Items where Author is "Semsarian, Christopher"

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Number of items: 8.

Article

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)

This list was generated on Thu Jun 27 02:57:45 2019 AEST.