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

DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects

NOTCH1 变异体的 DNA 甲基化分析揭示了非综合征型先天性心脏缺陷的首个表观遗传特征

Dombrowsky, Gregor; van der Laan, Liselot; Silva, Ananília; Breckpot, Jeroen; Audain, Enrique; Wilsdon, Anna; Levy, Michael A; Vos, Niels; Mannens, Marcel; Wang, Jiao; Jain, Anjali; Lesurf, Robert; Winlaw, David; Bezzina, Connie R; Thomas, Mary Ann; Caliebe, Almuth; Klaassen, Sabine; Berger, Felix; Dittrich, Sven; Stiller, Brigitte; Abdul-Khaliq, Hashim; Dähnert, Ingo; Bu'Lock, Frances; Loughna, Siobhan; Brook, J David; Mital, Seema; Russell, Robert B; Pickardt, Thomas; Bauer, Ulrike; Kramer, Hans-Heiner; Uebing, Anselm; Henneman, Peter; Sadikovic, Bekim; Postma, Alex; Hitz, Marc-Phillip

Prognostic Value of Speckle Tracking Echocardiography-Derived Strain in Unmasking Risk for Arrhythmias in Children with Myocarditis

斑点追踪超声心动图衍生应变在揭示儿童心肌炎患者心律失常风险中的预后价值

Rolfs, Nele; Huber, Cynthia; Opgen-Rhein, Bernd; Altmann, Isabell; Anderheiden, Felix; Hecht, Tobias; Fischer, Marcus; Wiegand, Gesa; Reineker, Katja; Voges, Inga; Kiski, Daniela; Frede, Wiebke; Boehne, Martin; Khedim, Malika; Messroghli, Daniel; Klingel, Karin; Schwarzkopf, Eicke; Pickardt, Thomas; Schubert, Stephan; Lunze, Fatima I; Seidel, Franziska

Myocarditis and sports in the young: data from a nationwide registry on myocarditis-"MYKKE-Sport"

青少年心肌炎与运动:来自全国心肌炎登记处“MYKKE-Sport”的数据

Schöffl, Isabelle; Holler, Sophia; Dittrich, Sven; Pickardt, Thomas; Opgen-Rhein, Bernd; Boehne, Martin; Wannenmacher, Bardo; Reineke, Katja; Wiegand, Gesa; Hecht, Tobias; Kaestner, Michael; Messroghli, Daniel; Schubert, Stephan; Seidel, Franziska; Weigelt, Annika

[Less surgery and lower cost due to back pain in a care program with an interdisciplinary second opinion procedure : A controlled non-randomized intervention study based on claims data]

[一项基于理赔数据的对照非随机干预研究:采用跨学科第二诊疗意见的护理方案可减少因背痛引起的手术次数和降低医疗成本]

Wagner, Christoph J; Lindena, Gabriele; Ayyad, Grit; Otzdorff, Andrea; Marnitz, Ulf; Bienek, Karen; von Pickardt, Björn; Sehlen, Stephanie; Wyrwich, Werner

Le Cœur en Sabot: shape associations with adverse events in repaired tetralogy of Fallot

Le Cœur en Sabot:形状与法洛四联症修复不良事件的关联

Mîra, Anna; Lamata, Pablo; Pushparajah, Kuberan; Abraham, Georgina; Mauger, Charlène A; McCulloch, Andrew D; Omens, Jeffrey H; Bissell, Malenka M; Blair, Zach; Huffaker, Tyler; Tandon, Animesh; Engelhardt, Sandy; Koehler, Sven; Pickardt, Thomas; Beerbaum, Philipp; Sarikouch, Samir; Latus, Heiner; Greil, Gerald; Young, Alistair A; Hussain, Tarique

Pathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis-Further Impact of Heterozygous Immune Disorder Gene Variants?

心肌病致病基因变异是儿童心肌炎的根本原因——杂合免疫疾病基因变异的进一步影响?

Seidel, Franziska; Laser, Kai Thorsten; Klingel, Karin; Dartsch, Josephine; Theisen, Simon; Pickardt, Thomas; Holtgrewe, Manuel; Gärtner, Anna; Berger, Felix; Beule, Dieter; Milting, Hendrik; Schubert, Stephan; Klaassen, Sabine; Kühnisch, Jirko

Compensatory Upregulation of Anti-Beta-Adrenergic Receptor Antibody Levels Might Prevent Heart Failure Presentation in Pediatric Myocarditis

抗β-肾上腺素能受体抗体水平的代偿性上调可能预防儿童心肌炎患者出现心力衰竭。

Seidel, Franziska; Scheibenbogen, Carmen; Heidecke, Harald; Opgen-Rhein, Bernd; Pickardt, Thomas; Klingel, Karin; Berger, Felix; Messroghli, Daniel; Schubert, Stephan

Pathogenic Variants Associated With Dilated Cardiomyopathy Predict Outcome in Pediatric Myocarditis

与扩张型心肌病相关的致病变异可预测儿童心肌炎的预后

Seidel, Franziska; Holtgrewe, Manuel; Al-Wakeel-Marquard, Nadya; Opgen-Rhein, Bernd; Dartsch, Josephine; Herbst, Christopher; Beule, Dieter; Pickardt, Thomas; Klingel, Karin; Messroghli, Daniel; Berger, Felix; Schubert, Stephan; Kühnisch, Jirko; Klaassen, Sabine

RNA expression profiles and regulatory networks in human right ventricular hypertrophy due to high pressure load

高压负荷引起的人类右心室肥厚中的RNA表达谱和调控网络

Chouvarine, Philippe; Photiadis, Joachim; Cesnjevar, Robert; Scheewe, Jens; Bauer, Ulrike M M; Pickardt, Thomas; Kramer, Hans-Heiner; Dittrich, Sven; Berger, Felix; Hansmann, Georg

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

基因组变异的整合分析揭示了候选单倍体不足基因与先天性心脏病的新关联

Audain, Enrique; Wilsdon, Anna; Breckpot, Jeroen; Izarzugaza, Jose M G; Fitzgerald, Tomas W; Kahlert, Anne-Karin; Sifrim, Alejandro; Wünnemann, Florian; Perez-Riverol, Yasset; Abdul-Khaliq, Hashim; Bak, Mads; Bassett, Anne S; Benson, D Woodrow; Berger, Felix; Daehnert, Ingo; Devriendt, Koenraad; Dittrich, Sven; Daubeney, Piers Ef; Garg, Vidu; Hackmann, Karl; Hoff, Kirstin; Hofmann, Philipp; Dombrowsky, Gregor; Pickardt, Thomas; Bauer, Ulrike; Keavney, Bernard D; Klaassen, Sabine; Kramer, Hans-Heiner; Marshall, Christian R; Milewicz, Dianna M; Lemaire, Scott; Coselli, Joseph S; Mitchell, Michael E; Tomita-Mitchell, Aoy; Prakash, Siddharth K; Stamm, Karl; Stewart, Alexandre F R; Silversides, Candice K; Siebert, Reiner; Stiller, Brigitte; Rosenfeld, Jill A; Vater, Inga; Postma, Alex V; Caliebe, Almuth; Brook, J David; Andelfinger, Gregor; Hurles, Matthew E; Thienpont, Bernard; Larsen, Lars Allan; Hitz, Marc-Phillip