Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 40 Records) |
Query Trace: Death and TTN[original query] |
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Novel missense variant in TTN cosegregating with familial atrioventricular block. European journal of medical genetics 2019 8 63 (3): 103752. Liu Guohui, Yang Ziying, Chen Weiwei, Xu Junguang, Mao Liangwei, Yu Qinlin, Guo Jian, Xu Hui, Liu Fengxia, Sun Yan, Huang Hui, Peng Zhiyu, Sun Jun, Li Wei, Yang Pi |
Whole-Exome Sequencing Reveals Novel Genetic Variation for Dilated Cardiomyopathy in Pediatric Chinese Patients. Pediatric cardiology 2019 4 40 (5): 950-957. Dai Genyin, Pu Zhening, Cheng Xueying, Yin Jie, Chen Jun, Xu Ting, Zhang Han, Li Zewei, Chen Xuan, Chen Jinlong, Qin Yuming, Yang Shiw |
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 |
Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing. Molecular genetics & genomic medicine 2020 9 8 (11): e1504. Carnevale Alessandra, Rosas-Madrigal Sandra, Rosendo-Gutiérrez Rigoberto, López-Mora Enrique, Romero-Hidalgo Sandra, Avila-Vazzini Nydia, Jacobo-Albavera Leonor, Domínguez-Pérez Mayra, Vargas-Alarcón Gilberto, Pérez-Villatoro Fernando, Navarrete-Martínez Juana Inés, Villarreal-Molina María Tere |
Prognostic implications of pathogenic truncating variants in the TTN gene. International journal of cardiology 2020 May . Peña-Peña Maria Luisa, Ochoa Juan Pablo, Barriales-Villa Roberto, Cicerchia Marcos, Palomino-Doza Julián, Salazar-Mendiguchía Joel, Lamounier Arsonval, Trujillo Juan Pablo, Garcia-Giustiniani Diego, Fernandez Xusto, Ortiz-Genga Martin, Monserrat Lorenzo, Crespo-Leiro Maria Genero |
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 |
Reduced Systolic Function and Not Genetic Variants Determine Outcome in Pediatric and Adult Left Ventricular Noncompaction Cardiomyopathy. Frontiers in pediatrics 2021 9 9 722926. Schultze-Berndt Alina, Kühnisch Jirko, Herbst Christopher, Seidel Franziska, Al-Wakeel-Marquard Nadya, Dartsch Josephine, Theisen Simon, Knirsch Walter, Jenni Rolf, Greutmann Matthias, Oechslin Erwin, Berger Felix, Klaassen Sabi |
Next-Generation Sequencing Reveals Novel Genetic Variants for Dilated Cardiomyopathy in Pediatric Chinese Patients. Pediatric cardiology 2021 Aug . Wang Yan, Han Bo, Fan Youfei, Yi Yingchun, Lv Jianli, Wang Jing, Yang Xiaofei, Jiang Diandong, Zhao Lijian, Zhang Jianjun, Yuan H |
Clinical Significance of Variants in the TTN Gene in a Large Cohort of Patients With Sporadic Dilated Cardiomyopathy. Frontiers in cardiovascular medicine 2021 5 8 657689. Xiao Lei, Li Chenze, Sun Yang, Chen Yanghui, Wei Haoran, Hu Dong, Yu Ting, Li Xianqing, Jin Li, Shi Leming, Marian Ali J, Wang Dao W |
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, |
[Expression and clinical significance of SETD2 in maligant pleural mesothelioma]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases 2021 3 39 (2): 91-98. Yu M, Yu M, Zhu L J, Yuan X Y, Zhang |
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 |
Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndrome. Heart rhythm O2 2021 10 2 (5): 431-438. Giudicessi John R, Maleszewski Joseph J, Tester David J, Ackerman Michael |
Genetic Architecture of Acute Myocarditis and the Overlap With Inherited Cardiomyopathy. Circulation 2022 9 146 (15): 1123-1134. Lota Amrit S, Hazebroek Mark R, Theotokis Pantazis, Wassall Rebecca, Salmi Sara, Halliday Brian P, Tayal Upasana, Verdonschot Job, Meena Devendra, Owen Ruth, de Marvao Antonio, Iacob Alma, Yazdani Momina, Hammersley Daniel J, Jones Richard E, Wage Riccardo, Buchan Rachel, Vivian Fredrik, Hafouda Yakeen, Noseda Michela, Gregson John, Mittal Tarun, Wong Joyce, Robertus Jan Lukas, Baksi A John, Vassiliou Vassilios, Tzoulaki Ioanna, Pantazis Antonis, Cleland John G F, Barton Paul J R, Cook Stuart A, Pennell Dudley J, Garcia-Pavia Pablo, Cooper Leslie T, Heymans Stephane, Ware James S, Prasad Sanjay |
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 |
The prognostic value and immune landscape of a cuproptosis-related lncRNA signature in head and neck squamous cell carcinoma. Frontiers in genetics 2022 8 13 942785. Li Yao Jun, Li Hai Yan, Zhang Quan, Wei Sheng |
Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants. PloS one 2022 17 (8): e0273280. Przyby?a Weronika, Gjersvoll Paulsen Kirsti Marie, Mishra Charitra Kumar, Nygård Ståle, Engebretsen Solveig, Ruud Ellen, Trøen Gunhild, Beiske Klaus, Baumbusch Lars Oliv |
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 |
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank. Nature genetics 2022 Feb . Jurgens Sean J, Choi Seung Hoan, Morrill Valerie N, Chaffin Mark, Pirruccello James P, Halford Jennifer L, Weng Lu-Chen, Nauffal Victor, Roselli Carolina, Hall Amelia W, Oetjens Matthew T, Lagerman Braxton, vanMaanen David P, , Aragam Krishna G, Lunetta Kathryn L, Haggerty Christopher M, Lubitz Steven A, Ellinor Patrick |
Genetic Profile and Clinical Characteristics of Brugada Syndrome in the Chinese Population. Journal of cardiovascular development and disease 2022 11 9 (11): . Wang Lin-Lin, Chen Yang-Hui, Sun Yang, Huang Man, Wei Hao-Ran, Liu Hao, Xu Ke, Song Xiu-Li, Chen Peng, Tan Lun, Huang Jin, Li Zong-Zhe, Li Rui, Yu Ting, Ma Fei, Ding Hu, Wang Yan, Wang Dao-Wen, Wang Hong, Zhao Chun-X |
Genetic Determinants of Sudden Unexpected Death in Pediatrics. Genetics in medicine : official journal of the American College of Medical Genetics 2022 1 24 (4): 839-850. Koh Hyun Yong, Haghighi Alireza, Keywan Christine, Alexandrescu Sanda, Plews-Ogan Erin, Haas Elisabeth A, Brownstein Catherine A, Vargas Sara O, Haynes Robin L, Berry Gerard T, Holm Ingrid A, Poduri Annapurna H, Goldstein Richard |
The cuproptosis-related signature associated with the tumor environment and prognosis of patients with glioma. Frontiers in immunology 2022 13 998236. Wang Weichen, Lu Zhichao, Wang Maoyu, Liu Zongheng, Wu Bing, Yang Chengkai, Huan He, Gong Peip |
The mutational landscape of a US Midwestern breast cancer cohort reveals subtype-specific cancer drivers and prognostic markers. Human genomics 2023 7 17 (1): 64. Neetha Nanoth Vellichirammal, Yuan-De Tan, Peng Xiao, James Eudy, Oleg Shats, David Kelly, Michelle Desler, Kenneth Cowan, Chittibabu Gu |
Genetic Determinants of Atherogenic Indexes. Genes 2023 6 14 (6): . Tomas Texis, Susana Rivera-Mancía, Eloisa Colín-Ramírez, Raul Cartas-Rosado, David Koepsell, Kenneth Rubio-Carrasco, Mauricio Rodríguez-Dorantes, Vanessa Gonzalez-Covarrubi |
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 |
Prognostic prediction and multidimensional dissections of a macrophages M0-related gene signature in liver cancer. Frontiers in endocrinology 2023 4 14 1153562. Xu Xiaoming, Wang Jingz |
A Novel Nonsense Pathogenic TTN Variant Identified in a Patient with Severe Dilated Cardiomyopathy. Current issues in molecular biology 2023 3 45 (3): 2422-2430. Micolonghi Caterina, Fabiani Marco, Pagannone Erika, Savio Camilla, Ricci Marta, Caroselli Silvia, Gambioli Vittoria, Musumeci Beatrice, Germani Aldo, Tini Giacomo, Autore Camillo, Pizzuti Antonio, Visco Vincenzo, Rubattu Speranza, Petrucci Simona, Piane Mar |
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 |
Population-Level Prevalence of Rare Variants Associated With Atrial Fibrillation and its Impact on Patient Outcomes. JACC. Clinical electrophysiology 2023 1 . Kandola Manjinder S, Kulm Scott, Kim Luke K, Markowitz Steven M, Liu Christopher F, Thomas George, Ip James E, Lerman Bruce B, Elemento Olivier, Cheung Jim |
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- Page last updated:Apr 22, 2024
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