日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

QTc measurement using Apple Watch electrocardiogram in congenital long QT syndrome

使用 Apple Watch 心电图测量先天性长 QT 综合征的 QTc 间期

van Steijn, Nicole J; Bergeman, Auke T; van der Werf, Christian; Veenstra, Renee N A M; van de Vijver, Willem R; Helmink, Ole G; Somsen, G Aernout; Tulevski, Igor I; Knops, Reinoud E; Wilde, Arthur A M; Winter, Michiel M

European Reference Networks - a flagship activity of the EU in the field of rare and complex diseases: from 2017 to 2025

欧洲参考网络——欧盟在罕见病和复杂疾病领域的一项旗舰活动:2017年至2025年

Graessner, Holm; Ripp, Sophie; Pereira, Alberto M; Schaefer, Franz; Mathijssen, Irene; Blay, Jean-Yves; Mulders, Peter F A; Evangelista, Teresinha; Ligtenberg, Marjolijn J L; Wilde, Arthur A M; Ladenstein, Ruth; Lohse, Ansgar W; Mosca, Marta; Swart, Joost Frans; Hernández, Francisco; Fenaux, Pierre; Dollfus, Hélène; Verloes, Alain; Wagner, Thomas; Bodemer, Christine; Wijnen, Rene; Scarpa, Maurizio; Jondeau, Guillaume; Tumienė, Birutė; Gallina, Sandra; Arzimanoglou, Alexis; Sangiorgi, Luca

Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies

利用遗传性心肌病中共同的和相反的遗传机制

Kramarenko, Daria R; Haydarlou, Poeya; Powell, George J; Rämö, Joel T; Janan, Riyad; Prince, Claire; Zimmerman, Dominic S; Theotokis, Pantazis; Thami, Prisca K; Haas, Jan; Garnier, Sophie; Rühle, Frank; Poel, Edwin; Schmidt, Amand F; Day, Sharlene; Helms, Adam; Lampert, Rachel; Parikh, Victoria; Ingles, Jodie; Olivotto, Iacopo; Lakdawala, Neal; Owens, Anjali; Saberi, Sara; Stendhal, John; Ashley, Euan; Gray, Belinda; Russell, Mark W; Ryan, Thomas D; Rossano, Joseph W; Abrams, Dominic; Miller, Erin; Lin, Kimberly; Maurizi, Niccolo; Argiro, Alessia; Berry, Colin; Cooper, Rob; Flett, Andrew S; Gardner, Roy S; Greenwood, John P; Halliday, Brian P; Hutchings, David; Mahmod, Masliza; McCann, Gerry P; Page, Stephen P; Peebles, Charles; Raman, Betty; Swoboda, Peter; Varnava, Amanda; Wright, David; Prasad, Sanjay; Cook, Stuart; Tayal, Upsala Paz; Buchan, Rachel; Walsh, Roddy; Wilde, Arthur A M; Meder, Benjamin; Charron, Philippe; Goel, Anuj; Amin, Ahmad S; Ellinor, Patrick T; Aragam, Krishna G; Tadros, Rafik; Pinto, Yigal M; Ho, Carolyn Y; Watkins, Hugh; Ware, James S; Bezzina, Connie R; Jurgens, Sean J

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand

泰国SCN5A基因中一种罕见的非编码增强子变异导致布鲁加达综合征高发

Walsh, Roddy; Mauleekoonphairoj, John; Mengarelli, Isabella; Bosada, Fernanda M; Verkerk, Arie O; van Duijvenboden, Karel; Poovorawan, Yong; Wongcharoen, Wanwarang; Sutjaporn, Boosamas; Wandee, Pharawee; Chimparlee, Nitinan; Chokesuwattanaskul, Ronpichai; Vongpaisarnsin, Kornkiat; Dangkao, Piyawan; Wu, Cheng-I; Tadros, Rafik; Amin, Ahmad S; Lieve, Krystien V V; Postema, Pieter G; Kooyman, Maarten; Beekman, Leander; Sahasatas, Dujdao; Amnueypol, Montawatt; Krittayaphong, Rungroj; Prechawat, Somchai; Anannab, Alisara; Makarawate, Pattarapong; Ngarmukos, Tachapong; Phusanti, Keerapa; Veerakul, Gumpanart; Kingsbury, Zoya; Newington, Taksina; Maheswari, Uma; Ross, Mark T; Grace, Andrew; Lambiase, Pier D; Behr, Elijah R; Schott, Jean-Jacques; Redon, Richard; Barc, Julien; Christoffels, Vincent M; Wilde, Arthur A M; Nademanee, Koonlawee; Bezzina, Connie R; Khongphatthanayothin, Apichai

Inositol 1,4,5-Trisphosphate Receptor 1 Gain-of-Function Increases the Risk for Cardiac Arrhythmias in Mice and Humans

肌醇1,4,5-三磷酸受体1功能获得性突变增加小鼠和人类发生心律失常的风险

Sun, Bo; Ni, Mingke; Li, Yanhui; Song, Zhenpeng; Wang, Hui; Zhu, Hai-Lei; Wei, Jinhong; Belke, Darrell; Cai, Shitian; Guo, Wenting; Yao, Jinjing; Tian, Shanshan; Estillore, John Paul; Wang, Ruiwu; Søndergaard, Mads Toft; Brohus, Malene; Rohde, Palle Duun; Mu, Yongxin; Vallmitjana, Alexander; Benitez, Raul; Hove-Madsen, Leif; Overgaard, Michael Toft; Fishman, Glenn I; Chen, Ju; Sanatani, Shubhayan; Wilde, Arthur A M; Fill, Michael; Ramos-Franco, Josefina; Nyegaard, Mette; Chen, S R Wayne

Epicardial adipose tissue and malignant ventricular arrhythmias in phospholamban p.(Arg14del) variant carriers

磷蛋白p.(Arg14del)变异携带者的心外膜脂肪组织和恶性室性心律失常

Mahmoud, Belend; Cox, Moniek G P J; de Brouwer, Remco; van der Heide, Myrthe Y C; Gorter, Thomas M; Meems, Laura M G; Wilde, Arthur A M; van Veldhuisen, Dirk J; de Boer, Rudolf A; Westenbrink, B Daan

Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings

在一般人群和不同临床环境中评估肥厚型心肌病的多基因评分

Zheng, Sean L; Jurgens, Sean J; McGurk, Kathryn A; Xu, Xiao; Grace, Chris; Theotokis, Pantazis I; Buchan, Rachel J; Francis, Catherine; de Marvao, Antonio; Curran, Lara; Bai, Wenjia; Pua, Chee Jian; Tang, Hak Chiaw; Jorda, Paloma; van Slegtenhorst, Marjon A; Verhagen, Judith M A; Harper, Andrew R; Ormondroyd, Elizabeth; Chin, Calvin W L; Pantazis, Antonis; Baksi, John; Halliday, Brian P; Matthews, Paul; Pinto, Yigal M; Walsh, Roddy; Amin, Ahmad S; Wilde, Arthur A M; Cook, Stuart A; Prasad, Sanjay K; Barton, Paul J R; O'Regan, Declan P; Lumbers, R T; Goel, Anuj; Tadros, Rafik; Michels, Michelle; Watkins, Hugh; Bezzina, Connie R; Ware, James S

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

大规模全基因组关联分析揭示肥厚型心肌病的新遗传位点和机制

Tadros, Rafik; Zheng, Sean L; Grace, Christopher; Jordà, Paloma; Francis, Catherine; West, Dominique M; Jurgens, Sean J; Thomson, Kate L; Harper, Andrew R; Ormondroyd, Elizabeth; Xu, Xiao; Theotokis, Pantazis I; Buchan, Rachel J; McGurk, Kathryn A; Mazzarotto, Francesco; Boschi, Beatrice; Pelo, Elisabetta; Lee, Michael; Noseda, Michela; Varnava, Amanda; Vermeer, Alexa M C; Walsh, Roddy; Amin, Ahmad S; van Slegtenhorst, Marjon A; Roslin, Nicole M; Strug, Lisa J; Salvi, Erika; Lanzani, Chiara; de Marvao, Antonio; Roberts, Jason D; Tremblay-Gravel, Maxime; Giraldeau, Genevieve; Cadrin-Tourigny, Julia; L'Allier, Philippe L; Garceau, Patrick; Talajic, Mario; Gagliano Taliun, Sarah A; Pinto, Yigal M; Rakowski, Harry; Pantazis, Antonis; Bai, Wenjia; Baksi, John; Halliday, Brian P; Prasad, Sanjay K; Barton, Paul J R; O'Regan, Declan P; Cook, Stuart A; de Boer, Rudolf A; Christiaans, Imke; Michels, Michelle; Kramer, Christopher M; Ho, Carolyn Y; Neubauer, Stefan; Matthews, Paul M; Wilde, Arthur A M; Tardif, Jean-Claude; Olivotto, Iacopo; Adler, Arnon; Goel, Anuj; Ware, James S; Bezzina, Connie R; Watkins, Hugh

Accumulating evidence for epicardial ablation in malignant forms of Brugada syndrome: summary of two randomized clinical trials

越来越多的证据表明,心外膜消融术对恶性布鲁加达综合征有效:两项随机临床试验的总结

Postema, Pieter G; Behr, Elijah R; Wilde, Arthur A M

Extreme phenotypes of the female athlete's heart: a sports-specific cardiac magnetic resonance imaging study

女性运动员心脏的极端表型:一项针对特定运动的心脏磁共振成像研究

van Hattum, Juliette C; van Diepen, Maarten A; Verwijs, Sjoerd M; Boekholdt, S Matthijs; van Randen, Adrienne; Groenink, Maarten; Planken, R Nils; Moen, Maarten H; Daems, Joëlle J N; Prakken, Niek H J; van de Sande, Danny A J P; Velthuis, Birgitta K; de Vries, Suzanna; Walhout, Ronald J; Pinto, Yigal M; Wilde, Arthur A M; Jørstad, Harald T