Items where Author is "Ingles, Jodie"

Article

Paratz, Elizabeth D. and Jennings, Garry and Timbs, Susan and Bray, Janet E. and Ingles, Jodie and Page, Greg and Vandenberg, Jamie and La Gerche, Andre (2025) Cardiac arrest in Australia: a call to action. Australian Health Review, 49 (2). ISSN 0156-5788

La Gerche, Andre and Paratz, Elizabeth D. and Bray, Janet E. and Jennings, Garry and Page, Greg and Timbs, Susan and Vandenberg, Jamie I. and Abhayaratna, Walter and Chow, Clara K. and Dennis, Mark and Figtree, Gemma A. and Kovacic, Jason C. and Maris, Jessica and Nehme, Ziad and Parsons, Sarah and Pflaumer, Andreas and Puranik, Rajesh and Stub, Dion and Freitas, Edwin and Zecchin, Robert and Cartledge, Susie and Haskins, Brian and Ingles, Jodie (2024) A Call to Action to Improve Cardiac Arrest Outcomes: A Report From the National Summit for Cardiac Arrest. Heart, Lung and Circulation, 33 (11). pp.1507-1522. ISSN 14439506

Thomson, Kate L. and Jiang, Connie and Richardson, Ebony and Westphal, Dominik S. and Burkard, Tobias and Wolf, Cordula M. and Vatta, Matteo and Harrison, Steven M. and Ingles, Jodie and Bezzina, Connie R. and Kroncke, Brett M. and Vandenberg, Jamie I. and Ng, Chai-Ann (2024) Clinical interpretation of KCNH2 variants using a robust PS3/BS3 functional patch-clamp assay. Human Genetics and Genomics Advances, 5 (2). p. 100270. ISSN 26662477

Gray, Michael P and Fatkin, Diane and Ingles, Jodie and Robertson, Elizabeth N and Figtree, Gemma A (2024) Genetic testing in cardiovascular disease. Medical Journal of Australia, 220 (8). pp.428-434. ISSN 0025-729X

Ma, Joanne G. and O’Neill, Matthew J. and Richardson, Ebony and Thomson, Kate L. and Ingles, Jodie and Muhammad, Ayesha and Solus, Joseph F. and Davogustto, Giovanni and Anderson, Katherine C. and Shoemaker, M. Benjamin and Stergachis, Andrew B. and Floyd, Brendan J. and Dunn, Kyla and Parikh, Victoria N. and Chubb, Henry and Perrin, Mark J. and Roden, Dan M. and Vandenberg, Jamie I. and Ng, Chai-Ann and Glazer, Andrew M. (2024) Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome–Associated Variants. Circulation: Genomic and Precision Medicine, 17 (4). ISSN 2574-8300

Austin, Rachel and Brown, Jaye S. and Casauria, Sarah and Madelli, Evanthia O. and Mattiske, Tessa and Boughtwood, Tiffany and Metke, Alejandro and Davis, Andrew and Horton, Ari E. and Winlaw, David and Das, Debjani and Soka, Magdalena and Giannoulatou, Eleni and Rath, Emma M. and Haan, Eric and Blue, Gillian M. and Vohra, Jitendra and Atherton, John J. and van Spaendonck-Zwarts, Karin and Cox, Kathy and Burnett, Leslie and Wallis, Mathew and Haas, Matilda and Quinn, Michael C.J. and Pachter, Nicholas and Poplawski, Nicola K. and Stark, Zornitza and Bagnall, Richard D. and Weintraub, Robert G. and Pantaleo, Sarah-Jane and Lunke, Sebastian and De Fazio, Paul and Thompson, Tina and James, Paul and Chang, Yuchen and Fatkin, Diane and Macciocca, Ivan and Ingles, Jodie and Dunwoodie, Sally L. and Semsarian, Chris and McGaughran, Julie and Ades, Lesley and Enriquez, Annabel and McLean, Alison and Smyth, Renee and Alankarage, Dimithu and Fatkin, Diane and McNamara, James and Soka, Magdalena and Almog, Morgan and Fear, Vanessa and Medi, Caroline and Stark, Zornitza and Al-Shinnag, Mohammad and Fine, Miriam and Metke, Alejandro and Sy, Raymond and Atherton, John J. and Finlay, Keri and Milnes, Di and Tang, Dotti and Austin, Rachel and Garza, Denisse and Milward, Michael and Taylor, Jessica and Bagnall, Richard D. and Giannoulatou, Eleni and Morrish, Ansley and Taylor, Shelby and Barnett, Chris and Gongolidis, Laura and Morwood, Jim and Tchan, Michel and Blue, Gillian M. and Gray, Belinda and Mountain, Helen and Thompson, Tina and Bodek, Simon and Greer, Cassie and Mowat, David and Thorpe, Jordan and Boggs, Kirsten and Haan, Eric and Ng, Chai-Ann and Trainer, Alison and Bogwitz, Michael and Haas, Mathilda and Nowak, Natalie and Trivedi, Gunjan and Boughtwood, Tiffany and Hanna, Bernadette and Martinez, Noelia Nunez and Valente, Giulia and Bray, Alessandra and Harvey, Richard and Ohanian, Monique and van Spaendonck-Zwarts, Karin and Brion, Marie-Jo and Hayward, Janette and O’Sullivan, Sinead and Vandenberg, Jamie and Brown, Jaye and Herrera, Carmen and Overkov, Angela and Verma, Kunal and Richardson, Rob Bryson and Hill, Adam and Pachter, Nicholas and Vidgen, Miranda and Burnett, Leslie and Hollingsworth, Georgie and Patel, Chirag and Vohra, Jitendra and Burns, Charlotte and Hollway, Georgina and Perrin, Mark and Waddel-Smith, Kathryn and Cao, Michelle and Horton, Ari E. and Perry, Matthew and Wallis, Mathew and Carr, Will and Howting, Denise and Pflaumer, Andreas and Weintraub, Robert G. and Casauria, Sarah and Ingles, Jodie and Phillips, Peta and Wilson, Meredith and Chalinor, Heather and Isbister, Joanne and Phuong, Thuan and Winlaw, David and Chang, Yuchen and Jackson, Matilda and Pope-Couston, Rachel and Worgan, Lisa and Chapman, Gavin and James, Paul and Poplawski, Nicola K. and Wornham, Linda and Charitou, Theosodia and Jane-Pantaleo, Sarah and Punni, Preeti and Wu, Kathy and Chong, Belinda and Johnson, Renee and Quinn, Michael C.J. and Yeates, Laura and Collins, Felicity and Kelly, Andrew and Quinn, Michael and Zentner, Dominica and Correnti, Gemma and King-Smith, Sarah and Rajagopalan, Sulekha and Cox, Kathy and Kirk, Edwin and Raju, Hariharan and Cunningham, Fiona and Kummerfeld, Sarah and Rath, Emma M. and Das, Debjani and Lassman, Timo and Regan, Matthew and Davis, Jason and Lipton, Jonathon and Rogers, Jonathan and Davis, Andrew and Lunke, Sebastian and Ryan, Mark and De Fazio, Paul and Macciocca, Ivan and Sandaradura, Sarah and de Silva, Michelle and MacIntyre, Paul and Schonrock, Nicole and Den Elzen, Nicola and Madelli, Evanthia O. and Scuffham, Paul and Devery, Sophie and Mallawaarachchi, Amali and Semsarian, Chris and Dobbins, Julia and Mansour, Julia and Sherburn, Isabella and Dunwoodie, Sally L. and Martin, Ellenore and Sherlock, Mary-Clare and Dwyer, Nathan and Mathew, Jacob and Singer, Emma and Elbracht-Leong, Stefanie and Mattiske, Tessa and Smerdon, Carla and Elliott, David and McGaughran, Julie and Smith, Janine (2024) A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship. Genetics in Medicine Open, 2. p. 101842. ISSN 29497744

Leslie, Felicity and Avis, Suzanne R. and Bagnall, Richard D. and Bendall, Jason and Briffa, Tom and Brouwer, Isabel and Butters, Alexandra and Figtree, Gemma A. and La Gerche, Andre and Gray, Belinda and Nedkoff, Lee and Page, Gregory and Paratz, Elizabeth and Semsarian, Christopher and Sy, Raymond W. and du Toit-Prinsloo, Lorraine and Yeates, Laura and Sweeting, Joanna and Ingles, Jodie (2023) The New South Wales Sudden Cardiac Arrest Registry: A Data Linkage Cohort Study. Heart, Lung and Circulation, 32 (9). pp.1069-1075. ISSN 14439506

Hoorntje, Edgar T. and Burns, Charlotte and Marsili, Luisa and Corden, Ben and Parikh, Victoria N. and te Meerman, Gerard J. and Gray, Belinda and Adiyaman, Ahmet and Bagnall, Richard D. and Barge-Schaapveld, Daniela Q.C.M. and van den Berg, Maarten P. and Bootsma, Marianne and Bosman, Laurens P. and Correnti, Gemma and Duflou, Johan and Eppinga, Ruben N. and Fatkin, Diane and Fietz, Michael and Haan, Eric and Jongbloed, Jan D.H. and Hauer, Arnaud D. and Lam, Lien and van Lint, Freyja H.M. and Lota, Amrit and Marcelis, Carlo and McCarthy, Hugh J. and van Mil, Anneke M. and Oldenburg, Rogier A. and Pachter, Nicholas and Planken, R. Nils and Reuter, Chloe and Semsarian, Christopher and van der Smagt, Jasper J. and Thompson, Tina and Vohra, Jitendra and Volders, Paul G.A. and van Waning, Jaap I. and Whiffin, Nicola and van den Wijngaard, Arthur and Amin, Ahmad S. and Wilde, Arthur A.M. and van Woerden, Gijs and Yeates, Laura and Zentner, Dominica and Ashley, Euan A. and Wheeler, Matthew T. and Ware, James S. and van Tintelen, J. Peter and Ingles, Jodie (2023) Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation: Genomic and Precision Medicine, 16 (1). ISSN 2574-8300

Jiang, Connie and Richardson, Ebony and Farr, Jessica and Hill, Adam P. and Ullah, Rizwan and Kroncke, Brett M. and Harrison, Steven M. and Thomson, Kate L. and Ingles, Jodie and Vandenberg, Jamie I. and Ng, Chai-Ann (2022) A calibrated functional patch-clamp assay to enhance clinical variant interpretation in KCNH2-related long QT syndrome. The American Journal of Human Genetics, 109 (7). pp.1199-1207. ISSN 00029297

Jordan, Elizabeth and Peterson, Laiken and Ai, Tomohiko and Asatryan, Babken and Bronicki, Lucas and Brown, Emily and Celeghin, Rudy and Edwards, Matthew and Fan, Judy and Ingles, Jodie and James, Cynthia A. and Jarinova, Olga and Johnson, Renee and Judge, Daniel P. and Lahrouchi, Najim and Lekanne Deprez, Ronald H. and Lumbers, R. Thomas and Mazzarotto, Francesco and Medeiros Domingo, Argelia and Miller, Rebecca L. and Morales, Ana and Murray, Brittney and Peters, Stacey and Pilichou, Kalliopi and Protonotarios, Alexandros and Semsarian, Christopher and Shah, Palak and Syrris, Petros and Thaxton, Courtney and van Tintelen, J. Peter and Walsh, Roddy and Wang, Jessica and Ware, James and Hershberger, Ray E. (2021) Evidence-Based Assessment of Genes in Dilated Cardiomyopathy. Circulation, 144 (1). pp.7-19. ISSN 0009-7322

Lacaze, Paul and Sebra, Robert and Riaz, Moeen and Ingles, Jodie and Tiller, Jane and Thompson, Bryony A. and James, Paul A. and Fatkin, Diane and Semsarian, Christopher and Reid, Christopher M. and Tonkin, Andrew M. and Winship, Ingrid and Schadt, Eric and McNeil, John J. (2021) Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent. npj Genomic Medicine, 6 (1). ISSN 2056-7944

Semsarian, Christopher and Ingles, Jodie and Ross, Samantha Barratt and Dunwoodie, Sally L. and Bagnall, Richard D. and Kovacic, Jason C. (2021) Precision Medicine in Cardiovascular Disease: Genetics and Impact on Phenotypes. Journal of the American College of Cardiology, 77 (20). pp.2517-2530. ISSN 07351097

Gray, Belinda and Semsarian, Christopher and Fatkin, Diane and Ingles, Jodie and Atherton, John J. and Davis, Andrew M. and Sanders, Prashanthan and Pachter, Nicholas and Skinner, Jonathan R. and Stiles, Martin K. (2020) Patients with Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus Statement. Heart, Lung and Circulation. ISSN 14439506

Minoche, Andre E. and Horvat, Claire and Johnson, Renee and Gayevskiy, Velimir and Morton, Sarah U and Drew, Alexander P and Woo, Kerhan and Statham, Aaron L and Lundie, Ben and Bagnall, Richard D and Ingles, Jodie and Semsarian, Christopher and Seidman, Jonathan G and Seidman, Christine E and Dinger, Marcel E and Cowley, Mark J and Fatkin, Diane (2018) Response to Brodehl et al. Genetics in Medicine, ePub. ISSN 1098-3600 (Not OA)

Bagnall, Richard D and Ingles, Jodie and Dinger, Marcel E and Cowley, Mark J and Ross, Samantha Barratt and Minoche, André E. and Lal, Sean and Turner, Christian and Colley, Alison and Rajagopalan, Sulekha and Berman, Yemima and Ronan, Anne and Fatkin, Diane and Semsarian, Christopher (2018) Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology, 72 (4). pp.419-429. ISSN 1558-3597 (Not OA)

Minoche, Andre E. and Horvat, Claire and Johnson, Renee and Gayevskiy, Velimir and Morton, Sarah U and Drew, Alexander P and Woo, Kerhan and Statham, Aaron L. and Lundie, Ben and Bagnall, Richard D and Ingles, Jodie and Semsarian, Christopher and Seidman, Jonathan G and Seidman, Christine E and Dinger, Marcel E and Cowley, Mark J and Fatkin, Diane (2018) Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy. Genetics in Medicine, ePub. ISSN 1098-3600 (Not OA)

Ingles, Jodie and Zodgekar, Poonam R and Yeates, Laura and Macciocca, Ivan and Semsarian, Christopher and Fatkin, Diane (2012) Guidelines for genetic testing of inherited cardiac disorders. Heart Lung and Circulation, 20 (11). pp.681-7. ISSN 1444-2892 (PP OA)