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Veronique Vitart

DR

 https://orcid.org/0000-0002-4991-3797

Accepting PhD Students

Search results

  • 2012

    Genome-wide association uncovers shared genetic effects among personality traits and mood states

    Luciano, M., Huffman, J. E., Arias-Vásquez, A., Vinkhuyzen, A. A. E., Middeldorp, C. M., Giegling, I., Payton, A., Davies, G., Zgaga, L., Janzing, J., Ke, X., Galesloot, T., Hartmann, A. M., Ollier, W., Tenesa, A., Hayward, C., Verhagen, M., Montgomery, G. W., Hottenga, J-J., Konte, B., & 24 othersStarr, J. M., Vitart, V., Vos, P. E., Madden, P. A. F., Willemsen, G., Konnerth, H., Horan, M. A., Porteous, D. J., Campbell, H., Vermeulen, S. H., Heath, A. C., Wright, A., Polasek, O., Kovacevic, S. B., Hastie, N. D., Franke, B., Boomsma, D. I., Martin, N. G., Rujescu, D., Wilson, J. F., Buitelaar, J., Pendleton, N., Rudan, I. & Deary, I. J., 1 Sept 2012, In: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 159B, 6, p. 684-695

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

    Verhoeven, V. J. M., Hysi, P. G., Saw, S-M., Vitart, V., Mirshahi, A., Guggenheim, J. A., Cotch, M. F., Yamashiro, K., Baird, P. N., Mackey, D. A., Wojciechowski, R., Ikram, M. K., Hewitt, A. W., Duggal, P., Janmahasatian, S., Khor, C-C., Fan, Q., Zhou, X., Young, T. L., Tai, E-S., & 75 othersGoh, L-K., Li, Y-J., Aung, T., Vithana, E., Teo, Y-Y., Tay, W., Sim, X., Rudan, I., Hayward, C., Wright, A. F., Polasek, O., Campbell, H., Wilson, J. F., Fleck, B. W., Nakata, I., Yoshimura, N., Yamada, R., Matsuda, F., Ohno-Matsui, K., Nag, A., McMahon, G., St Pourcain, B., Lu, Y., Rahi, J. S., Cumberland, P. M., Bhattacharya, S., Simpson, C. L., Atwood, L. D., Li, X., Raffel, L. J., Murgia, F., Portas, L., Despriet, D. D. G., van Koolwijk, L. M. E., Wolfram, C., Lackner, K. J., Tönjes, A., Mägi, R., Lehtimäki, T., Kähönen, M., Esko, T., Metspalu, A., Rantanen, T., Pärssinen, O., Klein, B. E., Meitinger, T., Spector, T. D., Oostra, B. A., Smith, A. V., de Jong, P. T. V. M., Hofman, A., Amin, N., Karssen, L. C., Rivadeneira, F., Vingerling, J. R., Eiríksdóttir, G., Gudnason, V., Döring, A., Bettecken, T., Uitterlinden, A. G., Williams, C., Zeller, T., Castagné, R., Oexle, K., van Duijn, C. M., Iyengar, S. K., Mitchell, P., Wang, J. J., Höhn, R., Pfeiffer, N., Bailey-Wilson, J. E., Stambolian, D., Wong, T-Y., Hammond, C. J. & Klaver, C. C. W., Sept 2012, In: Human Genetics. 131, 9, p. 1467-80 14 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Uncovering Networks from Genome-Wide Association Studies via Circular Genomic Permutation

    Cabrera, C. P., Navarro, P., Huffman, J. E., Wright, A. F., Hayward, C., Campbell, H., Wilson, J. F., Rudan, I., Hastie, N. D., Vitart, V. & Haley, C. S., Sept 2012, In: G3: Genes | Genomes | Genetics. 2, 9, p. 1067-75 9 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

    MUTHER Consortium, DIAGRAM Consortium, Manning, A. K., Hivert, M-F., Scott, R. A., Grimsby, J. L., Bouatia-Naji, N., Chen, H., Rybin, D., Liu, C-T., Bielak, L. F., Prokopenko, I., Amin, N., Barnes, D., Cadby, G., Hottenga, J-J., Ingelsson, E., Jackson, A. U., Johnson, T., Kanoni, S., Ladenvall, C., & 31 othersLagou, V., Lahti, J., Lecoeur, C., Liu, Y., Martinez-Larrad, M. T., Montasser, M. E., Navarro, P., Perry, J. R. B., Rasmussen-Torvik, L. J., Salo, P., Sattar, N., Shungin, D., Strawbridge, R. J., Tanaka, T., van Duijn, C. M., An, P., de Andrade, M., Andrews, J. S., Aspelund, T., Atalay, M., Aulchenko, Y., Balkau, B., Bandinelli, S., Campbell, H., Hayward, C., Rudan, I., Vitart, V., Wild, S. H., Wilson, J. F., Wright, A. F. & Zgaga, L., Jun 2012, In: Nature Genetics. 44, 6, p. 659-U81 13 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • A genome-wide association search for type 2 diabetes genes in African Americans

    DIAGRAM Consortium, Palmer, N. D., McDonough, C. W., Hicks, P. J., Roh, B. H., Wing, M. R., An, S. S., Hester, J. M., Cooke, J. N., Bostrom, M. A., Rudock, M. E., Talbert, M. E., Lewis, J. P., Ferrara, A., Lu, L., Ziegler, J. T., Sale, M. M., Divers, J., Shriner, D., Adeyemo, A., & 31 othersRotimi, C. N., Ng, M. C. Y., Langefeld, C. D., Freedman, B. I., Bowden, D. W., Voight, B. F., Scott, L. J., Steinthorsdottir, V., Morris, A. P., Dina, C., Welch, R. P., Zeggini, E., Huth, C., Aulchenko, Y. S., Thorleifsson, G., McCulloch, L. J., Ferreira, T., Grallert, H., Amin, N., Wu, G., Willer, C. J., Raychaudhuri, S., McCarroll, S. A., Navarro, P., Rudan, I., Campbell, H., Wilson, J. F., Hayward, C., Vitart, V., Wild, S. H. & Wright, A. F., 2012, In: PLoS ONE. 7, 1, p. 1-14 14 p., e29202.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Analysis of Blood Lipid Traits Using Regional Heritability Mapping

    Shirali, M., Pong-Wong, R., Navarro, P., Hayward, C., Vitart, V., Rudan, I., Campbell, H., Hastie, N., Wright, A. & Haley, C., 2012, p. P279 204.

    Research output: Contribution to conference › Abstract

  • Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

    Murabito, J. M., White, C. C., Kavousi, M., Sun, Y. V., Feitosa, M. F., Nambi, V., Lamina, C., Schillert, A., Coassin, S., Bis, J. C., Broer, L., Crawford, D. C., Franceschini, N., Frikke-Schmidt, R., Haun, M., Holewijn, S., Huffman, J. E., Hwang, S-J., Kiechl, S., Kollerits, B., & 109 othersMontasser, M. E., Nolte, I. M., Rudock, M. E., Senft, A., Teumer, A., van der Harst, P., Vitart, V., Waite, L. L., Wood, A. R., Wassel, C. L., Absher, D. M., Allison, M. A., Amin, N., Arnold, A., Asselbergs, F. W., Aulchenko, Y., Bandinelli, S., Barbalic, M., Boban, M., Brown-Gentry, K., Couper, D. J., Criqui, M. H., Dehghan, A., den Heijer, M., Dieplinger, B., Ding, J., Dörr, M., Espinola-Klein, C., Felix, S. B., Ferrucci, L., Folsom, A. R., Fraedrich, G., Gibson, Q., Goodloe, R., Gunjaca, G., Haltmayer, M., Heiss, G., Hofman, A., Kieback, A., Kiemeney, L. A., Kolcic, I., Kullo, I. J., Kritchevsky, S. B., Lackner, K. J., Li, X., Lieb, W., Lohman, K., Meisinger, C., Melzer, D., Mohler, E. R., Mudnic, I., Mueller, T., Navis, G., Oberhollenzer, F., Olin, J. W., O'Connell, J., O'Donnell, C. J., Palmas, W., Penninx, B. W., Petersmann, A., Polasek, O., Psaty, B. M., Rantner, B., Rice, K., Rivadeneira, F., Rotter, J. I., Seldenrijk, A., Stadler, M., Summerer, M., Tanaka, T., Tybjaerg-Hansen, A., Uitterlinden, A. G., van Gilst, W. H., Vermeulen, S. H., Wild, S. H., Wild, P. S., Willeit, J., Zeller, T., Zemunik, T., Zgaga, L., Assimes, T. L., Blankenberg, S., Boerwinkle, E., Campbell, H., Cooke, J. P., de Graaf, J., Herrington, D., Kardia, S. L. R., Mitchell, B. D., Murray, A., Münzel, T., Newman, A. B., Oostra, B. A., Rudan, I., Shuldiner, A. R., Snieder, H., van Duijn, C. M., Völker, U., Wright, A. F., Wichmann, H-E., Wilson, J. F., Witteman, J. C. M., Liu, Y., Hayward, C., Borecki, I. B., Ziegler, A., North, K. E., Cupples, L. A. & Kronenberg, F., 2012, In: Circulation: Cardiovascular Genetics. 5, 1, p. 100-12 13 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Discovery and fine mapping of serum protein loci through transethnic meta-analysis

    LifeLines Cohort Study, Franceschini, N., van Rooij, F. J. A., Prins, B. P., Feitosa, M. F., Karakas, M., Eckfeldt, J. H., Folsom, A. R., Kopp, J., Vaez, A., Andrews, J. S., Baumert, J., Boraska, V., Broer, L., Hayward, C., Ngwa, J. S., Okada, Y., Polasek, O., Westra, H-J., Wang, Y. A., & 31 othersDel Greco M, F., Glazer, N. L., Kapur, K., Kema, I. P., Lopez, L. M., Schillert, A., Smith, A. V., Winkler, C. A., Zgaga, L., Bandinelli, S., Bergmann, S., Boban, M., Bochud, M., Chen, Y. D., Davies, G., Dehghan, A., Ding, J., Doering, A., Durda, J. P., Ferrucci, L., Franco, O. H., Franke, L., Gunjaca, G., Hofman, A., Starr, J. M., Vitart, V., Campbell, H., Deary, I. J., Rudan, I., Wilson, J. F. & Wright, A. F., 2012, In: American Journal of Human Genetics. 91, 4, p. 744-53 10 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Evidence of Inbreeding Depression on Human Height

    on behalf of the ROHgen Consortium, McQuillan, R., Eklund, N., Pirastu, N., Kuningas, M., McEvoy, B. P., Esko, T., Corre, T., Davies, G., Kaakinen, M., Lyytikäinen, L-P., Kristiansson, K., Havulinna, A. S., Gögele, M., Vitart, V., Tenesa, A., Aulchenko, Y., Hayward, C., Johansson, A., Boban, M., & 31 othersUlivi, S., Robino, A., Boraska, V., Igl, W., Wild, S. H., Zgaga, L., Amin, N., Theodoratou, E., Polašek, O., Girotto, G., Lopez, L. M., Sala, C., Lahti, J., Laatikainen, T., Prokopenko, I., Kals, M., Viikari, J., Yang, J., Pouta, A., Estrada, K., Starr, J. M., Farrington, S. M., Campbell, H., Porteous, D., Hastie, N. D., Wright, A. F., Dunlop, M., Rudan, I., Deary, I. J., Visscher, P. M. & Wilson, J. F., 2012, In: PLoS Genetics. 8, 7, e1002655.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • FTO genotype is associated with phenotypic variability of body mass index

    Yang, J., Loos, R. J. F., Powell, J. E., Medland, S. E., Speliotes, E. K., Chasman, D. I., Rose, L. M., Thorleifsson, G., Steinthorsdottir, V., Mägi, R., Waite, L., Smith, A. V., Yerges-Armstrong, L. M., Monda, K. L., Hadley, D., Mahajan, A., Li, G., Kapur, K., Vitart, V., Huffman, J. E., & 152 othersWang, S. R., Palmer, C., Esko, T., Fischer, K., Zhao, J. H., Demirkan, A., Isaacs, A., Feitosa, M. F., Luan, J., Heard-Costa, N. L., White, C., Jackson, A. U., Preuss, M., Ziegler, A., Eriksson, J., Kutalik, Z., Frau, F., Nolte, I. M., Van Vliet-Ostaptchouk, J. V., Hottenga, J-J., Jacobs, K. B., Verweij, N., Goel, A., Medina-Gomez, C., Estrada, K., Bragg-Gresham, J. L., Sanna, S., Sidore, C., Tyrer, J., Teumer, A., Prokopenko, I., Mangino, M., Lindgren, C. M., Assimes, T. L., Shuldiner, A. R., Hui, J., Beilby, J. P., McArdle, W. L., Hall, P., Haritunians, T., Zgaga, L., Kolcic, I., Polasek, O., Zemunik, T., Oostra, B. A., Junttila, M. J., Grönberg, H., Schreiber, S., Peters, A., Hicks, A. A., Stephens, J., Foad, N. S., Laitinen, J., Pouta, A., Kaakinen, M., Willemsen, G., Vink, J. M., Wild, S. H., Navis, G., Asselbergs, F. W., Homuth, G., John, U., Iribarren, C., Harris, T., Launer, L., Gudnason, V., O'Connell, J. R., Boerwinkle, E., Cadby, G., Palmer, L. J., James, A. L., Musk, A. W., Ingelsson, E., Psaty, B. M., Beckmann, J. S., Waeber, G., Vollenweider, P., Hayward, C., Wright, A. F., Rudan, I., Groop, L. C., Metspalu, A., Khaw, K. T., van Duijn, C. M., Borecki, I. B., Province, M. A., Wareham, N. J., Tardif, J-C., Huikuri, H. V., Cupples, L. A., Atwood, L. D., Fox, C. S., Boehnke, M., Collins, F. S., Mohlke, K. L., Erdmann, J., Schunkert, H., Hengstenberg, C., Stark, K., Lorentzon, M., Ohlsson, C., Cusi, D., Staessen, J. A., Van der Klauw, M. M., Pramstaller, P. P., Kathiresan, S., Jolley, J. D., Ripatti, S., Jarvelin, M-R., de Geus, E. J. C., Boomsma, D. I., Penninx, B., Wilson, J. F., Campbell, H., Chanock, S. J., van der Harst, P., Hamsten, A., Watkins, H., Hofman, A., Witteman, J. C., Zillikens, M. C., Uitterlinden, A. G., Rivadeneira, F., Zillikens, M. C., Kiemeney, L. A., Vermeulen, S. H., Abecasis, G. R., Schlessinger, D., Schipf, S., Stumvoll, M., Tönjes, A., Spector, T. D., North, K. E., Lettre, G., McCarthy, M. I., Berndt, S. I., Heath, A. C., Madden, P. A. F., Nyholt, D. R., Montgomery, G. W., Martin, N. G., McKnight, B., Strachan, D. P., Hill, W. G., Snieder, H., Ridker, P. M., Thorsteinsdottir, U., Stefansson, K., Frayling, T. M., Hirschhorn, J. N., Goddard, M. E. & Visscher, P. M., 2012, In: Nature. 490, 7419, p. 267-272 6 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Genome-wide analysis of epistasis in body mass index using multiple human populations

    Wei, W., Hemani, G., Gyenesei, A., Vitart, V., Navarro, P., Hayward, C., Cabrera-Cardenas, C., Huffman, J. E., Knott, S. A., Hicks, A. A., Rudan, I., Pramstaller, P. P., Wild, S. H., Wilson, J. F., Campbell, H., Hastie, N. D., Wright, A. F. & Haley, C. S., 2012, In: European Journal of Human Genetics. 20, 8, p. 857-62 6 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Genome-wide association and functional follow-up reveals new loci for kidney function

    CARDIoGRAM Consortium, Pattaro, C., Köttgen, A., Teumer, A., Garnaas, M., Böger, C. A., Fuchsberger, C., Olden, M., Chen, M-H., Tin, A., Taliun, D., Li, M., Gao, X., Gorski, M., Yang, Q., Hundertmark, C., Foster, M. C., O'Seaghdha, C. M., Glazer, N., Isaacs, A., & 31 othersLiu, C-T., Smith, A. V., O'Connell, J. R., Struchalin, M., Tanaka, T., Li, G., Johnson, A. D., Gierman, H. J., Feitosa, M., Hwang, S-J., Atkinson, E. J., Lohman, K., Cornelis, M. C., Johansson, Å., Tönjes, A., Dehghan, A., Chouraki, V., Holliday, E. G., Sorice, R., Kutalik, Z., Lehtimäki, T., Esko, T., Wild, S. H., Wright, A. F., Campbell, H., Hastie, N., Vitart, V., Colhoun, H., Rudan, I., Wilson, J. F. & Hayward, C., 2012, In: PLoS Genetics. 8, 3, p. e1002584

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations

    DIAGRAM Consortium, Demirkan, A., van Duijn, C. M., Ugocsai, P., Isaacs, A., Pramstaller, P. P., Liebisch, G., Wilson, J. F., Johansson, Å., Rudan, I., Aulchenko, Y. S., Kirichenko, A. V., Janssens, A. C. J. W., Jansen, R. C., Gnewuch, C., Domingues, F. S., Pattaro, C., Wild, S. H., Jonasson, I., Polasek, O., & 31 othersZorkoltseva, I. V., Hofman, A., Karssen, L. C., Struchalin, M., Floyd, J., Igl, W., Biloglav, Z., Broer, L., Pfeufer, A., Pichler, I., Campbell, S., Zaboli, G., Kolcic, I., Rivadeneira, F., Huffman, J., Hastie, N. D., Uitterlinden, A., Franke, L., Franklin, C. S., Vitart, V., Nelson, C. P., Preuss, M., Bis, J. C., O'Donnell, C. J., Franceschini, N., Witteman, J. C. M., Axenovich, T., Oostra, B. A., Hayward, C., Wright, A. F. & Campbell, H., 2012, In: PLoS Genetics. 8, 2, p. e1002490

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

    Boraska, V., Day-Williams, A., Franklin, C. S., Elliott, K. S., Panoutsopoulou, K., Tachmazidou, I., Albrecht, E., Bandinelli, S., Beilin, L. J., Bochud, M., Cadby, G., Ernst, F., Evans, D. M., Hayward, C., Hicks, A. A., Huffman, J., Huth, C., James, A. L., Klopp, N., Kolcic, I., & 46 othersKutalik, Z., Lawlor, D. A., Musk, A. W., Pehlic, M., Pennell, C. E., Perry, J. R. B., Peters, A., Polasek, O., St Pourcain, B., Ring, S. M., Salvi, E., Schipf, S., Staessen, J. A., Teumer, A., Timpson, N., Vitart, V., Warrington, N. M., Yaghootkar, H., Zemunik, T., Zgaga, L., An, P., Anttila, V., Borecki, I. B., Holmen, J., Ntalla, I., Palotie, A., Pietiläinen, K. H., Wedenoja, J., Winsvold, B. S., Dedoussis, G. V., Kaprio, J., Province, M. A., Zwart, J-A., Burnier, M., Campbell, H., Cusi, D., Smith, G. D., Frayling, T. M., Gieger, C., Palmer, L. J., Pramstaller, P. P., Rudan, I., Völzke, H., Wichmann, H-E., Wright, A. F. & Zeggini, E., 2012, In: PLoS ONE. 7, 3, p. e31369

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

    DIAbetes Genetics Replication and Meta-analysis (DIAGRAM) Consortium, Scott, R. A., Lagou, V., Welch, R. P., Wheeler, E., Montasser, M. E., Luan, J., Mägi, R., Strawbridge, R. J., Rehnberg, E., Gustafsson, S., Kanoni, S., Rasmussen-Torvik, L. J., Yengo, L., Lecoeur, C., Shungin, D., Sanna, S., Sidore, C., Johnson, P. C. D., Jukema, J. W., & 31 othersJohnson, T., Mahajan, A., Verweij, N., Thorleifsson, G., Hottenga, J-J., Shah, S., Smith, A. V., Sennblad, B., Gieger, C., Salo, P., Perola, M., Timpson, N. J., Evans, D. M., Pourcain, B. S., Wu, Y., Andrews, J. S., Hui, J., Bielak, L. F., Navarro, P., Vitart, V., Hayward, C., Fraser, R. M., Bolton, J. L., Wild, S. H., Hastie, N. D., Rudan, I., Campbell, H., Wilson, J. F., Wright, A. F., Price, J. F. & Morris, A., 2012, In: Nature Genetics. 44, 9, p. 991-1005 15 p.

    Research output: Contribution to journal › Article › peer-review

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  • Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

    DIAGRAM+ Consortium, Dastani, Z., Hivert, M-F., Timpson, N., Perry, J. R. B., Yuan, X., Scott, R. A., Henneman, P., Heid, I. M., Kizer, J. R., Lyytikäinen, L-P., Fuchsberger, C., Tanaka, T., Morris, A. P., Small, K., Isaacs, A., Beekman, M., Coassin, S., Lohman, K., Qi, L., & 31 othersKanoni, S., Pankow, J. S., Uh, H-W., Wu, Y., Bidulescu, A., Rasmussen-Torvik, L. J., Greenwood, C. M. T., Ladouceur, M., Grimsby, J., Manning, A. K., Liu, C-T., Kooner, J., Mooser, V. E., Vollenweider, P., Kapur, K. A., Chambers, J., Wareham, N. J., Langenberg, C., Wilson, J. G., Navarro, P., Morris, A., Rudan, I., Campbell, H., Wilson, J. F., Hayward, C., Sharp, S. J., Vitart, V., Wild, S. H., Wright, A. F., Thompson, J. R. & Hastie, N. D., 2012, In: PLoS Genetics. 8, 3, p. e1002607

    Research output: Contribution to journal › Article › peer-review

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  • Regional heritability mapping for the dissection of complex traits

    Nagamine, Y., Pong-Wong, R., Navarro, P., Shirali, M., Uemoto, Y., Huffman, J., Vitart, V., Hayward, C., Riggio, V., Matika, O., Bishop, S., Rudan, I., Campbell, H., Hastie, N., Wright, A. & Haley, C., 2012, p. P21 74.

    Research output: Contribution to conference › Abstract

  • Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

    EUROSPAN Consortium, Zaboli, G., Ameur, A., Igl, W., Johansson, Å., Hayward, C., Vitart, V., Campbell, S., Zgaga, L., Polasek, O., Schmitz, G., van Duijn, C., Oostra, B., Pramstaller, P., Hicks, A., Meitinger, T., Rudan, I., Wright, A., Wilson, J. F., Campbell, H., & 1 othersGyllensten, U., 2012, In: European Journal of Human Genetics. 20, 1, p. 77-83 7 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • 2011

    Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function

    International Lung Cancer Consortium, Soler Artigas, M., Loth, D. W., Wain, L. V., Gharib, S. A., Obeidat, M., Tang, W., Zhai, G., Zhao, J. H., Smith, A. V., Huffman, J. E., Albrecht, E., Jackson, C. M., Evans, D. M., Cadby, G., Fornage, M., Manichaikul, A., Lopez, L. M., Johnson, T., Aldrich, M. C., & 31 othersAspelund, T., Barroso, I., Campbell, H., Cassano, P. A., Couper, D. J., Eiriksdottir, G., Franceschini, N., Garcia, M., Gieger, C., Gislason, G. K., Grkovic, I., Hammond, C. J., Hancock, D. B., Harris, T. B., Ramasamy, A., Heckbert, S. R., Deary, I. J., Harris, S. E., Henderson, J., Hunter, M. L., Kerr, S. M., Morris, A., Porteous, D. J., Starr, J. M., Rudan, I., Vitart, V., Wild, S. H., Wright, A. F., Zgaga, L., Wilson, J. F. & Hayward, C., Nov 2011, In: Nature Genetics. 43, 11, p. 1082-90 9 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
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  • Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

    AortaGen Consortium, CardioGram, KidneyGen Consortium, CKDGen Consortium, CHARGE Consortium Heart Failure, EchoGen Consortium, Cardiogenics Consortium, LifeLines Cohort Study, Wain, L. V., Verwoert, G. C., O'Reilly, P. F., Shi, G., Johnson, T., Johnson, A. D., Bochud, M., Rice, K. M., Henneman, P., Smith, A. V., Ehret, G. B., Amin, N., Larson, M. G., Mooser, V., Hadley, D., Doerr, M., Bis, J. C., Aspelund, T., Esko, T., & 31 othersJanssens, A. C. J. W., Zhao, J. H., Heath, S., Laan, M., Fu, J., Pistis, G., Luan, J., Arora, P., Lucas, G., Pirastu, N., Pichler, I., Jackson, A. U., Webster, R. J., Zhang, F., Peden, J. F., Schmidt, H., Tanaka, T., Campbell, H., Igl, W., Milaneschi, Y., Hottenga, J-J., Vitart, V., Lopez, L. M., Navarro, P., Wild, S. H., Davies, G., Starr, J., Rudan, I., Hayward, C., Deary, I. J. & Wilson, J. F., Oct 2011, In: Nature Genetics. 43, 10, p. 1005-11 7 p.

    Research output: Contribution to journal › Article › peer-review

  • Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults

    Huffman, J. E., Knezevic, A., Vitart, V., Kattla, J., Adamczyk, B., Novokmet, M., Igl, W., Pucic, M., Zgaga, L., Johannson, Å., Redzic, I., Gornik, O., Zemunik, T., Polasek, O., Kolcic, I., Pehlic, M., Koeleman, C. A. M., Campbell, S., Wild, S. H., Hastie, N. D., & 9 othersCampbell, H., Gyllensten, U., Wuhrer, M., Wilson, J. F., Hayward, C., Rudan, I., Rudd, P. M., Wright, A. F. & Lauc, G., 9 Sept 2011, In: Human Molecular Genetics. 20, 24, p. 5000-11 12 p.

    Research output: Contribution to journal › Article › peer-review

  • Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates

    Wei, W., Hemani, G., Hicks, A. A., Vitart, V., Cabrera-Cardenas, C., Navarro, P., Huffman, J., Hayward, C., Knott, S. A., Rudan, I., Pramstaller, P. P., Wild, S. H., Wilson, J. F., Campbell, H., Dunlop, M. G., Hastie, N., Wright, A. F. & Haley, C. S., 19 Aug 2011, In: PLoS ONE. 6, 8, e23836.

    Research output: Contribution to journal › Article › peer-review

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  • Genetic Predictors of Fibrin D-Dimer Levels in Healthy Adults

    Smith, N. L., Huffman, J. E., Strachan, D. P., Huang, J., Dehghan, A., Trompet, S., Lopez, L. M., Shin, S-Y., Baumert, J., Vitart, V., Bis, J. C., Wild, S. H., Rumley, A., Yang, Q., Uitterlinden, A. G., Stott, D. J., Davies, G., Carter, A. M., Thorand, B., Polašek, O., & 46 othersMcKnight, B., Campbell, H., Rudnicka, A. R., Chen, M-H., Buckley, B. M., Harris, S. E., Peters, A., Pulanic, D., Lumley, T., de Craen, A. J. M., Liewald, D. C., Gieger, C., Campbell, S., Ford, I., Gow, A. J., Luciano, M., Porteous, D. J., Guo, X., Sattar, N., Tenesa, A., Cushman, M., Slagboom, P. E., Visscher, P. M., Spector, T. D., Illig, T., Rudan, I., Bovill, E. G., Wright, A. F., McArdle, W. L., Tofler, G., Hofman, A., Westendorp, R. G. J., Starr, J. M., Grant, P. J., Karakas, M., Hastie, N. D., Psaty, B. M., Wilson, J. F., Lowe, G. D. O., O'Donnell, C. J., Witteman, J. C. M., Jukema, J. W., Deary, I. J., Soranzo, N., Koenig, W. & Hayward, C., Apr 2011, In: Circulation. 123, 17, p. 1864-1872 9 p.

    Research output: Contribution to journal › Article › peer-review

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  • Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

    Global BPgen Consortium, NASH CRN, GIANT consortium, MAGIC Investigators, GOLD Consortium, MAGIC, on behalf of Procardis Consortium, DIAGRAM Consortium, GIANT consortium & Navarro, P., 1 Mar 2011, In: PLoS Genetics. 7, 3, p. 1-13 13 p., e1001324.

    Research output: Contribution to journal › Article › peer-review

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  • Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson's Disease

    Facheris, M. F., Hicks, A. A., Minelli, C., Hagenah, J. M., Kostic, V., Campbell, S., Hayward, C., Volpato, C. B., Pattaro, C., Vitart, V., Wright, A., Campbell, H., Klein, C. & Pramstaller, P. P., Mar 2011, In: Journal of Molecular Neuroscience. 43, 3, p. 246-250 5 p.

    Research output: Contribution to journal › Article › peer-review

  • A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample

    SpiroMeta Consortium, Obeidat, M., Wain, L. V., Shrine, N., Kalsheker, N., Soler Artigas, M., Repapi, E., Burton, P. R., Johnson, T., Ramasamy, A., Zhao, J. H., Zhai, G., Huffman, J. E., Vitart, V., Albrecht, E., Igl, W., Hartikainen, A-L., Pouta, A., Cadby, G., Hui, J., & 31 othersPalmer, L. J., Hadley, D., McArdle, W. L., Rudnicka, A. R., Barroso, I., Loos, R. J. F., Wareham, N. J., Mangino, M., Soranzo, N., Spector, T. D., Gläser, S., Homuth, G., Völzke, H., Deloukas, P., Granell, R., Henderson, J., Grkovic, I., Jankovic, S., Zgaga, L., Polašek, O., Rudan, I., Wright, A. F., Campbell, H., Wild, S. H., Wilson, J. F., Heinrich, J., Imboden, M., Probst-Hensch, N. M., Gyllensten, U., Johansson, Å. & Hayward, C., 2011, In: PLoS ONE. 6, 5, p. e19382

    Research output: Contribution to journal › Article › peer-review

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  • Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

    International Consortium for Blood Pressure Genome-wide Association Studies (ICBP-GWAS), Fox, E. R., Young, J. H., Li, Y., Dreisbach, A. W., Keating, B. J., Musani, S. K., Liu, K., Morrison, A. C., Ganesh, S., Kutlar, A., Ramachandran, V. S., Polak, J. F., Fabsitz, R. R., Dries, D. L., Farlow, D. N., Redline, S., Adeyemo, A., Hirschorn, J. N., Sun, Y. V., & 31 othersWyatt, S. B., Penman, A. D., Palmas, W., Rotter, J. I., Townsend, R. R., Doumatey, A. P., Tayo, B. O., Mosley, T. H., Lyon, H. N., Kang, S. J., Rotimi, C. N., Cooper, R. S., Franceschini, N., Curb, J. D., Martin, L. W., Eaton, C. B., Kardia, S. L. R., Taylor, H. A., Caulfield, M. J., Ehret, G. B., Johnson, T., Chakravarti, A., Zhu, X., Levy, D., Wild, S. H., Rudan, I., Vitart, V., Campbell, H., Hayward, C., Wright, A. F. & Wilson, J. F., 2011, In: Human Molecular Genetics. 20, 11, p. 2273-84 12 p.

    Research output: Contribution to journal › Article › peer-review

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  • Copy number variation across European populations

    Chen, W., Hayward, C., Wright, A. F., Hicks, A. A., Vitart, V., Knott, S., Wild, S. H., Pramstaller, P. P., Wilson, J. F., Rudan, I. & Porteous, D. J., 2011, In: PLoS ONE. 6, 8, p. e23087

    Research output: Contribution to journal › Article › peer-review

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  • CUBN is a gene locus for albuminuria

    CKDGen Consortium, Böger, C. A., Chen, M-H., Tin, A., Olden, M., Köttgen, A., de Boer, I. H., Fuchsberger, C., O'Seaghdha, C. M., Pattaro, C., Teumer, A., Liu, C-T., Glazer, N. L., Li, M., O'Connell, J. R., Tanaka, T., Peralta, C. A., Kutalik, Z., Luan, J., Zhao, J. H., & 31 othersHwang, S-J., Akylbekova, E., Kramer, H., van der Harst, P., Smith, A. V., Lohman, K., de Andrade, M., Hayward, C., Kollerits, B., Tönjes, A., Aspelund, T., Ingelsson, E., Eiriksdottir, G., Launer, L. J., Harris, T. B., Shuldiner, A. R., Mitchell, B. D., Arking, D. E., Franceschini, N., Boerwinkle, E., Egan, J., Hernandez, D., Reilly, M., Townsend, R. R., Lumley, T., Siscovick, D. S., Psaty, B. M., Campbell, H., Vitart, V., Hastie, N. D. & Rudan, I., 2011, In: Journal of the American Society of Nephrology. 22, 3, p. 555-70 16 p.

    Research output: Contribution to journal › Article › peer-review

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  • Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

    International Consortium for Blood Pressure Genome-Wide Association Studies, Ehret, G. B., Munroe, P. B., Rice, K. M., Bochud, M., Johnson, A. D., Chasman, D. I., Smith, A. V., Tobin, M. D., Verwoert, G. C., Hwang, S-J., Pihur, V., Vollenweider, P., O'Reilly, P. F., Amin, N., Bragg-Gresham, J. L., Teumer, A., Glazer, N. L., Launer, L., Zhao, J. H., & 31 othersAulchenko, Y., Heath, S., Sõber, S., Parsa, A., Luan, J., Arora, P., Dehghan, A., Zhang, F., Lucas, G., Hicks, A. A., Jackson, A. U., Peden, J. F., Tanaka, T., Wild, S. H., Rudan, I., Igl, W., Milaneschi, Y., Parker, A. N., Fava, C., Chambers, J. C., Fox, E. R., Kumari, M., Go, M. J., van der Harst, P., Kao, W. H. L., Sjögren, M., Vitart, V., Campbell, H., Hayward, C., Wright, A. F. & Wilson, J. F., 2011, In: Nature. 478, 7367, p. 103-109 7 p.

    Research output: Contribution to journal › Article › peer-review

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  • SNP mistyping in genotyping arrays--an important cause of spurious association in case-control studies

    Mitry, D., Campbell, H., Charteris, D. G., Fleck, B. W., Tenesa, A., Dunlop, M. G., Hayward, C., Wright, A. F. & Vitart, V., 2011, In: Genetic Epidemiology. 35, 5, p. 423-6 4 p.

    Research output: Contribution to journal › Article › peer-review

  • Variants in STAT5B associate with serum TC and LDL-C levels

    Kornfeld, J-W., Isaacs, A., Vitart, V., Pospisilik, J. A., Meitinger, T., Gyllensten, U., Wilson, J. F., Rudan, I., Campbell, H., Penninger, J. M., Sexl, V., Moriggl, R., van Duijn, C., Pramstaller, P. P. & Hicks, A. A., 2011, In: The Journal of Clinical Endocrinology & Metabolism (JCEM). 96, 9, p. E1496-501

    Research output: Contribution to journal › Article › peer-review

  • 2010

    Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation

    Lauc, G., Essafi, A., Huffman, J. E., Hayward, C., Knezevic, A., Kattla, J. J., Polasek, O., Gornik, O., Vitart, V., Abrahams, J. L., Pucic, M., Novokmet, M., Redzic, I., Campbell, S., Wild, S. H., Borovecki, F., Wang, W., Kolcic, I., Zgaga, L., Gyllensten, U., & 6 othersWilson, J. F., Wright, A. F., Hastie, N. D., Campbell, H., Rudd, P. M. & Rudan, I., Dec 2010, In: PLoS Genetics. 6, 12, p. - 14 p., e1001256.

    Research output: Contribution to journal › Article › peer-review

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  • New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8

    Vitart, V., Bencić, G., Hayward, C., Skunca Herman, J., Huffman, J., Campbell, S., Bućan, K., Navarro, P., Gunjaca, G., Marin, J., Zgaga, L., Kolcić, I., Polasek, O., Kirin, M., Hastie, N. D., Wilson, J. F., Rudan, I., Campbell, H., Vatavuk, Z., Fleck, B., & 1 othersWright, A., 1 Nov 2010, In: Human Molecular Genetics. 19, 21, p. 4304-4311 8 p.

    Research output: Contribution to journal › Article › peer-review

  • The TCF7L2 diabetes risk variant is associated with HbA₁(C) levels: a genome-wide association meta-analysis

    Franklin, C. S., Aulchenko, Y. S., Huffman, J. E., Vitart, V., Hayward, C., Polašek, O., Knott, S., Zgaga, L., Zemunik, T., Rudan, I., Campbell, H., Wright, A. F., Wild, S. H. & Wilson, J. F., Nov 2010, In: Annals of Human Genetics. 74, 6, p. 471-478 8 p.

    Research output: Contribution to journal › Article › peer-review

  • Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndrome

    McKeigue, P. M., Campbell, H., Wild, S., Vitart, V., Hayward, C., Rudan, I., Wright, A. & Wilson, J. F., Jun 2010, In: International Journal of Epidemiology. 39, 3, p. 907-918 12 p.

    Research output: Contribution to journal › Article › peer-review

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  • Meta-analysis and imputation refines the association of 15q25 with smoking quantity

    Liu, J. Z., Tozzi, F., Waterworth, D. M., Pillai, S. G., Muglia, P., Middleton, L., Berrettini, W., Knouff, C. W., Yuan, X., Waeber, G., Vollenweider, P., Preisig, M., Wareham, N. J., Zhao, J. H., Loos, R. J. F., Barroso, I., Khaw, K. T., Grundy, S., Barter, P., Mahley, R., & 86 othersKesaniemi, A., McPherson, R., Vincent, J. B., Strauss, J., Kennedy, J. L., Farmer, A., McGuffin, P., Day, R., Matthews, K., Bakke, P., Gulsvik, A., Lucae, S., Ising, M., Brueckl, T., Horstmann, S., Wichmann, H. E., Rawal, R., Dahmen, N., Lamina, C., Polasek, O., Zgaga, L., Huffman, J., Campbell, S., Kooner, J., Chambers, J. C., Burnett, M. S., Devaney, J. M., Pichard, A. D., Kent, K. M., Satler, L., Lindsay, J. M., Waksman, R., Epstein, S., Wilson, J., Wild, S. H., Campbell, H., Vitart, V., Reilly, M. P., Li, M. Y., Qu, L., Wilensky, R., Matthai, W., Hakonarson, H. H., Rader, D. J., Franke, A., Wittig, M., Schafer, A., Uda, M., Terracciano, A., Xiao, X., Busonero, F., Scheet, P., Schlessinger, D., St Clair, D., Rujescu, D., Abecasis, G. R., Grabe, H. J., Teumer, A., Volzke, H., Petersmann, A., John, U., Rudan, I., Hayward, C., Wright, A. F., Kolcic, I., Wright, B. J., Thompson, J. R., Balmforth, A. J., Hall, A. S., Samani, N. J., Anderson, C. A., Ahmad, T., Mathew, C. G., Parkes, M., Satsangi, J., Caulfield, M., Munroe, P. B., Farrall, M., Dominiczak, A., Worthington, J., Thomson, W., Eyre, S., Barton, A., Mooser, V., Francks, C. & Marchini, J., May 2010, In: Nature Genetics. 42, 5, p. 436-440 5 p.

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  • Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

    Wellcome Trust Case Control Consor, Smith, N. L., Chen, M-H., Dehghan, A., Strachan, D. P., Basu, S., Soranzo, N., Hayward, C., Rudan, I., Sabater-Lleal, M., Bis, J. C., de Maat, M. P. M., Rumley, A., Kong, X., Yang, Q., Williams, F. M. K., Vitart, V., Campbell, H., Maelarstig, A., Wiggins, K. L., & 31 othersVan Duijn, C. M., McArdle, W. L., Pankow, J. S., Johnson, A. D., Silveira, A., McKnight, B., Uitterlinden, A. G., Aleksic, N., Meigs, J. B., Peters, A., Koenig, W., Cushman, M., Kathiresan, S., Rotter, J. I., Bovill, E. G., Hofman, A., Boerwinkle, E., Tofler, G. H., Peden, J. F., Psaty, B. M., Leebeek, F., Folsom, A. R., Larson, M. G., Spector, T. D., Wright, A., Wilson, J. F., Hamsten, A., Lumley, T., Witteman, J. C. M., Tang, W. & O'Donnell, C. J., 30 Mar 2010, In: Circulation. 121, 12, p. 1382-U45 30 p.

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  • A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

    EUROSPAN Consortium, Pattaro, C., De Grandi, A., Vitart, V., Hayward, C., Franke, A., Aulchenko, Y. S., Johansson, A., Wild, S. H., Melville, S. A., Isaacs, A., Polasek, O., Ellinghaus, D., Kolcic, I., Noethlings, U., Zgaga, L., Zemunik, T., Gnewuch, C., Schreiber, S., Campbell, S., & 14 othersHastie, N., Boban, M., Meitinger, T., Oostra, B. A., Riegler, P., Minelli, C., Wright, A. F., Campbell, H., van Duijn, C. M., Gyllensten, U., Wilson, J. F., Krawczak, M., Rudan, I. & Pramstaller, P. P., 11 Mar 2010, In: BMC Medical Genetics. 11, 41, p. - 17 p.

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  • Genetic comparison of a Croatian isolate and CEPH European founders

    Navarro, P., Vitart, V., Hayward, C., Tenesa, A., Zgaga, L., Juricic, D., Polasek, O., Hastie, N. D., Rudan, I., Campbell, H., Wright, A. F., Haley, C. S. & Knott, S. A., Feb 2010, In: Genetic Epidemiology. 34, 2, p. 140-5 6 p.

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  • Heritabilities of Ocular Biometrical Traits in Two Croatian Isolates with Extended Pedigrees

    Vitart, V., Bencic, G., Hayward, C., Herman, J. S., Huffman, J., Campbell, S., Bucan, K., Zgaga, L., Kolcic, I., Polasek, O., Campbell, H., Wright, A., Vatavuk, Z. & Rudan, I., Feb 2010, In: Investigative Ophthalmology & Visual Science (IOVS). 51, 2, p. 737-743 7 p.

    Research output: Contribution to journal › Article › peer-review

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  • New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

    DIAGRAM Consortium, Dupuis, J., Langenberg, C., Prokopenko, I., Saxena, R., Soranzo, N., Jackson, A. U., Wheeler, E., Glazer, N. L., Bouatia-Naji, N., Gloyn, A. L., Lindgren, C. M., Mägi, R., Morris, A. P., Randall, J., Johnson, T., Elliott, P., Rybin, D., Thorleifsson, G., Steinthorsdottir, V., & 31 othersHenneman, P., Grallert, H., Dehghan, A., Hottenga, J. J., Franklin, C. S., Navarro, P., Song, K., Goel, A., Perry, J. R. B., Egan, J. M., Lajunen, T., Grarup, N., Sparsø, T., Doney, A., Voight, B. F., Stringham, H. M., Li, M., Kanoni, S., Shrader, P., Cavalcanti-Proença, C., Kumari, M., Qi, L., Timpson, N. J., Hayward, C., Vitart, V., Wild, S. H., Morris, A., Rudan, I., Wright, A. F., Campbell, H. & Wilson, J. F., Feb 2010, In: Nature Genetics. 42, 2, p. 105-116 12 p.

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  • Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116))

    Dupuis, J., Langenberg, C., Prokopenko, I., Saxena, R., Soranzo, N., Jackson, A. U., Wheeler, E., Glazer, N. L., Bouatia-Naji, N., Gloyn, A. L., Lindgren, C. M., Mägi, R., Morris, A. P., Randall, J., Johnson, T., Elliott, P., Rybin, D., Thorleifsson, G., Steinthorsdottir, V., Henneman, P., & 287 othersGrallert, H., Dehghan, A., Hottenga, J. J., Franklin, C. S., Navarro, P., Song, K., Goel, A., Perry, J. R. B., Egan, J. M., Lajunen, T., Grarup, N., Sparsø, T., Doney, A., Voight, B. F., Stringham, H. M., Li, M., Kanoni, S., Shrader, P., Cavalcanti-Proença, C., Kumari, M., Qi, L., Timpson, N. J., Gieger, C., Zabena, C., Rocheleau, G., Ingelsson, E., An, P., O'Connell, J., Luan, JA., Elliott, A., McCarroll, S. A., Payne, F., Roccasecca, R. M., Pattou, F., Sethupathy, P., Ardlie, K., Ariyurek, Y., Balkau, B., Barter, P., Beilby, J. P., Ben-Shlomo, Y., Benediktsson, R., Bennett, A. J., Bergmann, S., Bochud, M., Boerwinkle, E., Bonnefond, A., Bonnycastle, L. L., Borch-Johnsen, K., Böttcher, Y., Brunner, E., Bumpstead, S. J., Charpentier, G., Chen, Y. D. I., Chines, P., Clarke, R., Coin, L. J. M., Cooper, M. N., Cornelis, M., Crawford, G., Crisponi, L., Day, I. N. M., De Geus, E. J. C., Delplanque, J., Dina, C., Erdos, M. R., Fedson, A. C., Fischer-Rosinsky, A., Forouhi, N. G., Fox, C. S., Frants, R., Franzosi, M. G., Galan, P., Goodarzi, M. O., Graessler, J., Groves, C. J., Grundy, S., Gwilliam, R., Gyllensten, U., Hadjadj, S., Hallmans, G., Hammond, N., Han, X., Hartikainen, A. L., Hassanali, N., Hayward, C., Heath, S. C., Hercberg, S., Herder, C., Hicks, A. A., Hillman, D. R., Hingorani, A. D., Hofman, A., Hui, J., Hung, J., Isomaa, B., Johnson, P. R. V., Jørgensen, T., Jula, A., Kaakinen, M., Kaprio, J., Kesaniemi, Y. A., Kivimaki, M., Knight, B., Koskinen, S., Kovacs, P., Kyvik, K. O., Lathrop, G. M., Lawlor, D. A., Le Bacquer, O., Lecoeur, C., Li, Y., Lyssenko, V., Mahley, R., Mangino, M., Manning, A. K., Martínez-Larrad, M. T., McAteer, J. B., McCulloch, L. J., McPherson, R., Meisinger, C., Melzer, D., Meyre, D., Mitchell, B. D., Morken, M. A., Mukherjee, S., Naitza, S., Narisu, N., Neville, M. J., Oostra, B. A., Orr, M., Pakyz, R., Palmer, C. N. A., Paolisso, G., Pattaro, C., Pearson, D., Peden, J. F., Pedersen, N. L., Perola, M., Pfeiffer, A. F. H., Pichler, I., Polasek, O., Posthuma, D., Potter, S. C., Pouta, A., Province, M. A., Psaty, B. M., Rathmann, W., Rayner, N. W., Rice, K., Ripatti, S., Rivadeneira, F., Roden, M., Rolandsson, O., Sandbaek, A., Sandhu, M., Sanna, S., Sayer, A. A., Scheet, P., Scott, L. J., Seedorf, U., Sharp, S. J., Shields, B., Sigursson, G., Sijbrands, E. J. G., Silveira, A., Simpson, L., Singleton, A., Smith, N. L., Sovio, U., Swift, A., Syddall, H., Syvänen, A. C., Tanaka, T., Thorand, B., Tichet, J., Tönjes, A., Tuomi, T., Uitterlinden, A. G., Van Dijk, K. W., Van Hoek, M., Varma, D., Visvikis-Siest, S., Vitart, V., Vogelzangs, N., Waeber, G., Wagner, P. J., Walley, A., Walters, G. B., Ward, K. L., Watkins, H., Weedon, M. N., Wild, S. H., Willemsen, G., Witteman, J. C. M., Yarnell, J. W. G., Zeggini, E., Zelenika, D., Zethelius, B., Zhai, G., Zhao, J. H., Zillikens, M. C., Consortium, D., Consortium, G., Consortium, G. B., Borecki, I. B., Loos, R. J. F., Meneton, P., Magnusson, P. K. E., Nathan, D. M., Williams, G. H., Hattersley, A. T., Silander, K., Salomaa, V., Smith, G. D., Bornstein, S. R., Schwarz, P., Spranger, J., Karpe, F., Shuldiner, A. R., Cooper, C., Dedoussis, G. V., Serrano-Ríos, M., Morris, A. D., Lind, L., Palmer, L. J., Hu, F. B., Franks, P. W., Ebrahim, S., Marmot, M., Kao, W. H. L., Pankow, J. S., Sampson, M. J., Kuusisto, J., Laakso, M., Hansen, T., Pedersen, O., Pramstaller, P. P., Wichmann, H. E., Illig, T., Rudan, I., Wright, A. F., Stumvoll, M., Campbell, H., Wilson, J. F., Hamsten, A., Bergman, R. N., Buchanan, T. A., Collins, F. S., Mohlke, K. L., Tuomilehto, J., Valle, T. T., Altshuler, D., Rotter, J. I., Siscovick, D. S., Penninx, B. W. J. H., Boomsma, D. I., Deloukas, P., Spector, T. D., Frayling, T. M., Ferrucci, L., Kong, A., Thorsteinsdottir, U., Stefansson, K., Van Duijn, C. M., Aulchenko, Y. S., Cao, A., Scuteri, A., Schlessinger, D., Uda, M., Ruokonen, A., Jarvelin, M. R., Waterworth, D. M., Vollenweider, P., Peltonen, L., Mooser, V., Abecasis, G. R., Wareham, N. J., Sladek, R., Froguel, P., Watanabe, R. M., Meigs, J. B., Groop, L., Boehnke, M., McCarthy, M. I., Florez, J. C. & Barroso, I., 17 Jan 2010, In: Nature Genetics. 42, 5

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  • Genome-wide association study identifies five loci associated with lung function

    Wellcome Trust Case Control Consortium, Repapi, E., Sayers, I., Wain, L. V., Burton, P. R., Johnson, T., Obeidat, M., Zhao, J. H., Ramasamy, A., Zhai, G., Vitart, V., Huffman, J. E., Igl, W., Albrecht, E., Deloukas, P., Henderson, J., Granell, R., McArdle, W. L., Rudnicka, A. R., Barroso, I., & 31 othersLoos, R. J. F., Wareham, N. J., Mustelin, L., Rantanen, T., Surakka, I., Imboden, M., Wichmann, H. E., Grkovic, I., Jankovic, S., Zgaga, L., Hartikainen, A-L., Peltonen, L., Gyllensten, U., Johansson, A., Zaboli, G., Campbell, H., Wild, S. H., Wilson, J. F., Gläser, S., Homuth, G., Völzke, H., Mangino, M., Soranzo, N., Spector, T. D., Polasek, O., Rudan, I., Wright, A., MacLeod, A. K., Morris, A., Porteous, D. J. & Hayward, C., Jan 2010, In: Nature Genetics. 42, 1, p. 36-44 9 p.

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  • Modeling of Environmental Effects in Genome-Wide Association Studies Identifies SLC2A2 and HP as Novel Loci Influencing Serum Cholesterol Levels

    EUROSPAN Consortium, Igl, W., Johansson, A., Wilson, J. F., Wild, S. H., Polasek, O., Hayward, C., Vitart, V., Hastie, N., Rudan, P., Gnewuch, C., Schmitz, G., Meitinger, T., Pramstaller, P. P., Hicks, A. A., Oostra, B. A., van Duijn, C. M., Rudan, I., Wright, A., Campbell, H., & 1 othersGyllensten, U., Jan 2010, In: PLoS Genetics. 6, 1, p. - 10 p., e1000798.

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  • Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

    MAGIC, Speliotes, E. K., Willer, C. J., Berndt, S. I., Monda, K. L., Thorleifsson, G., Jackson, A. U., Allen, H. L., Lindgren, C. M., Luan, J., Mägi, R., Randall, J. C., Vedantam, S., Winkler, T. W., Qi, L., Workalemahu, T., Heid, I. M., Steinthorsdottir, V., Stringham, H. M., Weedon, M. N., & 31 othersWheeler, E., Wood, A. R., Ferreira, T., Weyant, R. J., Segrè, A. V., Estrada, K., Liang, L., Nemesh, J., Park, J-H., Gustafsson, S., Kilpeläinen, T. O., Yang, J., Bouatia-Naji, N., Esko, T., Feitosa, M. F., Kutalik, Z., Mangino, M., Raychaudhuri, S., Scherag, A., Smith, A. V., Welch, R., Zhao, J. H., Campbell, H., Hayward, C., Vitart, V., Wild, S. H., Zgaga, L., Rudan, I., Wilson, J. F., Wright, A. F. & Visscher, P. M., 2010, In: Nature Genetics. 42, 11, p. 937-48 12 p.

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  • Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways

    WTCCC, Soranzo, N., Sanna, S., Wheeler, E., Gieger, C., Radke, D., Dupuis, J., Bouatia-Naji, N., Langenberg, C., Prokopenko, I., Stolerman, E., Sandhu, M. S., Heeney, M. M., Devaney, J. M., Reilly, M. P., Ricketts, S. L., Stewart, A. F. R., Voight, B. F., Willenborg, C., Wright, B., & 31 othersAltshuler, D., Arking, D., Balkau, B., Barnes, D., Boerwinkle, E., Böhm, B., Bonnefond, A., Bonnycastle, L. L., Boomsma, D. I., Bornstein, S. R., Böttcher, Y., Bumpstead, S., Burnett-Miller, M. S., Campbell, H., Cao, A., Chambers, J., Clark, R., Collins, F. S., Coresh, J., de Geus, E. J. C., Dei, M., Deloukas, P., Döring, A., Egan, J. M., Elosua, R., Hayward, C., Rudan, I., Vitart, V., Wild, S. H., Wilson, J. F. & Wright, A. F., 2010, In: Diabetes . 59, 12, p. 3229-39 11 p.

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  • Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

    Polasek, O., Hayward, C., Bellenguez, C., Vitart, V., Kolcić, I., McQuillan, R., Saftić, V., Gyllensten, U., Wilson, J. F., Rudan, I., Wright, A. F., Campbell, H. & Leutenegger, A-L., 2010, In: BMC Genomics. 11, p. 139

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  • New loci associated with kidney function and chronic kidney disease

    Köttgen, A., Pattaro, C., Böger, C. A., Fuchsberger, C., Olden, M., Glazer, N. L., Parsa, A., Gao, X., Yang, Q., Smith, A. V., O'Connell, J. R., Li, M., Schmidt, H., Tanaka, T., Isaacs, A., Ketkar, S., Hwang, S-J., Johnson, A. D., Dehghan, A., Teumer, A., & 112 othersParé, G., Atkinson, E. J., Zeller, T., Lohman, K., Cornelis, M. C., Probst-Hensch, N. M., Kronenberg, F., Tönjes, A., Hayward, C., Aspelund, T., Eiriksdottir, G., Launer, L. J., Harris, T. B., Rampersaud, E., Mitchell, B. D., Arking, D. E., Boerwinkle, E., Struchalin, M., Cavalieri, M., Singleton, A., Giallauria, F., Metter, J., de Boer, I. H., Haritunians, T., Lumley, T., Siscovick, D., Psaty, B. M., Zillikens, M. C., Oostra, B. A., Feitosa, M., Province, M., de Andrade, M., Turner, S. T., Schillert, A., Ziegler, A., Wild, P. S., Schnabel, R. B., Wilde, S., Munzel, T. F., Leak, T. S., Illig, T., Klopp, N., Meisinger, C., Wichmann, H-E., Koenig, W., Zgaga, L., Zemunik, T., Kolcic, I., Minelli, C., Hu, F. B., Johansson, A., Igl, W., Zaboli, G., Wild, S. H., Wright, A. F., Campbell, H., Ellinghaus, D., Schreiber, S., Aulchenko, Y. S., Felix, J. F., Rivadeneira, F., Uitterlinden, A. G., Hofman, A., Imboden, M., Nitsch, D., Brandstätter, A., Kollerits, B., Kedenko, L., Mägi, R., Stumvoll, M., Kovacs, P., Boban, M., Campbell, S., Endlich, K., Völzke, H., Kroemer, H. K., Nauck, M., Völker, U., Polasek, O., Vitart, V., Badola, S., Parker, A. N., Ridker, P. M., Kardia, S. L. R., Blankenberg, S., Liu, Y., Curhan, G. C., Franke, A., Rochat, T., Paulweber, B., Prokopenko, I., Wang, W., Gudnason, V., Shuldiner, A. R., Coresh, J., Schmidt, R., Ferrucci, L., Shlipak, M. G., van Duijn, C. M., Borecki, I., Krämer, B. K., Rudan, I., Gyllensten, U., Wilson, J. F., Witteman, J. C., Pramstaller, P. P., Rettig, R., Hastie, N., Chasman, D. I., Kao, W. H., Heid, I. M. & Fox, C. S., 2010, In: Nature Genetics. 42, 5, p. 376-384 9 p.

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  • 2009

    Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations

    Hicks, A. A., Pramstaller, P. P., Johansson, A., Vitart, V., Rudan, I., Ugocsai, P., Aulchenko, Y., Franklin, C. S., Liebisch, G., Erdmann, J., Jonasson, I., Zorkoltseva, I. V., Pattaro, C., Hayward, C., Isaacs, A., Hengstenberg, C., Campbell, S., Gnewuch, C., Janssens, A. C. W., Kirichenko, A. V., & 26 othersKönig, I. R., Marroni, F., Polsek, O., Demirkan, A., Kolcic, I., Schwienbacher, C., Igl, W., Biloglav, Z., Witteman, J. C. M., Pichler, I., Zaboli, G., Axenovich, T. I., Peters, A., Schreiber, S., Wichmann, H-E., Schunkert, H., Hastie, N., Oostra, B. A., Wild, S. H., Meitinger, T., Gyllensten, U., van Duijn, C. M., Wilson, J. F., Wright, A., Schmitz, G. & Campbell, H., Oct 2009, In: PLoS Genetics. 5, 10, 11 p., e1000672.

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