Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium von Siland, J E, Geelhoed, B, Roselli, C, Wang, B, Lin, H J, Weiss, S, Trompet, S, van den Berg, M E, Soliman, E Z, Chen, L Y, Ford, I, Jukema, J W, Macfarlane, P W, Kornej, J, Lin, H, Lunetta, K L, Kavousi, M, Kors, J A, Ikram, M A, Guo, X, Yao, J, Dörr, M, Felix, S B, Völker, U, Sotoodehnia, N, Arking, D E, Stricker, B H, Heckbert, S R, Lubitz, S A, Benjamin, E J, Alonso, A, Ellinor, P T, van der Harst, P, Rienstra, M

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Genome-wide association studies of atrial fibrillation: past, present, and future von Sinner, Moritz F, Ellinor, Patrick T, Meitinger, Thomas, Benjamin, Emelia J, Kääb, Stefan

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Familial aggregation in lone atrial fibrillation von ELLINOR, Patrick T, YOERGER, Danita M, RUSKIN, Jeremy N, MACRAE, Calum A

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Association analyses based on false discovery rate implicate new loci for coronary artery disease von Nelson, Christopher P, Goel, Anuj, Butterworth, Adam S, Kanoni, Stavroula, Webb, Tom R, Marouli, Eirini, Zeng, Lingyao, Ntalla, Ioanna, Lai, Florence Y, Hopewell, Jemma C, Giannakopoulou, Olga, Jiang, Tao, Hamby, Stephen E, Di Angelantonio, Emanuele, Assimes, Themistocles L, Bottinger, Erwin P, Chambers, John C, Clarke, Robert, Palmer, Colin N A, Cubbon, Richard M, Ellinor, Patrick, Ermel, Raili, Evangelou, Evangelos, Franks, Paul W, Grace, Christopher, Gu, Dongfeng, Hingorani, Aroon D, Howson, Joanna M M, Ingelsson, Erik, Kastrati, Adnan, Kessler, Thorsten, Kyriakou, Theodosios, Lehtimäki, Terho, Lu, Xiangfeng, Lu, Yingchang, März, Winfried, McPherson, Ruth, Metspalu, Andres, Pujades-Rodriguez, Mar, Ruusalepp, Arno, Schadt, Eric E, Schmidt, Amand F, Sweeting, Michael J, Zalloua, Pierre A, AlGhalayini, Kamal, Keavney, Bernard D, Kooner, Jaspal S, Loos, Ruth J F, Patel, Riyaz S, Rutter, Martin K, Tomaszewski, Maciej, Tzoulaki, Ioanna, Zeggini, Eleftheria, Erdmann, Jeanette, Dedoussis, George, Björkegren, Johan L M, Schunkert, Heribert, Farrall, Martin, Danesh, John, Samani, Nilesh J, Watkins, Hugh, Deloukas, Panos

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Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation von Ellinor, P T, Moore, R K, Patton, K K, Ruskin, J N, Pollak, M R, MacRae, C A

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Molecular determinants of Ca2+ selectivity and ion permeation in L-type Ca2+ channels von JIAN YANG, ELLINOR, P. T, SATHER, W. A, JI-FANG ZHANG, TSIEN, R. W

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Distinctive pharmacology and kinetics of cloned neuronal Ca2+ channels and their possible counterparts in mammalian CNS neurons von ZHANG, J.-F, RANDALL, A. D, ELLINOR, P. T, HORNE, W. A, SATHER, W. A, TANABE, T, SCHWARZ, T. L, TSIEN, R. W

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Monogenic atrial fibrillation as pathophysiological paradigms von Mahida, S., Lubitz, S. A., Rienstra, M., Milan, D. J., Ellinor, P. T.

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Molecular determinants of voltage-dependent inactivation in calcium channels von Zhang, Ji-Fang, Ellinor, Patrick T, Aldrich, Richard W, Tsien, Richard W

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Structural determinants of the blockade of N-type calcium channels by a peptide neurotoxin von Ellinor, Patrick T, Zhang, Ji-Fang, Horne, William A, Tsien, Richard W

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Functional expression of a rapidly inactivating neuronal calcium channel von Ellinor, Patrick T, Zhang, Ji-Fang, Randall, Andrew D, Zhou, Mei, Schwarz, Thomas L, Tsien, Richard W, Horne, William A

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Myocyte-Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2–Mediated Myocarditis von Tucker, Nathan R., Chaffin, Mark, Bedi, Kenneth C., Papangeli, Irinna, Akkad, Amer-Denis, Arduini, Alessandro, Hayat, Sikander, Eraslan, Gökcen, Muus, Christoph, Bhattacharyya, Roby P., Stegmann, Christian M., Margulies, Kenneth B., Ellinor, Patrick T.

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Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies von Lipov, A, Jurgens, S J, Mazzarotto, F, Allouba, M, Pirruccello, J P, Aguib, Y, Gennarelli, M, Yacoub, M, Ellinor, P T, Bezzina, C R, Walsh, R

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A polygenic risk score predicts atrial fibrillation in patients with coronary artery disease without severe systolic dysfunction von Sandhu, R, Liu, Y, Dron, J S, Moorthy, M V, Cook, N R, Chasman, D I, Ellinor, P T, Albert, C M

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Mutant Desmocollin-2 Causes Arrhythmogenic Right Ventricular Cardiomyopathy von Heuser, Arnd, Plovie, Eva R., Ellinor, Patrick T., Grossmann, Katja S., Shin, Jordan T., Wichter, Thomas, Basson, Craig T., Lerman, Bruce B., Sasse-Klaassen, Sabine, Thierfelder, Ludwig, MacRae, Calum A., Gerull, Brenda

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Large-scale genetic and multi-omics analyses identify molecular pathways underlying dilated cardiomyopathy von Jurgens, S J, Gaziano, L, Garnier, S, Krijger Juarez, C, Kany, S, Zheng, S, Biddinger, K, Tadros, R, Ware, J S, Schmidt, A F, Amin, A S, Ellinor, P T, Charron, P, Aragam, K G, Bezzina, C R

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Assessment of aortic valve function in over 47,000 people using deep learning von Kany, S, Ramo, J, Hou, C, Jurgens, S, Nauffal, V, Cunningham, J, Lau, E, Butte, A, Ho, J, Olgin, J, Elmariah, S, Lindsay, M, Ellinor, P, Pirruccello, J P

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cDNA cloning of a dihydropyridine-sensitive calcium channel from rat aorta. Evidence for the existence of alternatively spliced forms von Koch, W J, Ellinor, P T, Schwartz, A

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Expressivity of familial hypercholesterolemia variants in 1 million individuals von Koyama, S., Yu, Z., Choi, S.H., Klarin, D., Huffman, J., Trinh, M., Ravi, A., Dron, J., Hornsby, W., Damrauer, S., Chang, K.-M., Assimes, T., Tsao, P., Rader, D., Peloso, G., Ellinor, P., Cho, K., Sun, Y., Wilson, P., Natarajan, P.

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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure von Henry, Albert, Roselli, Carolina, Sveinbjörnsson, Garðar, Fatemifar, Ghazaleh, Hedman, Åsa K., Morley, Michael P., Helgadottir, Anna, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Andersson, Charlotte, Backman, Joshua D., Biggs, Mary L., Brandimarto, Jeffrey, Buckbinder, Leonard, Carey, David J., Chasman, Daniel I., Chen, Xu, Chung, Jonathan, Cook, James P., Delgado, Graciela E., Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C., Esko, Tõnu, Finan, Chris, Gottdiener, John S., Gross, Stefan, Guðbjartsson, Daníel F., Gutmann, Rebecca, Haggerty, Christopher M., Hyde, Craig L., Ingelsson, Erik, Jukema, J. Wouter, Kavousi, Maryam, Khaw, Kay-Tee, Kleber, Marcus E., Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, Lotta, Luca A., Luan, Jian’an, März, Winfried, Melander, Olle, Mordi, Ify R., Morgan, Thomas, Morris, Andrew D., Morris, Andrew P., Morrison, Alanna C., Nelson, Christopher P., Niessner, Alexander, Niiranen, Teemu, O’Donoghue, Michelle L., Owens, Anjali T., Parry, Helen M., Perola, Markus, Rice, Kenneth M., Ridker, Paul M., Rotter, Jerome I., Salo, Perttu, Salomaa, Veikko, Smelser, Diane T., Stender, Steen, Stott, David J., Tammesoo, Mari-Liis, Taylor, Kent D., Teder-Laving, Maris, Thorsteinsdottir, Unnur, Torp-Pedersen, Christian, Trompet, Stella, Tyl, Benoit, Uitterlinden, Andre G., Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A., Wareham, Nicholas J., Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L., Yerges-Armstrong, Laura M., Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, McMurray, John J. V., Yang, Jian, Visscher, Peter M., Malarstig, Anders, Holm, Hilma, Sattar, Naveed, Holmes, Michael V., Cappola, Thomas P., Hingorani, Aroon D., Kuchenbaecker, Karoline, Ellinor, Patrick T., Smith, J. Gustav, Vasan, Ramachandran S., Swerdlow, Daniel I., Lumbers, R. Thomas

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