Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 214 Records) |
| Query Trace: MYH7[original query] |
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| [Clinical and genetic analysis of eight children with Primary hypertrophic cardiomyopathy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 9 40 (10): 1211-1216. Qiqing Sun, Fangjie Wang, Linbo Su, Kun He, Yingying Li, Chanjuan Hao, Wei Li, Jun G |
| Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study. JACC. Heart failure 2023 8 . Mark Jansen, Remco de Brouwer, Fahima Hassanzada, Angela E Schoemaker, Amand F Schmidt, Maria D Kooijman-Reumerman, Valentina Bracun, Martijn G Slieker, Dennis Dooijes, Alexa M C Vermeer, Arthur A M Wilde, Ahmad S Amin, Ronald H Lekanne Deprez, Johanna C Herkert, Imke Christiaans, Rudolf A de Boer, Jan D H Jongbloed, J Peter van Tintelen, Folkert W Asselbergs, Annette F Ba |
| Late gadolinium enhancement distribution patterns in non-ischemic dilated cardiomyopathy: Genotype-phenotype correlation. European heart journal. Cardiovascular Imaging 2023 8 . Fernando de Frutos, Juan Pablo Ochoa, Ana Isabel Fernández, María Gallego-Delgado, Marina Navarro-Peñalver, Guillem Casas, María Teresa Basurte, José María Larrañaga-Moreira, María Victoria Mogollón, Ainhoa Robles-Mezcua, Pablo Elpidio García-Granja, Vicente Climent, Julián Palomino-Doza, Ana García-Álvarez, María Brion, Ramón Brugada, Juan Jiménez-Jáimez, Antoni Bayes-Genis, Tomas Ripoll-Vera, María Luisa Peña-Peña, José F Rodríguez-Palomares, Josefa Gonzalez-Carrillo, Eduardo Villacorta, Maria Angeles Espinosa, Pablo Garcia-Pavia, Jesus G Mirel |
| Long-Term Prevalence of Systolic Dysfunction in MYBPC3 Versus MYH7-Related Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 2023 7 e003832. Matteo Beltrami, Elisa Fedele, Carlo Fumagalli, Francesco Mazzarotto, Francesca Girolami, Cecilia Ferrantini, Raffaele Coppini, Lorenzo Tofani, Bruno Bertaccini, Corrado Poggesi, Iacopo Olivot |
| A Family with Myh7 Mutation and Different Forms of Cardiomyopathies. Biomedicines 2023 7 11 (7): . Bianca Iulia Catrina, Florina Batar, Georgiana Baltat, Cornel Ioan Bitea, Andreea Puia, Oana Stoia, Sorin Radu Fleac?, Minodora Teodo |
| MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2023 7 . Luisa Marsili, Freyja H M van Lint, Francesco Russo, Karin Y van Spaendonck-Zwarts, Flavie Ader, Marie-Line Bichon, Laurence Faivre, Arjan C Houweling, Bertrand Isidor, Ronald H Lekanne Deprez, Moniek G P J Cox, Arthur A M Wilde, Benoit Mazel, Sandra Mercier, Dennis Dooijes, Gilles Millat, Karine Nguyen, Jan G Post, Pascale Richard, Irma van de Beek, Alexa M C Vermeer, Ludolf Boven, Jan D H Jongbloed, J Peter van Tintelen, |
| The Definition of Sarcomeric and Non-Sarcomeric Gene Mutations in Hypertrophic Cardiomyopathy Patients: A Multicenter Diagnostic Study Across Türkiye. Anatolian journal of cardiology 2023 7 . Veysel Oktay, Omaç Tüfekçio?lu, Dilek Çicek Y?lmaz, Ersel Onrat, Dilay Karabulut, Murat Çelik, Akif Serhat Balc?o?lu, Mehmet Murat Sucu, Güllü Özdemir, Hakk? Kaya, Mehmet K??, Bar?? Güven, Oktay Ba?dato?lu, Fatma Nihan Turhan Ça?lar, Uygar Ça?da? Yüksel, ?rfan Veysel Düzen, Ahmet Barutçu, Özgüç Semih ?im?ir, ?brahim Ba?ar?c?, Af?in Parspur, Onur Dalg?ç, Fatma Özlem Ar?can Özlük, Mert Evlice, Saim Sa?, Muhammed Furkan Deniz, Arslan Öcal, Emine Gazi, Taner ?en, Osman Özdabako?lu, Nermin Bayar Çak?c?, Eren Ozan Bak?r, Ay?egül Ülgen Kunak, Gizem Çayl?, Aybike Gül Ta?delen, Ercan Ak?it, ?efika Uslu Çil, Hüseyin On |
| Genetic landscape in Russian patients with familial left ventricular noncompaction. Frontiers in cardiovascular medicine 2023 6 10 1205787. Alexey N Meshkov, Roman P Myasnikov, Anna V Kiseleva, Olga V Kulikova, Evgeniia A Sotnikova, Maria M Kudryavtseva, Anastasia A Zharikova, Sergey N Koretskiy, Elena A Mershina, Vasily E Ramensky, Marija Zaicenoka, Yuri V Vyatkin, Maria S Kharlap, Tatiana G Nikityuk, Valentin E Sinitsyn, Mikhail G Divashuk, Vladimir A Kutsenko, Elena N Basargina, Vladimir I Barskiy, Nataliya A Sdvigova, Olga P Skirko, Irina A Efimova, Maria S Pokrovskaya, Oxana M Drapki |
| Data mining on identifying diagnosis and prognosis biomarkers in head and neck squamous carcinoma. Scientific reports 2023 6 13 (1): 10020. Guoyuan Ju, Zhangyu Yao, Yanbin Zhao, Xiaotong Zhao, Fangzhou L |
| 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 |
| Genetic profile and genotype-phenotype correlations in childhood cardiomyopathy. Archives of cardiovascular diseases 2023 5 . Chloé Wanert, Fedoua El Louali, Sarab Al Dybiat, Karine Nguyen, Stéphane Zaffran, Caroline Ovae |
| End-stage Hypertrophic Cardiomyopathy with Advanced Heart Failure in Patients Carrying MYH7 R453 Variants: A Case Series. Internal medicine (Tokyo, Japan) 2023 3 . Naito Susumu, Higo Shuichiro, Kameda Satoshi, Ogawa Shou, Tabata Tomoka, Akazawa Yasuhiro, Nakamura Daisuke, Nakamoto Kei, Sera Fusako, Kuramoto Yuki, Aasano Yoshihiro, Hikoso Shungo, Miyagawa Shigeru, Sakata Yasus |
| Cardiomyocyte Apoptosis Is Associated with Contractile Dysfunction in Stem Cell Model of MYH7 E848G Hypertrophic Cardiomyopathy. International journal of molecular sciences 2023 3 24 (5): . Loiben Alexander M, Chien Wei-Ming, Friedman Clayton E, Chao Leslie S-L, Weber Gerhard, Goldstein Alex, Sniadecki Nathan J, Murry Charles E, Yang Kai-Ch |
| The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2023 11 . Lisa M Verheul, Martijn H van der Ree, Sanne A Groeneveld, Bart A Mulder, Imke Christiaans, Gijs F L Kapel, Marco Alings, Marianne Bootsma, Daniela Q C M Barge-Schaapveld, Jippe C Balt, Sing-Chien Yap, Ingrid P C Krapels, Rachel M A Ter Bekke, Paul G A Volders, Saskia N van der Crabben, Pieter G Postema, Arthur A M Wilde, Dennis Dooijes, Annette F Baas, Rutger J Hassi |
| [Clinical phenotype and genetic analysis of patients with left ventricular noncompaction caused by the biallelic mutation of MYBPC3 and MYH7]. Zhonghua xin xue guan bing za zhi 2023 11 51 (11): 1160-1165. Y H Zhang, X Y Li, B R Song, Y L Wang, J R Zhang, Y L R |
| Identification of concealed cardiomyopathy using next-generation sequencing-based genetic testing in Korean patients initially diagnosed with idiopathic ventricular fibrillation. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2023 11 25 (11): . Joo Hee Jeong, Yun Gi Kim, Suk-Kyu Oh, Hyoung Seok Lee, Yun Young Choi, Kyongjin Min, 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 |
| 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 |
| Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review. The Indian journal of medical research 2023 10 158 (2): 119-135. Linda Koshy, Sanjay Ganapathi, Panniyammakal Jeemon, M Madhuma, Y Vysakh, L R Lakshmikanth, Sivadasanpillai Harikrishn |
| Whole exome germline sequencing in early-onset prostate cancer patients: Genomic findings and clinical outcomes. The Prostate 2023 10 . Nava Siegelmann-Danieli, Victoria Neiman, Avital Bareket-Samish, Racheli Berger, Asaf Peretz, Hillel Alapi, Erez Tsur, Tal Patalon, Daniella Beller, Galit Rimler, Gabriel Chodick, Mordechai Shoh |
| Exploring novel MYH7 gene variants using in silico analyses in Korean patients with cardiomyopathy. BMC medical genomics 2024 9 17 (1): 225. Oc-Hee Kim, Jihyun Kim, Youngjun Kim, Soyoung Lee, Beom Hee Lee, Bong-Jo Kim, Hyun-Young Park, Mi-Hyun Pa |
| Association of Multiple Nonhypertrophic Cardiomyopathy-Related Genetic Variants and Outcomes in Patients With Hypertrophic Cardiomyopathy. JACC. Heart failure 2024 9 . Takashi Hiruma, Shunsuke Inoue, Zhehao Dai, Seitaro Nomura, Toru Kubo, Kenta Sugiura, Atsushi Suzuki, Takeshi Kashimura, Shouji Matsushima, Takanobu Yamada, Takashige Tobita, Manami Katoh, Toshiyuki Ko, Masamichi Ito, Junichi Ishida, Eisuke Amiya, Masaru Hatano, Norifumi Takeda, Eiki Takimoto, Hiroshi Akazawa, Hiroyuki Morita, Junichi Yamaguchi, Takayuki Inomata, Hiroyuki Tsutsui, Hiroaki Kitaoka, Hiroyuki Aburatani, Norihiko Takeda, Issei Komu |
| The French hypertrophic cardiomyopathy gene register: A systematic large gene screening for hypertrophic cardiomyopathy. International journal of cardiology 2024 9 417 132542. Albert Hagège, Tania Puscas, Mohamed El Hachmi, Alessandro Parodi, Anne Bacher, Benoit Funalot, Karim Wahbi, Xavier Jeunemaître, Thibaud Damy, Clarisse Billon, |
| Case report: Additional variants induced sudden cardiac death among pediatric ACM with DSG2 homozygous mutant genotype: a report of three cases. Frontiers in genetics 2024 9 15 1428796. Meng Wei, Yifei Li, Xiaoliang Liu, Kaiyu Zhou, Yu Qiu, Lei Liu, Lili Huang, Zhongqiang L |
| Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network. Neurology 2024 8 103 (4): e209697. Sara Bortolani, Marco Savarese, Gaetano Vattemi, Silvia Bonanno, Yuri M Falzone, Alessia Pugliese, Guido Primiano, Cristina Sancricca, Diego Lopergolo, Giulia Greco, Chiara Gemelli, Sabrina Ravaglia, Roberta P Bencivenga, Daniele Velardo, Francesca Magri, Maria L Valentino, Marta Cheli, Eleonora Torchia, Matteo Lucchini, Antonio Petrucci, Giulia Ricci, Matteo Garibaldi, Guja Astrea, Anna Rubegni, Corrado I Angelini, Alessandra Ariatti, Filippo M Santorelli, Alessandra Ruggieri, Giovanni Antonini, Gabriele Siciliano, Massimiliano Filosto, Massimiliano Mirabella, Rocco Liguori, Giacomo P Comi, Lucia Ruggiero, Marina Grandis, Roberto Massa, Alessandro Malandrini, Serenella Servidei, Tiziana E Mongini, Carmelo Rodolico, Antonio Toscano, Stefano C Previtali, Paola Tonin, Jordi Diaz-Manera, Mauro Monforte, Enzo Ricci, Lorenzo Maggi, Giorgio Tas |
| Genetic testing and human leukocyte antigen in patients with hypertrophic cardiomyopathy and connective tissue diseases. Frontiers in genetics 2024 8 15 1432670. Daigo Hiraya, Nobuyuki Murakoshi, Miyako Igarashi, DongZhu Xu, Tomoko Ishi |
| Clinical exome sequencing unravels the diverse spectrum of genetic heterogeneity and genotype-phenotype correlations in hypertrophic cardiomyopathy. International journal of cardiology 2024 6 132273. Sivadasanpillai Harikrishnan, Linda Koshy, Sanjay Ganapathi, Panniyammakal Jeemon, N K Ramya Das, Madhusoodanan Urulangodi, M Madhuma, Y Vysakh, Anjana Subran, L R Lakshmikan |
| Cardiomyopathy in children: a single-centre, retrospective study of genetic and clinical characteristics. BMJ paediatrics open 2024 6 8 (1): . Qiqing Sun, Jun Guo, Yaodong Zhang, Ruili Zheng, Kun He, Yuanying Chen, Chanjuan Hao, Zhenhua Xie, Fangjie Wa |
| Influence of Clinical Aspects and Genetic Factors on Feline HCM Severity and Development. Veterinary sciences 2024 5 11 (5): . Victoria Korobova, Yulia Kruglo |
| Searching for genetic determinants for left ventricular non-compaction. Quantitative imaging in medicine and surgery 2024 10 14 (10): 7046-7060. Micha? Spa?ek, Aneta Kusi?ska, Jan Spa?ek, Zbigniew Siudak, Beata Wo?akowska-Kap?on, Wioletta Adamus-Bia? |
| Prevalence, Penetrance, and Phenotypic Manifestation of Cardiomyopathy-Associated Genetic Variants in the General Population: Insights from a Mayo Clinic Biobank Study. Mayo Clinic proceedings 2024 10 . Marta Figueiral, Alessia Paldino, Matheus Vernet Machado Bressan Wilke, Joseph D Farris, Jan Verheijen, John R Giudicessi, Michael J Ackerman, Janet E Olson, Jennifer Arroyo, Rory J Olson, Eric W Klee, Naveen L Perei |
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