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ISSN 2574-8300

61. Clinical Characteristics of SCN5A p.R965C Carriers: A Common Founder Variant Predisposing to Brugada Syndrome in Thailand. (June 2021)

Authors:
Chimparlee, Nitinan; Prechawat, Somchai; Khongphatthanayothin, Apichai; Mauleekoonphairoj, John; Lekchuensakul, Sarin; Wongcharoen, Wanwarang; Makarawate, Pattarapong; Sahasatas, Dujdao; Krittayaphong, Rungroj; Amnueypol, Montawatt; Anannab, Alisara; Ngarmukos, Tachapong; Vardhanabhuti, Saran; Su...
Journal:
Circulation
Issue:
Volume 14:Number 3(2021)
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Journal Article
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63. Clinical Findings and Diagnostic Yield of Arrhythmogenic Cardiomyopathy Through Genomic Screening of Pathogenic or Likely Pathogenic Desmosome Gene Variants. (19th April 2021)

Authors:
Carruth, Eric D.; Beer, Dominik; Alsaid, Amro; Schwartz, Marci L.B.; McMinn, Megan; Kelly, Melissa A.; Buchanan, Adam H.; Nevius, Christopher D.; Calkins, Hugh; James, Cynthia A.; Murray, Brittney; Tichnell, Crystal; Matsumura, Martin E.; Kirchner, H. Lester; Fornwalt, Brandon K.; Sturm, Amy C.; ...
Journal:
Circulation
Issue:
Volume 14:Number 2(2021)
Page Start:
e003302
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Journal Article
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64. Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot. (30th July 2021)

Authors:
Reuter, Miriam S.; Chaturvedi, Rajiv R.; Jobling, Rebekah K.; Pellecchia, Giovanna; Hamdan, Omar; Sung, Wilson W.L.; Nalpathamkalam, Thomas; Attaluri, Pratyusha; Silversides, Candice K.; Wald, Rachel M.; Marshall, Christian R.; Williams, Simon G.; Keavney, Bernard D.; Thiruvahindrapuram, Bhooma; ...
Journal:
Circulation
Issue:
Volume 14:Number 4(2021)
Page Start:
e003410
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Journal Article
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65. Clinical Impact of Copy Number Variation on the Genetic Diagnosis of Syndromic Aortopathies. (30th July 2021)

Authors:
Takeda, Norifumi; Inuzuka, Ryo; Yagi, Hiroki; Morita, Hiroyuki; Ando, Masahiko; Yamauchi, Haruo; Taniguchi, Yuki; Porto, Kristine Joyce; Kanaya, Tsubasa; Ishiura, Hiroyuki; Mitsui, Jun; Tsuji, Shoji; Toda, Tatsushi; Ono, Minoru; Komuro, Issei
Journal:
Circulation
Issue:
Volume 14:Number 4(2021)
Page Start:
e003458
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Journal Article
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67. Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population. (1st February 2022)

Authors:
Paludan-Müller, Christian; Larsen, Simon; Ahlberg, Gustav; Andreasen, Laura; Monfort, Laia M.; Svendsen, Jesper H.; Jespersen, Thomas; Bundgaard, Henning; Kanters, Jørgen K.; Olesen, Morten S.
Journal:
Circulation
Issue:
Volume 15:Number 1(2022)
Page Start:
e003574
Record Type:
Journal Article
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68. Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population. (February 2022)

Authors:
Paludan-Müller, Christian; Larsen, Simon; Ahlberg, Gustav; Andreasen, Laura; Monfort, Laia M.; Svendsen, Jesper H.; Jespersen, Thomas; Bundgaard, Henning; Kanters, Jørgen K.; Olesen, Morten S.
Journal:
Circulation
Issue:
Volume 15:Number 1(2022)
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Journal Article
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69. Clinical Outcomes and Sustainability of Using CYP2C19 Genotype–Guided Antiplatelet Therapy After Percutaneous Coronary Intervention. (April 2018)

Authors:
Lee, Craig R.; Sriramoju, Vindhya B.; Cervantes, Alexandra; Howell, Lucius A.; Varunok, Nicholas; Madan, Shivanshu; Hamrick, Kasey; Polasek, Melissa J.; Lee, John Andrew; Clarke, Megan; Cicci, Jonathan D.; Weck, Karen E.; Stouffer, George A.
Journal:
Circulation
Issue:
Volume 11:Number 4(2018)
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Journal Article
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70. Clinical Profile of Cardiac Involvement in Danon Disease: A Multicenter European Registry. (December 2020)

Authors:
Lotan, Dor; Salazar-Mendiguchía, Joel; Mogensen, Jens; Rathore, Faizan; Anastasakis, Aris; Kaski, Juan; Garcia-Pavia, Pablo; Olivotto, Iacopo; Charron, Philippe; Biagini, Elena; Baban, Anwar; Limongelli, Giuseppe; Ashram, Waddah; Wasserstrum, Yishay; Galvin, Joseph; Zorio, Esther; Iacovoni, Attil...
Journal:
Circulation
Issue:
Volume 13:Number 6(2020)
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Journal Article
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