BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
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 cardiomyopathyEuropean 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 ReviewFrontiers 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 analysisFunctional & 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 DiscussionCurrent 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 CardiomyopathyFolia Biologica 2014; 60(1): 28 doi: 10.14712/fb2014060010028
6
Samira Kalayinia, Hamidreza Goodarzynejad, Majid Maleki, Nejat Mahdieh. Next generation sequencing applications for cardiovascular diseaseAnnals 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 developmentWIREs 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 FamilyChinese 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 cardiomyopathiesPLOS 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 correctionFuture 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 targetsBiochemical 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 ToolboxCirculation 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 DeathFrontiers 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 GeneticsSpringerBriefs 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 CardiomyopathiesInternational 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 ApproachesStem 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 proteomicsFrontiers 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 Disorders2017; : 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 levelsOrphanet 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 SequencingCirculation: Cardiovascular Genetics 2014; 7(5): 701 doi: 10.1161/CIRCGENETICS.113.000129
22
Cecilia Vecoli. CardiomyocytesMethods 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 GenomdatenMedizinische 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 Genomics2020; : 77 doi: 10.1016/B978-0-12-812532-8.00002-1