Items where Author is "Semsarian, Christopher"

Lim, Seakcheng and Mangala, Melissa M. and Holliday, Mira and Cserne Szappanos, Henrietta and Barratt-Ross, Samantha and Li, Serena and Thorpe, Jordan and Liang, Whitney and Ranpura, Ginell N. and Vandenberg, Jamie I. and Semsarian, Christopher and Hill, Adam P. and Hool, Livia C. (2024) Reduced connexin-43 expression, slow conduction and repolarisation dispersion in a model of hypertrophic cardiomyopathy. Disease Models & Mechanisms, 17 (8). ISSN 1754-8403

Stark, Zornitza and Boughtwood, Tiffany and Haas, Matilda and Braithwaite, Jeffrey and Gaff, Clara L. and Goranitis, Ilias and Spurdle, Amanda B. and Hansen, David P. and Hofmann, Oliver and Laing, Nigel and Metcalfe, Sylvia and Newson, Ainsley J. and Scott, Hamish S. and Thorne, Natalie and Ward, Robyn L. and Dinger, Marcel E. and Best, Stephanie and Long, Janet C. and Grimmond, Sean M. and Pearson, John and Waddell, Nicola and Barnett, Christopher P. and Cook, Matthew and Field, Michael and Fielding, David and Fox, Stephen B. and Gecz, Jozef and Jaffe, Adam and Leventer, Richard J. and Lockhart, Paul J. and Lunke, Sebastian and Mallett, Andrew J. and McGaughran, Julie and Mileshkin, Linda and Nones, Katia and Roscioli, Tony and Scheffer, Ingrid E. and Semsarian, Christopher and Simons, Cas and Thomas, David M. and Thorburn, David R. and Tothill, Richard and White, Deborah and Dunwoodie, Sally and Simpson, Peter T. and Phillips, Peta and Brion, Marie-Jo and Finlay, Keri and Quinn, Michael CJ. and Mattiske, Tessa and Tudini, Emma and Boggs, Kirsten and Murray, Sean and Wells, Kathy and Cannings, John and Sinclair, Andrew H. and Christodoulou, John and North, Kathryn N. (2023) Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare. The American Journal of Human Genetics, 110 (3). pp.419-426. ISSN 00029297

Cserne Szappanos, Henrietta and Viola, Helena M. and Ito, Danica W. and Lim, Seakcheng and Mangala, Melissa and Holliday, Mira and Barratt Ross, Samantha and Semsarian, Christopher and Hill, Adam and Dixon, Rose E. and Hool, Livia C. (2023) Cytoskeletal disarray increases arrhythmogenic vulnerability during sympathetic stimulation in a model of hypertrophic cardiomyopathy. Scientific Reports, 13 (1). ISSN 2045-2322

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

Semsarian, Christopher and Gray, Belinda and Haugaa, Kristina H. and Lampert, Rachel and Sharma, Sanjay and Kovacic, Jason C. (2022) Athletic Activity for Patients With Hypertrophic Cardiomyopathy and Other Inherited Cardiovascular Diseases. Journal of the American College of Cardiology, 80 (13). pp.1268-1283. ISSN 07351097

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

Holliday, Mira and Ross, Samantha Barratt and Lim, Seakcheng and Mangala, Melissa and Hill, Adam P and Szappanos, Henrietta Cserne and Hool, Livia and Semsarian, Christopher (2018) Development of induced pluripotent stem cells from a patient with hypertrophic cardiomyopathy who carries the pathogenic myosin heavy chain 7 mutation p.Arg403Gln. Stem Cell Research, 33. pp.269-273. ISSN 18735061 (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) 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)

Weintraub, Robert G and Semsarian, Christopher and Macdonald, Peter S (2017) Dilated cardiomyopathy. Lancet, 390. pp.400-414. ISSN 1474-547X (N/A)

Viola, Helena and Johnstone, Vicky and Szappanos, Henrietta Cserne and Richman, Tara and Tsoutsman, Tatiana and Filipovska, Aleksandra and Semsarian, Christopher and Hool, Livia (2016) The L-type Ca(2+) channel facilitates abnormal metabolic activity in the cTnI-G203S mouse model of hypertrophic cardiomyopathy. The Journal of Physiology, 594 (14). pp.4051-4070. ISSN 1469-7793 (PMC OA)

Costa, Mauro W and Guo, Guanglan and Wolstein, Orit and Vale, Molly and Castro, Maria L and Wang, Libin and Otway, Robyn and Riek, Peter and Cochrane, Natalie and Furtado, Milena B and Semsarian, Christopher and Weintraub, Robert G and Yeoh, Thomas and Hayward, Christopher S and Keogh, Anne and Macdonald, Peter S and Feneley, Michael P and Graham, Robert M and Seidman, Jonathan G and Seidman, Christine E and Rosenthal, Nadia and Fatkin, Diane and Harvey, Richard P (2013) Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy. Circulation: Cardiovascular Genetics, 6 (3). pp.238-47. ISSN 1942-3268 (PMC 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)