What do we do and how do we do it? Assessing genetic counselling in the modern era

por Yeates, Laura, McEwen, Alison, Ingles, Jodie
Publicado 2020

Infusion of Sibling Marrow in a Patient with Purine Nucleoside Phosphorylase Deficiency Leads to Split Mixed Donor Chimerism and Normal Immunity

por Yeates, Laura, Slatter, Mary A., Gennery, Andrew R.
Publicado 2017

Evaluating a custom-designed aid to improve communication of genetic results in families with hypertrophic cardiomyopathy: study protocol for a randomised controlled trial

por Burns, Charlotte, Yeates, Laura, Semsarian, Christopher, Ingles, Jodie
Publicado 2019

Needs analysis of parents following sudden cardiac death in the young

por McDonald, Kristie, Sharpe, Louise, Yeates, Laura, Semsarian, Christopher, Ingles, Jodie
Publicado 2020

Diabetes and the Metabolic Syndrome: Possibilities of a New Breath Test in a Dolphin Model

por Schivo, Michael, Aksenov, Alexander A., Yeates, Laura C., Pasamontes, Alberto, Davis, Cristina E.
Publicado 2013

Holt-Oram syndrome in two families diagnosed with left ventricular noncompaction and conduction disease

por Ross, Samantha Barratt, Bagnall, Richard D., Yeates, Laura, Sy, Raymond W., Semsarian, Christopher
Publicado 2018

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

por Puranik, Rajesh, Gray, Belinda, Lackey, Helen, Yeates, Laura, Parker, Geoffrey, Duflou, Johan, Semsarian, Christopher
Publicado 2014

Rare desmin variant causing penetrant life-threatening arrhythmic cardiomyopathy

por Oomen, Ad W.G.J., Jones, Katherine, Yeates, Laura, Semsarian, Christopher, Ingles, Jodie, Sy, Raymond W.
Publicado 2018

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

por Yeates, Laura, Gardner, Karen, Do, Judy, van den Heuvel, Lieke, Fleming, Gabrielle, Semsarian, Christopher, McEwen, Alison, Adlard, Leesa, Ingles, Jodie
Publicado 2022

Longitudinal assessment of structural phenotype in Brugada syndrome using cardiac magnetic resonance imaging

por Isbister, Julia C., Gray, Belinda, Offen, Sophie, Yeates, Laura, Naoum, Chris, Medi, Caroline, Raju, Hariharan, Semsarian, Christopher, Puranik, Rajesh, Sy, Raymond W.
Publicado 2022

The Australian Genetic Heart Disease Registry: Protocol for a Data Linkage Study

por Butters, Alexandra, Blanch, Bianca, Kemp-Casey, Anna, Do, Judy, Yeates, Laura, Leslie, Felicity, Semsarian, Christopher, Nedkoff, Lee, Briffa, Tom, Ingles, Jodie, Sweeting, Joanna
Publicado 2023

Metabolite Content Profiling of Bottlenose Dolphin Exhaled Breath

por Aksenov, Alexander A., Yeates, Laura, Pasamontes, Alberto, Siebe, Craig, Zrodnikov, Yuriy, Simmons, Jason, McCartney, Mitchell M., Deplanque, Jean-Pierre, Wells, Randall S., Davis, Cristina E.
Publicado 2014

Preclinical alterations in cardiac energetics amongst sarcomere mutation carriers in hypertrophic cardiomyopathy

por Lloyd, Rachael, Grover, Suchi, Parnham, Susie F, Lou, Pey Wen, Bradbrook, Craig, Yeates, Laura, Correnti, Gemma, Haan, Eric, Atherton, John J, Semsarian, Christopher, Selvanayagam, Joseph
Publicado 2015

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

por 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.
Publicado 2018

Genetic architecture of left ventricular noncompaction in adults

por 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
Publicado 2020

A prospective longitudinal study of health-related quality of life and psychological wellbeing after an implantable cardioverter-defibrillator in patients with genetic heart diseas...

por van den Heuvel, Lieke M., Sarina, Tanya, Sweeting, Joanna, Yeates, Laura, Bates, Kezia, Spinks, Catherine, O’Donnell, Catherine, Sears, Samuel F., McGeechan, Kevin, Semsarian, Christopher, Ingles, Jodie
Publicado 2022

The burden of splice-disrupting variants in inherited heart disease and unexplained sudden cardiac death

por Singer, Emma S., Crowe, Joshua, Holliday, Mira, Isbister, Julia C., Lal, Sean, Nowak, Natalie, Yeates, Laura, Burns, Charlotte, Rajagopalan, Sulekha, Macciocca, Ivan, King, Ingrid, Wacker, Julie, Ingles, Jodie, Weintraub, Robert G., Semsarian, Christopher, Bagnall, Richard D.
Publicado 2023

Overcoming the challenges of studying conservation physiology in large whales: a review of available methods

por Hunt, Kathleen E., Moore, Michael J., Rolland, Rosalind M., Kellar, Nicholas M., Hall, Ailsa J., Kershaw, Joanna, Raverty, Stephen A., Davis, Cristina E., Yeates, Laura C., Fauquier, Deborah A., Rowles, Teresa K., Kraus, Scott D.
Publicado 2013

The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic

por Stafford, Fergus, Krishnan, Neesha, Richardson, Ebony, Butters, Alexandra, Hespe, Sophie, Burns, Charlotte, Gray, Belinda, Medi, Caroline, Nowak, Natalie, Isbister, Julia C., Raju, Hariharan, Richmond, David, Ryan, Mark P., Singer, Emma S., Sy, Raymond W., Yeates, Laura, Bagnall, Richard D., Semsarian, Christopher, Ingles, Jodie
Publicado 2022

Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant

por Hoorntje, Edgar T., Burns, Charlotte, Marsili, Luisa, Corden, Ben, Parikh, Victoria N., te Meerman, Gerard J., Gray, Belinda, Adiyaman, Ahmet, Bagnall, Richard D., Barge-Schaapveld, Daniela Q.C.M., van den Berg, Maarten P., Bootsma, Marianne, Bosman, Laurens P., Correnti, Gemma, Duflou, Johan, Eppinga, Ruben N., Fatkin, Diane, Fietz, Michael, Haan, Eric, Jongbloed, Jan D.H., Hauer, Arnaud D., Lam, Lien, van Lint, Freyja H.M., Lota, Amrit, Marcelis, Carlo, McCarthy, Hugh J., van Mil, Anneke M., Oldenburg, Rogier A., Pachter, Nicholas, Planken, R. Nils, Reuter, Chloe, Semsarian, Christopher, van der Smagt, Jasper J., Thompson, Tina, Vohra, Jitendra, Volders, Paul G.A., van Waning, Jaap I., Whiffin, Nicola, van den Wijngaard, Arthur, Amin, Ahmad S., Wilde, Arthur A.M., van Woerden, Gijs, Yeates, Laura, Zentner, Dominica, Ashley, Euan A., Wheeler, Matthew T., Ware, James S., van Tintelen, J. Peter, Ingles, Jodie
Publicado 2022