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ArticlesPeer ReviewedFull Text
Dilated cardiomyopathy
Author / Creator:Weintraub, Robert G, Dr ; Semsarian, Christopher, Prof ; Macdonald, Peter, MD
Publisher:England: Elsevier Ltd
Journal title:The Lancet (British edition), 2017-07, Vol.390 (10092), p.400-414
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Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study
Author / Creator:Yeates, Laura ; McDonald, Kristie ; Burns, Charlotte ; Semsarian, Christopher ; Carter, Stacy ; Ingles, Jodie
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2022-02, Vol.30 (2), p.187-193
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A Prospective Study of Sudden Cardiac Death among Children and Young Adults
Author / Creator:Bagnall, Richard D ; Weintraub, Robert G ; Ingles, Jodie ; Duflou, Johan ; Yeates, Laura ; Lam, Lien ; Davis, Andrew M ; Thompson, Tina ; Connell, Vanessa ; Wallace, Jennie ; Naylor, Charles ; Crawford, Jackie ; Love, Donald R ; Hallam, Lavinia ; White, Jodi ; Lawrence, Christopher ; Lynch, Matthew ; Morgan, Natalie ; James, Paul ; du Sart, Desirée ; Puranik, Rajesh ; Langlois, Neil ; Vohra, Jitendra ; Winship, Ingrid ; Atherton, John ; McGaughran, Julie ; Skinner, Jonathan R ; Semsarian, Christopher
Publisher:United States: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2016-06, Vol.374 (25), p.2441-2452
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Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel
Author / Creator:Kelly, Melissa A ; Caleshu, Colleen ; Morales, Ana ; Buchan, Jillian ; Wolf, Zena ; Harrison, Steven M ; Cook, Stuart ; Dillon, Mitchell W ; Garcia, John ; Haverfield, Eden ; Jongbloed, Jan D H ; Macaya, Daniela ; Manrai, Arjun ; Orland, Kate ; Richard, Gabriele ; Spoonamore, Katherine ; Thomas, Matthew ; Thomson, Kate ; Vincent, Lisa M ; Walsh, Roddy ; Watkins, Hugh ; Whiffin, Nicola ; Ingles, Jodie ; van Tintelen, J Peter ; Semsarian, Christopher ; Ware, James S ; Hershberger, Ray ; Funke, Birgit
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2018-03, Vol.20 (3), p.351-359
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Perceptions of genetic variant reclassification in patients with inherited cardiac disease
Author / Creator:Wong, Eugene K. ; Bartels, Kirsten ; Hathaway, Julie ; Burns, Charlotte ; Yeates, Laura ; Semsarian, Christopher ; Krahn, Andrew D. ; Virani, Alice ; Ingles, Jodie
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2019-07, Vol.27 (7), p.1134-1142
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ArticlesPeer ReviewedFull Text
Molecular autopsy in victims of inherited arrhythmias
Author / Creator:Semsarian, Christopher, MBBS, PhD, MPH ; Ingles, Jodie, BBiomedSci, GradDipGenCouns, PhD, MPH
Publisher:Japan: John Wiley & Sons, Inc
Journal title:Journal of arrhythmia, 2016-10, Vol.32 (5), p.359-365
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Prognostic impact of atrial fibrillation in hypertrophic cardiomyopathy: a systematic review
Author / Creator:Alphonse, Patricia ; Virk, Sohaib ; Collins, Jhonna ; Campbell, Timothy ; Thomas, Stuart P. ; Semsarian, Christopher ; Kumar, Saurabh
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Clinical research in cardiology, 2021-04, Vol.110 (4), p.544-554
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Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death
Author / Creator:Singer, Emma S. ; Ross, Samantha B. ; Skinner, Jon R. ; Weintraub, Robert G. ; Ingles, Jodie ; Semsarian, Christopher ; Bagnall, Richard D.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2021-01, Vol.23 (1), p.86-93
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Genetic architecture of left ventricular noncompaction in adults
Author / Creator:Ross, Samantha Barratt ; Singer, Emma S. ; Driscoll, Elizabeth ; Nowak, Natalie ; Yeates, Laura ; Puranik, Rajesh ; Sy, Raymond W. ; Rajagopalan, Sulekha ; Barratt, Alexandra ; Ingles, Jodie ; Bagnall, Richard D. ; Semsarian, Christopher
Publisher:London: Nature Publishing Group UK
Journal title:Human genome variation, 2020-10, Vol.7 (1), p.33-33, Article 33
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Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy
Author / Creator:Ingles, Jodie ; Sarina, Tanya ; Yeates, Laura ; Hunt, Lauren ; Macciocca, Ivan ; McCormack, Louise ; Winship, Ingrid ; McGaughran, Julie ; Atherton, John ; Semsarian, Christopher
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2013-12, Vol.15 (12), p.972-977
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ArticlesPeer ReviewedFull Text
Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment
Author / Creator:Das K, Jipin ; Ingles, Jodie ; Bagnall, Richard D. ; Semsarian, Christopher
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2014-04, Vol.16 (4), p.286-293
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Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy
Author / Creator:Minoche, Andre E. ; Horvat, Claire ; Johnson, Renee ; Gayevskiy, Velimir ; Morton, Sarah U. ; Drew, Alexander P. ; Woo, Kerhan ; Statham, Aaron L. ; Lundie, Ben ; Bagnall, Richard D. ; Ingles, Jodie ; Semsarian, Christopher ; Seidman, J. G. ; Seidman, Christine E. ; Dinger, Marcel E. ; Cowley, Mark J. ; Fatkin, Diane
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2019-03, Vol.21 (3), p.650-662
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ArticlesPeer ReviewedFull Text
Global MicroRNA Profiling of the Mouse Ventricles during Development of Severe Hypertrophic Cardiomyopathy and Heart Failure
Author / Creator:Bagnall, Richard D. ; Tsoutsman, Tatiana ; Shephard, Rhian E. ; Ritchie, William ; Semsarian, Christopher
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-09, Vol.7 (9), p.e44744-e44744
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An ALPK3 truncation variant causing autosomal dominant hypertrophic cardiomyopathy is partially rescued by mavacamten
Author / Creator:Leinhos, Lisa ; Robinson, Paul ; Poloni, Giulia ; Broadway-Stringer, Sophie ; Beglov, Julia ; Lokman, Adam B. ; Douglas, Gillian ; Nuthay, Sajjad ; Fonseka, Oveena ; Schmid, Manuel ; Singer, Evie ; Hooper, Charlotte ; Thomson, Kate ; Bagnall, Richard D. ; Ingles, Jodie ; Semsarian, Christopher ; Ormondroyd, Elizabeth ; Toepfer, Christopher N. ; Davies, Benjamin ; Redwood, Charles ; Watkins, Hugh ; Gehmlich, Katja
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2025-03, Vol.15 (1), p.10090-14, Article 10090
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Cytoskeletal disarray increases arrhythmogenic vulnerability during sympathetic stimulation in a model of hypertrophic cardiomyopathy
Author / Creator:Cserne Szappanos, Henrietta ; Viola, Helena M. ; Ito, Danica W. ; Lim, Seakcheng ; Mangala, Melissa ; Holliday, Mira ; Barratt Ross, Samantha ; Semsarian, Christopher ; Hill, Adam ; Dixon, Rose E. ; Hool, Livia C.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2023-07, Vol.13 (1), p.11296-11296, Article 11296
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Cardiovascular genomics and sudden cardiac death in the young
Author / Creator:Isbister, Julia ; Semsarian, Christopher
Publisher:Sydney: Royal Australian College of General Practitioners
Journal title:Australian journal of general practice, 2019-03, Vol.48 (3), p.90-95
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Using codesign focus groups to develop an online COmmunity suPporting familiEs after Sudden Cardiac Death (COPE-SCD) in the young
Author / Creator:Yeates, Laura ; Gardner, Karen ; Do, Judy ; van den Heuvel, Lieke ; Fleming, Gabrielle ; Semsarian, Christopher ; McEwen, Alison ; Adlard, Leesa ; Ingles, Jodie
Publisher:London: British Medical Journal Publishing Group
Journal title:BMJ open, 2022-08, Vol.12 (8), p.e053785
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Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome
Author / Creator:Gray, Belinda ; Gnanappa, Ganesh Kumar ; Bagnall, Richard D. ; Femia, Giuseppe ; Yeates, Laura ; Ingles, Jodie ; Burns, Charlotte ; Puranik, Rajesh ; Grieve, Stuart M. ; Semsarian, Christopher ; Sy, Raymond W.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2018-04, Vol.13 (4), p.e0195594-e0195594
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Risk of Sudden Death and Outcome in Patients With Hypertrophic Cardiomyopathy With Benign Presentation and Without Risk Factors
Author / Creator:Spirito, Paolo, MD ; Autore, Camillo, MD ; Formisano, Francesco, MD ; Assenza, Gabriele Egidy, MD ; Biagini, Elena, MD ; Haas, Tammy S., RN ; Bongioanni, Sergio, MD ; Semsarian, Christopher, MD ; Devoto, Emmanuela, MD ; Musumeci, Beatrice, MD ; Lai, Francesco, MD ; Yeates, Laura, BSc ; Conte, Maria Rosa, MD ; Rapezzi, Claudio, MD ; Boni, Luca, MD ; Maron, Barry J., MD
Publisher:United States: Elsevier Inc
Journal title:The American journal of cardiology, 2014-05, Vol.113 (9), p.1550-1555
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Comparison of conventional autopsy and magnetic resonance imaging in determining the cause of sudden death in the young
Author / Creator:Puranik, Rajesh ; Gray, Belinda ; Lackey, Helen ; Yeates, Laura ; Parker, Geoffrey ; Duflou, Johan ; Semsarian, Christopher
Publisher:England: BioMed Central Ltd
Journal title:Journal of cardiovascular magnetic resonance, 2014-06, Vol.16 (1), p.44-44, Article 44
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Showing 1 to 20 of 116 results

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Dilated cardiomyopathy

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Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study

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A Prospective Study of Sudden Cardiac Death among Children and Young Adults

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Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel

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Perceptions of genetic variant reclassification in patients with inherited cardiac disease

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Molecular autopsy in victims of inherited arrhythmias

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Prognostic impact of atrial fibrillation in hypertrophic cardiomyopathy: a systematic review

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Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death

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Genetic architecture of left ventricular noncompaction in adults

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Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy

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Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment

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Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy

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Global MicroRNA Profiling of the Mouse Ventricles during Development of Severe Hypertrophic Cardiomyopathy and Heart Failure

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An ALPK3 truncation variant causing autosomal dominant hypertrophic cardiomyopathy is partially rescued by mavacamten

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Cytoskeletal disarray increases arrhythmogenic vulnerability during sympathetic stimulation in a model of hypertrophic cardiomyopathy

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Cardiovascular genomics and sudden cardiac death in the young

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Using codesign focus groups to develop an online COmmunity suPporting familiEs after Sudden Cardiac Death (COPE-SCD) in the young

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Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome

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Risk of Sudden Death and Outcome in Patients With Hypertrophic Cardiomyopathy With Benign Presentation and Without Risk Factors

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Comparison of conventional autopsy and magnetic resonance imaging in determining the cause of sudden death in the young

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