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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.
Article126 days agoGenome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels
Bengt Sennblad, Saonli Basu, Johanna Mazur, Pierre Suchon, Ángel Martínez-Pérez, Astrid van Hylckama Vlieg, Vinh Trương, Yuhuang Li, Jesper R. Gådin, Weihong Tang, Vera Grossman, Hugoline G. de Haan, Niklas Handin, Angela Silveira, Juan Carlos Souto, Anders Franco‐Cereceda, Pierre‐Emmanuel Morange, France Gagnon, José Manuel Soria, Per Eriksson, Anders Hamsten, Lars Mäegdefessel, Frits R. Rosendaal, Philipp S. Wild, Aaron R. Folsom, David‐Alexandre Trégouët, Maria Sabater‐Lleal (2016). Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels. Human Molecular Genetics, pp. ddw401-ddw401, DOI: 10.1093/hmg/ddw401.
Article126 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.
Article126 days agoElucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus
David Stacey, Lingyan Chen, Paulina J. Stanczyk, Joanna M. M. Howson, Amy M. Mason, Stephen Burgess, Stephen MacDonald, Jonathan Langdown, Harriett McKinney, Kate Downes, Neda Farahi, James E. Peters, Saonli Basu, James S. Pankow, Weihong Tang, Nathan Pankratz, Maria Sabater‐Lleal, Paul S. de Vries, Nicholas L. Smith, Abbas Dehghan, Adam S. Heath, Alanna C. Morrison, Alex P. Reiner, Andrew D. Johnson, Anne Richmond, Annette Peters, Astrid van Hylckama Vlieg, Barbara McKnight, Bruce M. Psaty, Caroline Hayward, Cavin Ward‐Caviness, Christopher J. O’Donnell, Daniel I. Chasman, David P. Strachan, David‐Alexandre Trégouët, Dennis O. Mook‐Kanamori, Dipender Gill, Florian Thibord, Folkert W. Asselbergs, Frank W.G. Leebeek, Frits R. Rosendaal, Gail Davies, Georg Homuth, Gerard Temprano, Harry Campbell, Herman A. Taylor, Jan Bressler, Jennifer E. Huffman, Jerome I. Rotter, Jie Yao, James F. Wilson, Joshua C. Bis, Julie Hahn, Karl C. Desch, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Lisa R. Yanek, Marcus E. Kleber, Martina Mueller, Maryam Kavousi, Massimo Mangino, Matthew P. Conomos, Melissa Liu, Michael R. Brown, Min-A Jhun, Ming‐Huei Chen, Moniek P.M. de Maat, Patricia A. Peyser, Paul Elliot, Peng Wei, Philipp S. Wild, Pierre‐Emmanuel Morange, Pim van der Harst, Qiong Yang, Ngoc‐Quynh Le, Riccardo E. Marioni, Ruifang Li, Scott M. Damrauer, Simon R. Cox, Stella Trompet, Stephan B. Felix, Uwe Völker, Wolfgang Köenig, J. Wouter Jukema, Xiuqing Guo, Amy D. Gelinas, Daniel J. Schneider, Nebojša Janjić, Nilesh J. Samani, Shu Ye, Charlotte Summers, Edwin R. Chilvers, John Danesh, Dirk S. Paul (2022). Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus. Nature Communications, 13(1), DOI: 10.1038/s41467-022-28729-3.
Article126 days agoPublisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus
David Stacey, Lingyan Chen, Paulina J. Stanczyk, Joanna M. M. Howson, Amy M. Mason, Stephen Burgess, Stephen MacDonald, Jonathan Langdown, Harriett McKinney, Kate Downes, Neda Farahi, James E. Peters, Saonli Basu, James S. Pankow, Weihong Tang, Nathan Pankratz, Maria Sabater‐Lleal, Paul S. de Vries, Nicholas L. Smith, Abbas Dehghan, Adam S. Heath, Alanna C. Morrison, Alex P. Reiner, Andrew D. Johnson, Anne Richmond, Annette Peters, Astrid van Hylckama Vlieg, Barbara McKnight, Bruce M. Psaty, Caroline Hayward, Cavin Ward‐Caviness, Christopher J. O’Donnell, Daniel I. Chasman, David P. Strachan, David‐Alexandre Trégouët, Dennis O. Mook‐Kanamori, Dipender Gill, Florian Thibord, Folkert W. Asselbergs, Frank W.G. Leebeek, Frits R. Rosendaal, Gail Davies, Georg Homuth, Gerard Temprano, Harry Campbell, Herman A. Taylor, Jan Bressler, Jennifer E. Huffman, Jerome I. Rotter, Jie Yao, James F. Wilson, Joshua C. Bis, Julie Hahn, Karl C. Desch, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Lisa R. Yanek, Marcus E. Kleber, Maryam Kavousi, Massimo Mangino, Matthew P. Conomos, Melissa Liu, Michael R. Brown, Min-A Jhun, Ming‐Huei Chen, Moniek P.M. de Maat, Patricia A. Peyser, Paul Elliot, Peng Wei, Philipp S. Wild, Pierre‐Emmanuel Morange, Pim van der Harst, Qiong Yang, Ngoc‐Quynh Le, Riccardo E. Marioni, Ruifang Li, Scott M. Damrauer, Simon R. Cox, Stella Trompet, Stephan B. Felix, Uwe Völker, Wolfgang Köenig, J. Wouter Jukema, Xiuqing Guo, Amy D. Gelinas, Daniel J. Schneider, Nebojša Janjić, Nilesh J. Samani, Shu Ye, Charlotte Summers, Edwin R. Chilvers, John Danesh, Dirk S. Paul, Martina Mueller (2022). Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus. , 13 (1), DOI: https://doi.org/10.1038/s41467-022-29641-6.
Corrigendum44 days ago