Open Access Research article

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

Luca A Lotta12, Mark Wang2, Jin Yu2, Ida Martinelli1, Fuli Yu2, Serena M Passamonti1, Dario Consonni3, Emanuela Pappalardo1, Marzia Menegatti1, Steven E Scherer2, Lora L Lewis2, Humeira Akbar2, Yuanqing Wu2, Matthew N Bainbridge2, Donna M Muzny2, Pier M Mannucci1, Richard A Gibbs2* and Flora Peyvandi1*

Author Affiliations

1 Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, U.O.S. Dipartimentale per la Diagnosi e la Terapia delle Coagulopatie, Fondazione IRCCS Cà Granda - Ospedale Maggiore Policlinico, Università degli Studi di Milano and Luigi Villa Foundation, Milan, Italy

2 Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA

3 Unit of Epidemiology, Fondazione IRCCS Cà Granda - Ospedale Maggiore Policlinico, Università degli Studi di Milano, Milan, Italy

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BMC Medical Genomics 2012, 5:7  doi:10.1186/1755-8794-5-7

Published: 21 February 2012

Additional files

Additional file 1:

Supplementary Material. Supplementary Tables and Figures.

Format: DOCX Size: 241KB Download file

Open Data

Additional file 2:

target and tiled regions. target and tiled genomic coordinate-intervals.

Format: TXT Size: 133KB Download file

Open Data