Items where Author is "Wilde, Arthur A.M."

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

Gigli, Marta and Stolfo, Davide and Graw, Sharon L. and Merlo, Marco and Gregorio, Caterina and Nee Chen, Suet and Dal Ferro, Matteo and PaldinoMD, Alessia and De Angelis, Giulia and Brun, Francesca and Jirikowic, Jean and Salcedo, Ernesto E. and Turja, Sylvia and Fatkin, Diane and Johnson, Renee and van Tintelen, J. Peter and Te Riele, Anneline S.J.M. and Wilde, Arthur A.M. and Lakdawala, Neal K. and Picard, Kermshlise and Miani, Daniela and Muser, Daniele and Maria Severini, Giovanni and Calkins, Hugh and James, Cynthia A. and Murray, Brittney and Tichnell, Crystal and Parikh, Victoria N. and Ashley, Euan A. and Reuter, Chloe and Song, Jiangping and Judge, Daniel P. and McKenna, William J. and Taylor, Matthew R.G. and Sinagra, Gianfranco and Mestroni, Luisa (2021) Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants. Circulation, 144 (20). pp.1600-1611. ISSN 0009-7322