Citation of this article
Corresponding Author of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (6321)
All Articles published online
|
Oct 26, 2012 (publication date) through Dec 8, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Cardiology
ISSN
1949-8462
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Faita F, Vecoli C, Foffa I, Andreassi MG. Next generation sequencing in cardiovascular diseases. World J Cardiol 2012; 4(10): 288-295 [PMID: 23110245 DOI: 10.4330/wjc.v4.i10.288] |
|---|---|
| URL: | https://www.wjgnet.com/1949-8462/full/v4/i10/288.htm |
| Number | Citing Articles |
| 1 |
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy. European Heart Journal 2014; 35(39): 2733 doi: 10.1093/eurheartj/ehu284
|
| 2 |
Szilvia Fiatal, Róza Ádány. Application of Single-Nucleotide Polymorphism-Related Risk Estimates in Identification of Increased Genetic Susceptibility to Cardiovascular Diseases: A Literature Review. Frontiers in Public Health 2018; 5 doi: 10.3389/fpubh.2017.00358
|
| 3 |
Diksha Pandey, P. Onkara Perumal. A scoping review on deep learning for next-generation RNA-Seq. data analysis. Functional & Integrative Genomics 2023; 23(2) doi: 10.1007/s10142-023-01064-6
|
| 4 |
Georgia Sarquella-Brugada, Sergi Cesar, Maria Dolores Zambrano, Anna Fernandez-Falgueras, Victoria Fiol, Anna Iglesias, Francesc Torres, Oscar Garcia-Algar, Elena Arbelo, Josep Brugada, Ramon Brugada, Oscar Campuzano. Electrocardiographic Assessment and Genetic Analysis in Neonates: a Current Topic of Discussion. Current Cardiology Reviews 2018; 15(1): 30 doi: 10.2174/1573403X14666180913114806
|
| 5 |
Pavol Tomašov, M. Minárik, D. Zemánek, P. Čadová, S. Homolová, K. Čurila, M. Pěnička, L. Benešová, B. Belšánová, P. Gregor, J. Veselka. Genetic Testing in the Management of Relatives of Patients with Hypertrophic Cardiomyopathy. Folia Biologica 2014; 60(1): 28 doi: 10.14712/fb2014060010028
|
| 6 |
Samira Kalayinia, Hamidreza Goodarzynejad, Majid Maleki, Nejat Mahdieh. Next generation sequencing applications for cardiovascular disease. Annals of Medicine 2018; 50(2): 91 doi: 10.1080/07853890.2017.1392595
|
| 7 |
Russell A. Gould, Lina M. Aboulmouna, Jeffrey D. Varner, Jonathan T. Butcher. Hierarchical approaches for systems modeling in cardiac development. WIREs Systems Biology and Medicine 2013; 5(3): 289 doi: 10.1002/wsbm.1217
|
| 8 |
Yan-ping Ruan, Chao-xia Lu, Xiao-yi Zhao, Rui-juan Liang, Hui Lian, Michael Routledge, Wei Wu, Xue Zhang, Zhong-jie Fan. Restrictive Cardiomyopathy Resulting from a Troponin I Type 3 Mutation in a Chinese Family. Chinese Medical Sciences Journal 2016; 31(1): 1 doi: 10.1016/S1001-9294(16)30015-3
|
| 9 |
Cinzia Forleo, Anna Maria D’Erchia, Sandro Sorrentino, Caterina Manzari, Matteo Chiara, Massimo Iacoviello, Andrea Igoren Guaricci, Delia De Santis, Rita Leonarda Musci, Antonino La Spada, Vito Marangelli, Graziano Pesole, Stefano Favale, Tomohiko Ai. Targeted next-generation sequencing detects novel gene–phenotype associations and expands the mutational spectrum in cardiomyopathies. PLOS ONE 2017; 12(7): e0181842 doi: 10.1371/journal.pone.0181842
|
| 10 |
Roberto R. Expósito, Jorge González-Domínguez. BigDEC: A multi-algorithm Big Data tool based on the k-mer spectrum method for scalable short-read error correction. Future Generation Computer Systems 2024; 154: 314 doi: 10.1016/j.future.2024.01.011
|
| 11 |
Simona Todisco, Biagia Musio, Vito Pesce, Maria Maddalena Cavalluzzi, Giuseppe Petrosillo, Gianluigi La Piana, Maria Noemi Sgobba, Nikola Schlosserová, Lucas Cafferati Beltrame, Rosa Di Lorenzo, Vincenzo Tragni, Domenico Marzulli, Lorenzo Guerra, Anna De Grassi, Vito Gallo, Mariateresa Volpicella, Luigi Leonardo Palese, Giovanni Lentini, Ciro Leonardo Pierri. Targeting mitochondrial impairment for the treatment of cardiovascular diseases: From hypertension to ischemia-reperfusion injury, searching for new pharmacological targets. Biochemical Pharmacology 2023; 208: 115405 doi: 10.1016/j.bcp.2022.115405
|
| 12 |
Jarryd M. Campbell, Katherine A. Hartjes, Timothy J. Nelson, Xiaolei Xu, Stephen C. Ekker. New and TALENted Genome Engineering Toolbox. Circulation Research 2013; 113(5): 571 doi: 10.1161/CIRCRESAHA.113.301765
|
| 13 |
Francesco Danilo Tiziano, Vincenzo Palmieri, Maurizio Genuardi, Paolo Zeppilli. The Role of Genetic Testing in the Identification of Young Athletes with Inherited Primitive Cardiac Disorders at Risk of Exercise Sudden Death. Frontiers in Cardiovascular Medicine 2016; 3 doi: 10.3389/fcvm.2016.00028
|
| 14 |
C. Alexander Valencia, M. Ali Pervaiz, Ammar Husami, Yaping Qian, Kejian Zhang. Next Generation Sequencing Technologies in Medical Genetics. SpringerBriefs in Genetics 2013; : 75 doi: 10.1007/978-1-4614-9032-6_8
|
| 15 |
Andreas Brodehl, Anna Gaertner-Rommel, Hendrik Milting.
FLNC
(Filamin-C)
. Circulation: Cardiovascular Genetics 2017; 10(6) doi: 10.1161/CIRCGENETICS.117.001959
|
| 16 |
Quynh Nguyen, Kenji Rowel Q. Lim, Toshifumi Yokota. Genome Editing for the Understanding and Treatment of Inherited Cardiomyopathies. International Journal of Molecular Sciences 2020; 21(3): 733 doi: 10.3390/ijms21030733
|
| 17 |
Benedetta M. Motta, Peter P. Pramstaller, Andrew A. Hicks, Alessandra Rossini. The Impact of CRISPR/Cas9 Technology on Cardiac Research: From Disease Modelling to Therapeutic Approaches. Stem Cells International 2017; 2017: 1 doi: 10.1155/2017/8960236
|
| 18 |
Vivek Sarohi, Sanchari Chakraborty, Trayambak Basak. Exploring the cardiac ECM during fibrosis: A new era with next-gen proteomics. Frontiers in Molecular Biosciences 2022; 9 doi: 10.3389/fmolb.2022.1030226
|
| 19 |
Guoliang Wang, Vivan Niewiadonski, Jianping Li, Ruirui Ji, Wenxin Zou, Daniel J. Penny, Yuxin Fan. Next Generation Sequencing Based Clinical Molecular Diagnosis of Human Genetic Disorders. 2017; : 243 doi: 10.1007/978-3-319-56418-0_12
|
| 20 |
Yazhou Cui, Xiaoyan Zhou, Jinxiang Han. China launched a pilot project to improve its rare disease healthcare levels. Orphanet Journal of Rare Diseases 2014; 9(1) doi: 10.1186/1750-1172-9-14
|
| 21 |
Po-Yen Wu, Raghu Chandramohan, John H. Phan, William T. Mahle, J. William Gaynor, Kevin O. Maher, May D. Wang. Cardiovascular Transcriptomics and Epigenomics Using Next-Generation Sequencing. Circulation: Cardiovascular Genetics 2014; 7(5): 701 doi: 10.1161/CIRCGENETICS.113.000129
|
| 22 |
Cecilia Vecoli. Cardiomyocytes. Methods in Molecular Biology 2015; 1299: 51 doi: 10.1007/978-1-4939-2572-8_4
|
| 23 |
N. Mathieu, B. Löhnhardt, R. Grütz, P. Weil, J. Drepper, M. Krawczak. Ethische und rechtliche Implikationen der Speicherung humaner Genomdaten. Medizinische Genetik 2013; 25(2): 278 doi: 10.1007/s11825-013-0380-1
|
| 24 |
Ronald M. Paranal, Polakit Teekakirikul, Carolyn Y. Ho, Diane Fatkin, Christine E. Seidman. Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics. 2020; : 77 doi: 10.1016/B978-0-12-812532-8.00002-1
|