Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study von Behr, Elijah R, Savio-Galimberti, Eleonora, Barc, Julien, Holst, Anders G, Petropoulou, Evmorfia, Prins, Bram P, Jabbari, Javad, Torchio, Margherita, Berthet, Myriam, Mizusawa, Yuka, Yang, Tao, Nannenberg, Eline A, Dagradi, Federica, Weeke, Peter, Bastiaenan, Rachel, Ackerman, Michael J, Haunso, Stig, Leenhardt, Antoine, Kääb, Stefan, Probst, Vincent, Redon, Richard, Sharma, Sanjay, Wilde, Arthur, Tfelt-Hansen, Jacob, Schwartz, Peter, Roden, Dan M, Bezzina, Connie R, Olesen, Morten, Darbar, Dawood, Guicheney, Pascale, Crotti, Lia, Jamshidi, Yalda

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Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24 von Hedberg-Oldfors, Carola, Abramsson, Alexandra, Osborn, Daniel P S, Danielsson, Olof, Fazlinezhad, Afsoon, Nilipour, Yalda, Hübbert, Laila, Nennesmo, Inger, Visuttijai, Kittichate, Bharj, Jaipreet, Petropoulou, Evmorfia, Shoreim, Azza, Vona, Barbara, Ahangari, Najmeh, López, Marcela Dávila, Doosti, Mohammad, Banote, Rakesh Kumar, Maroofian, Reza, Edling, Malin, Taherpour, Mehdi, Zetterberg, Henrik, Karimiani, Ehsan Ghayoor, Oldfors, Anders, Jamshidi, Yalda

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Digenic inheritance of mutations in the cardiac troponin ( TNNT2 ) and cardiac beta myosin heavy chain ( MYH7 ) as the cause of severe dilated cardiomyopathy von Petropoulou, Evmorfia, Soltani, Mohammadhossein, Firoozabadi, Ali Dehghani, Namayandeh, Seyedeh Mahdieh, Crockford, Jade, Maroofian, Reza, Jamshidi, Yalda

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Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization von Bersell, Kevin R., Yang, Tao, Mosley, Jonathan D., Glazer, Andrew M., Hale, Andrew T., Kryshtal, Dmytro O., Kim, Kyungsoo, Steimle, Jeffrey D., Brown, Jonathan D., Salem, Joe-Elie, Campbell, Courtney C., Hong, Charles C., Wells, Quinn S., Johnson, Amanda N., Short, Laura, Blair, Marcia A., Behr, Elijah R., Petropoulou, Evmorfia, Jamshidi, Yalda, Benson, Mark D., Keyes, Michelle J., Ngo, Debby, Vasan, Ramachandran S., Yang, Qiong, Gerszten, Robert E., Shaffer, Christian, Parikh, Shan, Sheng, Quanhu, Kannankeril, Prince J., Moskowitz, Ivan P., York, John D., Wang, Thomas J., Knollmann, Bjorn C., Roden, Dan M.

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The genetics of pro‐arrhythmic adverse drug reactions von Petropoulou, Evmorfia, Jamshidi, Yalda, Behr, Elijah R.

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Transcriptional dysregulation underlies both a monogenic arrhythmia syndrome and common modifier of cardiac repolarization von Bersell, Kevin R., Yang, Tao, Mosley, Jonathan D., Glazer, Andrew M., Hale, Andrew T., Kryshtal, Dmytro O., Kim, Kyungsoo, Steimle, Jeffrey D., Brown, Jonathan D., Salem, Joe-Elie, Campbell, Courtney C., Hong, Charles C., Wells, Quinn S., Johnson, Amanda N., Short, Laura, Blair, Marcia A., Behr, Elijah R., Petropoulou, Evmorfia, Jamshidi, Yalda, Benson, Mark D., Keyes, Michelle J., Ngo, Debby, Vasan, Ramachandran S., Yang, Qiong, Gerszten, Robert E., Shaffer, Christian, Parikh, Shan, Sheng, Quanhu, Kannankeril, Prince J., Moskowitz, Ivan P., York, John D., Wang, Thomas J., Knollmann, Bjorn C., Roden, Dan M.

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Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization von Bersell, Kevin R., Yang, Tao, Mosley, Jonathan D., Glazer, Andrew M., Hale, Andrew T., Kryshtal, Dmytro O., Kim, Kyungsoo, Steimle, Jeffrey D., Brown, Jonathan D., Salem, Joe-Elie, Campbell, Courtney C., Hong, Charles C., Wells, Quinn S., Johnson, Amanda N., Short, Laura, Blair, Marcia A., Behr, Elijah R., Petropoulou, Evmorfia, Jamshidi, Yalda, Benson, Mark D., Keyes, Michelle J., Ngo, Debby, Vasan, Ramachandran S., Yang, Qiong, Gerszten, Robert E., Shaffer, Christian, Parikh, Shan, Sheng, Quanhu, Kannankeril, Prince J., Moskowitz, Ivan P., York, John D., Wang, Thomas J., Knollmann, Bjorn C., Roden, Dan M.

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Coagulation Gene Expression Profiling in Infants With Necrotizing Enterocolitis von Giuliani, Stefano, Tan, Yew‐Wei, Zheng, Dongling, Petropoulou, Evmorfia, Sohail, Ali, Bradley, Sarah, Richards, Justin, Kennea, Nigel, Jamshidi, Yalda

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