Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hanne M. Boen"'
Autor:
Hanne M. Boen, Maaike Alaerts, Inge Goovaerts, Johan B. Saenen, Constantijn Franssen, Anne Vorlat, Tom Vermeulen, Hein Heidbuchel, Lut Van Laer, Bart Loeys, Emeline M. Van Craenenbroeck
Publikováno v:
Cardio-Oncology, Vol 10, Iss 1, Pp 1-12 (2024)
Abstract Background Variants in cardiomyopathy genes have been identified in patients with cancer therapy-related cardiac dysfunction (CTRCD), suggesting a genetic predisposition for the development of CTRCD. The diagnostic yield of genetic testing i
Externí odkaz:
https://doaj.org/article/d722bd93cc5b4cb3bf0e63ce250ce1f0
Autor:
Hanne M. Boen, Bert Vandendriessche, Jolien Schippers, Laura Rabaut, Aleksandra Nijak-Paeske, Peter Ponsaerts, Emeline M. Van Craenenbroeck, Bart Loeys, Maaike Alaerts
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103536- (2024)
Truncating variants in TTN (TTNtv) are present in 15–25 % of patients with idiopathic dilated cardiomyopathy. Interestingly, the pathogenicity of TTNtv seems to be linked to their location within the gene. More proximal I-band TTNtv (TTNtvI) harbou
Externí odkaz:
https://doaj.org/article/c3299bc2be0e424f95b05a7926882f59
Autor:
Hanne M. Boen, Maaike Alaerts, Lut Van Laer, Johan B. Saenen, Inge Goovaerts, Jarl Bastianen, Pieter Koopman, Philippe Vanduynhoven, Elke De Vuyst, Michael Rosseel, Hein Heidbuchel, Emeline M. Van Craenenbroeck, Bart Loeys
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
BackgroundVariants in the MYBPC3 gene are a frequent cause of hypertrophic cardiomyopathy (HCM) but display a large phenotypic heterogeneity. Founder mutations are often believed to be more benign as they prevailed despite potential negative selectio
Externí odkaz:
https://doaj.org/article/ff57bde99f3543aea920e69875af395f
Autor:
Hanne M Boen, Constantijn Franssen
Publikováno v:
European journal of preventive cardiology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6402ac87eeb21b4a858b1989d7d373c1
https://doi.org/10.1093/eurjpc/zwad104
https://doi.org/10.1093/eurjpc/zwad104
Autor:
Hanne M. Boen, Bart L. Loeys, Maaike Alaerts, Johan B. Saenen, Inge Goovaerts, Lut Van Laer, Anne Vorlat, Tom Vermeulen, Constantijn Franssen, Patrick Pauwels, Inez Rodrigus, Hein Heidbuchel, Emeline M Van Craenenbroeck
Publikováno v:
Journal of heart and lung transplantation
BACKGROUND: The importance of genetic testing for cardiomyopathies has increased in the last decade. However, in heart transplant patients with former cardiomyopathy, genetic testing in retrospect is not routinely performed. We hypothesize that the y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cbd6227ab31927e953c2d9775f116ac
https://pubmed.ncbi.nlm.nih.gov/36123002
https://pubmed.ncbi.nlm.nih.gov/36123002
Autor:
Arthur van den Wijngaard, Carlo Marcelis, Ingrid P.C. Krapels, Yvonne M. Hoedemaekers, Apollonia T. J. M. Helderman-van den Enden, Debby M.E.I. Hellebrekers, Job A J Verdonschot, Esther Brusse, Godelieve R.F. Claes, Hanne M Boen, Imke Christiaans, Janneke G. J. Hoeijmakers, Marlies Kempers, Pieter Koopman, Bart Loeys, Han G. Brunner, Stephane Heymans, Els K. Vanhoutte, Amber de Haan, Jaap I. van Waning, Ronald H. Lekanne Deprez, Annette F. Baas, Dennis Dooijes, Emeline M. Van Craenenbroeck, Daniela Q.C.M. Barge-Schaapveld, Folkert W. Asselbergs
Publikováno v:
Human mutation
Human Mutation, 41(6), 1091-1111. Wiley
Human Mutation
Human mutation, 41(6), 1091-1111. Wiley-Liss Inc.
Human Mutation, 41, 6, pp. 1091-1111
Human Mutation: Variation, Informatics and Disease, 41(6), 1091-1111. WILEY
Human Mutation, 41, 1091-1111
Human Mutation, 41(6), 1091-1111. Wiley
Human Mutation
Human mutation, 41(6), 1091-1111. Wiley-Liss Inc.
Human Mutation, 41, 6, pp. 1091-1111
Human Mutation: Variation, Informatics and Disease, 41(6), 1091-1111. WILEY
Human Mutation, 41, 1091-1111
Filamin C (FLNC) variants are associated with cardiac and muscular phenotypes. Originally, FLNC variants were described in myofibrillar myopathy (MFM) patients. Later, high‐throughput screening in cardiomyopathy cohorts determined a prominent role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28396717dc8ea773ff9ba4327b2e6ff1
http://hdl.handle.net/1942/34568
http://hdl.handle.net/1942/34568
