HuGE Literature Finder
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| Metabolite Signature in the Carriers of Pathogenic Genetic Variants for Cardiomyopathy: A Population-Based METSIM Study. Metabolites 2022 May 12 (5): . Ravi Rowmika, Fernandes Silva Lilian, Vangipurapu Jagadish, Maria Maleeha, Raivo Joose, Helisalmi Seppo, Laakso Mark |
| Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality. JAMA cardiology 2022 5 7 (7): 723-732. Patel Aniruddh P, Dron Jacqueline S, Wang Minxian, Pirruccello James P, Ng Kenney, Natarajan Pradeep, Lebo Matthew, Ellinor Patrick T, Aragam Krishna G, Khera Amit |
| Diagnostic yield of genetic testing in heart transplant recipients with prior cardiomyopathy. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation 2022 5 41 (9): 1218-1227. Boen Hanne M, Loeys Bart L, Alaerts Maaike, Saenen Johan B, Goovaerts Inge, Van Laer Lut, Vorlat Anne, Vermeulen Tom, Franssen Constantijn, Pauwels Patrick, Rodrigus Inez, Heidbuchel Hein, Van Craenenbroeck Emeline |
| Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure. JAMA cardiology 2021 5 6 (8): 891-901. Akhtar Mohammed Majid, Lorenzini Massimiliano, Pavlou Menelaos, Ochoa Juan Pablo, O'Mahony Constantinos, Restrepo-Cordoba Maria Alejandra, Segura-Rodriguez Diego, Bermúdez-Jiménez Francisco, Molina Pilar, Cuenca Sofia, Ader Flavie, Larrañaga-Moreira Jose M, Sabater-Molina Maria, Garcia-Alvarez Maria I, Arantzamendi Larraitz Gaztañaga, Truszkowska Grazyna, Ortiz-Genga Martin, Ruiz Itziar Solla, Nielsen Søren Kristian, Rasmussen Torsten Bloch, Robles Mezcua Ainhoa, Alvarez-Rubio Jorge, Eiskjaer Hans, Gautel Mathias, Garcia-Pinilla José M, Ripoll-Vera Tomas, Mogensen Jens, Limeres Freire Javier, Rodríguez-Palomares Jose F, Peña-Peña Maria Luisa, Rangel-Sousa Diego, Palomino-Doza Julian, Arana Achaga Xabier, Bilinska Zofia, Zamarreño Golvano Estibaliz, Climent Vincent, Peñalver Marina Navarro, Barriales-Villa Roberto, Charron Philippe, Yotti Raquel, Zorio Esther, Jiménez-Jáimez Juan, Garcia-Pavia Pablo, Elliott Perry M, |
| Genetic evaluation of cardiomyopathies in Qatar identifies enrichment of pathogenic sarcomere gene variants and possible founder disease mutations in the Arabs. Molecular genetics & genomic medicine 2021 6 9 (7): e1709. Al-Shafai Kholoud N, Al-Hashemi Mohammed, Manickam Chidambaram, Musa Rania, Selvaraj Senthil, Syed Najeeb, Vempalli Fazulur, Ali Muneera, Yacoub Magdi, Estivill Xavi |
| Molecular analysis of dilated and left ventricular noncompaction cardiomyopathies in Egyptian children. Cardiology in the young 2021 5 32 (2): 295-300. Mehaney Dina A, Haghighi Alireza, Embaby Amira K, Zeyada Reham A, Darwish Rania K, Elfeel Nesrine S, Abouelhoda Mohamed, El-Saiedi Sonia A, Gohar Nadida A, Seliem Zeinab |
| 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 |
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.
Nature communications 2020 May 11 (1): 2254. Pirruccello James P, Bick Alexander, Wang Minxian, Chaffin Mark, Friedman Samuel, Yao Jie, Guo Xiuqing, Venkatesh Bharath Ambale, Taylor Kent D, Post Wendy S, Rich Stephen, Lima Joao A C, Rotter Jerome I, Philippakis Anthony, Lubitz Steven A, Ellinor Patrick T, Khera Amit V, Kathiresan Sekar, Aragam Krishna |
| Genetic Basis and Genotype-Phenotype Correlations in Han Chinese Patients with Idiopathic Dilated Cardiomyopathy. Scientific reports 2020 2 10 (1): 2226. Zhang Xin-Lin, Xie Jun, Lan Rong-Fang, Kang Li-Na, Wang Lian, Xu Wei, Xu Bi |
| Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies. Journal of translational medicine 2018 9 16 (1): 241. Lu Chaoxia, Wu Wei, Liu Fang, Yang Kunqi, Li Jiacheng, Liu Yaping, Wang Rongrong, Si Nuo, Gao Peng, Liu Yongtai, Zhang Shuyang, Zhang X |
| Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity. Clinical genetics 2018 11 95 (3): 356-367. Richard Pascale, Ader Flavie, Roux Maguelonne, Donal Erwan, Eicher Jean-Christophe, Aoutil Nadia, Huttin Olivier, Selton-Suty Christine, Coisne Damien, Jondeau Guillaume, Damy Thibaud, Mansencal Nicolas, Casalta Anne-Claire, Michel Nicolas, Haentjens Julie, Faivre Laurence, Lavoute Cecile, Nguyen Karine, Tregouët David-Alexandre, Habib Gilbert, Charron Philip |
| Titin-Truncating Variants Increase the Risk of Cardiovascular Death in Patients With Hypertrophic Cardiomyopathy. The Canadian journal of cardiology 2017 Jun . Zhang Ce, Zhang Hongju, Wu Guixin, Luo Xiaoliang, Zhang Channa, Zou Yubao, Wang Hu, Hui Rutai, Wang Jizheng, Song L |
| High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation. PloS one 2017 12 12 (12): e0189489. Klauke Baerbel, Gaertner-Rommel Anna, Schulz Uwe, Kassner Astrid, Zu Knyphausen Edzard, Laser Thorsten, Kececioglu Deniz, Paluszkiewicz Lech, Blanz Ute, Sandica Eugen, van den Bogaerdt Antoon J, van Tintelen J Peter, Gummert Jan, Milting Hendr |
| 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 |
| Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy. European heart journal 2015 Sep 36 (34): 2327-37. Akinrinade Oyediran, Ollila Laura, Vattulainen Sanna, Tallila Jonna, Gentile Massimiliano, Salmenperä Pertteli, Koillinen Hannele, Kaartinen Maija, Nieminen Markku S, Myllykangas Samuel, Alastalo Tero-Pekka, Koskenvuo Juha W, Heliö Tii |
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