Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Jacob Tfelt‐Hansen"'
Autor:
Steffan Noe Christiansen, Jeppe Dyrberg Andersen, Marie-Louise Kampmann, Jing Liu, Mikkel Meyer Andersen, Jacob Tfelt-Hansen, Niels Morling
Publikováno v:
Epigenetics, Vol 17, Iss 12, Pp 1636-1645 (2022)
The Infinium MethylationEPIC BeadChip (EPIC) is a reliable method for measuring the DNA methylation of more than 850,000 CpG positions. In clinical and forensic settings, it is critical to be able to work with low DNA amounts without risking reduced
Externí odkaz:
https://doaj.org/article/924f15373a08427dbd28fa99f965e87b
Autor:
Reza Jabbari, Javad Jabbari, Charlotte Glinge, Bjarke Risgaard, Stefan Sattler, Bo Gregers Winkel, Christian Juhl Terkelsen, Hans-Henrik Tilsted, Lisette Okkels Jensen, Mikkel Hougaard, Stig Haunsø, Thomas Engstrøm, Christine M. Albert, Jacob Tfelt-Hansen
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-6 (2017)
Abstract Background Cohort studies have revealed an increased risk for ventricular fibrillation (VF) and sudden cardiac death (SCD) in patients with atrial fibrillation (AF). In this study, we hypothesized that single nucleotide polymorphisms (SNP) p
Externí odkaz:
https://doaj.org/article/a16e21d87a6742e7bf6838d57e9ce28a
Autor:
Steffan Noe Christiansen, Stine Bøttcher Jacobsen, Jeppe Dyrberg Andersen, Marie-Louise Kampmann, Linea Christine Trudsø, Kristine Boisen Olsen, Jacob Tfelt-Hansen, Jytte Banner, Niels Morling
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 6, p 2790 (2021)
Sudden cardiac death (SCD) is a diagnostic challenge in forensic medicine. In a relatively large proportion of the SCDs, the deaths remain unexplained after autopsy. This challenge is likely caused by unknown disease mechanisms. Changes in DNA methyl
Externí odkaz:
https://doaj.org/article/a9d198574f0b4fa2b66c289775394c26
Autor:
Peter Lichtner, Pharawee Wandee, John Mauleekoonphairoj, Apichai Khongphatthanayothin, Pattarapong Makarawate, Yong Poovorawan, Thomas Meitinger, Dujdao Sahasatas, Somchai Prechawat, Rungroj Krittayaphong, Boosamas Sutjaporn, Charlotte Glinge, Ahmad S. Amin, Arthur A.M. Wilde, Fleur V.Y. Tjong, Montawatt Amnueypol, Alisara Anannab, Rafik Tadros, Tachapong Ngarmukos, Connie R. Bezzina, Krystien V.V. Lieve, Duangdao Wichadakul, Roddy Walsh, Gumpanart Veerakul, Michael W.T. Tanck, Sunchai Payungporn, Jacob Tfelt-Hansen, Wanwarang Wongcharoen, Koonlawee Nademanee
Publikováno v:
Heart rhythm, 17(12), 2145-2153. Elsevier
BACKGROUND: Mutations in SCN5A are rarely found in Thai patients with Brugada syndrome (BrS). Recent evidence suggested that common genetic variations may underlie BrS in a complex inheritance model. OBJECTIVE: The purpose of this study was to find c
Autor:
Bernard Belhassen, Vincent Probst, Ruben Casado-Arroyo, Jean-Sylvain Hermida, Guy Zahavi, Laurens P Bosman, Anne Rollin, Giulio Conte, Esther Zorio, Rob W Roudijk, Carla Giustetto, Josef Kautzner, Firat Duru, Xavier Waintraub, Gabriele Paglino, J. Peter van Tintelen, Elijah R. Behr, Jacob Tfelt-Hansen, Philippe Maury, Francisco Bermúdez-Jiménez, Sandro Ninni, Stepan Havranek, Estelle Gandjbakhch, Alessio Gasperetti, Simone Sala, Josep Brugada, Dominique Lacroix, Chris Miles, Frederic Sacher, Laurent Fauchier, Paolo Della Bella, Christian de Chillou, Anneline S.J.M. te Riele, Elena Arbelo, Petr Peichl, Srijita Sen-Chowdhry, Alexandros Protonotarios, Mikael Laredo, Giovanni Peretto, Anat Milman, Richard N.W. Hauer, Leonardo Calò, Guillaume Duthoit, Antoine Andorin, Jean-Marc Sellal, Eyal Nof, Nicolas Badenco, Konstantinos P. Letsas, Roy Beinart, Bertrand Pierre
Publikováno v:
Europace
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
EUROPACE
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
EUROPACE
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Aims In arrhythmogenic cardiomyopathy (ACM), sustained ventricular tachycardia (VT) typically displays a left bundle branch block (LBBB) morphology while a right bundle branch block (RBBB) morphology is rare. The present study assesses the VT morphol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a568005e23b57a5e7f4c3acf8ccdc8d
https://hdl.handle.net/10668/19774
https://hdl.handle.net/10668/19774
Autor:
Giulio Conte, Kengo Kusano, David C Johnson, P. Delise, Shingo Maeda, Domenico Corrado, Belinda Gray, Leonardo Calò, Gi-Byoung Nam, Ruben Casado-Arroyo, Georgia Sarquella-Brugada, Aviram Hochstadt, Jean-Baptiste Gourraud, Christian Veltmann, Jacob Tfelt-Hansen, Silvia G Priori, Camilla H Jespersen, Ramon Brugada, Kenzo Hirao, Anat Milman, Carla Giustetto, Yuka Mizusawa, Jimmy Jm Juang, Giuseppe Allocca, Vincent Probst, Antoine Leenhardt, Pieter G. Postema, Bernard Belhassen, Andrea Mazzanti, Pedro Brugada, Elijah R. Behr, Elena Arbelo, Josep Brugada, T Kamakura, Antoine Andorin, Masahiko Takagi, Isabelle Denjoy, Yoshihide Takahashi, Fiorenzo Gaita, Zhengrong Huang, Arthur A.M. Wilde, Sung Hwan Kim, Takeshi Aiba, Gan-Xin Yan
Publikováno v:
Circulation. Genomic and precision medicine, 14(5). Lippincott Williams and Wilkins Ltd.
Milman, A, Behr, E R, Gray, B, Johnson, D C, Andorin, A, Hochstadt, A, Gourraud, J-B, Maeda, S, Takahashi, Y, Jm Juang, J, Kim, S-H, Kamakura, T, Aiba, T, Postema, P G, Mizusawa, Y, Denjoy, I, Giustetto, C, Conte, G, Huang, Z, Sarquella-Brugada, G, Mazzanti, A, Jespersen, C H, Arbelo, E, Brugada, R, Calo, L, Corrado, D, Casado-Arroyo, R, Allocca, G, Takagi, M, Delise, P, Brugada, J, Tfelt-Hansen, J, Priori, S G, Veltmann, C, Yan, G-X, Brugada, P, Gaita, F, Leenhardt, A, Wilde, A A M, Kusano, K F, Nam, G-B, Hirao, K, Probst, V & Belhassen, B 2021, ' Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events : Insights From the SABRUS in 392 Probands ', Circulation. Genomic and precision medicine, vol. 14, no. 5, e003222 . https://doi.org/10.1161/CIRCGEN.120.003222
Circulation-Genomic and Precision Medicine
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Milman, A, Behr, E R, Gray, B, Johnson, D C, Andorin, A, Hochstadt, A, Gourraud, J-B, Maeda, S, Takahashi, Y, Jm Juang, J, Kim, S-H, Kamakura, T, Aiba, T, Postema, P G, Mizusawa, Y, Denjoy, I, Giustetto, C, Conte, G, Huang, Z, Sarquella-Brugada, G, Mazzanti, A, Jespersen, C H, Arbelo, E, Brugada, R, Calo, L, Corrado, D, Casado-Arroyo, R, Allocca, G, Takagi, M, Delise, P, Brugada, J, Tfelt-Hansen, J, Priori, S G, Veltmann, C, Yan, G-X, Brugada, P, Gaita, F, Leenhardt, A, Wilde, A A M, Kusano, K F, Nam, G-B, Hirao, K, Probst, V & Belhassen, B 2021, ' Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events : Insights From the SABRUS in 392 Probands ', Circulation. Genomic and precision medicine, vol. 14, no. 5, e003222 . https://doi.org/10.1161/CIRCGEN.120.003222
Circulation-Genomic and Precision Medicine
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Background: Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, SCN5A. However, genetic studies of patients with BrS with arrhythmic events have been limited. We sought to compare various clinical, ECG, and electro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4996f0a0777debaf7d4e6c5402d63c04
https://pure.amc.nl/en/publications/genotypephenotype-correlation-of-scn5a-genotype-in-patients-with-brugada-syndrome-and-arrhythmic-events(30208168-1225-4d88-9df0-8b320cc73dcd).html
https://pure.amc.nl/en/publications/genotypephenotype-correlation-of-scn5a-genotype-in-patients-with-brugada-syndrome-and-arrhythmic-events(30208168-1225-4d88-9df0-8b320cc73dcd).html
Autor:
Lennart J. Blom, Ingrid P.C. Krapels, Bo Gregers Winkel, Sanne A Groeneveld, Greg Mellor, Elijah R. Behr, Jacob Tfelt-Hansen, Bianca van Rees, Chiara Scrocco, Johannes Bargehr, Andrew D. Krahn, Paul G.A. Volders, Rutger J. Hassink, Bode Ensam
Publikováno v:
Circulation-Arrhythmia and Electrophysiology, 14(3):009089, 296-305. LIPPINCOTT WILLIAMS & WILKINS
Background: Familial cascade screening is well established in patients with heritable cardiac disease and in cases of sudden arrhythmic death syndrome. The clinical benefit of family screening in idiopathic ventricular fibrillation (IVF) is unknown.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c9ffd4431bda1ebbdb157fb30417fca
https://cris.maastrichtuniversity.nl/en/publications/1d14a670-eafe-4db2-a944-4b5c7bb0abe0
https://cris.maastrichtuniversity.nl/en/publications/1d14a670-eafe-4db2-a944-4b5c7bb0abe0
Autor:
Stine B Jacobsen, Kristine Boisen Olsen, Linea Christine Trudsø, Jacob Tfelt-Hansen, Jeppe Dyrberg Andersen, Jytte Banner, Niels Morling, Steffan Noe Christiansen, Marie-Louise Kampmann
Publikováno v:
International Journal of Molecular Sciences
Christiansen, S N, Jacobsen, S B, Andersen, J D, Kampmann, M L, Trudsø, L C, Olsen, K B, Tfelt-Hansen, J, Banner, J & Morling, N 2021, ' Differential methylation in the GSTT1 regulatory region in sudden unexplained death and sudden unexpected death in epilepsy ', International Journal of Molecular Sciences, vol. 22, no. 6, 2790 . https://doi.org/10.3390/ijms22062790
International Journal of Molecular Sciences, Vol 22, Iss 2790, p 2790 (2021)
Volume 22
Issue 6
Christiansen, S N, Jacobsen, S B, Andersen, J D, Kampmann, M L, Trudsø, L C, Olsen, K B, Tfelt-Hansen, J, Banner, J & Morling, N 2021, ' Differential methylation in the GSTT1 regulatory region in sudden unexplained death and sudden unexpected death in epilepsy ', International Journal of Molecular Sciences, vol. 22, no. 6, 2790 . https://doi.org/10.3390/ijms22062790
International Journal of Molecular Sciences, Vol 22, Iss 2790, p 2790 (2021)
Volume 22
Issue 6
Sudden cardiac death (SCD) is a diagnostic challenge in forensic medicine. In a relatively large proportion of the SCDs, the deaths remain unexplained after autopsy. This challenge is likely caused by unknown disease mechanisms. Changes in DNA methyl
Autor:
Elijah R. Behr, Peter J. Fleming, Alban-Elouen Baruteau, Marta C. Cohen, Amie Jaye, Leonie C.H. Wong, Pritha Chanana, Michael A. Simpson, Belinda Gray, David J. Tester, Jacob Tfelt-Hansen, Michael J. Ackerman, Iona Jeffrey, Jared M. Evans, Margaret J. Evans
Publikováno v:
Gray, B, Tester, D J, Wong, L C, Chanana, P, Jaye, A, Evans, J M, Baruteau, A E, Evans, M, Fleming, P, Jeffrey, I, Cohen, M, Tfelt-Hansen, J, Simpson, M A, Ackerman, M J & Behr, E R 2019, ' Noncardiac genetic predisposition in sudden infant death syndrome ', Genetics in Medicine, vol. 21, no. 3, pp. 641–649 . https://doi.org/10.1038/s41436-018-0131-4
Gray, B, Tester, D J, Wong, L C, Chanana, P, Jaye, A, Evans, J M, Baruteau, A-E, Evans, M, Fleming, P, Jeffrey, I, Cohen, M, Tfelt-Hansen, J, Simpson, M A, Ackerman, M J & Behr, E R 2018, ' Noncardiac genetic predisposition in sudden infant death syndrome ', Genetics in Medicine . https://doi.org/10.1038/s41436-018-0131-4
Gray, B, Tester, D J, Wong, L C, Chanana, P, Jaye, A, Evans, J M, Baruteau, A-E, Evans, M, Fleming, P, Jeffrey, I, Cohen, M, Tfelt-Hansen, J, Simpson, M A, Ackerman, M J & Behr, E R 2018, ' Noncardiac genetic predisposition in sudden infant death syndrome ', Genetics in Medicine . https://doi.org/10.1038/s41436-018-0131-4
PURPOSE: Sudden infant death syndrome (SIDS) is the commonest cause of sudden death of an infant; however, the genetic basis remains poorly understood. We aimed to identify noncardiac genes underpinning SIDS and determine their prevalence compared wi
Autor:
Charles Antzelevitch, Ahmad S. Amin, Bo Gregers Winkel, Dan M. Roden, Stefan Kääb, Jonathan R. Skinner, Seiko Ohno, Julien Barc, Birgit Stallmeyer, Carla Giustetto, Connie R. Bezzina, Francesco Mazzarotto, Tomas Robyns, Carlo Napolitano, Stellan Mörner, Doris Škorić-Milosavljević, Sven Dittmann, Kenichiro Yamagata, Sonia Van Dooren, Anniek Corveleyn, Carlo de Asmundis, Ramon Brugada, K Usuda, Yuji Tanaka, Sven Zumhagen, Tadashi Nakajima, Johan Saenen, Elijah R. Behr, Hector Barajas-Martinez, Stéphane Bézieau, Masao Yoshinaga, Georgia Sarquella-Brugada, Paul G.A. Volders, Juan R. Gimeno, Lia Crotti, Charlotte Glinge, Andrea Mazzanti, Ingrid P.C. Krapels, Nicola Whiffin, Sebastian Clauss, Yoshiaki Kaneko, James S. Ware, Minoru Horie, Keiko Shimamoto, Isabelle Denjoy, Pieter G. Postema, Christian Krijger, Takeshi Aiba, Masahiko Kurabayashi, Pyotr G. Platonov, Regina Sebastiano, Cristina Gil Ortuño, Annika Rydberg, Roddy Walsh, Michael J. Ackerman, Hideki Itoh, M. Benjamin Shoemaker, Can Hasdemir, Pascale Guicheney, J. Martijn Bos, Frederic Sacher, Takeru Makiyama, Julieta Lazarte, Maarten P. van den Berg, Dominique Babuty, David J. Tester, Silvia Castelletti, Jacques Mansourati, Antoine Leenhardt, Paul A. van der Zwaag, Sanjay Sharma, Elena Arbelo, Candan Celen, Pier D. Lambiase, Maria Christina Kotta, Johannes Steinfurt, Jean-Baptiste Gourraud, Pedro Brugada, Wataru Shimizu, Josep Brugada, Jørgen K. Kanters, Eline A. Nannenberg, Silvia G. Priori, Mary N. Sheppard, Richard Redon, Morten S. Olesen, Jeroen Breckpot, Britt M. Beckmann, Naomasa Makita, Martin Borggrefe, Rafik Tadros, Jean-Jacques Schott, Jacob Tfelt-Hansen, Steven A. Lubitz, Hatice Şahin, Najim Lahrouchi, Michael Papadakis, Daisuke Hazeki, Kenshi Hayashi, Oscar Campuzano, Katja E. Odening, Federica Dagradi, Eric Schulze-Bahr, Boris Rudic, Hiroki Kimoto, Vincent Probst, Jason D. Roberts, Raphaël P. Martins, Bart Loeys, Daniela F. Giachino, F. Kyndt, Kimie Ohkubo, Taisuke Ishikawa, Catarina Lundin, Lut Van Laer, Patrick T. Ellinor, Maria Sabater Molina, Peter J. Schwartz, Annika Winbo
Publikováno v:
Nantes Referral Center for inherited cardiac arrhythmia 2021, ' Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls ', Genetics In Medicine, vol. 23, pp. 47–58 . https://doi.org/10.1038/s41436-020-00946-5
Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, 2020, ⟨10.1038/s41436-020-⟩
Genetics in Medicine, 47-58. Nature Publishing Group
ISSUE=1;STARTPAGE=47;ENDPAGE=58;ISSN=1098-3600;TITLE=Genetics in Medicine
Genetics in medicine
Walsh, Roddy; Lahrouchi, Najim; Tadros, Rafik; Kyndt, Florence; Glinge, Charlotte; Postema, Pieter G; Amin, Ahmad S; Nannenberg, Eline A; Ware, James S; Whiffin, Nicola; Mazzarotto, Francesco; Škorić-Milosavljević, Doris; Krijger, Christian; Arbelo, Elena; Babuty, Dominique; Barajas-Martinez, Hector; Beckmann, Britt M; Bézieau, Stéphane; Bos, J Martijn; Breckpot, Jeroen; ... (2021). Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genetics in medicine, 23(1), pp. 47-58. Springer Nature 10.1038/s41436-020-00946-5
Genetics in medicine, 23(1), 47-58. Lippincott Williams and Wilkins
Genetics in Medicine, 23(1), 47-58. Nature Publishing Group
Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, 2020, ⟨10.1038/s41436-020-⟩
Genetics in Medicine, 47-58. Nature Publishing Group
ISSUE=1;STARTPAGE=47;ENDPAGE=58;ISSN=1098-3600;TITLE=Genetics in Medicine
Genetics in medicine
Walsh, Roddy; Lahrouchi, Najim; Tadros, Rafik; Kyndt, Florence; Glinge, Charlotte; Postema, Pieter G; Amin, Ahmad S; Nannenberg, Eline A; Ware, James S; Whiffin, Nicola; Mazzarotto, Francesco; Škorić-Milosavljević, Doris; Krijger, Christian; Arbelo, Elena; Babuty, Dominique; Barajas-Martinez, Hector; Beckmann, Britt M; Bézieau, Stéphane; Bos, J Martijn; Breckpot, Jeroen; ... (2021). Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genetics in medicine, 23(1), pp. 47-58. Springer Nature 10.1038/s41436-020-00946-5
Genetics in medicine, 23(1), 47-58. Lippincott Williams and Wilkins
Genetics in Medicine, 23(1), 47-58. Nature Publishing Group
Purpose: Stringent variant interpretation guidelines can lead to high rates of variants of uncertain significance (VUS) for genetically heterogeneous disease like long QT syndrome (LQTS) and Brugada syndrome (BrS). Quantitative and disease-specific c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::193437f5ba4e2e30da09bd570e67f778
http://hdl.handle.net/10044/1/82315
http://hdl.handle.net/10044/1/82315