Multiple QTL influence the serum Lp(a) concentration: A genome-wide linkage screen in the PROCARDIS study Tekijä Barlera, Specchia, C, Farrall, M, Chiodini, B, Franzosi, MG, Rust, S, Nicolis, E, Consortium, PROCARDIS

Anaesthesiological strategies in elective craniotomy: randomized, equivalence, open trial – The <it>NeuroMorfeo </it>trial Tekijä Guzzetti Stefano, Barlera Simona, Masson Serge, Latini Roberto, Franzosi Maria Grazia, Citerio Giuseppe, Pesenti Antonio

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Quantitative trait genetic linkage analysis of body mass index in familial coronary artery disease. Tekijä Specchia, C, Barlera, S, Chiodini, B, Nicolis, E, Farrall, M, Peden, J, Collins, R, Watkins, H, Tognoni, G, Franzosi, MG

Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS study. Tekijä Barlera, S, Specchia, C, Farrall, M, Chiodini, B, Franzosi, MG, Rust, S, Green, F, Nicolis, E, Peden, J, Assmann, G, Collins, R, Hamsten, A, Tognoni, G, Watkins, H

Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study. Tekijä Mälarstig, A, Buil, A, Souto, J, Clarke, R, Blanco-Vaca, F, Fontcuberta, J, Peden, J, Andersen, M, Silveira, A, Barlera, S, Seedorf, U, Watkins, H, Almasy, L, Hamsten, A, Soria, J

COMMON GENETIC VARIANTS ASSOCIATED WITH LOW Lp(a) KRINGLE-IV COPY NUMBER, HIGH Lp(a) CONCENTRATION, AND INCREASED RISK OF CORONARY HEART DISEASE Tekijä Seedorf, U, Peden, J, Hopewell, J, Kyriakou, T, Goel, A, Heath, S, Parish, S, Barlera, S, Grazia, M, Rust, S, Bennett, D, Silveira, A, Malarstig, A, Green, F, Lathrop, M, Gigante, B, Leander, K, de Faire, U, Clarke, R, Hamsten, A, Collins, R, Watkins, H, Consortium, PROCARDIS

Genetic variants associated with Lp(a) lipoprotein level and coronary disease. Tekijä Clarke, R, Peden, J, Hopewell, J, Kyriakou, T, Goel, A, Heath, S, Parish, S, Barlera, S, Franzosi, MG, Rust, S, Bennett, D, Silveira, A, Malarstig, A, Green, F, Lathrop, M, Gigante, B, Leander, K, de Faire, U, Seedorf, U, Hamsten, A, Collins, R, Watkins, H, Farrall, M

ASSOCIATION STUDY OF CORONARY ARTERY DISEASE (CAD) USING HUMANCVD 50K CHIP Tekijä Goel, A, Clarke, R, Hopewell, J, Kyriakou, T, Heath, S, Parish, S, Barlera, S, Franzosi, MG, Rust, S, Bennett, D, Silveira, A, Malarstig, A, Green, F, Lathrop, M, Gigante, B, Leander, K, Faire, U, Seedorf, U, Hamsten, A, Collins, R, Watkins, H, Farrall, M, Peden, J, Consortium, PROCARDIS

Influence of pentraxin 3 (PTX3) genetic variants on myocardial infarction risk and PTX3 plasma levels. Tekijä Elisa Barbati, Claudia Specchia, Massimo Villella, Marco Luciano Rossi, Simona Barlera, Barbara Bottazzi, Luisa Crociati, Carmela d'Arienzo, Raffaele Fanelli, Cecilia Garlanda, Francesca Gori, Ruggiero Mango, Alberto Mantovani, Giuseppe Merla, Enrico B Nicolis, Silvia Pietri, Patrizia Presbitero, Yukio Sudo, Alessandro Villella, Maria Grazia Franzosi

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Common Genetic Variants Associated With Higher Lp(a) Concentrations and Increased Risk of Coronary Heart Disease Tekijä Clarke, R, Peden, J, Hopewell, J, Kyriakou, T, Goel, A, Heath, S, Parish, S, Barlera, S, Grazia, M, Negri, M, Rust, S, Bennett, D, Silveira, A, Malarstig, A, Green, F, Lathrop, M, Gigante, B, Leander, K, de Faire, U, Seedorf, U, Hamsten, A, Collins, R, Watkins, H, Consortium, PROCARDIS

Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Tekijä Holliday, E, Maguire, J, Evans, T, Koblar, SA, Jannes, J, Sturm, J, Hankey, G, Baker, R, Golledge, J, Parsons, M, Malik, R, McEvoy, M, Biros, E, Lewis, MD, Lincz, L, Peel, R, Oldmeadow, C, Smith, W, Moscato, P, Barlera, S, Bevan, S, Bis, J, Boerwinkle, E, Boncoraglio, G, Brott, T