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The last 5 uploaded publications
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Emelia Benjamin, Eric Boerwinkle, Gregory M. Marcus, Ingrid E. Christophersen, J. Gustav Smith, Jason D. Roberts, Laura M. Raffield, M. Benjamin Shoemaker, Michael Cho, Michael J. Cutler, Michiel Rienstra, Mina K. Chung, Morten S. Olesen, Moritz F. Sinner, Nona Sotoodehnia, Paulus Kirchhof, Ruth J. F. Loos, Saman Nazarian, Sanghamitra Mohanty, Scott M. Damrauer, Stefan Kääb, Susan R. Heckbert, Susan Redline, Svati H. Shah, Toshihiro Tanaka, Yusuke Ebana, Gonçalo R. Abecasis, Xiaodong Bai, Suganthi Balasubramanian, Aris Baras, Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson, Valerie N. Morrill, Nicholas Marston, Lu‐Chen Weng, James P. Pirruccello, Davíð O. Arnar, Daníel F. Guðbjartsson, Helene Mantineo, Aenne S. von Falkenhausen, Arnljot Tveit, Bastiaan Geelhoed, Carolina Roselli, David R. Van Wagoner, Dawood Darbar, Doreen Haase, Elsayed Z. Soliman, Giovanni Davogustto, Goo Jun, Hugh Calkins, Jeffrey L. Anderson, Jennifer A. Brody, Jennifer L. Halford, John Barnard, John E. Hokanson, Jonathan D. Smith, Joshua C. Bis, Kendra A. Young, Linda Johnson, Lorenz Risch, Lorne J. Gula, Lydia Coulter Kwee, Mark Chaffin, Michael Kühne, Michael Preuß, Namrata Gupta, Navid A. Nafissi, Nicholas L. Smith, Peter M. Nilsson, Pim van der Harst, Quinn S. Wells, Renae Judy, Renate B. Schnabel, Renée Johnson, Roelof A.J. Smit, Stacey Gabriel, Stacey Knight, Tetsushi Furukawa, Thomas W. Blackwell, Victor Nauffal, Xin Wang, Yuan‐I Min, Zachary T. Yoneda, Zachary Laksman, Connie R. Bezzina, Álvaro Alonso, Bruce M. Psaty, Christine M. Albert, Dan E. Arking, Dan M. Roden, Daniel I. Chasman, Daniel J. Rader, David Conen, David D. McManus, Diane Fatkin (2025). Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk. , 57(3), DOI: https://doi.org/10.1038/s41588-025-02074-9.
Article12 days agoThe impact of common and rare genetic variants on bradyarrhythmia development
Lu‐Chen Weng, Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall, Valerie N. Morrill, Xin Wang, Victor Nauffal, Yan V. Sun, Dominik Beer, Simon Lee, Girish N. Nadkarni, ThuyVy Duong, Biqi Wang, Tomasz Czuba, Thomas R. Austin, Zachary T. Yoneda, Daniel J. Friedman, Anne Clayton, Matthew C. Hyman, Renae Judy, Allan C. Skanes, Kate M. Orland, Timothy Treu, Matthew T. Oetjens, Álvaro Alonso, Elsayed Z. Soliman, Honghuang Lin, Kathryn L. Lunetta, Jesper van der Pals, Tariq Z. Issa, Navid A. Nafissi, Heidi T. May, Peter Leong‐Sit, Carolina Roselli, Seung Hoan Choi, Goncalo Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Andrew Blumenfeld, Boris Boutkov, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Adam J. Mansfield, Evan K. Maxwell, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Razvan Panea, Tommy Polanco, Ayesha Rasool, William Salerno, Jeffrey Staples, Marcus B. Jones, Lyndon J. Mitnaul, Habib Khan, Stacey Knight, Richard Karlsson Linnér, Connie R. Bezzina, Samuli Ripatti, Susan R. Heckbert, J. Michael Gaziano, Ruth J. F. Loos, Bruce M. Psaty, J. Gustav Smith, Emelia Benjamin, Dan E. Arking, Daniel J. Rader, Svati H. Shah, Dan M. Roden, Scott M. Damrauer, Lee L. Eckhardt (2025). The impact of common and rare genetic variants on bradyarrhythmia development. , 57(1), DOI: https://doi.org/10.1038/s41588-024-01978-2.
Article12 days agoSequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Ingrid E. Christophersen, Nona Sotoodehnia, Michiel Rienstra, Renée Johnson, Laura M. Raffield, Giovanni Davogustto, Kendra A. Young, Mark Chaffin, Peter M. Nilsson, Gregory M. Marcus, Michael J. Cutler, David R. Van Wagoner, Stefan Kääb, Christine M. Albert, Elsayed Z. Soliman, Joshua C. Bis, Patrick T. Ellinor, Daníel F. Guðbjartsson, Lydia Coulter Kwee, Nicholas L. Smith, Jason D. Roberts, Xin Wang, John Barnard, Daniel I. Chasman, Eric Boerwinkle, Thomas W. Blackwell, Kathryn L. Lunetta, Susan Redline, Jennifer A. Brody, Arnljot Tveit, Toshihiro Tanaka, Bruce M. Psaty, Andrea Natale, Linda Johnson, Connie R. Bezzina, Christian T. Ruff, Steven A. Lubitz, David D. McManus, J. Gustav Smith, Doreen Haase, Saman Nazarian, James P. Pirruccello, Moritz F. Sinner, Victor Nauffal, Jeffrey L. Anderson, Michael Cho, Jennifer L. Halford, Dan M. Roden, Lorne J. Gula, Garðar Sveinbjörnsson, Tetsushi Furukawa, Marc S. Sabatine, Susan R. Heckbert, Stacey Gabriel, Quinn S. Wells, Dan E. Arking, Emelia Benjamin, Kāri Stefánsson, David Conen, Sanghamitra Mohanty, Seung Hoan Choi, Dawood Darbar, Ruth J. F. Loos, Christopher M. Haggerty, Nicholas Marston, Morten Olesen, John E. Hokanson, Hugh Calkins, Valerie N. Morrill, Lorenz Risch, Namrata Gupta, Svati H. Shah, Matthew C. Hill, Navid A. Nafissi, Pim van der Harst, Roelof A.J. Smit, Diane Fatkin, Álvaro Alonso, Davíð O. Arnar, Hilma Hólm, Paulus Kirchhof, Daniel J. Rader, Bastiaan Geelhoed, Aenne S. von Falkenhausen, Stacey Knight, Renate B. Schnabel, Helene Mantineo, Yusuke Ebana, Ling Xiao, Zachary Laksman, Michael Preuß, Sean J. Jurgens, Yuan‐I Min, M. Benjamin Shoemaker, Scott M. Damrauer, Mina K. Chung, Lu‐Chen Weng, Goo Jun, Renae Judy, Carolina Roselli (2025). Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk. , DOI: https://doi.org/10.17615/8dr2-g803.
Article12 days agoSequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Ingrid E. Christophersen, Nona Sotoodehnia, Michiel Rienstra, Renée Johnson, Laura M. Raffield, Giovanni Davogustto, Kendra A. Young, Mark Chaffin, Peter M. Nilsson, Gregory M. Marcus, Michael J. Cutler, David R. Van Wagoner, Stefan Kääb, Christine M. Albert, Elsayed Z. Soliman, Joshua C. Bis, Patrick T. Ellinor, Daníel F. Guðbjartsson, Lydia Coulter Kwee, Nicholas L. Smith, Jason D. Roberts, Xin Wang, John Barnard, Daniel I. Chasman, Eric Boerwinkle, Thomas W. Blackwell, Kathryn L. Lunetta, Susan Redline, Jennifer A. Brody, Arnljot Tveit, Toshihiro Tanaka, Bruce M. Psaty, Andrea Natale, Linda Johnson, Connie R. Bezzina, Christian T. Ruff, Steven A. Lubitz, David D. McManus, J. Gustav Smith, Doreen Haase, Saman Nazarian, James P. Pirruccello, Moritz F. Sinner, Victor Nauffal, Jeffrey L. Anderson, Michael Cho, Jennifer L. Halford, Dan M. Roden, Lorne J. Gula, Garðar Sveinbjörnsson, Tetsushi Furukawa, Marc S. Sabatine, Susan R. Heckbert, Stacey Gabriel, Quinn S. Wells, Dan E. Arking, Emelia Benjamin, Kāri Stefánsson, David Conen, Sanghamitra Mohanty, Seung Hoan Choi, Dawood Darbar, Ruth J. F. Loos, Christopher M. Haggerty, Nicholas Marston, Morten Olesen, John E. Hokanson, Hugh Calkins, Valerie N. Morrill, Lorenz Risch, Namrata Gupta, Svati H. Shah, Matthew C. Hill, Navid A. Nafissi, Pim van der Harst, Roelof A.J. Smit, Diane Fatkin, Álvaro Alonso, Davíð O. Arnar, Hilma Hólm, Paulus Kirchhof, Daniel J. Rader, Bastiaan Geelhoed, Aenne S. von Falkenhausen, Stacey Knight, Renate B. Schnabel, Helene Mantineo, Yusuke Ebana, Ling Xiao, Zachary Laksman, Michael Preuß, Sean J. Jurgens, Yuan‐I Min, M. Benjamin Shoemaker, Scott M. Damrauer, Mina K. Chung, Lu‐Chen Weng, Goo Jun, Renae Judy, Carolina Roselli (2025). Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk. , DOI: https://doi.org/10.17615/8dr2-g803.
Article12 days agoRare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis
Alexandria Hall, Brandon K. Fornwalt, Chrissy Austin-Tse, Mark Chaffin, B.E. Cade, J Lee, Mary Pettinger, Lichun Weng, Braxton D. Mitchell, Susan Redline, Nona Sotoodehnia, E Boerwinkle, Hsingchi Lin, E.Z Soliman, Álvaro Alonso, Xiuqing Guo, Hai Lin, G.N. Nadkarni, Arden Moscati, Jelena Kornej, Seung‐Hyuk Choi, Cynthia M. Haggerty, Terri Blackwell, Tooraj Mirshahi, Jacob A. Brody, D.E. Arking, Bruce M. Psaty, Jerome I. Rotter, Sean J. Jurgens, J.L Halford, Carolina Roselli, Charles Kooperberg, S.A. Lubitz, Patrick T. Ellinor, Kathryn L. Lunetta, Eric A. Whitsel, Christina J. Lee, Marco Perez, Ruth J. F. Loos, S.S Rich, Susan R. Heckbert, K.L. Wiggins, Emelia Benjamin, A. Correa, Heidi L. Rehm, Valerie N. Morrill, Braxton Lagerman, Ramachandran S. Vasan (2024). Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis. , DOI: https://doi.org/10.17615/c1sy-3719.
Article12 days ago