Items where Author is "Bootsma, Marianne"

Article

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

Copier, Jaël S and Bootsma, Marianne and Ng, Chai A and Wilde, Arthur A M and Bertels, Robin A and Bikker, Hennie and Christiaans, Imke and van der Crabben, Saskia N and Hol, Janna A and Koopmann, Tamara T and Knijnenburg, Jeroen and Lommerse, Aafke A J and van der Smagt, Jasper J and Bezzina, Connie R and Vandenberg, Jamie I and Verkerk, Arie O and Barge-Schaapveld, Daniela Q C M and Lodder, Elisabeth M (2022) Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance. Human Molecular Genetics, 32 (7). pp.1072-1082. ISSN 0964-6906