Items where Author is "Fatkin, Diane"

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Guo, Yang and Merten, Anna-Lena and Schöler, Ulrike and Yu, Ze-Yan and Cvetkovska, Jasmina and Fatkin, Diane and Feneley, Michael P. and Martinac, Boris and Friedrich, Oliver (2020) In vitro cell stretching technology (IsoStretcher) as an approach to unravel Piezo1-mediated cardiac mechanotransduction. Progress in Biophysics and Molecular Biology. ISSN 00796107

Iismaa, Siiri E. and Hesselson, Stephanie and McGrath-Cadell, Lucy and Muller, David W. and Fatkin, Diane and Giannoulatou, Eleni and Kovacic, Jason and Graham, Robert M. (2020) Spontaneous Coronary Artery Dissection and Fibromuscular Dysplasia: Vasculopathies With a Predilection for Women. Heart, Lung and Circulation. ISSN 14439506

Ntalla, Ioanna and Weng, Lu-Chen and Cartwright, James H. and Hall, Amelia Weber and Sveinbjornsson, Gardar and Tucker, Nathan R. and Choi, Seung Hoan and Chaffin, Mark D. and Roselli, Carolina and Barnes, Michael R. and Mifsud, Borbala and Warren, Helen R. and Hayward, Caroline and Marten, Jonathan and Cranley, James J. and Concas, Maria Pina and Gasparini, Paolo and Boutin, Thibaud and Kolcic, Ivana and Polasek, Ozren and Rudan, Igor and Araujo, Nathalia M. and Lima-Costa, Maria Fernanda and Ribeiro, Antonio Luiz P. and Souza, Renan P. and Tarazona-Santos, Eduardo and Giedraitis, Vilmantas and Ingelsson, Erik and Mahajan, Anubha and Morris, Andrew P. and Del Greco M, Fabiola and Foco, Luisa and Gögele, Martin and Hicks, Andrew A. and Cook, James P. and Lind, Lars and Lindgren, Cecilia M. and Sundström, Johan and Nelson, Christopher P. and Riaz, Muhammad B. and Samani, Nilesh J. and Sinagra, Gianfranco and Ulivi, Sheila and Kähönen, Mika and Mishra, Pashupati P. and Mononen, Nina and Nikus, Kjell and Caulfield, Mark J. and Dominiczak, Anna and Padmanabhan, Sandosh and Montasser, May E. and O’Connell, Jeff R. and Ryan, Kathleen and Shuldiner, Alan R. and Aeschbacher, Stefanie and Conen, David and Risch, Lorenz and Thériault, Sébastien and Hutri-Kähönen, Nina and Lehtimäki, Terho and Lyytikäinen, Leo-Pekka and Raitakari, Olli T. and Barnes, Catriona L. K. and Campbell, Harry and Joshi, Peter K. and Wilson, James F. and Isaacs, Aaron and Kors, Jan A. and van Duijn, Cornelia M. and Huang, Paul L. and Gudnason, Vilmundur and Harris, Tamara B. and Launer, Lenore J. and Smith, Albert V. and Bottinger, Erwin P. and Loos, Ruth J. F. and Nadkarni, Girish N. and Preuss, Michael H. and Correa, Adolfo and Mei, Hao and Wilson, James and Meitinger, Thomas and Müller-Nurasyid, Martina and Peters, Annette and Waldenberger, Melanie and Mangino, Massimo and Spector, Timothy D. and Rienstra, Michiel and van de Vegte, Yordi J. and van der Harst, Pim and Verweij, Niek and Kääb, Stefan and Schramm, Katharina and Sinner, Moritz F. and Strauch, Konstantin and Cutler, Michael J. and Fatkin, Diane and London, Barry and Olesen, Morten and Roden, Dan M. and Benjamin Shoemaker, M. and Gustav Smith, J. and Biggs, Mary L. and Bis, Joshua C. and Brody, Jennifer A. and Psaty, Bruce M. and Rice, Kenneth and Sotoodehnia, Nona and De Grandi, Alessandro and Fuchsberger, Christian and Pattaro, Cristian and Pramstaller, Peter P. and Ford, Ian and Wouter Jukema, J. and Macfarlane, Peter W. and Trompet, Stella and Dörr, Marcus and Felix, Stephan B. and Völker, Uwe and Weiss, Stefan and Havulinna, Aki S. and Jula, Antti and Sääksjärvi, Katri and Salomaa, Veikko and Guo, Xiuqing and Heckbert, Susan R. and Lin, Henry J. and Rotter, Jerome I. and Taylor, Kent D. and Yao, Jie and de Mutsert, Renée and Maan, Arie C. and Mook-Kanamori, Dennis O. and Noordam, Raymond and Cucca, Francesco and Ding, Jun and Lakatta, Edward G. and Qian, Yong and Tarasov, Kirill V. and Levy, Daniel and Lin, Honghuang and Newton-Cheh, Christopher H. and Lunetta, Kathryn L. and Murray, Alison D. and Porteous, David J. and Smith, Blair H. and Stricker, Bruno H. and Uitterlinden, André and van den Berg, Marten E. and Haessler, Jeffrey and Jackson, Rebecca D. and Kooperberg, Charles and Peters, Ulrike and Reiner, Alexander P. and Whitsel, Eric A. and Alonso, Alvaro and Arking, Dan E. and Boerwinkle, Eric and Ehret, Georg B. and Soliman, Elsayed Z. and Avery, Christy L. and Gogarten, Stephanie M. and Kerr, Kathleen F. and Laurie, Cathy C. and Seyerle, Amanda A. and Stilp, Adrienne and Assa, Solmaz and Abdullah Said, M. and Yldau van der Ende, M. and Lambiase, Pier D. and Orini, Michele and Ramirez, Julia and Van Duijvenboden, Stefan and Arnar, David O. and Gudbjartsson, Daniel F. and Holm, Hilma and Sulem, Patrick and Thorleifsson, Gudmar and Thorolfsdottir, Rosa B. and Thorsteinsdottir, Unnur and Benjamin, Emelia J. and Tinker, Andrew and Stefansson, Kari and Ellinor, Patrick T. and Jamshidi, Yalda and Lubitz, Steven A. and Munroe, Patricia B. (2020) Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nature Communications, 11 (1). ISSN 2041-1723

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

Fatkin, Diane and Johnson, Renee (2020) Variants of Uncertain Significance and “Missing Pathogenicity”. Journal of the American Heart Association, 9 (3). ISSN 2047-9980

Fatkin, Diane and Huttner, Inken G. and Johnson, Renee (2019) Genetics of atrial cardiomyopathy. Current Opinion in Cardiology, ePub. p. 1. ISSN 0268-4705

Adlam, David and Kovacic, Jason C and Iismaa, Siiri E and Al-Hussaini, Abtehale and Wong, Claire Mei Yi and Giannoulatou, Eleni and Sweeting, Michael and Muller, David and Wood, Alice and McGrath-Cadell, Lucy and Fatkin, Diane and Dunwoodie, Sally L and Harvey, Richard and Holloway, Cameron and Empana, Jean-Philippe and Graham, Robert M and Motreff, Pascal and Meneveau, Nicolas and Gilard, Martine and Rioufol, Gilles and Range, Grégoire and Brunel, Philippe and Delarche, Nicolas and Filippi, Emmanuelle and Le Bivic, Louis and Harbaoui, Brahim and Benamer, Hakim and Cayla, Guillaume and Varenne, Olivier and Manzo-Silberman, Stephane Peggy and Silvain, Johanne and Spaulding, Christian and Caussin, Christophe and Gerbaud, Edouard and Valy, Yann and Koning, René and Lhermusier, Thibault and Champin, Stanislas and Salengro, Emmanuel and Fluttaz, Arnaud and Zabalawi, Amer and Cottin, Yves and Teiger, Emmanuel and Saint-Etienne, Christophe and Ducrocq, Grégory and Marliere, Stéphanie and Boiffard, Emmanuel and Aubry, Pierre and Georges, Jean Louis and Benamer, Hakim and Bresson, Didier and De Poli, Fabien and Karrillon, Gaëtan and Roule, Vincent and Bali, Laurent and Valla, Mathieu and Gerbay, Antoine and Houpe, David and Dubreuil, Olivier and Monnier, Arsène and Mayaud, Norbert and Manchuelle, Aurélie and Commeau, Philippe and Bedossa, Marc and Nikpay, Majid and Goel, Anuj and Won, Hong-Hee and Hall, Leanne M. and Willenborg, Christina and Kanoni, Stavroula and Saleheen, Danish and Kyriakou, Theodosios and Nelson, Christopher P. and Hopewell, Jemma C. and Webb, Thomas R. and Zeng, Lingyao and Dehghan, Abbas and Alver, Maris and Armasu, Sebastian M and Auro, Kirsi and Bjonnes, Andrew and Chasman, Daniel I. and Chen, Shufeng and Ford, Ian and Franceschini, Nora and Gieger, Christian and Grace, Christopher and Gustafsson, Stefan and Huang, Jie and Hwang, Shih-Jen and Kim, Yun Kyoung and Kleber, Marcus E. and Lau, King Wai and Lu, Xiangfeng and Lu, Yingchang and Lyytikäinen, Leo P. and Mihailov, Evelin and Morrison, Alanna and Pervjakova, Natalia and Qu, Liming and Rose, Lynda M. and Salfati, Elias and Saxena, Richa and Scholz, Markus and Smith, Albert V. and Tikkanen, Emmi and Uitterlinden, Andre and Yang, Xueli and Zhang, Weihua and Zhao, Wei and de Andrade, Mariza and de Vries, Paul S. and van Zuydam, Natalie R. and Anand, Sonia S. and Bertram, Lars and Beutner, Frank and Dedoussis, George and Frossard, Philippe and Gauguier, Dominique and Goodall, Alison H. and Gottesman, Omri and Haber, Marc and Han, Bok-Ghee and Huang, Jianfeng and Jalilzadeh, Shapour and Kessler, Thorsten and Thiery, Joachim and Zalloua, Pierre A. and O'Donnell, Christopher J. and Reilly, Muredach P. and Assimes, Themistocles L. and Thompson, John R. and Erdmann, Jeanette and Clarke, Robert and Watkins, Hugh and Kathiresan, Sekar and McPherson, Ruth and Deloukas, Panos and Schunkert, Heribert and Samani, Nilesh J. and Farrall, Martin (2019) Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection. Journal of the American College of Cardiology, 73 (1). pp.58-66. ISSN 1558-3597 (Not OA)

Peters, Stacey and Kumar, Saurabh and Elliott, Perry and Kalman, Jonathan M. and Fatkin, Diane (2019) Arrhythmic Genotypes in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management. Heart Lung and Circulation, 28 (1). pp.31-38. ISSN 14439506 (Not OA)

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)

Bart, Nicole K. and Thomas, Liza and Korczyk, Dariusz and Atherton, John J. and Stewart, Graeme J. and Fatkin, Diane (2019) Amyloid Cardiomyopathy. Heart, Lung and Circulation. ISSN 14439506

Peters, Stacey and Johnson, Renee and Birch, Samuel and Zentner, Dominica and Hershberger, Ray E. and Fatkin, Diane (2019) Familial Dilated Cardiomyopathy. Heart, Lung and Circulation. ISSN 14439506

Gladding, Patrick A. and Legget, Malcolm and Fatkin, Diane and Larsen, Peter and Doughty, Robert (2019) Polygenic Risk Scores in Coronary Artery Disease and Atrial Fibrillation. Heart, Lung and Circulation. ISSN 14439506

Fatkin, Diane and Huttner, Inken G. and Kovacic, Jason C. and Seidman, J.G. and Seidman, Christine E. (2019) Precision Medicine in the Management of Dilated Cardiomyopathy. Journal of the American College of Cardiology, 74 (23). pp.2921-2938. ISSN 07351097

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)

Zhang, Hong and Dvornikov, Alexey V and Huttner, Inken G and Ma, Xiao and Santiago, Celine F and Fatkin, Diane and Xu, Xiaolei (2018) A Langendorff-like system to quantify cardiac pump function in adult zebrafish. Disease Models & Mechanisms, 11 (9). pp. dmm034819. ISSN 1754-8403 (PMC OA)

Fatkin, Diane (2018) ETV1 : A New Player in Atrial Remodeling. Circulation Research, 123 (5). pp.515-517. ISSN 0009-7330 (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)

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)

Roselli, Carolina and Chaffin, Mark D. and Weng, Lu-Chen and Aeschbacher, Stefanie and Ahlberg, Gustav and Albert, Christine M. and Almgren, Peter and Alonso, Alvaro and Anderson, Christopher D. and Aragam, Krishna G. and Arking, Dan E. and Barnard, John and Bartz, Traci M. and Benjamin, Emelia J. and Bihlmeyer, Nathan A. and Bis, Joshua C. and Bloom, Heather L. and Boerwinkle, Eric and Bottinger, Erwin B. and Brody, Jennifer A. and Calkins, Hugh and Campbell, Archie and Cappola, Thomas P. and Carlquist, John and Chasman, Daniel I. and Chen, Lin Y. and Chen, Yii-Der Ida and Choi, Eue-Keun and Choi, Seung Hoan and Christophersen, Ingrid E. and Chung, Mina K. and Cole, John W. and Conen, David and Cook, James and Crijns, Harry J. and Cutler, Michael J. and Damrauer, Scott M. and Daniels, Brian R. and Darbar, Dawood and Delgado, Graciela and Denny, Joshua C. and Dichgans, Martin and Dörr, Marcus and Dudink, Elton A. and Dudley, Samuel C. and Esa, Nada and Esko, Tonu and Eskola, Markku and Fatkin, Diane and Felix, Stephan B. and Ford, Ian and Franco, Oscar H. and Geelhoed, Bastiaan and Grewal, Raji P. and Gudnason, Vilmundur and Guo, Xiuqing and Gupta, Namrata and Gustafsson, Stefan and Gutmann, Rebecca and Hamsten, Anders and Harris, Tamara B. and Hayward, Caroline and Heckbert, Susan R. and Hernesniemi, Jussi and Hocking, Lynne J. and Hofman, Albert and Horimoto, Andrea R. V. R. and Huang, Jie and Huang, Paul L. and Huffman, Jennifer and Ingelsson, Erik and Ipek, Esra Gucuk and Ito, Kaoru and Jimenez-Conde, Jordi and Johnson, Renee and Jukema, J. Wouter and Kääb, Stefan and Kähönen, Mika and Kamatani, Yoichiro and Kane, John P. and Kastrati, Adnan and Kathiresan, Sekar and Katschnig-Winter, Petra and Kavousi, Maryam and Kessler, Thorsten and Kietselaer, Bas L. and Kirchhof, Paulus and Kleber, Marcus E. and Knight, Stacey and Krieger, Jose E. and Kubo, Michiaki and Launer, Lenore J. and Laurikka, Jari and Lehtimäki, Terho and Leineweber, Kirsten and Lemaitre, Rozenn N. and Li, Man and Lim, Hong Euy and Lin, Henry J. and Lin, Honghuang and Lind, Lars and Lindgren, Cecilia M. and Lokki, Marja-Liisa and London, Barry and Loos, Ruth J. F. and Low, Siew-Kee and Lu, Yingchang and Lyytikäinen, Leo-Pekka and Macfarlane, Peter W. and Magnusson, Patrik K. and Mahajan, Anubha and Malik, Rainer and Mansur, Alfredo J. and Marcus, Gregory M. and Margolin, Lauren and Margulies, Kenneth B. and März, Winfried and McManus, David D. and Melander, Olle and Mohanty, Sanghamitra and Montgomery, Jay A. and Morley, Michael P. and Morris, Andrew P. and Müller-Nurasyid, Martina and Natale, Andrea and Nazarian, Saman and Neumann, Benjamin and Newton-Cheh, Christopher and Niemeijer, Maartje N. and Nikus, Kjell and Nilsson, Peter and Noordam, Raymond and Oellers, Heidi and Olesen, Morten S. and Orho-Melander, Marju and Padmanabhan, Sandosh and Pak, Hui-Nam and Paré, Guillaume and Pedersen, Nancy L. and Pera, Joanna and Pereira, Alexandre and Porteous, David and Psaty, Bruce M. and Pulit, Sara L. and Pullinger, Clive R. and Rader, Daniel J. and Refsgaard, Lena and Ribasés, Marta and Ridker, Paul M. and Rienstra, Michiel and Risch, Lorenz and Roden, Dan M. and Rosand, Jonathan and Rosenberg, Michael A. and Rost, Natalia and Rotter, Jerome I. and Saba, Samir and Sandhu, Roopinder K. and Schnabel, Renate B. and Schramm, Katharina and Schunkert, Heribert and Schurman, Claudia and Scott, Stuart A. and Seppälä, Ilkka and Shaffer, Christian and Shah, Svati and Shalaby, Alaa A. and Shim, Jaemin and Shoemaker, M. Benjamin and Siland, Joylene E. and Sinisalo, Juha and Sinner, Moritz F. and Slowik, Agnieszka and Smith, Albert V. and Smith, Blair H. and Smith, J. Gustav and Smith, Jonathan D. and Smith, Nicholas L. and Soliman, Elsayed Z. and Sotoodehnia, Nona and Stricker, Bruno H. and Sun, Albert and Sun, Han and Svendsen, Jesper H. and Tanaka, Toshihiro and Tanriverdi, Kahraman and Taylor, Kent D. and Teder-Laving, Maris and Teumer, Alexander and Thériault, Sébastien and Trompet, Stella and Tucker, Nathan R. and Tveit, Arnljot and Uitterlinden, Andre G. and Van Der Harst, Pim and Van Gelder, Isabelle C. and Van Wagoner, David R. and Verweij, Niek and Vlachopoulou, Efthymia and Völker, Uwe and Wang, Biqi and Weeke, Peter E and Weijs, Bob and Weiss, Raul and Weiss, Stefan and Wells, Quinn S and Wiggins, Kerri L and Wong, Jorge A and Woo, Daniel and Worrall, Bradford B and Yang, Pil-Sung and Yao, Jie and Yoneda, Zachary T and Zeller, Tanja and Zeng, Lingyao and Lubitz, Steven A and Lunetta, Kathryn L and Ellinor, Patrick T (2018) Multi-ethnic genome-wide association study for atrial fibrillation. Nature Genetics, 50. pp.1225-1233. ISSN 1061-4036 (Not OA)

Fatkin, Diane and Cox, Charles D and Huttner, Inken G and Martinac, Boris (2018) Is There a Role for Genes in Exercise-Induced Atrial Cardiomyopathy? Heart Lung and Circulation, ePub. ISSN 14439506 (Not OA)

Fatkin, Diane (2018) Left Ventricular Diastolic Dysfunction in Hutchinson-Gilford Progeria Syndrome. JAMA Cardiology, ePub. ISSN 2380-6583 (Not OA)

Wang, Louis W and Kesteven, Scott H and Huttner, Inken G and Feneley, Michael P and Fatkin, Diane (2018) High-Frequency Echocardiography ― Transformative Clinical and Research Applications in Humans, Mice, and Zebrafish. Circulation Journal, ePub. ISSN 1346-9843 (OA)

Friedrich, Oliver and Schneidereit, D and Nikolaev, Yury A and Nikolova-Krstevski, Vesna and Schürmann, Sebastian and Wirth-Hücking, A and Merten, A L and Fatkin, Diane and Martinac, Boris (2017) Adding dimension to cellular mechanotransduction: Advances in biomedical engineering of multiaxial cell-stretch systems and their application to cardiovascular biomechanics and mechano-signaling. Progress in Biophysics and Molecular Biology, 130 (Part B). pp.170-191. ISSN 1873-1732 (PP OA)

Nikolova-Krstevski, Vesna and Wagner, Soeren and Yu, Ze Yan and Cox, Charles D and Cvetkovska, Jasmina and Hill, Adam P and Huttner, Inken G and Benson, Victoria and Werdich, Andreas A and MacRae, Calum and Feneley, Michael P and Friedrich, Oliver and Martinac, Boris and Fatkin, Diane (2017) Endocardial TRPC-6 Channels Act as Atrial Mechanosensors and Load-Dependent Modulators of Endocardial/Myocardial Cross-Talk. JACC: Basic to Translational Science, 2 (5). pp.575-590. ISSN 2452302X (PMC OA)

Fatkin, Diane and Santiago, Celine F and Huttner, Inken G and Lubitz, Steven A and Ellinor, Patrick T (2017) Genetics of Atrial Fibrillation: State of the Art in 2017. Heart Lung and Circulation, 26 (9). pp.894-901. ISSN 1444-2892 (PP 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 Johnson, Renee and McGaughran, Julie and Weintraub, Robert G and Atherton, John J (2017) Position Statement on the Diagnosis and Management of Familial Dilated Cardiomyopathy. Heart Lung and Circulation, 26 (11). pp.1127-1132. ISSN 1444-2892 (PP OA)

Fatkin, Diane and Huttner, Inken G (2017) Titin-truncating mutations in dilated cardiomyopathy. Current Opinion in Cardiology, 32 (3). pp.232-238. ISSN 0268-4705 (Not OA)

Fatkin, Diane and Johnson, Renee (2017) Are Double Mutations Double Trouble? Circulation. Cardiovascular Genetics, 10 (2). ISSN 1942-3268 (OA)

Furtado, Milena B and Wilmanns, Julia C and Chandran, Anjana and Perera, Joelle and Hon, Olivia and Biben, Christine and Willow, Taylor J and Nim, Hieu T and Kaur, Gurpreet and Simonds, Stephanie and Wu, Qizhu and Willians, David and Salimova, Ekaterina and Plachta, Nicolas and Denegre, James M and Murray, Stephen A and Fatkin, Diane and Cowley, Michael and Pearson, James T and Kaye, David and Ramialison, Mirana and Harvey, Richard P and Rosenthal, Nadia A and Costa, Mauro W (2017) Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling. JCI Insight, 2 (6). pp. e88271. ISSN 2379-3708 (PMC OA)

Wang, Louis W and Huttner, Inken G and Santiago, Celine F and Kesteven, Scott H and Yu, Ze-Yan and Feneley, Michael P and Fatkin, Diane (2017) Standardized echocardiographic assessment of cardiac function in normal adult zebrafish and heart disease models. Disease Models & Mechanisms, 10 (1). pp.63-76. ISSN 1754-8411 (OA)

Fatkin, Diane and Johnson, Renee and McGaughran, Julie and Weintraub, Robert G and Atherton, John J (2016) Diagnosis and Management of Familial Dilated Cardiomyopathy – Position Statement. CSANZ Position Statement. pp.1-12. ISSN (OA)

Wang, Louis W and Huttner, Inken G and Santiago, Celine F and Fatkin, Diane (2016) Bradycardia in Zebrafish Heart Failure: A True Physiological Response or Anesthetic-Induced Red Herring? Zebrafish, 13 (6). pp.475-476. ISSN 1557-8542 (PP OA)

Iyngkaran, Pupalan and Thomas, Merlin C and Johnson, Renee and French, John and Ilton, Marcus and McDonald, Peter and Hare, David L and Fatkin, Diane (2016) Contextualizing Genetics for Regional Heart Failure Care. Current Cardiology Reviews, 12 (3). pp.231-42. ISSN 1875-6557 (PMC OA)

Christensen, Alex Hørby and Chatelain, Franck C and Huttner, Inken G and Olesen, Morten Salling and Soka, Magdalena and Feliciangeli, Sylvain and Horvat, Claire and Santiago, Celine F and Vandenberg, Jamie I and Schmitt, Nicole and Olesen, Søren-Peter and Lesage, Florian and Fatkin, Diane (2016) The two-pore domain potassium channel, TWIK-1, has a role in the regulation of heart rate and atrial size. Journal of Molecular and Cellular Cardiology, 97. pp.24-35. ISSN 1095-8584 (PP 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)

Cannon, Leah and Yu, Ze-Yan and Marciniec, Tadeusz and Waardenberg, Ashley J and Iismaa, Siiri E and Nikolova-Krstevski, Vesna and Neist, Elysia and Ohanian, Monique and Qiu, Min Ru and Rainer, Stephen and Harvey, Richard P and Feneley, Michael P and Graham, Robert M and Fatkin, Diane (2015) Irreversible triggers for hypertrophic cardiomyopathy are established in the early postnatal period. Journal of the American College of Cardiology, 65 (6). pp.560-9. ISSN 1558-3597 (OA)

Wang, Louis W and Grygiel, John J and O'Neill, John H and Fatkin, Diane and Feneley, Michael P (2015) Snowflakes in the heart: an ultrasonic marker of severe hypercoagulability. Lancet, 385 (9964). p. 302. ISSN 1474-547X (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)

Yu, Ze-Yan and Tan, Ju-Chiat and McMahon, Aisling C and Iismaa, Siiri E and Xiao, Xiao-Hui and Kesteven, Scott H and Reichelt, Melissa E and Mohl, Marion C and Smith, Nicola J and Fatkin, Diane and Allen, David and Head, Stewart I and Graham, Robert M and Feneley, Michael P (2014) RhoA/ROCK signaling and pleiotropic α1A-adrenergic receptor regulation of cardiac contractility. PloS One, 9 (6). pp. e99024. ISSN 1932-6203 (Gold OA)

Liang, Bo and Soka, Magdalena and Christensen, Alex Horby and Olesen, Morten S and Larsen, Anders P and Knop, Filip K and Wang, Fan and Nielsen, Jonas B and Andersen, Martin N and Humphreys, David T and Mann, Stefan A and Huttner, Inken G and Vandenberg, Jamie I and Svendsen, Jesper H and Haunsø, Stig and Preiss, Thomas and Seebohm, Guiscard and Olesen, Søren-Peter and Schmitt, Nicole and Fatkin, Diane (2014) Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis. Journal of Molecular and Cellular Cardiology, 67. pp.69-76. ISSN 1095-8584 (PP OA)

Ballouz, Sara and Liu, Jason Y and Oti, Martin and Gaeta, Bruno and Fatkin, Diane and Bahlo, Melanie and Wouters, Merridee A (2014) Candidate disease gene prediction using Gentrepid: application to a genome-wide association study on coronary artery disease. Molecular genetics & Genomic Medicine, 2 (1). pp.44-57. ISSN 2324-9269 (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)

Priori, Silvia G and Wilde, Arthur A and Horie, Minoru and Cho, Yongkeun and Behr, Elijah R and Berul, Charles and Blom, Nico and Brugada, Josep and Chiang, Chern-En and Huikuri, Heikki and Kannankeril, Prince and Krahn, Andrew and Leenhardt, Antoine and Moss, Arthur and Schwartz, Peter J and Shimizu, Wataru and Tomaselli, Gordon and Tracy, Cynthia and Ackerman, Michael and Belhassen, Bernard and Estes, N A Mark and Fatkin, Diane and Kalman, Jonathan and Kaufman, Elizabeth and Kirchhof, Paulus and Schulze-Bahr, Eric and Wolpert, Christian and Vohra, Jitendra and Refaat, Marwan and Etheridge, Susan P and Campbell, Robert M and Martin, Edward T and Quek, Swee Chye (2013) Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes. Europace, 15 (10). pp.1389-406. ISSN 1532-2092 (OA)

Huttner, Inken G and Trivedi, Gunjan and Jacoby, Arie and Mann, Stefan A and Vandenberg, Jamie I and Fatkin, Diane (2013) A transgenic zebrafish model of a human cardiac sodium channel mutation exhibits bradycardia, conduction-system abnormalities and early death. Journal of molecular and cellular cardiology, 61. pp.123-32. ISSN 1095-8584 (Not OA)

Christensen, Alex Hørby and Fatkin, Diane (2013) Efficacy of carvedilol in pediatric heart failure. Future Cardiology, 9 (4). pp.475-8. ISSN 1744-8298 (Not 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)

Fatkin, Diane and Nikolova-Krstevski, Vesna (2013) Atrial cardiomyopathy an orphan disease or common disorder? Circulation. Cardiovascular genetics, 6 (1). pp.5-6. ISSN 1942-3268 (OA)

Fatkin, Diane (2013) Familial dilated cardiomyopathy. Decision Support in Medicine. Clinical Decision Support:CDS:Cardio, 2nd ed. ISSN NA (Book, OA not required)

Ballouz, Sara and Liu, Jason Y and George, Richard A and Bains, Naresh and Liu, Arthur and Oti, Martin and Gaeta, Bruno and Fatkin, Diane and Wouters, Merridee A (2013) Gentrepid V2.0: a web server for candidate disease gene prediction. BMC bioinformatics, 14. p. 249. ISSN 1471-2105 (PMC OA)

Ohanian, Monique and Humphreys, David T and Anderson, Elizabeth and Preiss, Thomas and Fatkin, Diane (2013) A heterozygous variant in the human cardiac miR-133 gene, MIR133A2, alters miRNA duplex processing and strand abundance. BMC genetics, 14. p. 18. ISSN 1471-2156 (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)

Mann, Stefan A and Castro, Maria L and Ohanian, Monique and Guo, Guanglan and Zodgekar, Poonam and Sheu, Angela and Stockhammer, Kathryn and Thompson, Tina and Playford, David and Subbiah, Rajesh and Kuchar, Dennis and Aggarwal, Anu and Vandenberg, Jamie I and Fatkin, Diane (2012) R222Q SCN5A mutation is associated with reversible ventricular ectopy and dilated cardiomyopathy. Journal of the American College of Cardiology, 60 (16). pp.1566-73. ISSN 1558-3597 (OA)

Ohanian, Monique and Otway, Robyn and Fatkin, Diane (2012) Heuristic methods for finding pathogenic variants in gene coding sequences. Journal of the American Heart Association, 1 (5). pp. e002642. ISSN 2047-9980 (PMC OA)

Zhang, Bao-Ting and Whitehead, Nicholas P and Gervasio, Othon L and Reardon, Trent F and Vale, Molly and Fatkin, Diane and Dietrich, Alexander and Yeung, Ella W and Allen, David G (2012) Pathways of Ca²⁺ entry and cytoskeletal damage following eccentric contractions in mouse skeletal muscle. Journal of applied physiology (Bethesda, Md. : 1985), 112 (12). pp.2077-86. ISSN 1522-1601 (PMC OA)

Mann, Stefan A and Otway, Robyn and Guo, Guanglan and Soka, Magdalena and Karlsdotter, Lina and Trivedi, Gunjan and Ohanian, Monique and Zodgekar, Poonam and Smith, Robert A and Wouters, Merridee A and Subbiah, Rajesh and Walker, Bruce and Kuchar, Dennis and Sanders, Prashanthan and Griffiths, Lyn and Vandenberg, Jamie I and Fatkin, Diane (2012) Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk. Journal of the American College of Cardiology, 59 (11). pp.1017-25. ISSN 1558-3597 (OA)

Granados-Riveron, Javier T and Pope, Mark and Bu'lock, Frances A and Thornborough, Christopher and Eason, Jacqueline and Setchfield, Kerry and Ketley, Ami and Kirk, Edwin P and Fatkin, Diane and Feneley, Michael P and Harvey, Richard P and Brook, J David (2012) Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations. Congenital heart disease, 7 (2). pp.151-9. ISSN 1747-0803 (PMC OA)

Humphreys, David T and Hynes, Carly J and Patel, Hardip R and Wei, Grace H and Cannon, Leah and Fatkin, Diane and Suter, Catherine M and Clancy, Jennifer L and Preiss, Thomas (2012) Complexity of murine cardiomyocyte miRNA biogenesis, sequence variant expression and function. PloS one, 7 (2). pp. e30933. ISSN 1932-6203 (Gold OA)

Fatkin, Diane (2012) Familial dilated cardiomyopathy: Current challenges and future directions. Global cardiology science & practice, 2012 (1). p. 8. ISSN 2305-7823 (PMC OA)

Vidal, Christopher and Bermeo, Sandra and Fatkin, Diane and Duque, Gustavo (2012) Role of the nuclear envelope in the pathogenesis of age-related bone loss and osteoporosis. BoneKEy reports, 1. p. 62. ISSN 2047-6396 (PMC OA)

This list was generated on Wed Nov 25 10:27:53 2020 AEDT.