| 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] |
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| 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 case. Russian Journal for Personalized Medicine 2023; 3(2) doi: 10.18705/2782-38062023-3-2-98-106
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| 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 Cardiomyopathy. Journal of the American Heart Association 2023; 12(13) doi: 10.1161/JAHA.123.029676
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| 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 Genes. JACC: Advances 2024; 3(2) doi: 10.1016/j.jacadv.2023.100767
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| 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 Association. Circulation: Cardiovascular Genetics 2016; 9(5) doi: 10.1161/HCG.0000000000000031
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| 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 Mutation. Korean Circulation Journal 2017; 47(2) doi: 10.4070/kcj.2016.0213
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| 6 |
Stephanie M. Ware. Genetics of paediatric cardiomyopathies. Current Opinion in Pediatrics 2017; 29(5) doi: 10.1097/MOP.0000000000000533
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| 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 Study. Journal of the American Heart Association 2021; 10(9) doi: 10.1161/JAHA.120.017731
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| 8 |
Teresa M. Lee, Erin Miller, Arthi Sridhar, Xiao Fan, Phillip J. Dexheimer, Neha Bansal, Justin Godown, Daphne T. Hsu, Paul Kantor, Sonya Kirmani, Ashwin K. Lal, Joseph W. Rossano, Jeffrey A. Towbin, Steven A. Webber, Ling Shi, Taye H. Hamza, Bruce J. Aronow, Surbhi Bhatnaghar, Lisa J. Martin, Jeffrey Schubert, Stephanie M. Ware, Wendy K. Chung, James D. Wilkinson, Steven E. Lipshultz. Pediatric cardiomyopathy illustrates the importance of reinterpreting the significance of genetic variants. Progress in Pediatric Cardiology 2024; 74 doi: 10.1016/j.ppedcard.2024.101732
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| 9 |
Rania Gargouri, Nihel Ammous-Boukhris, Manel Hssairi, Amor Mosbah, Mariem Jabeur, Wiem Feki, Zeineb Mnif, Raja Mokdad-Gargouri, Leila Abid, Lamia Gargouri. A novel likely pathogenic variant in the mitochondrial ribosomal protein L44 (MRPL44) associated with hypertrophic cardiomyopathy in Tunisian patients. Molecular Biology Reports 2025; 52(1) doi: 10.1007/s11033-025-10556-6
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| 10 |
Thomas D. Ryan, Steven J. Kindel, Matthew J. O’Connor. Heart Failure in the Child and Young Adult. 2026; doi: 10.1016/B978-0-443-13279-7.00016-X
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| 11 |
Elfriede Pahl, Stephanie M. Ware, Ling Shi, Steven D. Colan, Melanie D. Everitt, Lynn A. Sleeper, Arthi Sridhar, Jeffrey A. Schubert, Charles E. Canter, Daphne T. Hsu, Steven A. Webber, Paul F. Kantor, Joseph W. Rossano, Wendy K. Chung, Teresa M. Lee, Jeffrey A. Towbin, Ashwin K. Lal, Muhammad Tariq, Surbhi Bhatnagar, Phillip J. Dexheimer, Bruce J. Aronow, Lisa J. Martin, Erin M. Miller, Neha Bansal, Steven E. Lipshultz. Genotype-Phenotype Associations in Pediatric Hypertrophic Cardiomyopathy. JACC: Heart Failure 2026; doi: 10.1016/j.jchf.2026.103355
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| 12 |
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 treatment. Current Opinion in Organ Transplantation 2020; 25(3) doi: 10.1097/MOT.0000000000000755
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| 13 |
Diana Cimiotti, Heidi Budde, Roua Hassoun, Kornelia Jaquet. Genetic Restrictive Cardiomyopathy: Causes and Consequences—An Integrative Approach. International Journal of Molecular Sciences 2021; 22(2) doi: 10.3390/ijms22020558
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| 14 |
Thomas D. Ryan, Steven J. Kindel, Matthew J. O’Connor. Heart Failure in the Child and Young Adult. 2018; doi: 10.1016/B978-0-12-802393-8.00029-6
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| 15 |
Diana Cimiotti, Seyyed-Reza Sadat-Ebrahimi, Andreas Mügge, Kornelia Jaquet. New Insights on Cardiomyopathy. 2024; doi: 10.5772/intechopen.109896
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| 16 |
Stephanie M. Ware. Evaluation of genetic causes of cardiomyopathy in childhood. Cardiology in the Young 2015; 25(S2) doi: 10.1017/S1047951115000827
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| 17 |
Mohammed Shahab Uddin, Fayez AlShammari, Amr Esmail, Khaled Shafeen, Fahad Alnajim, Danah AlMohaimeed, Nujud Alessa, Wojod Alothman, Fay Aldenaini, Karthiga Gurumurthy, Maryam AlQannas. Rapidly Progressive Infantile Dilated Cardiomyopathy in Long–Olsen–Distelmaier Syndrome Associated with RRAGC NM_022157.4:c.343T>C, p.(Trp115Arg): A Case Report. Genes 2026; 17(9) doi: 10.3390/genes17091106
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| 18 |
Hamza El Hadi, Anne Freund, Steffen Desch, Holger Thiele, Nicolas Majunke. Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We?. Biomedicines 2023; 11(2) doi: 10.3390/biomedicines11020524
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| 19 |
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 Cardiomyopathy. Journal of the American College of Cardiology 2016; 67(5) doi: 10.1016/j.jacc.2015.10.093
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| 20 |
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 Cardiomyopathy. Circulation Journal 2021; 85(5) doi: 10.1253/circj.CJ-20-1008
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| 21 |
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 cardiomyopathy. American Journal of Medical Genetics Part A 2019; 179(4) doi: 10.1002/ajmg.a.61072
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| 22 |
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) doi: 10.1016/j.ppedcard.2015.01.008
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| 23 |
Dong Li, Ce Wang. Advances in symptomatic therapy for left ventricular non-compaction in children. Frontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1147362
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| 24 |
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 cardiomyopathy. PLOS ONE 2022; 17(9) doi: 10.1371/journal.pone.0275296
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| 25 |
Gulsah Yildirim, Memduh Dursun, Rıfat Arslan. Effect of trabeculated myocardial mass on left ventricle global and regional functions in noncompaction cardiomyopathy. World Journal of Cardiology 2021; 13(7): 211-222 doi: 10.4330/wjc.v13.i7.211
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| 26 |
Jeffrey Schubert, Muhammad Tariq, Gabrielle Geddes, Steven Kindel, Erin M. Miller, Stephanie M. Ware. Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy. Human Mutation 2018; 39(12) doi: 10.1002/humu.23661
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| 27 |
K. Wahbi, D. Bonnet. Transition et cardiomyopathies familiales. Archives des Maladies du Coeur et des Vaisseaux - Pratique 2021; 2021(297) doi: 10.1016/j.amcp.2021.01.008
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| 28 |
Stephanie M. Ware. Pediatric cardiomyopathy and the PCM Genes study: A summary with insights on genetic testing, variant interpretation, race and ethnicity. Progress in Pediatric Cardiology 2021; 63 doi: 10.1016/j.ppedcard.2021.101468
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| 29 |
Hugo R. Martinez, Gary S. Beasley, John Jefferies, Jeffrey A. Towbin. Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care. 2021; doi: 10.1007/978-1-4471-4999-6_89-2
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| 30 |
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 Children. 2019; doi: 10.1016/B978-1-4557-0760-7.00072-3
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| 31 |
Evan M. Harvey, Murad Almasri, Hugo R. Martinez. Cardiomyopathy - Disease of the Heart Muscle. 2021; doi: 10.5772/intechopen.97010
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| 32 |
Tony L. Brown, Theresa M. Meloche. Exome sequencing a review of new strategies for rare genomic disease research. Genomics 2016; 108(3-4) doi: 10.1016/j.ygeno.2016.06.003
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| 33 |
Franklyn P. Cladis, Brian Blasiole, Martin B. Anixter, James Gordon Cain, Peter J. Davis. A Practice of Anesthesia for Infants and Children. 2019; doi: 10.1016/B978-0-323-42974-0.00031-8
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| 34 |
Elise L. Kessler, Peter GJ Nikkels, Toon AB van Veen. Disturbed Desmoglein-2 in the intercalated disc of pediatric patients with dilated cardiomyopathy. Human Pathology 2017; 67 doi: 10.1016/j.humpath.2017.07.012
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| 35 |
Chalani D. Ellepola, Linda M. Knight, Peter Fischbach, Shriprasad R. Deshpande. Genetic Testing in Pediatric Cardiomyopathy. Pediatric Cardiology 2018; 39(3) doi: 10.1007/s00246-017-1779-2
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| 36 |
Hugo R. Martinez, Stephanie M. Ware, Marcus S. Schamberger, John J. Parent. Noncompaction cardiomyopathy and heterotaxy syndrome. Progress in Pediatric Cardiology 2017; 46 doi: 10.1016/j.ppedcard.2017.06.007
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| 37 |
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 Report. Genes 2023; 14(6) doi: 10.3390/genes14061177
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| 38 |
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> Mutation. Cardiology 2017; 137(3) doi: 10.1159/000465516
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| 39 |
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 cardiomyopathy. Molecular Case Studies 2017; 3(6) doi: 10.1101/mcs.a002055
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| 40 |
Svetlana Fetisova, Olesya Melnik, Elena Vasichkina, Tatyana Vershinina, Olga Kofeynikova, Alexandra Kozyreva, Yulia Fomicheva, Polina Sokolnikova, Sergey Zhuk, Tatyana Pervunina, Anna Kostareva. The clinical and genetic spectrum of pediatric hypertrophic cardiomyopathy manifesting before one year of age. Pediatric Research 2025; 98(4) doi: 10.1038/s41390-025-03989-z
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| 41 |
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 Cardiomyopathy. Journal of Cardiovascular Translational Research 2023; 16(6) doi: 10.1007/s12265-023-10461-y
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| 42 |
Hugo R. Martinez, Gary S. Beasley, Noah Miller, Jason F. Goldberg, John L. Jefferies. Clinical Insights Into Heritable Cardiomyopathies. Frontiers in Genetics 2021; 12 doi: 10.3389/fgene.2021.663450
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| 43 |
Hidekazu Ishida. Idiopathic Restrictive Cardiomyopathy in Children. Pediatric Cardiology and Cardiac Surgery 2021; 37(3) doi: 10.9794/jspccs.37.184
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| 44 |
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 cardiomyopathy. The American Journal of Human Genetics 2022; 109(2) doi: 10.1016/j.ajhg.2021.12.006
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