Results
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21.
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Sudden Cardiac Arrest and Rare Genetic Variants in the Community. [electronic resource] by
- Milano, Annalisa
- Blom, Marieke T
- Lodder, Elisabeth M
- van Hoeijen, Daniel A
- Barc, Julien
- Koopmann, Tamara T
- Bardai, Abdennasser
- Beekman, Leander
- Lichtner, Peter
- van den Berg, Maarten P
- Wilde, Arthur A M
- Bezzina, Connie R
- Tan, Hanno L
Producer: 20170106
In:
Circulation. Cardiovascular genetics vol. 9
Availability: No items available.
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22.
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Genetic variation in [electronic resource] by
- Veerman, Christiaan C
- Mengarelli, Isabella
- Koopman, Charlotte D
- Wilders, Ronald
- van Amersfoorth, Shirley C
- Bakker, Diane
- Wolswinkel, Rianne
- Hababa, Mariam
- de Boer, Teun P
- Guan, Kaomei
- Milnes, James
- Lodder, Elisabeth M
- Bakkers, Jeroen
- Verkerk, Arie O
- Bezzina, Connie R
Producer: 20200505
In:
Disease models & mechanisms vol. 12
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23.
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The Brugada Syndrome Susceptibility Gene [electronic resource] by
- Veerman, Christiaan C
- Podliesna, Svitlana
- Tadros, Rafik
- Lodder, Elisabeth M
- Mengarelli, Isabella
- de Jonge, Berend
- Beekman, Leander
- Barc, Julien
- Wilders, Ronald
- Wilde, Arthur A M
- Boukens, Bastiaan J
- Coronel, Ruben
- Verkerk, Arie O
- Remme, Carol Ann
- Bezzina, Connie R
Producer: 20170907
In:
Circulation research vol. 121
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24.
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Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart. [electronic resource] by
- Koopmann, Tamara T
- Adriaens, Michiel E
- Moerland, Perry D
- Marsman, Roos F
- Westerveld, Margriet L
- Lal, Sean
- Zhang, Taifang
- Simmons, Christine Q
- Baczko, Istvan
- dos Remedios, Cristobal
- Bishopric, Nanette H
- Varro, Andras
- George, Alfred L
- Lodder, Elisabeth M
- Bezzina, Connie R
Producer: 20150212
In:
PloS one vol. 9
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25.
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Dilation of the Aorta Ascendens Forms Part of the Clinical Spectrum of HCN4 Mutations. [electronic resource] by
- Vermeer, Alexa M C
- Lodder, Elisabeth M
- Thomas, Dierk
- Duijkers, Floor A M
- Marcelis, Carlo
- van Gorselen, Edwin O F
- Fortner, Philipp
- Buss, Sebastian J
- Mereles, Derliz
- Katus, Hugo A
- Wilde, Arthur A M
- Bezzina, Connie R
- Boekholdt, S Matthijs
- Schweizer, Patrick A
- Christiaans, Imke
Producer: 20180809
In:
Journal of the American College of Cardiology vol. 67
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26.
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GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum. [electronic resource] by
- Škorić-Milosavljević, Doris
- Tjong, Fleur V Y
- Barc, Julien
- Backx, Ad P C M
- Clur, Sally-Ann B
- van Spaendonck-Zwarts, Karin
- Oostra, Roelof-Jan
- Lahrouchi, Najim
- Beekman, Leander
- Bökenkamp, Regina
- Barge-Schaapveld, Daniela Q C M
- Mulder, Barbara J
- Lodder, Elisabeth M
- Bezzina, Connie R
- Postma, Alex V
Producer: 20200803
In:
American journal of medical genetics. Part A vol. 179
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27.
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Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys). [electronic resource] by
- Podliesna, Svitlana
- Delanne, Julian
- Miller, Lindsey
- Tester, David J
- Uzunyan, Merujan
- Yano, Shoji
- Klerk, Mischa
- Cannon, Bryan C
- Khongphatthanayothin, Apichai
- Laurent, Gabriel
- Bertaux, Geraldine
- Falcon-Eicher, Sylvie
- Wu, Shengnan
- Yen, Hai-Yun
- Gao, Hanlin
- Wilde, Arthur A M
- Faivre, Laurence
- Ackerman, Michael J
- Lodder, Elisabeth M
- Bezzina, Connie R
Producer: 20200902
In:
Heart rhythm vol. 16
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28.
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A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression. [electronic resource] by
- Bundgaard, Henning
- Jøns, Christian
- Lodder, Elisabeth M
- Izarzugaza, Jose M G
- Romero Herrera, Jose A
- Pehrson, Steen
- Tfelt-Hansen, Jacob
- Ahlberg, Gustav
- Olesen, Morten S
- Holst, Anders G
- Wellens, Hein
- de Villiers, Carin
- Hastings, Robert
- Stuart, Graham
- Brunak, Søren
- Wilde, Arthur A M
- Watkins, Hugh
- Christensen, Alex H
Producer: 20181211
In:
The New England journal of medicine vol. 379
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29.
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Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposure. [electronic resource] by
- Glinge, Charlotte
- Engstrøm, Thomas
- Midgley, Sofie E
- Tanck, Michael W T
- Madsen, Jeppe Ekstrand Halkjær
- Pedersen, Frants
- Ravn Jacobsen, Mia
- Lodder, Elisabeth M
- Al-Hussainy, Nour R
- Kjær Stampe, Niels
- Trebbien, Ramona
- Køber, Lars
- Gerds, Thomas
- Torp-Pedersen, Christian
- Fischer, Thea K
- Bezzina, Connie R
- Tfelt-Hansen, Jacob
- Jabbari, Reza
Producer: 20200511
In:
PloS one vol. 15
Availability: No items available.
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30.
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Correction: Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposure. [electronic resource] by
- Glinge, Charlotte
- Engstrøm, Thomas
- Midgley, Sofie E
- Tanck, Michael W T
- Madsen, Jeppe Ekstrand Halkjær
- Pedersen, Frants
- Jacobsen, Mia Ravn
- Lodder, Elisabeth M
- Al-Hussainy, Nour R
- Stampe, Niels Kjær
- Trebbien, Ramona
- Køber, Lars
- Gerds, Thomas
- Torp-Pedersen, Christian
- Fischer, Thea Kølsen
- Bezzina, Connie R
- Tfelt-Hansen, Jacob
- Jabbari, Reza
Publication details: PloS one 2020
In:
PloS one vol. 15
Availability: No items available.
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31.
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HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy. [electronic resource] by
- Milano, Annalisa
- Vermeer, Alexa M C
- Lodder, Elisabeth M
- Barc, Julien
- Verkerk, Arie O
- Postma, Alex V
- van der Bilt, Ivo A C
- Baars, Marieke J H
- van Haelst, Paul L
- Caliskan, Kadir
- Hoedemaekers, Yvonne M
- Le Scouarnec, Solena
- Redon, Richard
- Pinto, Yigal M
- Christiaans, Imke
- Wilde, Arthur A
- Bezzina, Connie R
Producer: 20141021
In:
Journal of the American College of Cardiology vol. 64
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32.
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Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemia. [electronic resource] by
- Marsman, Roos F J
- Bezzina, Connie R
- Freiberg, Fabian
- Verkerk, Arie O
- Adriaens, Michiel E
- Podliesna, Svitlana
- Chen, Chen
- Purfürst, Bettina
- Spallek, Bastian
- Koopmann, Tamara T
- Baczko, Istvan
- Dos Remedios, Cristobal G
- George, Alfred L
- Bishopric, Nanette H
- Lodder, Elisabeth M
- de Bakker, Jacques M T
- Fischer, Robert
- Coronel, Ruben
- Wilde, Arthur A M
- Gotthardt, Michael
- Remme, Carol Ann
Producer: 20140408
In:
Journal of the American College of Cardiology vol. 63
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33.
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Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly. [electronic resource] by
- Lahrouchi, Najim
- George, Aman
- Ratbi, Ilham
- Schneider, Ronen
- Elalaoui, Siham C
- Moosa, Shahida
- Bharti, Sanita
- Sharma, Ruchi
- Abu-Asab, Mones
- Onojafe, Felix
- Adadi, Najlae
- Lodder, Elisabeth M
- Laarabi, Fatima-Zahra
- Lamsyah, Yassine
- Elorch, Hamza
- Chebbar, Imane
- Postma, Alex V
- Lougaris, Vassilios
- Plebani, Alessandro
- Altmueller, Janine
- Kyrieleis, Henriette
- Meiner, Vardiella
- McNeill, Helen
- Bharti, Kapil
- Lyonnet, Stanislas
- Wollnik, Bernd
- Henrion-Caude, Alexandra
- Berraho, Amina
- Hildebrandt, Friedhelm
- Bezzina, Connie R
- Brooks, Brian P
- Sefiani, Abdelaziz
Producer: 20190405
In:
Nature communications vol. 10
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34.
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Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy. [electronic resource] by
- Heinig, Matthias
- Adriaens, Michiel E
- Schafer, Sebastian
- van Deutekom, Hanneke W M
- Lodder, Elisabeth M
- Ware, James S
- Schneider, Valentin
- Felkin, Leanne E
- Creemers, Esther E
- Meder, Benjamin
- Katus, Hugo A
- Rühle, Frank
- Stoll, Monika
- Cambien, François
- Villard, Eric
- Charron, Philippe
- Varro, Andras
- Bishopric, Nanette H
- George, Alfred L
- Dos Remedios, Cristobal
- Moreno-Moral, Aida
- Pesce, Francesco
- Bauerfeind, Anja
- Rüschendorf, Franz
- Rintisch, Carola
- Petretto, Enrico
- Barton, Paul J
- Cook, Stuart A
- Pinto, Yigal M
- Bezzina, Connie R
- Hubner, Norbert
Producer: 20180507
In:
Genome biology vol. 18
Availability: No items available.
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35.
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Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome. [electronic resource] by
- Lahrouchi, Najim
- Raju, Hariharan
- Lodder, Elisabeth M
- Papatheodorou, Efstathios
- Ware, James S
- Papadakis, Michael
- Tadros, Rafik
- Cole, Della
- Skinner, Jonathan R
- Crawford, Jackie
- Love, Donald R
- Pua, Chee J
- Soh, Bee Y
- Bhalshankar, Jaydutt D
- Govind, Risha
- Tfelt-Hansen, Jacob
- Winkel, Bo G
- van der Werf, Christian
- Wijeyeratne, Yanushi D
- Mellor, Greg
- Till, Jan
- Cohen, Marta C
- Tome-Esteban, Maria
- Sharma, Sanjay
- Wilde, Arthur A M
- Cook, Stuart A
- Bezzina, Connie R
- Sheppard, Mary N
- Behr, Elijah R
Producer: 20170717
In:
Journal of the American College of Cardiology vol. 69
Availability: No items available.
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36.
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The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy. [electronic resource] by
- Lahrouchi, Najim
- Raju, Hariharan
- Lodder, Elisabeth M
- Papatheodorou, Stathis
- Miles, Chris
- Ware, James S
- Papadakis, Michael
- Tadros, Rafik
- Cole, Della
- Skinner, Jonathan R
- Crawford, Jackie
- Love, Donald R
- Pua, Chee J
- Soh, Bee Y
- Bhalshankar, Jaydutt D
- Govind, Risha
- Tfelt-Hansen, Jacob
- Winkel, Bo G
- van der Werf, Christian
- Wijeyeratne, Yanushi D
- Mellor, Greg
- Till, Janice
- Cohen, Marta
- Tome-Esteban, Maria
- Sharma, Sanjay
- Wilde, Arthur A M
- Cook, Stuart A
- Sheppard, Mary N
- Bezzina, Connie R
- Behr, Elijah R
Producer: 20210203
In:
European journal of human genetics : EJHG vol. 28
Availability: No items available.
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37.
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GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. [electronic resource] by
- Lodder, Elisabeth M
- De Nittis, Pasquelena
- Koopman, Charlotte D
- Wiszniewski, Wojciech
- Moura de Souza, Carolina Fischinger
- Lahrouchi, Najim
- Guex, Nicolas
- Napolioni, Valerio
- Tessadori, Federico
- Beekman, Leander
- Nannenberg, Eline A
- Boualla, Lamiae
- Blom, Nico A
- de Graaff, Wim
- Kamermans, Maarten
- Cocciadiferro, Dario
- Malerba, Natascia
- Mandriani, Barbara
- Coban Akdemir, Zeynep Hande
- Fish, Richard J
- Eldomery, Mohammad K
- Ratbi, Ilham
- Wilde, Arthur A M
- de Boer, Teun
- Simonds, William F
- Neerman-Arbez, Marguerite
- Sutton, V Reid
- Kok, Fernando
- Lupski, James R
- Reymond, Alexandre
- Bezzina, Connie R
- Bakkers, Jeroen
- Merla, Giuseppe
Publication details: American journal of human genetics 09 2016
In:
American journal of human genetics vol. 99
Availability: No items available.
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38.
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GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. [electronic resource] by
- Lodder, Elisabeth M
- De Nittis, Pasquelena
- Koopman, Charlotte D
- Wiszniewski, Wojciech
- Moura de Souza, Carolina Fischinger
- Lahrouchi, Najim
- Guex, Nicolas
- Napolioni, Valerio
- Tessadori, Federico
- Beekman, Leander
- Nannenberg, Eline A
- Boualla, Lamiae
- Blom, Nico A
- de Graaff, Wim
- Kamermans, Maarten
- Cocciadiferro, Dario
- Malerba, Natascia
- Mandriani, Barbara
- Akdemir, Zeynep Hande Coban
- Fish, Richard J
- Eldomery, Mohammad K
- Ratbi, Ilham
- Wilde, Arthur A M
- de Boer, Teun
- Simonds, William F
- Neerman-Arbez, Marguerite
- Sutton, V Reid
- Kok, Fernando
- Lupski, James R
- Reymond, Alexandre
- Bezzina, Connie R
- Bakkers, Jeroen
- Merla, Giuseppe
Producer: 20170502
In:
American journal of human genetics vol. 99
Availability: No items available.
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39.
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Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing. [electronic resource] by
- Nicod, Jérôme
- Davies, Robert W
- Cai, Na
- Hassett, Carl
- Goodstadt, Leo
- Cosgrove, Cormac
- Yee, Benjamin K
- Lionikaite, Vikte
- McIntyre, Rebecca E
- Remme, Carol Ann
- Lodder, Elisabeth M
- Gregory, Jennifer S
- Hough, Tertius
- Joynson, Russell
- Phelps, Hayley
- Nell, Barbara
- Rowe, Clare
- Wood, Joe
- Walling, Alison
- Bopp, Nasrin
- Bhomra, Amarjit
- Hernandez-Pliego, Polinka
- Callebert, Jacques
- Aspden, Richard M
- Talbot, Nick P
- Robbins, Peter A
- Harrison, Mark
- Fray, Martin
- Launay, Jean-Marie
- Pinto, Yigal M
- Blizard, David A
- Bezzina, Connie R
- Adams, David J
- Franken, Paul
- Weaver, Tom
- Wells, Sara
- Brown, Steve D M
- Potter, Paul K
- Klenerman, Paul
- Lionikas, Arimantas
- Mott, Richard
- Flint, Jonathan
Producer: 20170907
In:
Nature genetics vol. 48
Availability: No items available.
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40.
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Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy. [electronic resource] by
- Roberts, Jason D
- Murphy, Nathaniel P
- Hamilton, Robert M
- Lubbers, Ellen R
- James, Cynthia A
- Kline, Crystal F
- Gollob, Michael H
- Krahn, Andrew D
- Sturm, Amy C
- Musa, Hassan
- El-Refaey, Mona
- Koenig, Sara
- Aneq, Meriam Åström
- Hoorntje, Edgar T
- Graw, Sharon L
- Davies, Robert W
- Rafiq, Muhammad Arshad
- Koopmann, Tamara T
- Aafaqi, Shabana
- Fatah, Meena
- Chiasson, David A
- Taylor, Matthew Rg
- Simmons, Samantha L
- Han, Mei
- van Opbergen, Chantal Jm
- Wold, Loren E
- Sinagra, Gianfranco
- Mittal, Kirti
- Tichnell, Crystal
- Murray, Brittney
- Codima, Alberto
- Nazer, Babak
- Nguyen, Duy T
- Marcus, Frank I
- Sobriera, Nara
- Lodder, Elisabeth M
- van den Berg, Maarten P
- Spears, Danna A
- Robinson, John F
- Ursell, Philip C
- Green, Anna K
- Skanes, Allan C
- Tang, Anthony S
- Gardner, Martin J
- Hegele, Robert A
- van Veen, Toon Ab
- Wilde, Arthur Am
- Healey, Jeff S
- Janssen, Paul Ml
- Mestroni, Luisa
- van Tintelen, J Peter
- Calkins, Hugh
- Judge, Daniel P
- Hund, Thomas J
- Scheinman, Melvin M
- Mohler, Peter J
Producer: 20200526
In:
The Journal of clinical investigation vol. 129
Availability: No items available.
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