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Veronique Vitart

DR

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

Accepting PhD Students

Search results

  • 2016

    New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk

    Lu, Y., Day, F. R., Gustafsson, S., Buchkovich, M. L., Na, J., Bataille, V., Cousminer, D. L., Dastani, Z., Drong, A. W., Esko, T., Evans, D. M., Falchi, M., Feitosa, M. F., Ferreira, T., Hedman, Å. K., Haring, R., Hysi, P. G., Iles, M. M., Justice, A. E., Kanoni, S., & 239 othersLagou, V., Li, R., Li, X., Locke, A., Lu, C., Mägi, R., Perry, J. R. B., Pers, T. H., Qi, Q., Sanna, M., Schmidt, E. M., Scott, W. R., Shungin, D., Teumer, A., Vinkhuyzen, A. A. E., Walker, R. W., Westra, H-J., Zhang, M., Zhang, W., Zhao, J. H., Zhu, Z., Afzal, U., Ahluwalia, T. S., Bakker, S. J. L., Bellis, C., Bonnefond, A., Borodulin, K., Buchman, A. S., Cederholm, T., Choh, A. C., Choi, H. J., Curran, J. E., de Groot, L. C. P. G. M., De Jager, P. L., Dhonukshe-Rutten, R. A. M., Enneman, A. W., Eury, E., Evans, D. S., Forsen, T., Friedrich, N., Fumeron, F., Garcia, M. E., Gärtner, S., Han, B-G., Havulinna, A. S., Hayward, C., Hernandez, D., Hillege, H., Ittermann, T., Kent, J. W., Kolcic, I., Laatikainen, T., Lahti, J., Mateo Leach, I., Lee, C. G., Lee, J-Y., Liu, T., Liu, Y., Lobbens, S., Loh, M., Lyytikäinen, L-P., Medina-Gomez, C., Michaëlsson, K., Nalls, M. A., Nielson, C. M., Oozageer, L., Pascoe, L., Paternoster, L., Polašek, O., Ripatti, S., Sarzynski, M. A., Shin, C. S., Narančić, N. S., Spira, D., Srikanth, P., Steinhagen-Thiessen, E., Sung, Y. J., Swart, K. M. A., Taittonen, L., Tanaka, T., Tikkanen, E., van der Velde, N., van Schoor, N. M., Verweij, N., Wright, A. F., Yu, L., Zmuda, J. M., Eklund, N., Forrester, T., Grarup, N., Jackson, A. U., Kristiansson, K., Kuulasmaa, T., Kuusisto, J., Lichtner, P., Luan, J., Mahajan, A., Männistö, S., Palmer, C. D., Ried, J. S., Scott, R. A., Stancáková, A., Wagner, P. J., Demirkan, A., Döring, A., Gudnason, V., Kiel, D. P., Kühnel, B., Mangino, M., Mcknight, B., Menni, C., O'Connell, J. R., Oostra, B. A., Shuldiner, A. R., Song, K., Vandenput, L., van Duijn, C. M., Vollenweider, P., White, C. C., Boehnke, M., Boettcher, Y., Cooper, R. S., Forouhi, N. G., Gieger, C., Grallert, H., Hingorani, A., Jørgensen, T., Jousilahti, P., Kivimaki, M., Kumari, M., Laakso, M., Langenberg, C., Linneberg, A., Luke, A., Mckenzie, C. A., Palotie, A., Pedersen, O., Peters, A., Strauch, K., Tayo, B. O., Wareham, N. J., Bennett, D. A., Bertram, L., Blangero, J., Blüher, M., Bouchard, C., Campbell, H., Cho, N. H., Cummings, S. R., Czerwinski, S. A., Demuth, I., Eckardt, R., Eriksson, J. G., Ferrucci, L., Franco, O. H., Froguel, P., Gansevoort, R. T., Hansen, T., Harris, T. B., Hastie, N., Heliövaara, M., Hofman, A., Jordan, J. M., Jula, A., Kähönen, M., Kajantie, E., Knekt, P. B., Koskinen, S., Kovacs, P., Lehtimäki, T., Lind, L., Liu, Y., Orwoll, E. S., Osmond, C., Perola, M., Pérusse, L., Raitakari, O. T., Rankinen, T., Rao, D. C., Rice, T. K., Rivadeneira, F., Rudan, I., Salomaa, V., Sørensen, T. I. A., Stumvoll, M., Tönjes, A., Towne, B., Tranah, G. J., Tremblay, A., Uitterlinden, A. G., van der Harst, P., Vartiainen, E., Viikari, J. S., Vitart, V., Vohl, M-C., Völzke, H., Walker, M., Wallaschofski, H., Wild, S., Wilson, J. F., Yengo, L., Bishop, D. T., Borecki, I. B., Chambers, J. C., Cupples, L. A., Dehghan, A., Deloukas, P., Fatemifar, G., Fox, C., Furey, T. S., Franke, L., Han, J., Hunter, D. J., Karjalainen, J., Karpe, F., Kaplan, R. C., Kooner, J. S., McCarthy, M. I., Murabito, J. M., Morris, A. P., Bishop, J. A. N., North, K. E., Ohlsson, C., Ong, K. K., Prokopenko, I., Richards, J. B., Schadt, E. E., Spector, T. D., Widén, E., Willer, C. J., Yang, J., Ingelsson, E., Mohlke, K. L., Hirschhorn, J. N., Pospisilik, J. A., Zillikens, M. C., Lindgren, C., Kilpeläinen, T. O. & Loos, R. J. F., 1 Feb 2016, In: Nature Communications. 7, p. 10495

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  • GWAS for executive function and processing speed suggests involvement of the CADM2 gene

    Generation Scotland, Ibrahim-Verbaas, C. A., Bressler, J., Debette, S., Schuur, M., Smith, A. V., Bis, J. C., Davies, G., Trompet, S., Smith, J. A., Wolf, C., Chibnik, L. B., Liu, Y., Vitart, V., Kirin, M., Petrovic, K., Polasek, O., Zgaga, L., Fawns-Ritchie, C., Hoffmann, P., & 31 othersKarjalainen, J., Lahti, J., Llewellyn, D. J., Schmidt, C. O., Mather, K. A., Chouraki, V., Sun, Q., Resnick, S. M., Rose, L. M., Oldmeadow, C., Stewart, M., Smith, B. H., Gudnason, V., Yang, Q., Mirza, S. S., Jukema, J. W., deJager, P. L., Harris, T. B., Liewald, D., Amin, N., Gow, A. J., Pattie, A., Starr, J. M., McLachlan, S., Porteous, D. J., Price, J. F., Rudan, I., Hayward, C., Wright, A. F., Wilson, J. F. & Deary, I., Feb 2016, In: Molecular Psychiatry. 21, p. 189-197

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  • Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

    ICBP Consortium, Pattaro, C., Teumer, A., Gorski, M., Chu, A. Y., Li, M., Mijatovic, V., Garnaas, M., Tin, A., Sorice, R., Li, Y., Taliun, D., Olden, M., Foster, M., Yang, Q., Chen, M-H., Pers, T. H., Johnson, A. D., Ko, Y-A., Fuchsberger, C., & 31 othersTayo, B., Nalls, M., Feitosa, M. F., Isaacs, A., Dehghan, A., d'Adamo, P., Adeyemo, A., Dieffenbach, A. K., Zonderman, A. B., Nolte, I. M., van der Most, P. J., Wright, A. F., Shuldiner, A. R., Morrison, A. C., Hofman, A., Smith, A. V., Dreisbach, A. W., Franke, A., Uitterlinden, A. G., Metspalu, A., Tonjes, A., Hayward, C., Campbell, H., Rudan, I., Wilson, J. F., Martin, N. G., Hastie, N., Polasek, O., Mitchell, P., Wild, S. H. & Vitart, V., 21 Jan 2016, In: Nature Communications. 7, 10023.

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  • 2015

    Integrative pathway genomics of lung function and airflow obstruction

    CHARGE Consortium; SpiroMeta Consortium, Gharib, S. A., Loth, D. W., Soler Artigas, M., Birkland, T. P., Wilk, J. B., Wain, L. V., Brody, J. A., Obeidat, M., Hancock, D. B., Tang, W., Rawal, R., Boezen, H. M., Imboden, M., Huffman, J. E., Lahousse, L., Alves, A. C., Manichaikul, A., Hui, J., Morrison, A. C., & 30 othersRamasamy, A., Smith, A. V., Gudnason, V., Surakka, I., Vitart, V., Evans, D. M., Strachan, D. P., Deary, I. J., Hofman, A., Gläser, S., Wilson, J. F., North, K. E., Zhao, J. H., Heckbert, S. R., Jarvis, D. L., Probst-Hensch, N., Schulz, H., Barr, R. G., Jarvelin, M-R., O'Connor, G. T., Kähönen, M., Cassano, P. A., Hysi, P. G., Dupuis, J., Hayward, C., Psaty, B. M., Hall, I. P., Parks, W. C., Tobin, M. D. & London, S. J., 22 Dec 2015, In: Human Molecular Genetics. 24, 23, p. 6836-48 13 p.

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

  • Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

    UK BiLEVE, Artigas, M. S., Wain, L. V., Miller, S., Kheirallah, A. K., Huffman, J. E., Ntalla, I., Shrine, N., Obeidat, M., Trochet, H., McArdle, W. L., Alves, A. C., Hui, J., Zhao, J. H., Joshi, P. K., Teumer, A., Albrecht, E., Imboden, M., Rawal, R., Lopez, L. M., & 31 othersMarten, J., Enroth, S., Surakka, I., Polasek, O., Lyytikäinen, L-P., Granell, R., Hysi, P. G., Flexeder, C., Mahajan, A., Beilby, J., Bossé, Y., Brandsma, C-A., Campbell, H., Gieger, C., Gläser, S., González, J. R., Grallert, H., Hammond, C. J., Harris, S. E., Hartikainen, A-L., Henderson, J., Navarro, P., Starr, J. M., Wild, S. H., Wright, A. F., Vitart, V., Rudan, I., Deary, I. J., Wilson, J. F., Morris, A. P. & Hayward, C., 4 Dec 2015, In: Nature Communications. 6, p. 8658

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  • Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C

    Generation Scotland, LifeLines Cohort Study & CHARGE Lipids Working Group, 12 Nov 2015, In: npj Aging and Mechanisms of Disease. 1, 1, 15011.

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  • Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank

    Wain, L. V., Shrine, N., Miller, S., Jackson, V. E., Ntalla, I., Artigas, M. S., Billington, C. K., Kheirallah, A. K., Allen, R., Cook, J. P., Probert, K., Obeidat, M., Bossé, Y., Hao, K., Postma, D. S., Paré, P. D., Ramasamy, A., Mägi, R., Mihailov, E., Reinmaa, E., & 138 othersMelén, E., O'Connell, J., Frangou, E., Delaneau, O., Freeman, C., Petkova, D., McCarthy, M., Sayers, I., Deloukas, P., Hubbard, R., Pavord, I., Hansell, A. L., Thomson, N. C., Zeggini, E., Morris, A. P., Marchini, J., Strachan, D. P., Tobin, M. D., Hall, I. P., Farrall, M., Barroso, I., Anderson, C. A., Botía, J., Vandrocova, J., Guelfi, S., D'Sa, K., Ryten, M., Trabzuni, D., Matarin, M., Hardy, J. A., Weale, M. E., Varghese, V., Forabosco, P., Farmer, A., McGuffin, P., Zgaga, L., Wilson, J. F., Wild, S. H., Campbell, H., Rudan, I., Smith, C., Walker, R., Liu, J. Z., Tozzi, F., Muglia, P., Waterworth, D. M., Pillai, S. G., Yuan, X., Mooser, V., Middleton, L., Kooner, J., Chambers, J. C., Berrettini, W., Knouff, C. W., Waeber, G., Vollenweider, P., Preisig, M., Wareham, N. J., Zhao, J. H., Loos, R. J. F., Khaw, K. T., Grundy, S., Barter, P., Mahley, R., Kesaniemi, A., McPherson, R., Vincent, J. B., Strauss, J., Kennedy, J. L., Day, R., Matthews, K., Bakke, P., Gulsvik, A., Lucae, S., Ising, M., Brueckl, T., Horstmann, S., Wichmann, H. E., Rawal, R., Wichmann, H. E., Lamina, C., Dahmen, N., Polasek, O., Kolcic, I., Huffman, J., Campbell, S., Vitart, V., Hayward, C., Wright, A. F., Burnett, M. S., Devaney, J. M., Pichard, A. D., Kent, K. M., Satler, L., Lindsay, J. M., Waksman, R., Epstein, S., Reilly, M. P., Li, M., Qu, L., Wilensky, R., Matthai, W., Hakonarson, H. H., Rader, D. J., Ellinghaus, D., Lieb, W., Franke, A., Uda, M., Busonero, F., Terracciano, A., Schlessinger, D., Xiao, X., Scheet, P., St Clair, D., Rujescu, D., Abecasis, G. R., Grabe, H. J., Teumer, A., Völzke, H., Petersmann, A., John, U., Wright, B. J., Thompson, J. R., Balmforth, A. J., Hall, A. S., Samani, N. J., Ahmad, T., Mathew, C. G., Parkes, M., Satsangi, J., Caulfield, M., Munroe, P. B., Dominiczak, A., Worthington, J., Thomson, W., Eyre, S., Barton, A. & Francks, C., 1 Oct 2015, In: The Lancet Respiratory Medicine. 3, 10, p. 769-781 13 p.

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  • The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

    CHARGE Consortium, Winkler, T. W., Justice, A. E., Graff, M., Barata, L., Feitosa, M. F., Chu, S., Czajkowski, J., Esko, T., Fall, T., Kilpeläinen, T. O., Lu, Y., Mägi, R., Mihailov, E., Pers, T. H., Rüeger, S., Teumer, A., Ehret, G. B., Ferreira, T., Heard-Costa, N. L., & 31 othersKarjalainen, J., Lagou, V., Mahajan, A., Neinast, M. D., Prokopenko, I., Simino, J., Teslovich, T. M., Jansen, R., Westra, H-J., White, C. C., Absher, D., Ahluwalia, T. S., Ahmad, S., Albrecht, E., Alves, A. C., Bragg-Gresham, J. L., de Craen, A. J. M., Bis, J. C., Bonnefond, A., Boucher, G., Cadby, G., Cheng, Y-C., Wild, S. H., Wilson, J. F., Campbell, H., Hastie, N., Morris, A. P., Wright, A. F., Hayward, C., Rudan, I. & Vitart, V., Oct 2015, In: PLoS Genetics. 11, 10, p. e1005378

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  • Multicohort analysis of the maternal age effect on recombination

    Martin, H. C., Christ, R., Hussin, J. G., O'Connell, J., Gordon, S., Mbarek, H., Hottenga, J-J., McAloney, K., Willemsen, G., Gasparini, P., Pirastu, N., Montgomery, G. W., Navarro, P., Soranzo, N., Toniolo, D., Vitart, V., Wilson, J. F., Marchini, J., Boomsma, D. I., Martin, N. G., & 1 othersDonnelly, P., 5 Aug 2015, In: Nature Communications. 6, p. 7846

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  • Directional dominance on stature and cognition in diverse human populations

    Joshi, P. K., Esko, T., Mattsson, H., Eklund, N., Gandin, I., Nutile, T., Jackson, A. U., Schurmann, C., Smith, A. V., Zhang, W., Okada, Y., Stančáková, A., Faul, J. D., Zhao, W., Bartz, T. M., Concas, M. P., Franceschini, N., Enroth, S., Vitart, V., Trompet, S., & 30 othersGuo, X., Chasman, D. I., O'Connel, J. R., Corre, T., Nongmaithem, S. S., Chen, Y., Mangino, M., Ruggiero, D., Campbell, A., Davies, G., Haley, C., Harris, S. E., Hastie, N. D., Kerr, S. M., Liewald, D. C. M., Navarro, P., Redmond, P., Wild, S., BioBank Japan Project, Morris, A. D., Starr, J. M., Deary, I. J., Pirastu, N., Wilson, J. G., Rudan, I., Porteous, D. J., Hayward, C., Wright, A. F., Campbell, H. & Wilson, J. F., 23 Jul 2015, In: Nature. 523, 7561, p. 459-462 4 p.

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  • Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models

    Spiliopoulou, A., Nagy, R., Bermingham, M. L., Huffman, J. E., Hayward, C., Vitart, V., Rudan, I., Campbell, H., Wright, A. F., Wilson, J. F., Pong-Wong, R., Agakov, F., Navarro, P. & Haley, C. S., 15 Jul 2015, In: Human Molecular Genetics. 24, 14, p. 4167-4182 15 p.

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  • Homozygous loss-of-function variants in European cosmopolitan and isolate populations

    Generation Scotland, UK10K, Kaiser, V. B., Svinti, V., Prendergast, J. G., Chau, Y-Y., Campbell, A., Patarcic, I., Barroso, I., Joshi, P. K., Hastie, N. D., Miljkovic, A., Taylor, M. S., Enroth, S., Memari, Y., Kolb-Kokocinski, A., Wright, A. F., Gyllensten, U., Durbin, R., Rudan, I., & 11 othersCampbell, H., Polašek, O., Johansson, Å., Sauer, S., Porteous, D. J., Fraser, R. M., Drake, C., Vitart, V., Hayward, C., Semple, C. A. & Wilson, J. F., 14 Jul 2015, In: Human Molecular Genetics.

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  • Recent genomic heritage in Scotland

    Generation Scotland, Amador, C., Huffman, J., Trochet, H., Campbell, A., Porteous, D., Wilson, J. F., Hastie, N., Vitart, V., Hayward, C., Navarro, P. & Haley, C. S., 6 Jun 2015, In: BMC Genomics. 16, 1, 437.

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  • Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

    Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium, Debette, S., Ibrahim Verbaas, C. A., Bressler, J., Schuur, M., Smith, A., Bis, J. C., Davies, G., Wolf, C., Gudnason, V., Chibnik, L. B., Yang, Q., deStefano, A. L., de Quervain, D. J. F., Srikanth, V., Lahti, J., Grabe, H. J., Smith, J. A., Priebe, L., Yu, L., & 31 othersKarbalai, N., Hayward, C., Wilson, J. F., Campbell, H., Petrovic, K., Fornage, M., Chauhan, G., Yeo, R., Boxall, R., Becker, J., Stegle, O., Mather, K. A., Chouraki, V., Sun, Q., Rose, L. M., Resnick, S., Oldmeadow, C., Kirin, M., Wright, A. F., Jonsdottir, M. K., Vitart, V., Hastie, N. D., Zgaga, L., Rudan, I., Polasek, O., Liewald, D. C., Gow, A. J., Pattie, A., Starr, J. M., Porteous, D. & Deary, I. J., 15 Apr 2015, In: Biological Psychiatry. 77, 8, p. 749-763 15 p.

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  • Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia

    Nagahama Study Group, Miyake, M., Yamashiro, K., Tabara, Y., Suda, K., Morooka, S., Nakanishi, H., Khor, C-C., Chen, P., Qiao, F., Nakata, I., Akagi-Kurashige, Y., Gotoh, N., Tsujikawa, A., Meguro, A., Kusuhara, S., Polasek, O., Hayward, C., Wright, A. F., Campbell, H., & 27 othersRichardson, A. J., Schache, M., Takeuchi, M., Mackey, D. A., Hewitt, A. W., Cuellar, G., Shi, Y., Huang, L., Yang, Z., Leung, K. H., Kao, P. Y. P., Yap, M. K. H., Yip, S. P., Moriyama, M., Ohno-Matsui, K., Mizuki, N., MacGregor, S., Vitart, V., Aung, T., Saw, S-M., Tai, E-S., Wong, T. Y., Cheng, C-Y., Baird, P. N., Yamada, R., Matsuda, F. & Yoshimura, N., 31 Mar 2015, In: Nature Communications. 6, 6689.

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  • Modulation of genetic associations with serum urate levels by body-mass-index in humans

    Huffman, J. E., Albrecht, E., Teumer, A., Mangino, M., Kapur, K., Johnson, T., Kutalik, Z., Pirastu, N., Pistis, G., Lopez, L. M., Haller, T., Salo, P., Goel, A., Li, M., Tanaka, T., Dehghan, A., Ruggiero, D., Malerba, G., Smith, A. V., Nolte, I. M., & 100 othersPortas, L., Phipps-Green, A., Boteva, L., Navarro, P., Johansson, A., Hicks, A. A., Polasek, O., Esko, T., Peden, J. F., Harris, S. E., Murgia, F., Wild, S. H., Tenesa, A., Tin, A., Mihailov, E., Grotevendt, A., Gislason, G. K., Coresh, J., D'Adamo, P., Ulivi, S., Vollenweider, P., Waeber, G., Campbell, S., Kolcic, I., Fisher, K., Viigimaa, M., Metter, J. E., Masciullo, C., Trabetti, E., Bombieri, C., Sorice, R., Döring, A., Reischl, E., Strauch, K., Hofman, A., Uitterlinden, A. G., Waldenberger, M., Wichmann, H-E., Davies, G., Gow, A. J., Dalbeth, N., Stamp, L., Smit, J. H., Kirin, M., Nagaraja, R., Nauck, M., Schurmann, C., Budde, K., Farrington, S. M., Theodoratou, E., Jula, A., Salomaa, V., Sala, C., Hengstenberg, C., Burnier, M., Mägi, R., Klopp, N., Kloiber, S., Schipf, S., Ripatti, S., Cabras, S., Soranzo, N., Homuth, G., Nutile, T., Munroe, P. B., Hastie, N., Campbell, H., Rudan, I., Cabrera, C., Haley, C., Franco, O. H., Merriman, T. R., Gudnason, V., Pirastu, M., Penninx, B. W., Snieder, H., Metspalu, A., Ciullo, M., Pramstaller, P. P., van Duijn, C. M., Ferrucci, L., Gambaro, G., Deary, I. J., Dunlop, M. G., Wilson, J. F., Gasparini, P., Gyllensten, U., Spector, T. D., Wright, A. F., Hayward, C., Watkins, H., Perola, M., Bochud, M., Kao, W. H. L., Caulfield, M., Toniolo, D., Völzke, H., Gieger, C., Köttgen, A. & Vitart, V., 26 Mar 2015, In: PLoS ONE. 10, 3, e0119752.

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  • Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

    CHARGE Inflammation working group, 13 Mar 2015, In: PLoS ONE. 10, 3, e0118859.

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  • Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

    Genome Netherlands Consortium, van Leeuwen, E. M., Karssen, L. C., Deelen, J., Isaacs, A., Medina-Gomez, C., Mbarek, H., Kanterakis, A., Trompet, S., Postmus, I., Verweij, N., van Enckevort, D. J., Huffman, J. E., White, C. C., Feitosa, M. F., Bartz, T. M., Manichaikul, A., Joshi, P. K., Peloso, G. M., Deelen, P., & 31 othersvan Dijk, F., Willemsen, G., de Geus, E. J., Milaneschi, Y., Penninx, B. W. J. H., Francioli, L. C., Menelaou, A., Pulit, S. L., Rivadeneira, F., Hofman, A., Oostra, B. A., Franco, O. H., Leach, I. M., Beekman, M., de Craen, A. J. M., Uh, H-W., Trochet, H., Hocking, L. J., Porteous, D. J., Sattar, N., Packard, C. J., Buckley, B. M., Brody, J. A., Bis, J. C., Campbell, H., Wilson, J. F., Hayward, C., Polasek, O., Vitart, V., Rudan, I. & Wright, A. F., 9 Mar 2015, In: Nature Communications. 6, 6 p., 6065.

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  • Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)

    Davies, G., Armstrong, N., Bis, J. C., Bressler, J., Chouraki, V., Giddaluru, S., Hofer, E., Ibrahim-Verbaas, C. A., Kirin, M., Lahti, J., van der Lee, S. J., Le Hellard, S., Liu, T., Marioni, R. E., Oldmeadow, C., Postmus, I., Smith, A. V., Smith, J. A., Thalamuthu, A., Thomson, R., & 109 othersVitart, V., Wang, J., Yu, L., Zgaga, L., Zhao, W., Boxall, R., Harris, S. E., Hill, W. D., Liewald, D. C., Luciano, M., Adams, H., Ames, D., Amin, N., Amouyel, P., Assareh, A. A., Au, R., Becker, J. T., Beiser, A., Berr, C., Bertram, L., Boerwinkle, E., Buckley, B. M., Campbell, H., Corley, J., De Jager, P. L., Dufouil, C., Eriksson, J. G., Espeseth, T., Faul, J. D., Ford, I., Generation Scotland, Gottesman, R. F., Griswold, M. E., Gudnason, V., Harris, T. B., Heiss, G., Hofman, A., Holliday, E. G., Huffman, J., Kardia, S. L. R., Kochan, N., Knopman, D. S., Kwok, J. B., Lambert, J-C., Lee, T., Li, G., Li, S-C., Loitfelder, M., Lopez, O. L., Lundervold, A. J., Lundqvist, A., Mather, K. A., Mirza, S. S., Nyberg, L., Oostra, B. A., Palotie, A., Papenberg, G., Pattie, A., Petrovic, K., Polasek, O., Psaty, B. M., Redmond, P., Reppermund, S., Rotter, J. I., Schmidt, H., Schuur, M., Schofield, P. W., Scott, R. J., Steen, V. M., Stott, D. J., van Swieten, J. C., Taylor, K. D., Trollor, J., Trompet, S., Uitterlinden, A. G., Weinstein, G., Widen, E., Windham, B. G., Jukema, J. W., Wright, A. F., Wright, M. J., Yang, Q., Amieva, H., Attia, J. R., Bennett, D. A., Brodaty, H., de Craen, A. J. M., Hayward, C., Ikram, M. A., Lindenberger, U., Nilsson, L-S., Porteous, D. J., Räikkönen, K., Reinvang, I., Rudan, I., Sachdev, P. S., Schmidt, R., Schofield, P. R., Srikanth, V., Starr, J. M., Turner, S. T., Weir, D. R., Wilson, J. F., Duijn, C. V., Launer, L., Fitzpatrick, A. L., Seshadri, S., Mosley Jr, T. H. & Deary, I. J., 28 Feb 2015, In: Molecular Psychiatry. 20, 2, p. 183-192 10 p.

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

    Open Access
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  • Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

    The CREAM Consortium, Li, Q., Wojciechowski, R., Simpson, C. L., Hysi, P. G., Verhoeven, V. J. M., Ikram, M. K., Höhn, R., Vitart, V., Hewitt, A. W., Oexle, K., Mäkelä, K-M., MacGregor, S., Pirastu, M., Fan, Q., Cheng, C-Y., St Pourcain, B., McMahon, G., Kemp, J. P., Northstone, K., & 31 othersRahi, J. S., Cumberland, P. M., Martin, N. G., Sanfilippo, P. G., Lu, Y., Wang, Y. X., Hayward, C., Polašek, O., Campbell, H., Bencic, G., Wright, A. F., Wedenoja, J., Zeller, T., Schillert, A., Mirshahi, A., Lackner, K., Yip, S. P., Yap, M. K. H., Ried, J. S., Gieger, C., Murgia, F., Wilson, J. F., Fleck, B., Yazar, S., Vingerling, J. R., Hofman, A., Uitterlinden, A., Rivadeneira, F., Amin, N., Karssen, L. & Oostra, B. A., Feb 2015, In: Human Genetics. 134, 2, p. 131-146 16 p.

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

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  • 2014

    Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus

    Lechner, J., Porter, L. F., Rice, A., Vitart, V., Armstrong, D. J., Schorderet, D. F., Munier, F. L., Wright, A. F., Inglehearn, C. F., Black, G. C., Simpson, D. A., Manson, F. & Willoughby, C. E., 15 Oct 2014, In: Human Molecular Genetics. 23, 20, p. 5527-35 9 p.

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

  • Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

    BMES GWAS Group, Hysi, P. G., Cheng, C-Y., Springelkamp, H., Macgregor, S., Bailey, J. N. C., Wojciechowski, R., Vitart, V., Nag, A., Hewitt, A. W., Höhn, R., Venturini, C., Mirshahi, A., Ramdas, W. D., Thorleifsson, G., Vithana, E., Khor, C-C., Stefansson, A. B., Liao, J., Haines, J. L., & 31 othersAmin, N., Wang, Y. X., Wild, P. S., Ozel, A. B., Li, J. Z., Fleck, B. W., Zeller, T., Staffieri, S. E., Teo, Y-Y., Cuellar-Partida, G., Luo, X., Allingham, R. R., Richards, J. E., Senft, A., Karssen, L. C., Zheng, Y., Bellenguez, C., Xu, L., Iglesias, A. I., Wilson, J. F., Kang, J. H., van Leeuwen, E. M., Jonsson, V., Thorsteinsdottir, U., Despriet, D. D. G., Ennis, S., Moroi, S. E., Martin, N. G., Jansonius, N. M., Yazar, S. & Tai, E-S., Oct 2014, In: Nature Genetics. 46, 10, p. 1126-1130 5 p.

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

  • Genome-Wide Meta-Analysis of Myopia and Hyperopia Provides Evidence for Replication of 11 Loci

    DCCT EDIC Res Grp, Simpson, C. L., Wojciechowski, R., Oexle, K., Murgia, F., Portas, L., Li, X., Verhoeven, V. J. M., Vitart, V., Schache, M., Hosseini, S. M., Hysi, P. G., Raffel, L. J., Cotch, M. F., Chew, E., Klein, B. E. K., Klein, R., Wong, T. Y., Van Duijn, C. M., Mitchell, R., & 31 othersSaw, S. M., Fossarello, M., Wang, J. J., Polasek, O., Campbell, H., Rudan, I., Oostra, B. A., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Amin, N., Karssen, L. C., Vingerling, J. R., Doering, A., Bettecken, T., Bencic, G., Gieger, C., Wichmann, H. -E., Wilson, J. F., Venturini, C., Fleck, B., Cumberland, P. M., Rahi, J. S., Hammond, C. J., Hayward, C., Wright, A. F., Paterson, A. D., Baird, P. N., Klaver, C. C. W., Rotter, J. I. & Pirastu, M., 18 Sept 2014, In: PLoS ONE. 9, 9, 19 p., 107110.

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

    Open Access
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  • Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study

    LifeLines Cohort Study Investigato, ICBP, CHARGE Consortium, Global Blood Pressure Genetics Gl, Vimaleswaran, K. S., Cavadino, A., Berry, D. J., Jorde, R., Dieffenbach, A. K., Lu, C., Alves, A. C., Heerspink, H. J. L., Tikkanen, E., Eriksson, J., Wong, A., Mangino, M., Jablonski, K. A., Nolte, I. M., Houston, D. K., Ahluwalia, T. S., & 34 othersvan der Most, P. J., Pasko, D., Zgaga, L., Thiering, E., Vitart, V., Fraser, R. M., Huffman, J. E., de Boer, R. A., Schoettker, B., Saum, K-U., McCarthy, M. I., Dupuis, J., Herzig, K-H., Sebert, S., Pouta, A., Laitinen, J., Kleber, M. E., Navis, G., Lorentzon, M., Jameson, K., Arden, N., Cooper, J. A., Acharya, J., Hardy, R., McLachlan, S., Theodoratou, E., Navarro, P., Wright, A. F., Polasek, O., Hayward, C., Wilson, J. F., Rudan, I., Campbell, H. & Price, J. F., Sept 2014, In: The Lancet Diabetes & Endocrinology. 2, 9, p. 719-729 11 p.

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

    Open Access
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  • Genome-wide association analysis identifies six new loci associated with forced vital capacity

    Generation Scotland, Jul 2014, In: Nature Genetics. 46, 7, p. 669-77 9 p.

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

  • A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness

    O'Connell, J., Gurdasani, D., Delaneau, O., Pirastu, N., Ulivi, S., Cocca, M., Traglia, M., Huang, J., Huffman, J. E., Rudan, I., McQuillan, R., Fraser, R. M., Campbell, H., Polasek, O., Asiki, G., Ekoru, K., Hayward, C., Wright, A. F., Vitart, V., Navarro, P., & 7 othersZagury, J-F., Wilson, J. F., Toniolo, D., Gasparini, P., Soranzo, N., Sandhu, M. S. & Marchini, J., 17 Apr 2014, In: PLoS Genetics. 10, 4, 21 p., e1004234.

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

    Open Access
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  • Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2

    Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group, Huang, J., Huffman, J. E., Yamkauchi, M., Trompet, S., Asselbergs, F. W., Sabater-Lleal, M., Trégouët, D-A., Chen, W-M., Smith, N. L., Kleber, M. E., Shin, S-Y., Becker, D. M., Tang, W., Dehghan, A., Johnson, A. D., Truong, V., Folkersen, L., Yang, Q., Oudot-Mellkah, T., & 31 othersBuckley, B. M., Moore, J. H., Williams, F. M. K., Campbell, H., Silbernagel, G., Vitart, V., Rudan, I., Tofler, G. H., Navis, G. J., Destefano, A., Wright, A. F., Chen, M-H., de Craen, A. J. M., Worrall, B. B., Rudnicka, A. R., Rumley, A., Bookman, E. B., Psaty, B. M., Chen, F., Keene, K. L., Franco, O. H., Böhm, B. O., Uitterlinden, A. G., Carter, A. M., Jukema, J. W., Sattar, N., Bis, J. C., Ikram, M. A., Wilson, J. F., Polasek, O. & Hayward, C., 27 Feb 2014, In: Arteriosclerosis, Thrombosis, and Vascular Biology. 34, 5, p. 1093-101 9 p.

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

  • The association between galactosylation of immunoglobulin G and body mass index

    Perkovic, M. N., Bakovic, M. P., Kristic, J., Novokmet, M., Huffman, J. E., Vitart, V., Hayward, C., Rudan, I., Wilson, J. F., Campbell, H., Polasek, O., Lauc, G. & Pivac, N., 3 Jan 2014, In: Progress in Neuro-Psychopharmacology and Biological Psychiatry. 48, p. 20-25 6 p.

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

  • Using Haplotype Mapping to Uncover the Missing Heritability: A Simulation Study

    Shirali, M., Pong-Wong, R., Knott, S., Hayward, C., Vitart, V., Rudan, I., Campbell, H., Hastie, N., Wright, A., Navarro, P. & Haley, C., 2014, (Unpublished) proceedings of the 10th World Congress in Ganetics Applied to Livestock Production.

    Research output: Chapter in Book/Report/Conference proceeding › Conference contribution

    File
  • 2013

    Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration

    Ansari, M., Mckeigue, P. M., Skerka, C., Hayward, C., Rudan, I., Vitart, V., Polasek, O., Armbrecht, A-M., Yates, J. R. W., Vatavuk, Z., Bencic, G., Kolcic, I., Oostra, B. A., Van Duijn, C. M., Campbell, S., Stanton, C. M., Huffman, J., Shu, X., Khan, J. C., Shahid, H., & 11 othersHarding, S. P., Bishop, P. N., Deary, I. J., Moore, A. T., Dhillon, B., Rudan, P., Zipfel, P. F., Sim, R. B., Hastie, N. D., Campbell, H. & Wright, A. F., 1 Dec 2013, In: Human Molecular Genetics. 22, 23, p. 4857-4869 13 p.

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

    Open Access
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  • Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function

    Parsa, A., Fuchsberger, C., Köttgen, A., O'Seaghdha, C. M., Pattaro, C., de Andrade, M., Chasman, D. I., Teumer, A., Endlich, K., Olden, M., Chen, M-H., Tin, A., Kim, Y. J., Taliun, D., Li, M., Feitosa, M., Gorski, M., Yang, Q., Hundertmark, C., Foster, M. C., & 139 othersGlazer, N., Isaacs, A., Rao, M., Smith, A. V., O'Connell, J. R., Struchalin, M., Tanaka, T., Li, G., Hwang, S-J., Atkinson, E. J., Lohman, K., Cornelis, M. C., Johansson, A., Tönjes, A., Dehghan, A., Couraki, V., Holliday, E. G., Sorice, R., Kutalik, Z., Lehtimäki, T., Esko, T., Deshmukh, H., Ulivi, S., Chu, A. Y., Murgia, F., Trompet, S., Imboden, M., Kollerits, B., Pistis, G., Harris, T. B., Launer, L. J., Aspelund, T., Eiriksdottir, G., Mitchell, B. D., Boerwinkle, E., Schmidt, H., Hofer, E., Hu, F., Demirkan, A., Oostra, B. A., Turner, S. T., Ding, J., Andrews, J. S., Freedman, B. I., Giulianini, F., Koenig, W., Illig, T., Döring, A., Wichmann, H-E., Zgaga, L., Zemunik, T., Boban, M., Minelli, C., Wheeler, H. E., Igl, W., Zaboli, G., Wild, S. H., Wright, A. F., Campbell, H., Ellinghaus, D., Nöthlings, U., Jacobs, G., Biffar, R., Ernst, F., Homuth, G., Kroemer, H. K., Nauck, M., Stracke, S., Völker, U., Völzke, H., Kovacs, P., Stumvoll, M., Mägi, R., Hofman, A., Uitterlinden, A. G., Rivadeneira, F., Aulchenko, Y. S., Polasek, O., Hastie, N., Vitart, V., Helmer, C., Wang, J. J., Stengel, B., Ruggiero, D., Bergmann, S., Kähönen, M., Viikari, J., Nikopensius, T., Province, M., Colhoun, H., Doney, A., Robino, A., Krämer, B. K., Portas, L., Ford, I., Buckley, B. M., Adam, M., Thun, G-A., Paulweber, B., Haun, M., Sala, C., Mitchell, R., Ciullo, M., Vollenweider, P., Raitakari, O., Metspalu, A., Palmer, C., Gasparini, P., Pirastu, M., Jukema, J. W., Probst-Hensch, N. M., Kronenberg, F., Toniolo, D., Gudnason, V., Shuldiner, A. R., Coresh, J., Schmidt, R., Ferrucci, L., van Duijn, C. M., Borecki, I., Kardia, S. L. R., Liu, Y., Curhan, G. C., Rudan, I., Gyllensten, U., Wilson, J. F., Franke, A., Pramstaller, P. P., Rettig, R., Prokopenko, I., Witteman, J., Hayward, C., Ridker, P. M., Bochud, M., Heid, I. M., Siscovick, D. S., Fox, C. S., Kao, W. L. & Böger, C. A., Dec 2013, In: Journal of the American Society of Nephrology. 24, 12, p. 2105-2117 13 p.

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

  • Inference of identity by descent in population isolates and optimal sequencing studies

    Glodzik, D., Navarro, P., Vitart, V., Hayward, C., McQuillan, R., Wild, S. H., Dunlop, M. G., Rudan, I., Campbell, H., Haley, C., Wright, A. F., Wilson, J. F. & McKeigue, P., Oct 2013, In: European Journal of Human Genetics. 21, 10, p. 1140-1145 6 p.

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

  • Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations

    SUNLIGHT consortium & The GEFOS consortium, Sept 2013, In: PLoS Genetics. 9, 9, 13 p., e1003796.

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

    Open Access
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  • Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics

    Hu, Y-J., Berndt, S. I., Gustafsson, S., Ganna, A., Hirschhorn, J., North, K. E., Ingelsson, E., Lin, D-Y., Genetic Investigation of ANthropometric Traits (GIANT) Consortium & Vitart, V., 8 Aug 2013, In: American Journal of Human Genetics. 93, 2, p. 236-48 13 p.

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

  • Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

    Consortium for Refractive Error and Myopia, Cheng, C-Y., Schache, M., Ikram, M. K., Young, T. L., Guggenheim, J. A., Vitart, V., Macgregor, S., Verhoeven, V. J. M., Barathi, V. A., Liao, J., Hysi, P. G., Bailey-Wilson, J. E., St Pourcain, B., Kemp, J. P., McMahon, G., Timpson, N. J., Evans, D. M., Montgomery, G. W., Mishra, A., & 31 othersWang, Y. X., Wang, J. J., Rochtchina, E., Polasek, O., Wright, A. F., Amin, N., van Leeuwen, E. M., Wilson, J. F., Pennell, C. E., van Duijn, C. M., de Jong, P. T. V. M., Vingerling, J. R., Zhou, X., Chen, P., Li, R., Tay, W-T., Zheng, Y., Chew, M., Burdon, K. P., Craig, J. E., Iyengar, S. K., Igo, R. P., Lass, J. H., Chew, E. Y., Haller, T., Mihailov, E., Metspalu, A., Wedenoja, J., Campbell, H., Fleck, B. & Rudan, I., 8 Aug 2013, In: American Journal of Human Genetics. 93, 2, p. 264-77 14 p.

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

  • Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment

    Kirin, M., Chandra, A., Charteris, D. G., Hayward, C., Campbell, S., Celap, I., Bencic, G., Vatavuk, Z., Kirac, I., Richards, A. J., Tenesa, A., Snead, M. P., Fleck, B. W., Singh, J., Harsum, S., Maclaren, R. E., den Hollander, A., Dunlop, M. G., Hoyng, C. B., Wright, A. F., & 3 othersCampbell, H., Vitart, V. & Mitry, D., 1 Aug 2013, In: Human Molecular Genetics. 22, 15, p. 3174-3185

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

  • Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies

    Joshi, P., Prendergast, J., Fraser, R. M., Huffman, J. E., Vitart, V., Hayward, C., McQuillan, R., Glodzik, D., Polašek, O., Hastie, N. D., Rudan, I., Campbell, H., Wright, A. F., Haley, C. S., Wilson, J. F. & Navarro, P., 16 Jul 2013, In: PLoS ONE. 8, 7, 6 p., e68604.

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

    Open Access
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  • Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

    DCCT/EDIC Research Group, Stambolian, D., Wojciechowski, R., Oexle, K., Pirastu, M., Li, X., Raffel, L. J., Cotch, M. F., Chew, E. Y., Klein, B., Klein, R., Wong, T. Y., Simpson, C. L., Klaver, C. C. W., van Duijn, C. M., Verhoeven, V. J. M., Baird, P. N., Vitart, V., Paterson, A. D., Mitchell, P., & 31 othersSaw, S. M., Fossarello, M., Kazmierkiewicz, K., Murgia, F., Portas, L., Schache, M., Richardson, A., Xie, J., Wang, J. J., Rochtchina, E., Viswanathan, A. C., Hayward, C., Wright, A. F., Polasek, O., Campbell, H., Rudan, I., Oostra, B. A., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Amin, N., Karssen, L. C., Vingerling, J. R., Hosseini, S. M., Döring, A., Bettecken, T., Vatavuk, Z., Gieger, C., Wichmann, H-E., Wilson, J. F. & Fleck, B., 1 Jul 2013, In: Human Molecular Genetics. 22, 13, p. 2754-2764 11 p.

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

  • Individual multi-locus heterozygosity is associated with lower morning plasma cortisol concentrations

    Zgaga, L., Vitart, V., Hayward, C., Kastelan, D., Polasek, O., Jakovljevic, M., Kolcic, I., Biloglav, Z., Wright, A. F., Campbell, H., Walker, B. R. & Rudan, I., Jul 2013, In: European Journal of Endocrinology. 169, 1, p. 59-64 6 p.

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

  • GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment

    The LifeLines Cohort Study, Rietveld, C. A., Medland, S. E., Derringer, J., Yang, J., Esko, T., Martin, N. W., Westra, H-J., Shakhbazov, K., Abdellaoui, A., Agrawal, A., Albrecht, E., Alizadeh, B. Z., Amin, N., Barnard, J., Baumeister, S. E., Benke, K. S., Bielak, L. F., Boatman, J. A., Boyle, P. A., & 31 othersDavies, G., de Leeuw, C., Eklund, N., Evans, D. S., Ferhmann, R., Fischer, K., Gieger, C., Gjessing, H. K., Hägg, S., Harris, J. R., Hayward, C., Holzapfel, C., Ibrahim-Verbaas, C. A., Ingelsson, E., Jacobsson, B., Joshi, P., Jugessur, A., Kaakinen, M., Kanoni, S., Karjalainen, J., Kolcic, I., Vitart, V., Campbell, H., Deary, I. J., Hastie, N. D., Liewald, D. C., Rudan, I., Starr, J. M., Wilson, J. F., Wright, A. F. & Visscher, P. M., 21 Jun 2013, In: Science. 340, 6139, p. 1467-1471 5 p.

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

    Open Access
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  • Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

    Global BPgen Consortium, den Hoed, M., Eijgelsheim, M., Esko, T., Brundel, B. J. J. M., Peal, D. S., Evans, D. M., Nolte, I. M., Segrè, A. V., Holm, H., Handsaker, R. E., Westra, H-J., Johnson, T., Isaacs, A., Yang, J., Lundby, A., Zhao, J. H., Kim, Y. J., Go, M. J., Almgren, P., & 31 othersBochud, M., Boucher, G., Cornelis, M. C., Gudbjartsson, D., Hadley, D., van der Harst, P., Hayward, C., den Heijer, M., Igl, W., Jackson, A. U., Kutalik, Z., Luan, J., Kemp, J. P., Kristiansson, K., Ladenvall, C., Lorentzon, M., Montasser, M. E., Njajou, O. T., O'Reilly, P. F., Padmanabhan, S., St Pourcain, B., Rankinen, T., Salo, P., Tanaka, T., Timpson, N. J., Vitart, V., Navarro, P., Polasek, O., Wild, S. H., Wilson, J. F. & Rudan, I., Jun 2013, In: Nature Genetics. 45, 6, p. 621- 14 p.

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

    Open Access
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  • Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

    Berndt, S. I., Gustafsson, S., Mägi, R., Ganna, A., Wheeler, E., Feitosa, M. F., Justice, A. E., Monda, K. L., Croteau-Chonka, D. C., Day, F. R., Esko, T., Fall, T., Ferreira, T., Gentilini, D., Jackson, A. U., Luan, J., Randall, J. C., Vedantam, S., Willer, C. J., Winkler, T. W., & 302 othersWood, A. R., Workalemahu, T., Hu, Y-J., Lee, S. H., Liang, L., Lin, D-Y., Min, J. L., Neale, B. M., Thorleifsson, G., Yang, J., Albrecht, E., Amin, N., Bragg-Gresham, J. L., Cadby, G., den Heijer, M., Eklund, N., Fischer, K., Goel, A., Hottenga, J-J., Huffman, J. E., Jarick, I., Johansson, A., Johnson, T., Kanoni, S., Kleber, M. E., König, I. R., Kristiansson, K., Kutalik, Z., Lamina, C., Lecoeur, C., Li, G., Mangino, M., McArdle, W. L., Medina-Gomez, C., Müller-Nurasyid, M., Ngwa, J. S., Nolte, I. M., Paternoster, L., Pechlivanis, S., Perola, M., Peters, M. J., Preuss, M., Rose, L. M., Shi, J., Shungin, D., Smith, A. V., Strawbridge, R. J., Surakka, I., Teumer, A., Trip, M. D., Tyrer, J., Van Vliet-Ostaptchouk, J. V., Vandenput, L., Waite, L. L., Zhao, J. H., Absher, D., Asselbergs, F. W., Atalay, M., Attwood, A. P., Balmforth, A. J., Basart, H., Beilby, J., Bonnycastle, L. L., Brambilla, P., Bruinenberg, M., Campbell, H., Chasman, D. I., Chines, P. S., Collins, F. S., Connell, J. M., Cookson, W. O., de Faire, U., de Vegt, F., Dei, M., Dimitriou, M., Edkins, S., Estrada, K., Evans, D. M., Farrall, M., Ferrario, M. M., Ferrières, J., Franke, L., Frau, F., Gejman, P. V., Grallert, H., Grönberg, H., Gudnason, V., Hall, A. S., Hall, P., Hartikainen, A-L., Hayward, C., Heard-Costa, N. L., Heath, A. C., Hebebrand, J., Homuth, G., Hu, F. B., Hunt, S. E., Hyppönen, E., Iribarren, C., Jacobs, K. B., Jansson, J-O., Jula, A., Kähönen, M., Kathiresan, S., Kee, F., Khaw, K-T., Kivimäki, M., Koenig, W., Kraja, A. T., Kumari, M., Kuulasmaa, K., Kuusisto, J., Laitinen, J. H., Lakka, T. A., Langenberg, C., Launer, L. J., Lind, L., Lindström, J., Liu, J., Liuzzi, A., Lokki, M-L., Lorentzon, M., Madden, P. A., Magnusson, P. K., Manunta, P., Marek, D., März, W., Mateo Leach, I., McKnight, B., Medland, S. E., Mihailov, E., Milani, L., Montgomery, G. W., Mooser, V., Mühleisen, T. W., Munroe, P. B., Musk, A. W., Narisu, N., Navis, G., Nicholson, G., Nohr, E. A., Ong, K. K., Oostra, B. A., Palmer, C. N. A., Palotie, A., Peden, J. F., Pedersen, N., Peters, A., Polasek, O., Pouta, A., Pramstaller, P. P., Prokopenko, I., Pütter, C., Radhakrishnan, A., Raitakari, O., Rendon, A., Rivadeneira, F., Rudan, I., Saaristo, T. E., Sambrook, J. G., Sanders, A. R., Sanna, S., Saramies, J., Schipf, S., Schreiber, S., Schunkert, H., Shin, S-Y., Signorini, S., Sinisalo, J., Skrobek, B., Soranzo, N., Stančáková, A., Stark, K., Stephens, J. C., Stirrups, K., Stolk, R. P., Stumvoll, M., Swift, A. J., Theodoraki, E. V., Thorand, B., Tregouet, D-A., Tremoli, E., Van der Klauw, M. M., van Meurs, J. B. J., Vermeulen, S. H., Viikari, J., Virtamo, J., Vitart, V., Waeber, G., Wang, Z., Widén, E., Wild, S. H., Willemsen, G., Winkelmann, B. R., Witteman, J. C. M., Wolffenbuttel, B. H. R., Wong, A., Wright, A. F., Zillikens, M. C., Amouyel, P., Boehm, B. O., Boerwinkle, E., Boomsma, D. I., Caulfield, M. J., Chanock, S. J., Cupples, L. A., Cusi, D., Dedoussis, G. V., Erdmann, J., Eriksson, J. G., Franks, P. W., Froguel, P., Gieger, C., Gyllensten, U., Hamsten, A., Harris, T. B., Hengstenberg, C., Hicks, A. A., Hingorani, A., Hinney, A., Hofman, A., Hovingh, K. G., Hveem, K., Illig, T., Jarvelin, M-R., Jöckel, K-H., Keinanen-Kiukaanniemi, S. M., Kiemeney, L. A., Kuh, D., Laakso, M., Lehtimäki, T., Levinson, D. F., Martin, N. G., Metspalu, A., Morris, A., Nieminen, M. S., Njølstad, I., Ohlsson, C., Oldehinkel, A. J., Ouwehand, W. H., Palmer, L. J., Penninx, B., Power, C., Province, M. A., Psaty, B. M., Qi, L., Rauramaa, R., Ridker, P. M., Ripatti, S., Salomaa, V., Samani, N. J., Snieder, H., Sørensen, T. I. A., Spector, T. D., Stefansson, K., Tönjes, A., Tuomilehto, J., Uitterlinden, A. G., Uusitupa, M., van der Harst, P., Vollenweider, P., Wallaschofski, H., Wareham, N. J., Watkins, H., Wichmann, H-E., Wilson, J. F., Abecasis, G. R., Assimes, T. L., Barroso, I., Boehnke, M., Borecki, I. B., Deloukas, P., Fox, C. S., Frayling, T., Groop, L. C., Haritunian, T., Heid, I. M., Hunter, D., Kaplan, R. C., Karpe, F., Moffatt, M. F., Mohlke, K. L., O'Connell, J. R., Pawitan, Y., Schadt, E. E., Schlessinger, D., Steinthorsdottir, V., Strachan, D. P., Thorsteinsdottir, U., van Duijn, C. M., Visscher, P. M., Di Blasio, A. M., Hirschhorn, J. N., Lindgren, C. M., Morris, A. P., Meyre, D., Scherag, A., McCarthy, M. I., Speliotes, E. K., North, K. E., Loos, R. J. F. & Ingelsson, E., May 2013, In: Nature Genetics. 45, 5, p. 501-512 12 p.

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  • Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

    CREAM, Diabet Control Complications Trial, WTCCC2, Fuchs' Genetics Multi-Ctr Study Gr, Verhoeven, V. J. M., Hysi, P. G., Wojciechowski, R., Fan, Q., Guggenheim, J. A., Hoehn, R., MacGregor, S., Hewitt, A. W., Nag, A., Cheng, C-Y., Yonova-Doing, E., Zhou, X., Ikram, M. K., Buitendijk, G. H. S., McMahon, G., Kemp, J. P., & 34 othersSt Pourcain, B., Simpson, C. L., Makela, K-M., Lehtimaki, T., Kahonen, M., Paterson, A. D., Hosseini, S. M., Wong, H. S., Xu, L., Jonas, J. B., Parssinen, O., Wedenoja, J., Yip, S. P., Ho, D. W. H., Pang, C. P., Chen, L. J., Burdon, K. P., Craig, J. E., Klein, B. E. K., Klein, R., Haller, T., Metspalu, A., Khor, C-C., Tai, E-S., Aung, T., Vithana, E., Tay, W-T., Barathi, V. A., Rudan, I., Hayward, C., Wright, A. F., Wilson, J. F., Fleck, B. & Vitart, V., Mar 2013, In: Nature Genetics. 45, 3, p. 314-318 5 p.

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  • Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

    LifeLines Cohort Study, Köttgen, A., Albrecht, E., Teumer, A., Vitart, V., Krumsiek, J., Hundertmark, C., Pistis, G., Ruggiero, D., O'Seaghdha, C. M., Haller, T., Yang, Q., Tanaka, T., Johnson, A. D., Kutalik, Z., Smith, A. V., Shi, J., Struchalin, M., Middelberg, R. P. S., Brown, M. J., & 31 othersGaffo, A. L., Pirastu, N., Li, G., Hayward, C., Zemunik, T., Huffman, J., Yengo, L., Zhao, J. H., Demirkan, A., Feitosa, M. F., Liu, X., Malerba, G., Lopez, L. M., van der Harst, P., Li, X., Kleber, M. E., Wild, S. H., Tenesa, A., Navarro, P., Hastie, N., Davies, G., Gow, A. J., Wilson, J. F., Farrington, S. M., Theodoratou, E., Polasek, O., Campbell, H., Rudan, I., Deary, I. J., Wright, A. F. & Dunlop, M. G., Feb 2013, In: Nature Genetics. 45, 2, p. 145-154 10 p.

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  • Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

    NEIGHBOR Consortium, Lu, Y., Vitart, V., Burdon, K. P., Khor, C. C., Bykhovskaya, Y., Mirshahi, A., Hewitt, A. W., Koehn, D., Hysi, P. G., Ramdas, W. D., Zeller, T., Vithana, E. N., Cornes, B. K., Tay, W-T., Tai, E. S., Cheng, C-Y., Liu, J., Foo, J-N., Saw, S. M., & 31 othersThorleifsson, G., Stefansson, K., Dimasi, D. P., Mills, R. A., Mountain, J., Ang, W., Hoehn, R., Verhoeven, V. J. M., Grus, F., Wolfs, R., Castagne, R., Lackner, K. J., Springelkamp, H., Yang, J., Jonasson, F., Leung, D. Y. L., Chen, L. J., Tham, C. C. Y., Rudan, I., Vatavuk, Z., Hayward, C., Gibson, J., Cree, A. J., Macleod, A., Ennis, S., Polasek, O., Campbell, H., Wilson, J. F., Viswanathan, A. C., Fleck, B. & Wright, A. F., Feb 2013, In: Nature Genetics. 45, 2, p. 155-163 9 p.

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  • Loci Associated with N-Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological Cancers

    Lauc, G., Huffman, J. E., Pučić, M., Zgaga, L., Adamczyk, B., Mužinić, A., Novokmet, M., Polsek, O., Gornik, O., Krištić, J., Keser, T., Vitart, V., Scheijen, B., Uh, H-W., Molokhia, M., Patrick, A. L., McKeigue, P., Kolčić, I., Lukić, I. K., Swann, O., & 19 othersvan Leeuwen, F. N., Ruhaak, L. R., Houwing-Duistermaat, J. J., Slagboom, P. E., Beekman, M., de Craen, A. J. M., Deelder, A. M., Zeng, Q., Wang, W., Hastie, N. D., Gyllensten, U., Wilson, J. F., Wuhrer, M., Wright, A. F., Rudd, P. M., Hayward, C., Aulchenko, Y., Campbell, H. & Rudan, I., 31 Jan 2013, In: PLoS Genetics. 9, 1, e1003225.

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  • The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits

    Uemoto, Y., Pong-Wong, R., Navarro, P., Vitart, V., Hayward, C., Wilson, J. F., Rudan, I., Campbell, H., Hastie, N. D., Wright, A. F. & Haley, C. S., 2013, In: Frontiers in Genetics. 4, p. 232

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  • 2012

    Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

    CARDIoGRAM Consortium, Chasman, D. I., Fuchsberger, C., Pattaro, C., Teumer, A., Böger, C. A., Endlich, K., 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. F., Hwang, S-J., Atkinson, E. J., Lohman, K., Cornelis, M. C., Johansson, A., Tönjes, A., Dehghan, A., Lambert, J-C., Holliday, E. G., Sorice, R., Kutalik, Z., Lehtimäki, T., Zgaga, L., Wild, S. H., Wright, A. F., Campbell, H., Hastie, N., Vitart, V., Colhoun, H., Rudan, I., Wilson, J. F. & Hayward, C., 15 Dec 2012, In: Human Molecular Genetics. 21, 24, p. 5329-5343 15 p.

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

  • Localising Loci underlying Complex Trait Variation Using Regional Genomic Relationship Mapping

    Nagamine, Y., Pong-Wong, R., Navarro, P., Vitart, V., Hayward, C., Rudan, I., Campbell, H., Wilson, J., Wild, S., Hicks, A. A., Pramstaller, P. P., Hastie, N., Wright, A. F. & Haley, C. S., Oct 2012, In: PLoS ONE. 7, 10, 12 p., e46501.

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  • Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene

    EUROSPAN Consortium, Johansson, A., Marroni, F., Hayward, C., Franklin, C. S., Kirichenko, A. V., Jonasson, I., Hicks, A. A., Vitart, V., Isaacs, A., Axenovich, T., Campbell, S., Floyd, J., Hastie, N., Knott, S., Lauc, G., Pichler, I., Rotim, K., Wild, S. H., Zorkoltseva, I. V., & 10 othersWilson, J. F., Rudan, I., Campbell, H., Pattaro, C., Pramstaller, P., Oostra, B. A., Wright, A. F., van Duijn, C. M., Aulchenko, Y. S. & Gyllensten, U., 6 Sept 2012, In: Obesity. 18, 4, p. 803-8 6 p.

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