檢索結果 - Elisabeth M. Lodder
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Dissection of a Quantitative Trait Locus for PR Interval Duration Identifies Tnni3k as a Novel Modulator of Cardiac Conduction 由 Elisabeth M. Lodder, Brendon P. Scicluna, Annalisa Milano, Albert Y. Sun, Hao Tang, Carol Ann Remme, Perry D. Moerland, Michael W.T. Tanck, Geoffrey S. Pitt, Douglas A. Marchuk, Connie R. Bezzina
出版 2012Artigo -
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Switch From Fetal to Adult <i>SCN5A</i> Isoform in Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease–Causing Mutatio... 由 Christiaan C. Veerman, Isabella Mengarelli, Elisabeth M. Lodder, Georgios Kosmidis, Milena Bellin, Miao Zhang, Sven Dittmann, Kaomei Guan, Arthur A.M. Wilde, Eric Schulze‐Bahr, Boris Greber, Connie R. Bezzina, Arie O. Verkerk
出版 2017Artigo -
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Reduced kinase function in two ultra‐rare <scp><i>TNNI3K</i></scp> variants in families with congenital junctional ectopic tachycardia 由 Caroline Pham, Tamara T. Koopmann, Jeffrey M. Vinocur, Nico A. Blom, Vivian Nogueira Silbiger, Kirti Mittal, Marianne Bootsma, Kaylin C. A. Palm, Sally‐Ann B. Clur, Daniela Q.C.M. Barge‐Schaapveld, Robert M. Hamilton, Elisabeth M. Lodder
出版 2024Artigo -
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Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart 由 Tamara T. Koopmann, Michiel Adriaens, Perry D. Moerland, Roos F. Marsman, Marinda Westerveld, Sean Lal, Taifang Zhang, Christine Q. Simmons, István Baczkó, Cristobal G. dos Remedios, Nanette H. Bishopric, András Varró, Alfred L. George, Elisabeth M. Lodder, Connie R. Bezzina
出版 2014Artigo -
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The Brugada Syndrome Susceptibility Gene <i>HEY2</i> Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity 由 Christiaan C. Veerman, Svitlana Podliesna, Rafik Tadros, Elisabeth M. Lodder, Isabella Mengarelli, Berend de Jonge, Leander Beekman, Julien Barc, Ronald Wilders, Arthur A.M. Wilde, Bastiaan J. Boukens, Ruben Coronel, Arie O. Verkerk, Carol Ann Remme, Connie R. Bezzina
出版 2017Artigo -
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Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark 由 Charlotte Glinge, Sára Rossetti, L Oestergaard, Niels Kjær Stampe, Thomas Hadberg Lynge, Regitze Gyldenholm Skals, Bo Gregers Winkel, Elisabeth M. Lodder, Connie R. Bezzina, Gunnar Gislason, Jytte Banner, Elijah R. Behr, Christian Torp‐Pedersen, Reza Jabbari, Jacob Tfelt‐Hansen
出版 2023Artigo -
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HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy 由 Annalisa Milano, Alexa M.C. Vermeer, Elisabeth M. Lodder, Julien Barc, Arie O. Verkerk, Alex V. Postma, Ivo A.C. van der Bilt, Marieke J.H. Baars, Paul L. van Haelst, Kadir Çalişkan, Yvonne M. Hoedemaekers, Solena Le Scouarnec, Richard Redon, Yigal M. Pinto, Imke Christiaans, Arthur A.M. Wilde, Connie R. Bezzina
出版 2014Artigo -
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Coxsackie and Adenovirus Receptor Is a Modifier of Cardiac Conduction and Arrhythmia Vulnerability in the Setting of Myocardial Ischemia 由 Roos F. Marsman, Connie R. Bezzina, Fabian Freiberg, Arie O. Verkerk, Michiel Adriaens, Svitlana Podliesna, Chen Chen, Bettina Purfürst, Bastian Spallek, Tamara T. Koopmann, István Baczkó, Cristobal G. dos Remedios, Alfred L. George, Nanette H. Bishopric, Elisabeth M. Lodder, Jacques M.T. de Bakker, Robert Fischer, Ruben Coronel, Arthur A.M. Wilde, Michael Gotthardt, Carol Ann Remme
出版 2013Artigo -
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Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant 由 Esmée van Drie, Jan D.H. Jongbloed, Edgar T. Hoorntje, Paul A. van der Zwaag, Moniek G.P.J. Cox, Ronald H. Lekanne Deprez, Arjan C. Houweling, Virginnio Proost, A. A. M. Wilde, Dennis Dooijes, Annette F. Baas, Anneline S.J.M. te Riele, Karin Y. van Spaendonck‐Zwarts, Elisabeth M. Lodder, J. Peter van Tintelen
出版 2025Artigo -
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Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies 由 Francesco Mazzarotto, Megan H. Hawley, Matteo Beltrami, Leander Beekman, Antonio de Marvao, Kathryn A. McGurk, Ben Statton, Beatrice Boschi, Francesca Girolami, Angharad M. Roberts, Elisabeth M. Lodder, Mona Allouba, Soha Romeih, Yasmine Aguib, A. John Baksi, Antonis Pantazis, Sanjay Prasad, Elisabetta Cerbai, Magdi H. Yacoub, Declan P. O’Regan, Stuart A. Cook, James S. Ware, Birgit Funke, Iacopo Olivotto, Connie R. Bezzina, Paul J.R. Barton, Roddy Walsh
出版 2021Artigo -
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Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome 由 Najim Lahrouchi, Hariharan Raju, Elisabeth M. Lodder, Efstathios Papatheodorou, James S. Ware, Michael Papadakis, Rafik Tadros, Della Cole, Jonathan R. Skinner, Jackie Crawford, Donald R. Love, Chee Jian Pua, Bee Y. Soh, Jaydutt Bhalshankar, Risha Govind, Jacob Tfelt‐Hansen, Bo Gregers Winkel, Christian van der Werf, Yanushi D. Wijeyeratne, Greg Mellor, Jan Till, Marta C. Cohen, Maite Tome, Sanjay Sharma, Arthur A.M. Wilde, Stuart A. Cook, Connie R. Bezzina, Mary N. Sheppard, Elijah R. Behr
出版 2017Artigo -
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The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy 由 Najim Lahrouchi, Hariharan Raju, Elisabeth M. Lodder, Efstathios Papatheodorou, Chris Miles, James S. Ware, Michael Papadakis, Rafik Tadros, Della Cole, Jonathan R. Skinner, Jackie Crawford, Donald R. Love, Chee Jian Pua, Bee Y. Soh, Jaydutt Bhalshankar, Risha Govind, Jacob Tfelt‐Hansen, Bo Gregers Winkel, Christian van der Werf, Yanushi D. Wijeyeratne, Greg Mellor, Janice Till, Marta C. Cohen, Maite Tome, Sanjay Sharma, Arthur A.M. Wilde, Stuart A. Cook, Mary N. Sheppard, Connie R. Bezzina, Elijah R. Behr
出版 2019Artigo -
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Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy 由 Matthias Heinig, Michiel Adriaens, Sebastian Schäfer, Hanneke W. M. van Deutekom, Elisabeth M. Lodder, James S. Ware, Valentin Schneider-Lunitz, Leanne E. Felkin, Esther E. Creemers, Benjamin Meder, Hugo A. Katus, Frank Rühle, Monika Stoll, François Cambien, Eric Villard, Philippe Charron, András Varró, Nanette H. Bishopric, Alfred L. George, Cristobal G. dos Remedios, Aida Moreno‐Moral, Francesco Pesce, Anja Bauerfeind, Franz Rüschendorf, Carola Rintisch, Enrico Petretto, Paul J.R. Barton, Stuart A. Cook, Yigal M. Pinto, Connie R. Bezzina, Norbert Hübner
出版 2017Artigo -
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GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability 由 Elisabeth M. Lodder, Pasquelena De Nittis, Charlotte D. Koopman, Wojciech Wiszniewski, Carolina Fischinger Moura de Souza, Najim Lahrouchi, Nicolas Guex, Valerio Napolioni, Federico Tessadori, Leander Beekman, Eline A. Nannenberg, Lamiae Boualla, Nico A. Blom, Wim de Graaff, Maarten Kamermans, Dario Cocciadiferro, Natascia Malerba, Barbara Mandriani, Zeynep H. Coban Akdemir, Richard J. Fish, Mohammad K. Eldomery, Ilham Ratbi, Arthur A.M. Wilde, Teun P. de Boer, William F. Simonds, Marguerite Neerman‐Arbez, V. Reid Sutton, Fernando Kok, James R. Lupski, Alexandre Reymond, Connie R. Bezzina, Jeroen Bakkers, Giuseppe Merla
出版 2016Artigo -
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Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing 由 Jérôme Nicod, R. W. Davies, Na Cai, Carl Hassett, Leo Goodstadt, Cormac Cosgrove, Benjamin K. Yee, Vikte Lionikaite, Rebecca E. McIntyre, Carol Ann Remme, Elisabeth M. Lodder, J.S. Gregory, Tertius Hough, Russell Joynson, Hayley Phelps, Barbara Nell, Clare Rowe, Joe Wood, Alison Walling, Nasrin Bopp, Amarjit Bhomra, Polinka Hernandez-Pliego, Jacques Callebert, R.M. Aspden, Nick P. Talbot, Peter A. Robbins, Mark E. Harrison, Martin Fray, Jean‐Marie Launay, Yigal M. Pinto, David A. Blizard, Connie R. Bezzina, David J. Adams, Paul Franken, Tom Weaver, Sara Wells, Steve D. M. Brown, Paul Potter, Paul Klenerman, Arimantas Lionikas, Richard Mott, Jonathan Flint
出版 2016Artigo -
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Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy 由 Jason D. Roberts, Nathaniel P. Murphy, Robert M. Hamilton, Ellen R. Lubbers, Cynthia A. James, Crystal F. Kline, Michael H. Gollob, Andrew D. Krahn, Amy C. Sturm, Hassan Musa, Mona El Refaey, Sara N. Koenig, Meriam Åström Aneq, Edgar T. Hoorntje, Sharon Graw, Robert Davies, Muhammad Rafiq, Tamara T. Koopmann, Shabana Aafaqi, Meena Fatah, David A. Chiasson, Matthew R.G. Taylor, Samantha L. Simmons, Mei Han, Chantal J.M. van Opbergen, Loren E. Wold, Gianfranco Sinagra, Kirti Mittal, Crystal Tichnell, Brittney Murray, Alberto Codima, Babak Nazer, Duy T. Nguyen, Gregory M. Marcus, Nara Sobriera, Elisabeth M. Lodder, Maarten P. van den Berg, Danna Spears, John F. Robinson, Philip C. Ursell, Anna K. Green, Allan C. Skanes, Anthony Tang, Martin J. Gardner, Robert A. Hegele, Toon A.B. van Veen, Arthur A.M. Wilde, Jeff S. Healey, Paul M.L. Janssen, Luisa Mestroni, J. Peter van Tintelen, Hugh Calkins, Daniel P. Judge, Thomas J. Hund, Melvin M. Scheinman, Peter J. Mohler
出版 2019Artigo
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