Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes

JOURNAL ARTICLE published December 2018 in Journal of Thrombosis and Haemostasis

Research funded by Nederlandse Organisatie voor Wetenschappelijk Onderzoek (912-03-033¦2003,916.56.157) | KWF Kankerbestrijding (RUL 99/1992) | Hartstichting (NHS208B086,NHS98.113) | Fondazione Cariplo (N. 2011-0524) | Italian Ministry of Health (N. RF-2009-1530493)

Authors: H.G. de Haan | A. van Hylckama Vlieg | L.A. Lotta | M.M. Gorski | P. Bucciarelli | I. Martinelli | T.P. Baglin | F. Peyvandi | F.R. Rosendaal | P. Amouyel | M. de Andrade | S. Basu | C. Berr | J.A. Brody | D. I Chasman | J.‐F. Dartigues | A.R. Folsom | M. Germain | J. Heit | J. Houwing‐Duitermaat | C. Kabrhel | P. Kraft | G. Le Gal | S. Lindström | R. Monajemi | P.‐E. Morange | B.M. Psaty | P.H. Reitsma | P.M. Ridker | L.M. Rose | N. Saut | E. Slagboom | D. Smadja | N.L. Smith | P. Suchon | W. Tang | K.D. Taylor | D.‐A. Trégouët | C. Tzourio | M.C.H. de Visser | L.‐C. Weng | K.L. Wiggins