Items where Author is "Ingles, Jodie"

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Number of items: 10.

Article

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)

This list was generated on Sat Feb 24 18:25:56 2024 AEDT.