HuGE Literature Finder
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Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC). Journal of cardiovascular electrophysiology 2018 Apr . Murray Brittney, Hoorntje Edgar T, Te Riele Anneline S J M, Tichnell Crystal, van der Heijden Jeroen F, Tandri Harikrishna, van den Berg Maarten P, Jongbloed Jan D H, Wilde Arthur A M, Hauer Richard N W, Calkins Hugh, Judge Daniel P, James Cynthia A, van Tintelen J Peter, Dooijes Denn |
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 |
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients. Circulation. Cardiovascular genetics 2017 Apr 10 (2): . Gómez Juan, Lorca Rebeca, Reguero Julian R, Morís César, Martín María, Tranche Salvador, Alonso Belén, Iglesias Sara, Alvarez Victoria, Díaz-Molina Beatriz, Avanzas Pablo, Coto Eliec |
Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction. Journal of genetics 2016 Jun 95 (2): 263-72. Kumar Surendra, Mishra Avshesh, Srivastava Anshika, Bhatt Mansi, Garg N, Agarwal S K, Pande Shantanu, Mittal Balr |
Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy. The American journal of cardiology 2016 Jan . Bongini Carolina, Ferrantini Cecilia, Girolami Francesca, Coppini Raffaele, Arretini Anna, Targetti Mattia, Bardi Sara, Castelli Gabriele, Torricelli Francesca, Cecchi Franco, Ackerman Michael J, Padeletti Luigi, Poggesi Corrado, Olivotto Iaco |
Targeted next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in patients and a cardiomyopathy risk group. Clinica chimica acta; international journal of clinical chemistry 2015 Jun 446 132-40. Glotov Andrey S, Kazakov Sergey V, Zhukova Elena A, Alexandrov Anton V, Glotov Oleg S, Pakin Vladimir S, Danilova Maria M, Poliakova Irina V, Niyazova Svetlana S, Chakova Natalia N, Komissarova Svetlana M, Kurnikova Elena A, Sarana Andrey M, Sherbak Sergey G, Sergushichev Alexey A, Shalyto Anatoly A, Baranov Vladislav |
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 |
Cardiac structural and sarcomere genes associated with cardiomyopathy exhibit marked intolerance of genetic variation. Circulation. Cardiovascular genetics 2012 Oct . Pan S, Caleshu CA, Dunn KE, Foti MJ, Moran MK, Soyinka O, Ashley EA |
Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients. PloS one 2011 6 (9): e24123. Srivastava Anshika, Garg Naveen, Mittal Tulika, Khanna Roopali, Gupta Shipra, Seth Prahlad Kishore, Mittal Balr |
Limited distribution of a cardiomyopathy-associated variant in India. Annals of human genetics 2010 Mar 74 (2): 184-8. Simonson Tatum S, Zhang Yuhua, Huff Chad D, Xing Jinchuan, Watkins W Scott, Witherspoon David J, Woodward Scott R, Jorde Lynn |
A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia. Nature genetics 2009 Feb 41 (2): 187-91. Dhandapany Perundurai S, Sadayappan Sakthivel, Xue Yali, Powell Gareth T, Rani Deepa Selvi, Nallari Prathiba, Rai Taranjit Singh, Khullar Madhu, Soares Pedro, Bahl Ajay, Tharkan Jagan Mohan, Vaideeswar Pradeep, Rathinavel Andiappan, Narasimhan Calambur, Ayapati Dharma Rakshak, Ayub Qasim, Mehdi S Qasim, Oppenheimer Stephen, Richards Martin B, Price Alkes L, Patterson Nick, Reich David, Singh Lalji, Tyler-Smith Chris, Thangaraj Kumarasa |
Shared genetic causes of cardiac hypertrophy in children and adults. The New England journal of medicine 2008 May 358 (18): 1899-908. Morita Hiroyuki, Rehm Heidi L, Menesses Andres, McDonough Barbara, Roberts Amy E, Kucherlapati Raju, Towbin Jeffrey A, Seidman J G, Seidman Christine |
Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study. Circulation 2006 Jun 113 (23): 2697-705. Morita Hiroyuki, Larson Martin G, Barr Scott C, Vasan Ramachandran S, O'Donnell Christopher J, Hirschhorn Joel N, Levy Daniel, Corey Diane, Seidman Christine E, Seidman J G, Benjamin Emelia |
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- Page last updated:Jun 22, 2022
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