Nonfamilial Hypertrophic Cardiomyopathy
Ingles Jodie, Burns, Charlotte, Bagnall, Richard D, Lam, Lien, Yeates, Laura, Sarina Tanya, Puranik Rajesh, Briffa, Tom, Atherton, John J, Driscoll, Tim, Semsarian Christopher
Published in Circulation. Cardiovascular genetics (01.04.2017)
Published in Circulation. Cardiovascular genetics (01.04.2017)
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Journal Article
Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study
Yeates, Laura, McDonald, Kristie, Burns, Charlotte, Semsarian, Christopher, Carter, Stacy, Ingles, Jodie
Published in European journal of human genetics : EJHG (01.02.2022)
Published in European journal of human genetics : EJHG (01.02.2022)
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Journal Article
What do we do and how do we do it? Assessing genetic counselling in the modern era
Yeates, Laura, McEwen, Alison, Ingles, Jodie
Published in European journal of human genetics : EJHG (01.09.2020)
Published in European journal of human genetics : EJHG (01.09.2020)
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Journal Article
A Prospective Study of Sudden Cardiac Death among Children and Young Adults
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
Published in The New England journal of medicine (23.06.2016)
Published in The New England journal of medicine (23.06.2016)
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Journal Article
Recommendations for clinical interpretation of variants found in non-coding regions of the genome
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
Published in Genome medicine (19.07.2022)
Published in Genome medicine (19.07.2022)
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Journal Article
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions
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.
Published in Genetics in medicine (01.01.2021)
Published in Genetics in medicine (01.01.2021)
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Journal Article
Hypertrophic Cardiomyopathy: Genetic Testing and Risk Stratification
Stafford, Fergus, Thomson, Kate, Butters, Alexandra, Ingles, Jodie
Published in Current cardiology reports (01.02.2021)
Published in Current cardiology reports (01.02.2021)
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Journal Article
Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes
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
Published in Circulation. Genomic and precision medicine (01.02.2019)
Published in Circulation. Genomic and precision medicine (01.02.2019)
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Journal Article
Molecular autopsy in victims of inherited arrhythmias
Semsarian, Christopher, MBBS, PhD, MPH, Ingles, Jodie, BBiomedSci, GradDipGenCouns, PhD, MPH
Published in Journal of arrhythmia (01.10.2016)
Published in Journal of arrhythmia (01.10.2016)
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Journal Article
The emerging role of the cardiac genetic counselor
Ingles, Jodie, BBiomedSc, GradDipGenCouns, Yeates, Laura, BSc, GradDipGenCouns, Semsarian, Christopher, MBBS, PhD
Published in Heart rhythm (01.12.2011)
Published in Heart rhythm (01.12.2011)
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Journal Article
Perceptions of genetic variant reclassification in patients with inherited cardiac disease
Wong, Eugene K, Bartels, Kirsten, Hathaway, Julie, Burns, Charlotte, Yeates, Laura, Semsarian, Christopher, Krahn, Andrew D, Virani, Alice, Ingles, Jodie
Published in European journal of human genetics : EJHG (01.07.2019)
Published in European journal of human genetics : EJHG (01.07.2019)
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Journal Article
Genetic architecture of left ventricular noncompaction in adults
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
Published in Human genome variation (15.10.2020)
Published in Human genome variation (15.10.2020)
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Journal Article
Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death
Singer, Emma S., Ross, Samantha B., Skinner, Jon R., Weintraub, Robert G., Ingles, Jodie, Semsarian, Christopher, Bagnall, Richard D.
Published in Genetics in medicine (01.01.2021)
Published in Genetics in medicine (01.01.2021)
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Journal Article
Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy
Ingles, Jodie, Sarina, Tanya, Yeates, Laura, Hunt, Lauren, Macciocca, Ivan, McCormack, Louise, Winship, Ingrid, McGaughran, Julie, Atherton, John, Semsarian, Christopher
Published in Genetics in medicine (01.12.2013)
Published in Genetics in medicine (01.12.2013)
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