BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
For: Tariq M, Ware SM. Importance of genetic evaluation and testing in pediatric cardiomyopathy. World J Cardiol 2014; 6(11): 1156-1165 [PMID: 25429328 DOI: 10.4330/wjc.v6.i11.1156]
URL: https://www.wjgnet.com/1949-8462/full/v6/i11/1156.htm
Number Citing Articles
1
I. V. Leontyeva, V. V. Presova. Hypertrophic cardiomyopathy in an athlete, occurring under the mask of sports remodeling. Secondary prevention of sudden cardiac death. Analysis of a clinical caseRussian Journal for Personalized Medicine 2023; 3(2): 98 doi: 10.18705/2782-38062023-3-2-98-106
2
Hirofumi Tsuru, Chika Yoshihara, Hidehiro Suginobe, Mizuki Matsumoto, Yoichiro Ishii, Jun Narita, Ryo Ishii, Renjie Wang, Atsuko Ueyama, Kazutoshi Ueda, Masaki Hirose, Kazuhisa Hashimoto, Hiroki Nagano, Ryosuke Tanaka, Takaharu Okajima, Keiichi Ozono, Hidekazu Ishida. Pathogenic Roles of Cardiac Fibroblasts in Pediatric Dilated CardiomyopathyJournal of the American Heart Association 2023; 12(13) doi: 10.1161/JAHA.123.029676
3
Michael B. Rosamilia, Alexandra M. Markunas, Priya S. Kishnani, Andrew P. Landstrom. Underrepresentation of Diverse Ancestries Drives Uncertainty in Genetic Variants Found in Cardiomyopathy-Associated GenesJACC: Advances 2024; 3(2): 100767 doi: 10.1016/j.jacadv.2023.100767
4
Seema Mital, Kiran Musunuru, Vidu Garg, Mark W. Russell, David E. Lanfear, Rajat M. Gupta, Kathleen T. Hickey, Michael J. Ackerman, Marco V. Perez, Dan M. Roden, Daniel Woo, Caroline S. Fox, Stephanie Ware. Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart AssociationCirculation: Cardiovascular Genetics 2016; 9(5): 448 doi: 10.1161/HCG.0000000000000031
5
Ji-won Hwang, Mi-Ae Jang, Shin Yi Jang, Soo Hyun Seo, Moon-Woo Seong, Sung Sup Park, Chang-Seok Ki, Duk-Kyung Kim. Diverse Phenotypic Expression of Cardiomyopathies in a Family with TNNI3 p.Arg145Trp MutationKorean Circulation Journal 2017; 47(2): 270 doi: 10.4070/kcj.2016.0213
6
Stephanie M. Ware. Genetics of paediatric cardiomyopathiesCurrent Opinion in Pediatrics 2017; 29(5): 534 doi: 10.1097/MOP.0000000000000533
7
Stephanie M. Ware, James D. Wilkinson, Muhammad Tariq, Jeffrey A. Schubert, Arthi Sridhar, Steven D. Colan, Ling Shi, Charles E. Canter, Daphne T. Hsu, Steven A. Webber, Debra A. Dodd, Melanie D. Everitt, Paul F. Kantor, Linda J. Addonizio, John L. Jefferies, Joseph W. Rossano, Elfriede Pahl, Paolo Rusconi, Wendy K. Chung, Teresa Lee, Jeffrey A. Towbin, Ashwin K. Lal, Surbhi Bhatnagar, Bruce Aronow, Phillip J. Dexheimer, Lisa J. Martin, Erin M. Miller, Lynn A. Sleeper, Hiedy Razoky, Jason Czachor, Steven E. Lipshultz. Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes StudyJournal of the American Heart Association 2021; 10(9) doi: 10.1161/JAHA.120.017731
8
Giulia De Angelis, Marco Bobbo, Alessia Paldino, Biancamaria D’Agata Mottolese, Alessandro Altinier, Matteo Dal Ferro, Marco Merlo, Gianfranco Sinagra. Cardiomyopathies in children: classification, diagnosis and treatmentCurrent Opinion in Organ Transplantation 2020; 25(3): 218 doi: 10.1097/MOT.0000000000000755
9
Diana Cimiotti, Heidi Budde, Roua Hassoun, Kornelia Jaquet. Genetic Restrictive Cardiomyopathy: Causes and Consequences—An Integrative ApproachInternational Journal of Molecular Sciences 2021; 22(2): 558 doi: 10.3390/ijms22020558
10
Thomas D. Ryan, Steven J. Kindel, Matthew J. O’Connor. Heart Failure in the Child and Young Adult2018; : 383 doi: 10.1016/B978-0-12-802393-8.00029-6
11
Diana Cimiotti, Seyyed-Reza Sadat-Ebrahimi, Andreas Mügge, Kornelia Jaquet. New Insights on Cardiomyopathy2024;  doi: 10.5772/intechopen.109896
12
Stephanie M. Ware. Evaluation of genetic causes of cardiomyopathy in childhoodCardiology in the Young 2015; 25(S2): 43 doi: 10.1017/S1047951115000827
13
Hamza El Hadi, Anne Freund, Steffen Desch, Holger Thiele, Nicolas Majunke. Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We?Biomedicines 2023; 11(2): 524 doi: 10.3390/biomedicines11020524
14
Rowida Almomani, Judith M.A. Verhagen, Johanna C. Herkert, Erwin Brosens, Karin Y. van Spaendonck-Zwarts, Angeliki Asimaki, Paul A. van der Zwaag, Ingrid M.E. Frohn-Mulder, Aida M. Bertoli-Avella, Ludolf G. Boven, Marjon A. van Slegtenhorst, Jasper J. van der Smagt, Wilfred F.J. van IJcken, Bert Timmer, Margriet van Stuijvenberg, Rob M. Verdijk, Jeffrey E. Saffitz, Frederik A. du Plessis, Michelle Michels, Robert M.W. Hofstra, Richard J. Sinke, J. Peter van Tintelen, Marja W. Wessels, Jan D.H. Jongbloed, Ingrid M.B.H. van de Laar. Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric CardiomyopathyJournal of the American College of Cardiology 2016; 67(5): 515 doi: 10.1016/j.jacc.2015.10.093
15
Hirofumi Tsuru, Hidekazu Ishida, Jun Narita, Ryo Ishii, Hidehiro Suginobe, Yoichiro Ishii, Renjie Wang, Shigetoyo Kogaki, Masaki Taira, Takayoshi Ueno, Yohei Miyashita, Hidetaka Kioka, Yoshihiro Asano, Yoshiki Sawa, Keiichi Ozono. Cardiac Fibroblasts Play Pathogenic Roles in Idiopathic Restrictive CardiomyopathyCirculation Journal 2021; 85(5): 677 doi: 10.1253/circj.CJ-20-1008
16
Deema Aljeaid, Ana Isabel Sanchez, Emily Wakefield, Sarah E. Chadwell, Nicole Moore, Carlos E. Prada, Wenying Zhang. Prevalence of pathogenic and likely pathogenic variants in the RASopathy genes in patients who have had panel testing for cardiomyopathyAmerican Journal of Medical Genetics Part A 2019; 179(4): 608 doi: 10.1002/ajmg.a.61072
17
Teresa M. Lee, Stephanie M. Ware. Toward personalized medicine: Does genetic diagnosis of pediatric cardiomyopathy influence patient management?Progress in Pediatric Cardiology 2015; 39(1): 43 doi: 10.1016/j.ppedcard.2015.01.008
18
Dong Li, Ce Wang. Advances in symptomatic therapy for left ventricular non-compaction in childrenFrontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1147362
19
Mizuki Matsumoto, Hirofumi Tsuru, Hidehiro Suginobe, Jun Narita, Ryo Ishii, Masaki Hirose, Kazuhisa Hashimoto, Renjie Wang, Chika Yoshihara, Atsuko Ueyama, Ryosuke Tanaka, Keiichi Ozono, Takaharu Okajima, Hidekazu Ishida, Akinori Kimura. Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathyPLOS ONE 2022; 17(9): e0275296 doi: 10.1371/journal.pone.0275296
20
Gulsah Yildirim, Memduh Dursun, Rıfat Arslan. Effect of trabeculated myocardial mass on left ventricle global and regional functions in noncompaction cardiomyopathyWorld Journal of Cardiology 2021; 13(7): 211-222 doi: 10.4330/wjc.v13.i7.211
21
Jeffrey Schubert, Muhammad Tariq, Gabrielle Geddes, Steven Kindel, Erin M. Miller, Stephanie M. Ware. Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathyHuman Mutation 2018; 39(12): 2083 doi: 10.1002/humu.23661
22
K. Wahbi, D. Bonnet. Transition et cardiomyopathies familialesArchives des Maladies du Coeur et des Vaisseaux - Pratique 2021; 2021(297): 14 doi: 10.1016/j.amcp.2021.01.008
23
Stephanie M. Ware. Pediatric cardiomyopathy and the PCM Genes study: A summary with insights on genetic testing, variant interpretation, race and ethnicityProgress in Pediatric Cardiology 2021; 63: 101468 doi: 10.1016/j.ppedcard.2021.101468
24
Hugo R. Martinez, Gary S. Beasley, John Jefferies, Jeffrey A. Towbin. Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care2021; : 1 doi: 10.1007/978-1-4471-4999-6_89-2
25
Scott I. Aydin, Nida Siddiqi, Christopher M. Janson, Sarah E. Norris, Giles J. Peek, Kimberly D. Beddows, Jacqueline M. Lamour, Daphne T. Hsu. Critical Heart Disease in Infants and Children2019; : 852 doi: 10.1016/B978-1-4557-0760-7.00072-3
26
Evan M. Harvey, Murad Almasri, Hugo R. Martinez. Cardiomyopathy - Disease of the Heart Muscle2021;  doi: 10.5772/intechopen.97010
27
Tony L. Brown, Theresa M. Meloche. Exome sequencing a review of new strategies for rare genomic disease researchGenomics 2016; 108(3-4): 109 doi: 10.1016/j.ygeno.2016.06.003
28
Franklyn P. Cladis, Brian Blasiole, Martin B. Anixter, James Gordon Cain, Peter J. Davis. A Practice of Anesthesia for Infants and Children2019; : 696 doi: 10.1016/B978-0-323-42974-0.00031-8
29
Elise L. Kessler, Peter GJ Nikkels, Toon AB van Veen. Disturbed Desmoglein-2 in the intercalated disc of pediatric patients with dilated cardiomyopathyHuman Pathology 2017; 67: 101 doi: 10.1016/j.humpath.2017.07.012
30
Chalani D. Ellepola, Linda M. Knight, Peter Fischbach, Shriprasad R. Deshpande. Genetic Testing in Pediatric CardiomyopathyPediatric Cardiology 2018; 39(3): 491 doi: 10.1007/s00246-017-1779-2
31
Hugo R. Martinez, Stephanie M. Ware, Marcus S. Schamberger, John J. Parent. Noncompaction cardiomyopathy and heterotaxy syndromeProgress in Pediatric Cardiology 2017; 46: 23 doi: 10.1016/j.ppedcard.2017.06.007
32
Ekaterina R. Tolmacheva, Jekaterina Shubina, Taisiya O. Kochetkova, Lubov’ V. Ushakova, Ekaterina L. Bokerija, Grigory S. Vasiliev, Galina V. Mikhaylovskaya, Ekaterina E. Atapina, Nadezhda V. Zaretskaya, Gennady T. Sukhikh, Denis V. Rebrikov, Dmitriy Yu. Trofimov. CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case ReportGenes 2023; 14(6): 1177 doi: 10.3390/genes14061177
33
Zarghuna M.A. Shinwari, Abdulrahman Almesned, Ali Alakhfash, Ahmad M. Al-Rashdan, Eissa Faqeih, Zainab Al-Humaidi, Ahmed Alomrani, Malak Alghamdi, Dilek Colak, Abdullah Alwadai, Monther Rababh, Majid Al-Fayyadh, Zuhair N. Al-Hassnan. The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous <b><i>ELAC2</i></b> MutationCardiology 2017; 137(3): 188 doi: 10.1159/000465516
34
Dale L. Bodian, Thierry Vilboux, Suchitra K. Hourigan, Callie L. Jenevein, Haresh Mani, Kathleen C. Kent, Alina Khromykh, Benjamin D. Solomon, Natalie S. Hauser. Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathyMolecular Case Studies 2017; 3(6): a002055 doi: 10.1101/mcs.a002055
35
Tomer Poleg, Marina Eskin-Schwartz, Regina Proskorovski-Ohayon, Ilana Aminov, Vadim Dolgin, Nadav Agam, Matan Jean, Amit Safran, Ofek Freund, Aviva Levitas, Yuval Konstantino, Ohad S. Birk, Roi Westreich, Moti Haim. Compound Heterozygosity for Late-Onset Cardiomyopathy-Causative ALPK3 Coding Variant and Novel Intronic Variant Cause Infantile Hypertrophic CardiomyopathyJournal of Cardiovascular Translational Research 2023; 16(6): 1325 doi: 10.1007/s12265-023-10461-y
36
Hugo R. Martinez, Gary S. Beasley, Noah Miller, Jason F. Goldberg, John L. Jefferies. Clinical Insights Into Heritable CardiomyopathiesFrontiers in Genetics 2021; 12 doi: 10.3389/fgene.2021.663450
37
Hidekazu Ishida. Idiopathic Restrictive Cardiomyopathy in ChildrenPediatric Cardiology and Cardiac Surgery 2021; 37(3): 184 doi: 10.9794/jspccs.37.184
38
Stephanie M. Ware, Surbhi Bhatnagar, Phillip J. Dexheimer, James D. Wilkinson, Arthi Sridhar, Xiao Fan, Yufeng Shen, Muhammad Tariq, Jeffrey A. Schubert, Steven D. Colan, Ling Shi, Charles E. Canter, Daphne T. Hsu, Neha Bansal, Steven A. Webber, Melanie D. Everitt, Paul F. Kantor, Joseph W. Rossano, Elfriede Pahl, Paolo Rusconi, Teresa M. Lee, Jeffrey A. Towbin, Ashwin K. Lal, Wendy K. Chung, Erin M. Miller, Bruce Aronow, Lisa J. Martin, Steven E. Lipshultz. The genetic architecture of pediatric cardiomyopathyThe American Journal of Human Genetics 2022; 109(2): 282 doi: 10.1016/j.ajhg.2021.12.006