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The last 5 uploaded publications
Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism
Marine Germain, Daniel I. Chasman, Hugoline G. de Haan, Weihong Tang, Sara Lindstrӧm, Lu‐Chen Weng, Mariza de Andrade, Marieke C. Visser, Kerri L. Wiggins, Pierre Suchon, Noémie Saut, David M. Smadja, Grégoire Le Gal, Astrid van Hylckama Vlieg, Antonio Di Narzo, Ke Hao, Christopher P. Nelson, Ares Rocañín-Arjó, Lasse Folkersen, Ramin Monajemi, Lynda M. Rose, Jennifer A. Brody, P. Eline Slagboom, Dylan Aïssi, France Gagnon, Jean‐François Deleuze, Panos Deloukas, Christophe Tzourio, Jean‐François Dartigues, Claudine Berr, Kent D. Taylor, Mete Civelek, Per Eriksson, Bruce M. Psaty, Jeanine Houwing-Duitermaat, Alison H. Goodall, François Cambien, Peter Kraft, Philippe Amouyel, Nilesh J. Samani, Saonli Basu, Paul M. Ridker, Frits R. Rosendaal, Christopher Kabrhel, Aaron R. Folsom, John A. Heit, Pieter H. Reitsma, David‐Alexandre Trégouët, Nicholas L. Smith, Pierre‐Emmanuel Morange (2015). Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism. The American Journal of Human Genetics, 96(4), pp. 532-542, DOI: 10.1016/j.ajhg.2015.01.019.
Article323 days agoTargeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes
Hugoline G. de Haan, Astrid van Hylckama Vlieg, Luca A. Lotta, Marcin M. Gorski, Paolo Bucciarelli, Ida Martinelli, Trevor Baglin, Flora Peyvandi, Frits R. Rosendaal, Philippe Amouyel, M. de Andrade, Saonli Basu, Claudine Berr, J.A. Brody, Daniel I. Chasman, Jean‐François Dartigues, Aaron R. Folsom, Marine Germain, John A. Heit, Jeanine Houwing-Duitermaat, Christopher Kabrhel, Peter Kraft, Grégoire Le Gal, Sara Lindstrӧm, Ramin Monajemi, Pierre‐Emmanuel Morange, B.M. Psaty, Pieter H. Reitsma, Paul M. Ridker, L.M. Rose, Noémie Saut, P. Eline Slagboom, David M. Smadja, Nicholas L. Smith, P. Suchon, W.H. Wilson Tang, Kent D. Taylor, David‐Alexandre Trégouët, Christophe Tzourio, Marieke C. Visser, Lu‐Chen Weng, K.L. Wiggins (2018). Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes. Journal of Thrombosis and Haemostasis, 16(12), pp. 2432-2441, DOI: 10.1111/jth.14279.
Article323 days agoPredicting Atrial Fibrillation After Stroke by Combining Polygenic Risk Scores and Clinical Features
Reinier W. P. Tack, Benjamin Yong‐Qiang Tan, Jasper R. Senff, Savvina Prapiadou, Tamara N. Kimball, Shaan Khurshid, Jeffrey M. Ashburner, Sean J. Jurgens, Sanjula Singh, Lu‐Chen Weng, Sophia Gunn, Carolina Roselli, Kathryn L. Lunetta, Emelia Benjamin, Patrick T. Ellinor, Jonathan Rosand, Ernst Mayerhofer, Steven A. Lubitz, Christopher D. Anderson (2025). Predicting Atrial Fibrillation After Stroke by Combining Polygenic Risk Scores and Clinical Features. , 56(4), DOI: https://doi.org/10.1161/strokeaha.124.050123.
Article4 days agoSequencing 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.
Article4 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.
Article4 days ago