirikul Polakit, Lo Cecilia |
Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study. Annals of translational medicine 2022 3 10 (3): 129. Shen Cheng, Xu Lei, Sun Xiaoning, Sun Aijun, Ge Jun |
Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT. Circulation research 2022 10 131 (10): 862-865. Andreasen Laura, Ahlberg Gustav, Ægisdottir Hildur M, Sveinbjörnsson Gardar, Lundegaard Pia R, Hartmann Jacob P, Paludan-Müller Christian, Hadji-Turdeghal Katra, Ghouse Jonas, Pehrson Steen, Jensen Henrik K, Riahi Sam, Hansen Jim, Sandgaard Niels, Sørensen Erik, Banasik Karina, Sækmose Susanne G, Bruun Mie T, Hjalgrim Henrik, Erikstrup Christian, Pedersen Ole B, Wittig Michael, Haunsø Stig, Ostrowski Sisse R, , Franke Andre, Brunak Søren, Kanters Jørgen K, Ellervik Christina, Bundgaard Henning, Ullum Henrik, Gudbjartsson Daniel F, Thorsteinsdottir Unnur, Holm Hilma, Arnar David O, Stefansson Kari, Svendsen Jesper H, Olesen Morten |
Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel. Orphanet journal of rare diseases 2022 10 17 (1): 394. Chen Jia, Li Hong, Guo Sicheng, Yang Zhe, Sun Shaoping, Zeng JunJie, Gou Hongjuan, Chen Yechang, Wang Feng, Lin Yanping, Huang Kun, Yue Hong, Ma Yuting, Lin Yu |
Genetic insight into sick sinus syndrome.
European heart journal 2021 May 42 (20): 1959-1971. Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
Case-control association study of congenital heart disease from a tertiary paediatric cardiac centre from North India. BMC pediatrics 2023 6 23 (1): 290. Prachi Kukshal, Radha O Joshi, Ajay Kumar, Shadab Ahamad, Prabhatha Rashmi Murthy, Yogesh Sathe, Krishna Manohar, Soma Guhathakurta, Subramanian Chellapp |
Whole exome sequencing with a focus on cardiac disease-associated genes in families of sudden unexplained deaths in Yunnan, southwest of China. BMC genomics 2023 2 24 (1): 57. Wei Si-Jie, Du Jin-Liang, Wang Yue-Bing, Qu Peng-Fei, Ma Lin, Sun Zhong-Chun, Tang Xue, Liu Kai, Xi Yan-Mei, Nie Sheng-Jie, Jia Peng-Lin, Long Wu, Qu Yong-Qiang, Li Yu-Hua, Lei Pu-Pi |
Single-Cell Reconstruction and Mutation Enrichment Analysis Identifies Dysregulated Cardiomyocyte and Endothelial Cells in Congenital Heart Disease. Physiological genomics 2023 10 . Richa Tambi, Binte Ashraf, Sharon Nandkishore, Shermin Sharafat, Faiza Kader, Nasna Nassir, Nesrin Mohamed, Awab Ahmed, Reem Abdel Hameid, Samah Alasrawi, Martina Brueckner, Wolfgang M Kuebler, Wendy Chung, Alawi Alsheikh-Ali, Roberto M Di Donato, Mohammed Uddin, Bakhrom K Berdi |
Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases. Scientific reports 2023 10 13 (1): 16769. Ishani Mhatre, Habiba Abdelhalim, William Degroat, Shreya Ashok, Bruce T Liang, Zeeshan Ahm |
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- Page last updated:Apr 22, 2024
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