Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy

od Chaix, Marie-A., Koopmann, Tamara T., Goyette, Philippe, Alikashani, Azadeh, Latour, Frédéric, Fatah, Meena, Hamilton, Robert M., Rioux, John D.
Izdano u HeartRhythm Case Rep (2016)

A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated with Brugada ECG Phenotype

od Hu, Dan, Barajas-Martinez, Hector, Burashnikov, Elena, Springer, Michael, Wu, Yuesheng, Varro, Andras, Pfeiffer, Ryan, Koopmann, Tamara T., Cordeiro, Jonathan M., Guerchicoff, Alejandra, Pollevick, Guido D., Antzelevitch, Charles
Izdano 2009

Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation

od Alders, Marielle, Koopmann, Tamara T., Christiaans, Imke, Postema, Pieter G., Beekman, Leander, Tanck, Michael W.T., Zeppenfeld, Katja, Loh, Peter, Koch, Karel T., Demolombe, Sophie, Mannens, Marcel M.A.M., Bezzina, Connie R., Wilde, Arthur A.M.
Izdano 2009

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

od 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.
Izdano 2014

Unique Cardiac Purkinje Fiber Transient Outward Current β-Subunit Composition: A Potential Molecular Link to Idiopathic Ventricular Fibrillation

od Xiao, Ling, Koopmann, Tamara T., Ördög, Balázs, Postema, Pieter G., Verkerk, Arie O., Iyer, Vivek, Sampson, Kevin J., Boink, Gerard J.J., Mamarbachi, Maya A., Varro, Andras, Jordaens, Luc, Res, Jan, Kass, Robert S., Wilde, Arthur A., Bezzina, C.R., Nattel, Stanley
Izdano u Circ Res (2013)

An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis

od Chatterjee, Diptendu, Fatah, Meena, Akdis, Deniz, Spears, Danna A, Koopmann, Tamara T, Mittal, Kirti, Rafiq, Muhammad A, Cattanach, Bruce M, Zhao, Qili, Healey, Jeff S, Ackerman, Michael J, Bos, Johan Martijn, Sun, Yu, Maynes, Jason T, Brunckhorst, Corinna, Medeiros-Domingo, Argelia, Duru, Firat, Saguner, Ardan M, Hamilton, Robert M
Izdano u Eur Heart J (2018)

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

od Watanabe, Hiroshi, Koopmann, Tamara T., Le Scouarnec, Solena, Yang, Tao, Ingram, Christiana R., Schott, Jean-Jacques, Demolombe, Sophie, Probst, Vincent, Anselme, Frédéric, Escande, Denis, Wiesfeld, Ans C.P., Pfeufer, Arne, Kääb, Stefan, Wichmann, H.-Erich, Hasdemir, Can, Aizawa, Yoshifusa, Wilde, Arthur A.M., Roden, Dan M., Bezzina, Connie R.
Izdano 2008

Usefulness of NGS for Diagnosis of Dominant Beta-Thalassemia and Unstable Hemoglobinopathies in Five Clinical Cases

od Rizzuto, Valeria, Koopmann, Tamara T., Blanco-Álvarez, Adoración, Tazón-Vega, Barbara, Idrizovic, Amira, Díaz de Heredia, Cristina, Del Orbe, Rafael, Pampliega, Miriam Vara, Velasco, Pablo, Beneitez, David, Santen, Gijs W. E., Waisfisz, Quinten, Elting, Mariet, Smiers, Frans J. W., de Pagter, Anne J., Kerkhoffs, Jean-Louis H., Harteveld, Cornelis L., Mañú-Pereira, Maria del Mar
Izdano u Front Physiol (2021)

Coxsackie and adenovirus receptor (CAR) is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemia

od 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
Izdano 2013

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

od Kolder, Iris C.R.M., Tanck, Michael W.T., Postema, Pieter G., Barc, Julien, Sinner, Moritz F., Zumhagen, Sven, Husemann, Anja, Stallmeyer, Birgit, Koopmann, Tamara T., Hofman, Nynke, Pfeufer, Arne, Lichtner, Peter, Meitinger, Thomas, Beckmann, Britt M., Myerburg, Robert J., Bishopric, Nanette H., Roden, Dan M., Kääb, Stefan, Wilde, Arthur A.M., Schott, Jean-Jacques, Schulze-Bahr, Eric, Bezzina, Connie R.
Izdano u Circ Cardiovasc Genet (2015)

A common genetic variant within SCN10A modulates cardiac SCN5A expression

od van den Boogaard, Malou, Smemo, Scott, Burnicka-Turek, Ozanna, Arnolds, David E., van de Werken, Harmen J.G., Klous, Petra, McKean, David, Muehlschlegel, Jochen D., Moosmann, Julia, Toka, Okan, Yang, Xinan H., Koopmann, Tamara T., Adriaens, Michiel E., Bezzina, Connie R., de Laat, Wouter, Seidman, Christine, Seidman, J.G., Christoffels, Vincent M., Nobrega, Marcelo A., Barnett, Phil, Moskowitz, Ivan P.
Izdano 2014

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

od Kapplinger, Jamie D., Tester, David J., Alders, Marielle, Benito, Begoña, Berthet, Myriam, Brugada, Josep, Brugada, Pedro, Fressart, Véronique, Guerchicoff, Alejandra, Harris-Kerr, Carole, Kamakura, Shiro, Kyndt, Florence, Koopmann, Tamara T., Miyamoto, Yoshihiro, Pfeiffer, Ryan, Pollevick, Guido D., Probst, Vincent, Zumhagen, Sven, Vatta, Matteo, Towbin, Jeffrey A., Shimizu, Wataru, Schulze-Bahr, Eric, Antzelevitch, Charles, Salisbury, Benjamin A., Guicheney, Pascale, Wilde, Arthur A. M., Brugada, Ramon, Schott, Jean-Jacques, Ackerman, Michael J.
Izdano 2009

Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes

od Yagihara, Nobue, Watanabe, Hiroshi, Barnett, Phil, Duboscq‐Bidot, Laetitia, Thomas, Atack C., Yang, Ping, Ohno, Seiko, Hasegawa, Kanae, Kuwano, Ryozo, Chatel, Stéphanie, Redon, Richard, Schott, Jean‐Jacques, Probst, Vincent, Koopmann, Tamara T., Bezzina, Connie R., Wilde, Arthur A. M., Nakano, Yukiko, Aiba, Takeshi, Miyamoto, Yoshihiro, Kamakura, Shiro, Darbar, Dawood, Donahue, Brian S., Shigemizu, Daichi, Tanaka, Toshihiro, Tsunoda, Tatsuhiko, Suda, Masayoshi, Sato, Akinori, Minamino, Tohru, Endo, Naoto, Shimizu, Wataru, Horie, Minoru, Roden, Dan M., Makita, Naomasa
Izdano u J Am Heart Assoc (2016)

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

od Cordell, Heather J., Bentham, Jamie, Topf, Ana, Zelenika, Diana, Heath, Simon, Mamasoula, Chrysovalanto, Cosgrove, Catherine, Blue, Gillian, Granados-Riveron, Javier, Setchfield, Kerry, Thornborough, Chris, Breckpot, Jeroen, Soemedi, Rachel, Martin, Ruairidh, Rahman, Thahira J., Hall, Darroch, van Engelen, Klaartje, Moorman, Antoon F.M., Zwinderman, Aelko H, Barnett, Phil, Koopmann, Tamara T., Adriaens, Michiel E., Varro, Andras, George, Alfred L., dos Remedios, Christobal, Bishopric, Nanette H., Bezzina, Connie R., O’Sullivan, John, Gewillig, Marc, Bu’Lock, Frances A., Winlaw, David, Bhattacharya, Shoumo, Devriendt, Koen, Brook, J. David, Mulder, Barbara J.M., Mital, Seema, Postma, Alex V., Lathrop, G. Mark, Farrall, Martin, Goodship, Judith A., Keavney, Bernard D.
Izdano 2013

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

od 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 R.G., Simmons, Samantha L., Han, Mei, van Opbergen, Chantal J.M., 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 A.B., Wilde, Arthur A.M., Healey, Jeff S., Janssen, Paul M.L., Mestroni, Luisa, van Tintelen, J. Peter, Calkins, Hugh, Judge, Daniel P., Hund, Thomas J., Scheinman, Melvin M., Mohler, Peter J.
Izdano u J Clin Invest (2019)

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

od Arking, Dan E., Pulit, Sara L., Crotti, Lia, van der Harst, Pim, Munroe, Patricia B., Koopmann, Tamara T., Sotoodehnia, Nona, Rossin, Elizabeth J., Morley, Michael, Wang, Xinchen, Johnson, Andrew D., Lundby, Alicia, Gudbjartsson, Daníel F., Noseworthy, Peter A., Eijgelsheim, Mark, Bradford, Yuki, Tarasov, Kirill V., Dörr, Marcus, Müller-Nurasyid, Martina, Lahtinen, Annukka M., Nolte, Ilja M., Smith, Albert Vernon, Bis, Joshua C., Isaacs, Aaron, Newhouse, Stephen J., Evans, Daniel S., Post, Wendy S., Waggott, Daryl, Lyytikäinen, Leo-Pekka, Hicks, Andrew A., Eisele, Lewin, Ellinghaus, David, Hayward, Caroline, Navarro, Pau, Ulivi, Sheila, Tanaka, Toshiko, Tester, David J., Chatel, Stéphanie, Gustafsson, Stefan, Kumari, Meena, Morris, Richard W., Naluai, Åsa T., Padmanabhan, Sandosh, Kluttig, Alexander, Strohmer, Bernhard, Panayiotou, Andrie G., Torres, Maria, Knoflach, Michael, Hubacek, Jaroslav A., Slowikowski, Kamil, Raychaudhuri, Soumya, Kumar, Runjun D., Harris, Tamara B., Launer, Lenore J., Shuldiner, Alan R., Alonso, Alvaro, Bader, Joel S., Ehret, Georg, Huang, Hailiang, Kao, W.H. Linda, Strait, James B., Macfarlane, Peter W., Brown, Morris, Caulfield, Mark J., Samani, Nilesh J., Kronenberg, Florian, Willeit, Johann, Smith, J. Gustav, Greiser, Karin H., zu Schwabedissen, Henriette Meyer, Werdan, Karl, Carella, Massimo, Zelante, Leopoldo, Heckbert, Susan R., Psaty, Bruce M., Rotter, Jerome I., Kolcic, Ivana, Polašek, Ozren, Wright, Alan F., Griffin, Maura, Daly, Mark J., Arnar, David O., Hólm, Hilma, Thorsteinsdottir, Unnur, Denny, Joshua C., Roden, Dan M., Zuvich, Rebecca L., Emilsson, Valur, Plump, Andrew S., Larson, Martin G., O'Donnell, Christopher J., Yin, Xiaoyan, Bobbo, Marco, D'Adamo, Adamo P., Iorio, Annamaria, Sinagra, Gianfranco, Carracedo, Angel, Cummings, Steven R., Nalls, Michael A., Jula, Antti, Kontula, Kimmo K., Marjamaa, Annukka, Oikarinen, Lasse, Perola, Markus, Porthan, Kimmo, Erbel, Raimund, Hoffmann, Per, Jöckel, Karl-Heinz, Kälsch, Hagen, Nöthen, Markus M., consortium, HRGEN, den Hoed, Marcel, Loos, Ruth J.F., Thelle, Dag S., Gieger, Christian, Meitinger, Thomas, Perz, Siegfried, Peters, Annette, Prucha, Hanna, Sinner, Moritz F., Waldenberger, Melanie, de Boer, Rudolf A., Franke, Lude, van der Vleuten, Pieter A., Beckmann, Britt Maria, Martens, Eimo, Bardai, Abdennasser, Hofman, Nynke, Wilde, Arthur A.M., Behr, Elijah R., Dalageorgou, Chrysoula, Giudicessi, John R., Medeiros-Domingo, Argelia, Barc, Julien, Kyndt, Florence, Probst, Vincent, Ghidoni, Alice, Insolia, Roberto, Hamilton, Robert M., Scherer, Stephen W., Brandimarto, Jeffrey, Margulies, Kenneth, Moravec, Christine E., Fabiola Del, Greco M., Fuchsberger, Christian, O'Connell, Jeffrey R., Lee, Wai K., Watt, Graham C.M., Campbell, Harry, Wild, Sarah H., El Mokhtari, Nour E., Frey, Norbert, Asselbergs, Folkert W., Leach, Irene Mateo, Navis, Gerjan, van den Berg, Maarten P., van Veldhuisen, Dirk J., Kellis, Manolis, Krijthe, Bouwe P., Franco, Oscar H., Hofman, Albert, Kors, Jan A., Uitterlinden, André G., Witteman, Jacqueline C.M., Kedenko, Lyudmyla, Lamina, Claudia, Oostra, Ben A., Abecasis, Gonçalo R., Lakatta, Edward G., Mulas, Antonella, Orrú, Marco, Schlessinger, David, Uda, Manuela, Markus, Marcello R.P., Völker, Uwe, Snieder, Harold, Spector, Timothy D., Ärnlöv, Johan, Lind, Lars, Sundström, Johan, Syvänen, Ann-Christine, Kivimaki, Mika, Kähönen, Mika, Mononen, Nina, Raitakari, Olli T., Viikari, Jorma S., Adamkova, Vera, Kiechl, Stefan, Brion, Maria, Nicolaides, Andrew N., Paulweber, Bernhard, Haerting, Johannes, Dominiczak, Anna F., Nyberg, Fredrik, Whincup, Peter H., Hingorani, Aroon, Schott, Jean-Jacques, Bezzina, Connie R., Ingelsson, Erik, Ferrucci, Luigi, Gasparini, Paolo, Wilson, James F., Rudan, Igor, Franke, Andre, Mühleisen, Thomas W., Pramstaller, Peter P., Lehtimäki, Terho J., Paterson, Andrew D., Parsa, Afshin, Liu, Yongmei, van Duijn, Cornelia, Siscovick, David S., Gudnason, Vilmundur, Jamshidi, Yalda, Salomaa, Veikko, Felix, Stephan B., Sanna, Serena, Ritchie, Marylyn D., Stricker, Bruno H., Stefansson, Kari, Boyer, Laurie A., Cappola, Thomas P., Olsen, Jesper V., Lage, Kasper, Schwartz, Peter J., Kääb, Stefan, Chakravarti, Aravinda, Ackerman, Michael J., Pfeufer, Arne, de Bakker, Paul I.W., Newton-Cheh, Christopher
Izdano 2014