Items where Author is "Seidman, Jonathan G"

Article

Horvat, Claire and Johnson, Renee and Lam, Lien and Munro, Jacob and Mazzarotto, Francesco and Roberts, Angharad M and Herman, Daniel S and Parfenov, Michael and Haghighi, Alireza and McDonough, Barbara and DePalma, Steven R and Keogh, Anne M and Macdonald, Peter S and Hayward, Christopher S and Roberts, Amy and Barton, Paul J R and Felkin, Leanne E and Giannoulatou, Eleni and Cook, Stuart A and Seidman, Jonathan G and Seidman, Christine E and Fatkin, Diane (2019) A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy. Genetics in Medicine, 21 (1). pp.133-143. ISSN 1098-3600 (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)

Huttner, Inken G and Wang, Louis W and Santiago, Celine F and Horvat, Claire and Johnson, Renee and Cheng, Delfine and von Frieling-Salewsky, Marion and Hillcoat, Karen and Bemand, Timothy J and Trivedi, Gunjan and Braet, Filip and Hesselson, Dan and Alford, Kevin and Hayward, Christopher S and Seidman, Jonathan G and Seidman, Christine E and Feneley, Michael P and Linke, Wolfgang A and Fatkin, Diane (2018) A-Band Titin Truncation in Zebrafish Causes Dilated Cardiomyopathy and Hemodynamic Stress Intolerance. Circulation: Genomic and Precision Medicine, 11 (8). pp. e002135. ISSN 2574-8300 (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)

Ito, Kaoru and Patel, Parth N and Gorham, Joshua M and McDonough, Barbara and DePalma, Steven R and Adler, Emily E and Lam, Lien and MacRae, Calum A and Mohiuddin, Syed M and Fatkin, Diane and Seidman, Christine E and Seidman, Jonathan G (2017) Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing. Proceedings of the National Academy of Sciences of the United States of America, 114 (29). pp.7689-7694. ISSN 1091-6490 (OA)

Fatkin, Diane and Lam, Lien and Herman, Daniel S and Benson, Craig C and Felkin, Leanne E and Barton, Paul J R and Walsh, Roddy and Candan, Sukru and Ware, James S and Roberts, Angharad M and Chung, Wendy and Smoot, Leslie and Bornaun, Helen and Keogh, Anne M and Macdonald, Peter S and Hayward, Christopher S and Seidman, Jonathan G and Roberts, Amy E and Cook, Stuart A and Seidman, Christine E (2016) Titin truncating mutations: A rare cause of dilated cardiomyopathy in the young. Progress in Pediatric Cardiology, 40. pp.41-45. ISSN 1058-9813 (PP OA)

Roberts, Angharad M and Ware, James S and Herman, Daniel S and Schafer, Sebastian and Baksi, John and Bick, Alexander G and Buchan, Rachel J and Walsh, Roddy and John, Shibu and Wilkinson, Samuel and Macdonald, Peter S and Keogh, Anne M and Hayward, Christopher S and Fatkin, Diane and Seidman, Jonathan G and Seidman, Christine E and Cook, Stuart A (2015) Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease. Science Translational Medicine, 7 (270). pp. 270ra6. ISSN 1946-6242 (PMC OA)

Fatkin, Diane and Seidman, Christine E and Seidman, Jonathan G (2014) Genetics and disease of ventricular muscle. Cold Spring Harbor Perspectives in Medicine, 4 (1). pp. a021063. ISSN 2157-1422 (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)