Результати пошуку - Elisabeth M. Lodder

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  1. 1
    Aquaporin Channels in the Heart—Physiology and Pathophysiology

    Aquaporin Channels in the Heart—Physiology and Pathophysiology за авторством Arie O. Verkerk, Elisabeth M. Lodder, Ronald Wilders

    Опубліковано 2019
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  2. 2
    The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology

    The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology за авторством Christiaan C. Veerman, Arthur A.M. Wilde, Elisabeth M. Lodder

    Опубліковано 2015
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  3. 3
    Dissection of a Quantitative Trait Locus for PR Interval Duration Identifies Tnni3k as a Novel Modulator of Cardiac Conduction

    Dissection of a Quantitative Trait Locus for PR Interval Duration Identifies Tnni3k as a Novel Modulator of Cardiac Conduction за авторством 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

    Опубліковано 2012
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  4. 4
    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 Mutation

    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... за авторством 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

    Опубліковано 2017
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  5. 5
    Reduced kinase function in two ultra‐rare <scp><i>TNNI3K</i></scp> variants in families with congenital junctional ectopic tachycardia

    Reduced kinase function in two ultra‐rare <scp><i>TNNI3K</i></scp> variants in families with congenital junctional ectopic tachycardia за авторством 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

    Опубліковано 2024
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  6. 6
    Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart

    Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart за авторством 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

    Опубліковано 2014
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  7. 7
    The Brugada Syndrome Susceptibility Gene <i>HEY2</i> Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity

    The Brugada Syndrome Susceptibility Gene <i>HEY2</i> Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity за авторством 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

    Опубліковано 2017
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  8. 8
    Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark

    Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark за авторством 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

    Опубліковано 2023
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  9. 9
    HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy

    HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy за авторством 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

    Опубліковано 2014
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  10. 10
    Coxsackie and Adenovirus Receptor Is a Modifier of Cardiac Conduction and Arrhythmia Vulnerability in the Setting of Myocardial Ischemia

    Coxsackie and Adenovirus Receptor Is a Modifier of Cardiac Conduction and Arrhythmia Vulnerability in the Setting of Myocardial Ischemia за авторством 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

    Опубліковано 2013
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  11. 11
    Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant

    Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant за авторством 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

    Опубліковано 2025
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  12. 12
    Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies

    Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies за авторством 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

    Опубліковано 2021
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  13. 13
    Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome

    Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome за авторством 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

    Опубліковано 2017
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  14. 14
    The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy

    The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy за авторством 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

    Опубліковано 2019
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  15. 15
    Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy

    Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy за авторством 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

    Опубліковано 2017
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  16. 16
    GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability

    GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability за авторством 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

    Опубліковано 2016
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  17. 17
    Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing

    Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing за авторством 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

    Опубліковано 2016
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  18. 18
    Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy

    Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy за авторством 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

    Опубліковано 2019
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