Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 44 Records) |
Query Trace: Hypertrophy and MYBPC3[original query] |
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The role of renin-angiotensin-aldosterone system polymorphisms in phenotypic expression of MYBPC3-related hypertrophic cardiomyopathy. European journal of human genetics : EJHG 2012 Oct 20 (10): 1071-7. Kolder Iris C R M, Michels Michelle, Christiaans Imke, Ten Cate Folkert J, Majoor-Krakauer Danielle, Danser Alexander H J, Lekanne Deprez Robert H, Tanck Michael W T, Wilde Arthur A M, Bezzina Connie R, Dooijes Denn |
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (9): 2358-65. Núñez Lucía, Gimeno-Blanes Juan Ramón, Rodríguez-García María Isabel, Monserrat Lorenzo, Zorio Esther, Coats Caroline, McGregor Christopher G, Hernandez del Rincón Juan Pedro, Castro-Beiras Alfonso, Hermida-Prieto Manu |
Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy. The American journal of cardiology 2013 Aug 112 (4): 585-9. Liu Wen, Liu Wenling, Hu Dayi, Zhu Tiangang, Ma Zhanfeng, Yang Jie, Xie Wenli, Li Cuilan, Li Lei, Yang Jingang, Li Tianchang, Bian Hong, Tong Qigua |
Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy. American heart journal 2013 Oct 166 (4): 775-82. Marsiglia Julia Daher Carneiro, Credidio Flávia Laghi, de Oliveira Théo Gremen Mimary, Reis Rafael Ferreira, Antunes Murillo de Oliveira, de Araujo Aloir Queiroz, Pedrosa Rodrigo Pinto, Barbosa-Ferreira João Marcos Bemfica, Mady Charles, Krieger José Eduardo, Arteaga-Fernandez Edmundo, Pereira Alexandre da Cos |
Gender differences in the clinical features of hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutations. Journal of cardiology 2015 May 65 (5): 423-8. Terauchi Yasunobu, Kubo Toru, Baba Yuichi, Hirota Takayoshi, Tanioka Katsutoshi, Yamasaki Naohito, Furuno Takashi, Kitaoka Hiroa |
Genetic variations of beta-MYH7 in Venezuelan patients with hypertrophic cardiomyopathy. Investigación clínica 2014 Mar 55 (1): 23-31. Rodríguez Rosalva, Guerrero David, Rivas Yoyna, Lacruz Andrea, Flores Yr |
Diltiazem treatment for pre-clinical hypertrophic cardiomyopathy sarcomere mutation carriers: a pilot randomized trial to modify disease expression. JACC. Heart failure 2015 Feb 3 (2): 180-8. Ho Carolyn Y, Lakdawala Neal K, Cirino Allison L, Lipshultz Steven E, Sparks Elizabeth, Abbasi Siddique A, Kwong Raymond Y, Antman Elliott M, Semsarian Christopher, González Arantxa, López Begoña, Diez Javier, Orav E John, Colan Steven D, Seidman Christine |
Circulating concentrations of a marker of type I collagen metabolism are associated with hypertrophic cardiomyopathy mutation status in ragdoll cats. The Journal of small animal practice 2015 Jun 56 (6): 360-5. Borgeat K, Dudhia J, Luis Fuentes V, Connolly D |
Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM. DNA and cell biology 2015 May 34 (5): 350-9. Selvi Rani Deepa, Nallari Pratibha, Dhandapany Perundurai S, Rani Jhansi, Meraj Khunza, Ganesan Mala, Narasimhan Calambur, Thangaraj Kumarasa |
A Long Term Follow-up Study of Carriers of Hypertrophic Cardiomyopathy Mutations. Heart, lung & circulation 2016 May . McTaggart Don R, Ogden Kathryn J, Marathe Jessica |
Cardiovascular magnetic resonance of mitral valve length in hypertrophic cardiomyopathy. Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance 2016 18 (1): 33. Tarkiainen Mika, Sipola Petri, Jalanko Mikko, Heliö Tiina, Laine Mika, Järvinen Vesa, Häyrinen Kaisu, Lauerma Kirsi, Kuusisto Johan |
MYBPC3 hypertrophic cardiomyopathy can be detected by using advanced ECG in children and young adults. Journal of electrocardiology 2016 Mar . Fernlund E, Liuba P, Carlson J, Platonov P G, Schlegel T |
[Mutation and clinical relevance in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy]. Zhonghua xin xue guan bing za zhi 2015 Aug 43 (8): 682-9. Jie Liu, Wenling Liu, Dayi Hu, Tiangang Zhu, Wen Liu, Zhanfeng Ma, Jie Yang, Wenli Xie, Cuilan Li, Lei Li, Guozhong P |
Clinical Characteristics and Long-Term Outcome of Hypertrophic Cardiomyopathy in Individuals With a MYBPC3 (Myosin-Binding Protein C) Founder Mutation. Circulation. Cardiovascular genetics 2017 8 10 (4): . van Velzen Hannah G, Schinkel Arend F L, Oldenburg Rogier A, van Slegtenhorst Marjon A, Frohn-Mulder Ingrid M E, van der Velden Jolanda, Michels Michel |
Association of Cardiomyopathy With MYBPC3 D389V and MYBPC3?25bpIntronic Deletion in South Asian Descendants. JAMA cardiology 2018 Apr . Viswanathan Shiv Kumar, Puckelwartz Megan J, Mehta Ashish, Ramachandra Chrishan J A, Jagadeesan Aravindakshan, Fritsche-Danielson Regina, Bhat Ratan V, Wong Philip, Kandoi Sangeetha, Schwanekamp Jennifer A, Kuffel Gina, Pesce Lorenzo L, Zilliox Michael J, Durai U Nalla B, Verma Rama Shanker, Molokie Robert E, Suresh Domodhar P, Khoury Philip R, Thomas Annie, Sanagala Thriveni, Tang Hak Chiaw, Becker Richard C, Knöll Ralph, Shim Winston, McNally Elizabeth M, Sadayappan Sakthiv |
Genetic characterization and genotype-phenotype associations in a large cohort of patients with hypertrophic cardiomyopathy - An ancillary study of the Portuguese registry of hypertrophic cardiomyopathy. International journal of cardiology 2018 Dec . Lopes Luis Rocha, Brito Dulce, Belo Adriana, Cardim Nuno, |
Novel electrocardiographic features in carriers of hypertrophic cardiomyopathy causing sarcomeric mutations. Journal of electrocardiology 2018 12 51 (6): 983-989. Jalanko Mikko, Heliö Tiina, Mustonen Pirjo, Kokkonen Jorma, Huhtala Heini, Laine Mika, Jääskeläinen Pertti, Tarkiainen Mika, Lauerma Kirsi, Sipola Petri, Laakso Markku, Kuusisto Johanna, Nikus Kje |
Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy. European journal of medical genetics 2019 9 63 (3): 103754. Robyns Tomas, Breckpot Jeroen, Nuyens Dieter, Vandenberk Bert, Corveleyn Anniek, Kuiperi Cuno, Van Aelst Lucas, Van Cleemput Johan, Willems R |
Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy. Journal of the American College of Cardiology 2019 4 73 (13): 1601-1611. van Waning Jaap I, Caliskan Kadir, Michels Michelle, Schinkel Arend F L, Hirsch Alexander, Dalinghaus Michiel, Hoedemaekers Yvonne M, Wessels Marja W, IJpma Arne S, Hofstra Robert M W, van Slegtenhorst Marjon A, Majoor-Krakauer Daniel |
MYBPC3 Haplotype Linked to Hypertrophic Cardiomyopathy in Rhesus Macaques (Macaca mulatta). Comparative medicine 2020 8 70 (5): 358-367. Oldt Robert F, Bussey Kimberly J, Settles Matthew L, Fass Joseph N, Roberts Jeffrey A, Reader J Rachel, Komandoor Srivathsan, Abrich Victor A, Kanthaswamy Sreethar |
Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 2020 8 13 (5): 396-405. Helms Adam S, Thompson Andrea D, Glazier Amelia A, Hafeez Neha, Kabani Samat, Rodriguez Juliani, Yob Jaime M, Woolcock Helen, Mazzarotto Francesco, Lakdawala Neal K, Wittekind Samuel G, Pereira Alexandre C, Jacoby Daniel L, Colan Steven D, Ashley Euan A, Saberi Sara, Ware James S, Ingles Jodie, Semsarian Christopher, Michels Michelle, Olivotto Iacopo, Ho Carolyn Y, Day Sharlene |
Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy. Revista portuguesa de cardiologia 2020 6 39 (6): 317-327. Toste Alexandra, Perrot Andreas, Özcelik Cemil, Cardim Nu |
Hypertrophic cardiomyopathy in myosin-binding protein C (MYBPC3) Icelandic founder mutation carriers. Open heart 2020 4 7 (1): e001220. Adalsteinsdottir Berglind, Burke Michael, Maron Barry J, Danielsen Ragnar, Lopez Begoña, Diez Javier, Jarolim Petr, Seidman Jonathan, Seidman Christine E, Ho Carolyn Y, Gunnarsson Gunnar |
Targeting the population for gene therapy with MYBPC3. Journal of molecular and cellular cardiology 2020 Oct . Carrier Luc |
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy. Forensic science international. Genetics 2021 2 52 102478. Mori Augusto Akira, Castro Lara Reinel de, Bortolin Raul Hernandes, Bastos Gisele Medeiros, Oliveira Victor Fernandes de, Ferreira Glaucio Monteiro, Hirata Thiago Dominguez Crespo, Fajardo Cristina Moreno, Sampaio Marcelo Ferraz, Moreira Dalmo Antonio Ribeiro, Pachón-Mateos José Carlos, Correia Edileide de Barros, Sousa Amanda Guerra de Moraes Rego, Brión Maria, Carracedo Angel, Hirata Rosario Dominguez Crespo, Hirata Mario Hiroyu |
MicroRNA expression profiles in familial hypertrophic cardiomyopathy with myosin-binding protein C3 (MYBPC3) gene mutations. BMC cardiovascular disorders 2022 6 22 (1): 278. Lin Li-Rong, Hu Xue-Qun, Lu Li-Hong, Dai Jia-Zhen, Lin Ning-Ning, Wang Re-Hua, Xie Zhang-Xin, Chen Xue-M |
Implications of structural right ventricular involvement in patients with hypertrophic cardiomyopathy. European heart journal. Quality of care & clinical outcomes 2022 2 9 (1): 34-41. Zhang Yu, Zhu Yuming, Zhang Mo, Liu Jie, Wu Guixin, Wang Jizheng, Sun Xiaolu, Wang Dong, Jiang Wen, Xu Lianjun, Kang Lianming, Song L |
South Asian-Specific MYBPC3 Deletion Carriers Display Hypercontraction and Impaired Diastolic Function Under Exercise Stress. Frontiers in cardiovascular medicine 2022 1 8 766339. Bazrafshan Sholeh, Sibilia Robert, Girgla Saavia, Viswanathan Shiv Kumar, Puckelwartz Megan J, Sangha Kiranpal S, Singh Rohit R, Kakroo Mashhood, Jandarov Roman, Harris David M, Rubinstein Jack, Becker Richard C, McNally Elizabeth M, Sadayappan Sakthiv |
Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers. Journal of cardiovascular translational research 2023 6 . Mark Jansen, A F Schmidt, J J M Jans, I Christiaans, S N van der Crabben, Y M Hoedemaekers, D Dooijes, J D H Jongbloed, L G Boven, R H Lekanne Deprez, A A M Wilde, J van der Velden, R A de Boer, J P van Tintelen, F W Asselbergs, A F Ba |
Three-dimensional echocardiography reveals early mitral valve alterations in hypertrophic cardiomyopathy genetic mutation carriers. International journal of cardiology 2023 11 131576. Nianwei Zhou, Ao Liu, Haobo Weng, Wen Liu, Fangyan Tian, Weipeng Zhao, Jing Ma, Wei Guo, Haiyan Chen, Cuizhen Pan, Xianhong S |
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- Page last updated:Apr 22, 2024
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