New Perspectives on the Prevalence of Hypertrophic Cardiomyopathy von Semsarian, Christopher, MBBS, PhD, MPH, Ingles, Jodie, GradDipGenCouns, PhD, MPH, Maron, Martin S., MD, Maron, Barry J., MD

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Time to Rethink the Genetic Architecture of Long QT Syndrome von Ingles, Jodie, Semsarian, Christopher

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Nonfamilial Hypertrophic Cardiomyopathy von Ingles Jodie, Burns, Charlotte, Bagnall, Richard D, Lam, Lien, Yeates, Laura, Sarina Tanya, Puranik Rajesh, Briffa, Tom, Atherton, John J, Driscoll, Tim, Semsarian Christopher

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Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study von Yeates, Laura, McDonald, Kristie, Burns, Charlotte, Semsarian, Christopher, Carter, Stacy, Ingles, Jodie

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

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Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing von Burns, Charlotte, Bagnall, Richard D, Lam, Lien, Semsarian, Christopher, Ingles, Jodie

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What do we do and how do we do it? Assessing genetic counselling in the modern era von Yeates, Laura, McEwen, Alison, Ingles, Jodie

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Conveying a probabilistic genetic test result to families with an inherited heart disease von Ingles, Jodie, BBiomedSc, GradDipGenCouns, PhD, Semsarian, Christopher, MBBS, PhD, FHRS

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Posttraumatic Stress and Prolonged Grief After the Sudden Cardiac Death of a Young Relative von Ingles, Jodie, Spinks, Catherine, Yeates, Laura, McGeechan, Kevin, Kasparian, Nadine, Semsarian, Christopher

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Recommendations for clinical interpretation of variants found in non-coding regions of the genome von Ellingford, Jamie M, Ahn, Joo Wook, Bagnall, Richard D, Baralle, Diana, Barton, Stephanie, Campbell, Chris, Downes, Kate, Ellard, Sian, Duff-Farrier, Celia, FitzPatrick, David R, Greally, John M, Ingles, Jodie, Krishnan, Neesha, Lord, Jenny, Martin, Hilary C, Newman, William G, O'Donnell-Luria, Anne, Ramsden, Simon C, Rehm, Heidi L, Richardson, Ebony, Singer-Berk, Moriel, Taylor, Jenny C, Williams, Maggie, Wood, Jordan C, Wright, Caroline F, Harrison, Steven M, Whiffin, Nicola

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Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions von Zhang, Xiaolei, Walsh, Roddy, Whiffin, Nicola, Buchan, Rachel, Midwinter, William, Wilk, Alicja, Govind, Risha, Li, Nicholas, Ahmad, Mian, Mazzarotto, Francesco, Roberts, Angharad, Theotokis, Pantazis I., Mazaika, Erica, Allouba, Mona, de Marvao, Antonio, Pua, Chee Jian, Day, Sharlene M., Ashley, Euan, Colan, Steven D., Michels, Michelle, Pereira, Alexandre C., Jacoby, Daniel, Ho, Carolyn Y., Olivotto, Iacopo, Gunnarsson, Gunnar T., Jefferies, John L., Semsarian, Chris, Ingles, Jodie, O’Regan, Declan P., Aguib, Yasmine, Yacoub, Magdi H., Cook, Stuart A., Barton, Paul J.R., Bottolo, Leonardo, Ware, James S.

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Molecular autopsy in victims of inherited arrhythmias von Semsarian, Christopher, MBBS, PhD, MPH, Ingles, Jodie, BBiomedSci, GradDipGenCouns, PhD, MPH

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Perceptions of genetic variant reclassification in patients with inherited cardiac disease von Wong, Eugene K, Bartels, Kirsten, Hathaway, Julie, Burns, Charlotte, Yeates, Laura, Semsarian, Christopher, Krahn, Andrew D, Virani, Alice, Ingles, Jodie

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Genetic architecture of left ventricular noncompaction in adults von 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

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Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes von Ingles, Jodie, Goldstein, Jennifer, Thaxton, Courtney, Caleshu, Colleen, Corty, Edward W, Crowley, Stephanie B, Dougherty, Kristen, Harrison, Steven M, McGlaughon, Jennifer, Milko, Laura V, Morales, Ana, Seifert, Bryce A, Strande, Natasha, Thomson, Kate, Peter van Tintelen, J, Wallace, Kathleen, Walsh, Roddy, Wells, Quinn, Whiffin, Nicola, Witkowski, Leora, Semsarian, Christopher, Ware, James S, Hershberger, Ray E, Funke, Birgit

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Hypertrophic Cardiomyopathy: Genetic Testing and Risk Stratification von Stafford, Fergus, Thomson, Kate, Butters, Alexandra, Ingles, Jodie

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The emerging role of the cardiac genetic counselor von Ingles, Jodie, BBiomedSc, GradDipGenCouns, Yeates, Laura, BSc, GradDipGenCouns, Semsarian, Christopher, MBBS, PhD

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Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death von Singer, Emma S., Ross, Samantha B., Skinner, Jon R., Weintraub, Robert G., Ingles, Jodie, Semsarian, Christopher, Bagnall, Richard D.

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Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy von Ingles, Jodie, Sarina, Tanya, Yeates, Laura, Hunt, Lauren, Macciocca, Ivan, McCormack, Louise, Winship, Ingrid, McGaughran, Julie, Atherton, John, Semsarian, Christopher

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Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment von Das K, Jipin, Ingles, Jodie, Bagnall, Richard D., Semsarian, Christopher

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