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  • Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts

    Moll, M., Sakornsakolpat, P., Shrine, N., Hobbs, B. D., DeMeo, D. L., John, C., Guyatt, A. L., McGeachie, M. J., Gharib, S. A., Obeidat, M., Lahousse, L., Wijnant, S. R. A., Brusselle, G., Meyers, D. A., Bleecker, E. R., Li, X., Tal-Singer, R., Manichaikul, A., Rich, S. S., Won, S. & 67 others, Kim, W. J., Do, A. R., Washko, G. R., Barr, R. G., Psaty, B. M., Bartz, T. M., Hansel, N. N., Barnes, K., Hokanson, J. E., Crapo, J. D., Lynch, D., Bakke, P., Gulsvik, A., Hall, I. P., Wain, L., Soler Artigas, M., Jackson, V. E., Strachan, D. P., Hui, J., James, A. L., Kerr, S. M., Polasek, O., Vitart, V., Marten, J., Rudan, I., Kähönen, M., Surakka, I., Gieger, C., Karrasch, S., Rawal, R., Schulz, H., Deary, I. J., Harris, S. E., Enroth, S., Gyllensten, U., Imboden, M., Probst-Hensch, N. M., Lehtimäki, T., Raitakari, O. T., Langenberg, C., Luan, J., Wareham, N., Zhao, J. H., Hayward, C., Murray, A., Porteous, D. J., Smith, B. H., Jarvelin, M. R., Wielscher, M., Joshi, P. K., Kentistou, K. A., Timmers, P. RHJ., Wilson, J. F., Cook, J. P., Lind, L., Mahajan, A., Morris, A. P., Ewert, R., Homuth, G., Stubbe, B., Weiss, S., Zeggini, E., Weiss, S. T., Silverman, E. K., Dudbridge, F., Tobin, M. D. & Cho, M. H., 7 Jul 2020, (E-pub ahead of print) In: The Lancet Respiratory Medicine. 8, 7, p. 696-708 13 p.

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  • Chronotype and sleep duration: The influence of season of assessment

    Allebrandt, K. V., Teder-Laving, M., Kantermann, T., Peters, A., Campbell, H., Rudan, I., Wilson, J. F., Metspalu, A. & Roenneberg, T., 28 Mar 2014, In: Chronobiology international. 31, 5, p. 731-740 10 p.

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  • Coffee consumption and kidney function: A Mendelian randomisation study

    Kennedy, O. J., Pirastu, N., Poole, R., Fallowfield, J., Hayes, P., Grzeszkowiak, E. J., Taal, M. W., Wilson, J., Parkes, J. & Roderick, P., 11 Dec 2019, (E-pub ahead of print) In: American Journal of Kidney Diseases.

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  • Common variants associated with plasma triglycerides and risk for coronary artery disease

    Do, R., Willer, C. J., Schmidt, E. M., Sengupta, S., Gao, C., Peloso, G. M., Gustafsson, S., Kanoni, S., Ganna, A., Chen, J., Buchkovich, M. L., Mora, S., Beckmann, J. S., Bragg-Gresham, J. L., Chang, H-Y., Demirkan, A., Den Hertog, H. M., Donnelly, L. A., Ehret, G. B., Esko, T. & 243 others, Feitosa, M. F., Ferreira, T., Fischer, K., Fontanillas, P., Fraser, R. M., Freitag, D. F., Gurdasani, D., Heikkilä, K., Hyppönen, E., Isaacs, A., Jackson, A. U., Johansson, A., Johnson, T., Kaakinen, M., Kettunen, J., Kleber, M. E., Li, X., Luan, J., Lyytikäinen, L-P., Magnusson, P. K. E., Mangino, M., Mihailov, E., Montasser, M. E., Müller-Nurasyid, M., Nolte, I. M., O'Connell, J. R., Palmer, C. D., Perola, M., Petersen, A-K., Sanna, S., Saxena, R., Service, S. K., Shah, S., Shungin, D., Sidore, C., Song, C., Strawbridge, R. J., Surakka, I., Tanaka, T., Teslovich, T. M., Thorleifsson, G., Van den Herik, E. G., Voight, B. F., Volcik, K. A., Waite, L. L., Wong, A., Wu, Y., Zhang, W., Absher, D., Asiki, G., Barroso, I., Been, L. F., Bolton, J. L., Bonnycastle, L. L., Brambilla, P., Burnett, M. S., Cesana, G., Dimitriou, M., Doney, A. S. F., Döring, A., Elliott, P., Epstein, S. E., Eyjolfsson, G. I., Gigante, B., Goodarzi, M. O., Grallert, H., Gravito, M. L., Groves, C. J., Hallmans, G., Hartikainen, A-L., Hayward, C., Hernandez, D., Hicks, A. A., Holm, H., Hung, Y-J., Illig, T., Jones, M. R., Kaleebu, P., Kastelein, J. J. P., Khaw, K-T., Kim, E., Klopp, N., Komulainen, P., Kumari, M., Langenberg, C., Lehtimäki, T., Lin, S-Y., Lindström, J., Loos, R. J. F., Mach, F., McArdle, W. L., Meisinger, C., Mitchell, B. D., Müller, G., Nagaraja, R., Narisu, N., Nieminen, T. V. M., Nsubuga, R. N., Olafsson, I., Ong, K. K., Palotie, A., Papamarkou, T., Pomilla, C., Pouta, A., Rader, D. J., Reilly, M. P., Ridker, P. M., Rivadeneira, F., Rudan, I., Ruokonen, A., Samani, N., Scharnagl, H., Seeley, J., Silander, K., Stančáková, A., Stirrups, K., Swift, A. J., Tiret, L., Uitterlinden, A. G., van Pelt, L. J., Vedantam, S., Wainwright, N., Wijmenga, C., Wild, S. H., Willemsen, G., Wilsgaard, T., Wilson, J. F., Young, E. H., Zhao, J. H., Adair, L. S., Arveiler, D., Assimes, T. L., Bandinelli, S., Bennett, F., Bochud, M., Boehm, B. O., Boomsma, D. I., Borecki, I. B., Bornstein, S. R., Bovet, P., Burnier, M., Campbell, H., Chakravarti, A., Chambers, J. C., Chen, Y-D. I., Collins, F. S., Cooper, R. S., Danesh, J., Dedoussis, G., de Faire, U., Feranil, A. B., Ferrières, J., Ferrucci, L., Freimer, N. B., Gieger, C., Groop, L. C., Gudnason, V., Gyllensten, U., Hamsten, A., Harris, T. B., Hingorani, A., Hirschhorn, J. N., Hofman, A., Hovingh, G. K., Hsiung, C. A., Humphries, S. E., Hunt, S. C., Hveem, K., Iribarren, C., Järvelin, M-R., Jula, A., Kähönen, M., Kaprio, J., Kesäniemi, A., Kivimaki, M., Kooner, J. S., Koudstaal, P. J., Krauss, R. M., Kuh, D., Kuusisto, J., Kyvik, K. O., Laakso, M., Lakka, T. A., Lind, L., Lindgren, C. M., Martin, N. G., März, W., McCarthy, M. I., McKenzie, C. A., Meneton, P., Metspalu, A., Moilanen, L., Morris, A., Munroe, P. B., Njølstad, I., Pedersen, N. L., Power, C., Pramstaller, P. P., Price, J. F., Psaty, B. M., Quertermous, T., Rauramaa, R., Saleheen, D., Salomaa, V., Sanghera, D. K., Saramies, J., Schwarz, P. E. H., Sheu, W. H-H., Shuldiner, A. R., Siegbahn, A., Spector, T. D., Stefansson, K., Strachan, D. P., Tayo, B. O., Tremoli, E., Tuomilehto, J., Uusitupa, M., van Duijn, C. M., Vollenweider, P., Wallentin, L., Wareham, N. J., Whitfield, J. B., Wolffenbuttel, B. H. R., Altshuler, D., Ordovas, J. M., Boerwinkle, E., Palmer, C. N. A., Thorsteinsdottir, U., Chasman, D. I., Rotter, J. I., Franks, P. W., Ripatti, S., Cupples, L. A., Sandhu, M. S., Rich, S. S., Boehnke, M., Deloukas, P., Mohlke, K. L., Ingelsson, E., Abecasis, G. R., Daly, M. J., Neale, B. M. & Kathiresan, S., Nov 2013, In: Nature Genetics. 45, 11, p. 1345-52 8 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 others, Altshuler, 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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  • Common variants at 6q22 and 17q21 are associated with intracranial volume

    Early Growth Genetics EGG Consorti, Cohorts Heart Aging Res Genomic Ep, Ikram, M. A., Fornage, M., Smith, A. V., Seshadri, S., Schmidt, R., Debette, S., Vrooman, H. A., Sigurdsson, S., Ropele, S., Taal, H. R., Mook-Kanamori, D. O., Coker, L. H., Longstreth, W. T., Niessen, W. J., DeStefano, A. L., Beiser, A., Zijdenbos, A. P., Struchalin, M., Jack, C. R. & 31 others, Rivadeneira, F., Uitterlinden, A. G., Knopman, D. S., Hartikainen, A-L., Pennell, C. E., Thiering, E., Steegers, E. A. P., Hakonarson, H., Heinrich, J., Palmer, L. J., Jarvelin, M-R., McCarthy, M. I., Grant, S. F. A., St Pourcain, B., Timpson, N. J., Smith, G. D., Sovio, U., Nalls, M. A., Au, R., Hofman, A., Gudnason, H., van der Lugt, A., Harris, T. B., Meeks, W. M., Vernooij, M. W., van Buchem, M. A., Catellier, D., Jaddoe, V. W. V., Gudnason, V., Windham, B. G. & Wilson, J. F., May 2012, In: Nature Genetics. 44, 5, p. 539-+ 7 p.

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  • Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

    Sotoodehnia, N., Isaacs, A., de Bakker, P. I. W., Doerr, M., Newton-Cheh, C., Nolte, I. M., van der Harst, P., Mueller, M., Eijgelsheim, M., Alonso, A., Hicks, A. A., Padmanabhan, S., Hayward, C., Smith, A. V., Polsek, O., Giovannone, S., Fu, J., Magnani, J. W., Marciante, K. D., Pfeufer, A. & 83 others, Gharib, S. A., Teumer, A., Li, M., Bis, J. C., Rivadeneira, F., Aspelund, T., Koettgen, A., Johnson, T., Rice, K., Sie, M. P. S., Wang, Y. A., Klopp, N., Fuchsberger, C., Wild, S. H., Leach, I. M., Estrada, K., Voelker, U., Wright, A., Asselbergs, F. W., Qu, J., Chakravarti, A., Sinner, M. F., Kors, J. A., Petersmann, A., Harris, T. B., Soliman, E. Z., Munroe, P. B., Psaty, B. M., Oostra, B. A., Cupples, L. A., Perz, S., de Boer, R. A., Uitterlinden, A. G., Voelzke, H., Spector, T. D., Liu, F-Y., Boerwinkle, E., Dominiczak, A. F., Rotter, J. I., van Herpen, G., Levy, D., Wichmann, H-E., van Gilst, W. H., Witteman, J. C. M., Kroemer, H. K., Kao, W. H. L., Heckbert, S. R., Meitinger, T., Hofman, A., Campbell, H., Folsom, A. R., van Veldhuisen, D. J., Schwienbacher, C., O'Donnell, C. J., Volpato, C. B., Caulfield, M. J., Connell, J. M., Launer, L., Lu, X., Franke, L., Fehrmann, R. S. N., Meerman, G. T., Groen, H. J. M., Weersma, R. K., van den Berg, L. H., Wijmenga, C., Ophoff, R. A., Navis, G., Rudan, I., Snieder, H., Wilson, J. F., Pramstaller, P. P., Siscovick, D. S., Wang, T. J., Gudnason, V., van Duijn, C. M., Felix, S. B., Fishman, G. I., Jamshidi, Y., Stricker, B. H. C., Samani, N. J., Kaeaeb, S. & Arking, D. E., Dec 2010, In: Nature Genetics. 42, 12, p. 1068-1076 11 p.

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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 others, Glazer, 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.

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  • Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

    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., Dunlop, M. G., Floyd, J., Hastie, N., Hofman, A., Knott, S., Kolcic, I., Pichler, I., Polasek, O. & 16 others, Rivadeneira, F., Tenesa, A., Uitterlinden, A. G., Wild, S. H., Zorkoltseva, I. V., Meitinger, T., Wilson, 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., Jan 2009, In: Human Molecular Genetics. 18, 2, p. 373-80 8 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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  • Comparison of participant information and informed consent forms of five European studies in genetic isolated populations

    EUROSPAN Consortium, Mascalzoni, D., Janssens, A. C. J. W., Stewart, A., Pramstaller, P., Gyllensten, U., Rudan, I., van Duijn, C. M., Wilson, J. F., Campbell, H. & Mc Quillan, R., Mar 2010, In: European Journal of Human Genetics. 18, 3, p. 296-302 7 p.

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  • Consistent long-range linkage disequilibrium generated by admixture in a Bantu-Semitic hybrid population

    Wilson, J. F. & Goldstein, D. B., 2000, In: American Journal of Human Genetics. 67, 4, p. 926-35 10 p.

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  • Contribution of common risk variants to multiple sclerosis in Orkney and Shetland

    Barnes, C. L. K., Hayward, C., Porteous, D. J., Campbell, H., Joshi, P. K. & Wilson, J. F., 4 Jun 2021, (E-pub ahead of print) In: European Journal of Human Genetics.

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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

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  • Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

    Iglesias, A. I., Vitart, V., Li, X., Yazar, S., Nag, A., Khawaja, A. P., Polašek, O., Siscovick, D., Mitchell, P., Chung Tham, Y., Haines, J. L., Kearns, L. S., Hayward, C., Shi, Y., van Leeuwen, E. M., Taylor, K. D., Blue Mountains Eye Study—GWAS group, Bonnemaijer, P., Rotter, J. I., Martin, N. G. & 33 others, Zeller, T., Mills, R. A., Souzeau, E., Staffieri, S. E., Jonas, J. B., Schmidtmann, I., Boutin, T., Kang, J. H., Lucas, S. E. M., Wong, T. Y., Beutel, M. E., NEIGHBORHOOD Consortium, Wellcome Trust Case Control Consortium 2 (WTCCC2), Uitterlinden, A. G., Vithana, E. N., Foster, P. J., Hysi, P. G., Hewitt, A. W., Khor, C. C., Pasquale, L. R., Montgomery, G. W., Klaver, C. C. W., Aung, T., Pfeiffer, N., Mackey, D. A., Hammond, C. J., Cheng, C-Y., Craig, J. E., Rabinowitz, Y. S., Wiggs, J. L., Burdon, K. P., van Duijn, C. M. & MacGregor, S., 14 May 2018, In: Nature Communications. 9, 1864.

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  • Defining the role of common variation in the genomic and biological architecture of adult human height

    Elect Med Records & Genom eMERGE C, MIGen Consortium, PAGE Consortium, LifeLines Cohort Study, Wood, A. R., Esko, T., Yang, J., Vedantam, S., Pers, T. H., Gustafsson, S., Chun, A. Y., Estrada, K., Luan, J., Kutalik, Z., Amin, N., Buchkovich, M. L., Croteau-Chonka, D. C., Day, F. R., Duan, Y., Fall, T. & 34 others, Fehrmann, R., Ferreira, T., Jackson, A. U., Karjalainen, J., Lo, K. S., Locke, A. E., Maegi, R., Mihailov, E., Porcu, E., Randall, J. C., Scherag, A., Vinkhuyzen, A. A. E., Westra, H-J., Winkler, T. W., Workalemahu, T., Zhao, J. H., Absher, D., Albrecht, E., Anderson, D., Baron, J., Beekman, M., Demirkan, A., Fraser, R. M., Bolton, J. L., Hayward, C., McLachlan, S., Wright, A. F., Campbell, H., Morris, A. D., Price, J. F., Rudan, I., Walker, M., Wilson, J. F. & Visscher, P. M., 5 Oct 2014, In: Nature Genetics. 46, 11, p. 1173-1186 14 p.

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  • Determinants of retinal microvascular features and their relationships in two European populations

    Kirin, M., Nagy, R., MacGillivray, T., Polasek, O., Hayward, C., Rudan, I., Campbell, H., Wild, S., Wright, A., Wilson, J. F. & Vitart, V., Aug 2017, In: Journal of Hypertension.

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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 others, Guo, 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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  • 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 others, Del 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.

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  • Discovery and refinement of loci associated with lipid levels

    Global Lipids Genetics Consortium, Willer, C. J., Schmidt, E. M., Sengupta, S., Peloso, G. M., Gustafsson, S., Kanoni, S., Ganna, A., Chen, J., Buchkovich, M. L., Mora, S., Beckmann, J. S., Bragg-Gresham, J. L., Chang, H-Y., Demirkan, A., Den Hertog, H. M., Do, R., Donnelly, L. A., Ehret, G. B., Esko, T. & 31 others, Feitosa, M. F., Ferreira, T., Fischer, K., Fontanillas, P., Fraser, R. M., Freitag, D. F., Gurdasani, D., Heikkilä, K., Hyppönen, E., Isaacs, A., Jackson, A. U., Johansson, A., Johnson, T., Kaakinen, M., Kettunen, J., Kleber, M. E., Li, X., Luan, J., Lyytikäinen, L-P., Magnusson, P. K. E., Mangino, M., Mihailov, E., Montasser, M. E., Bolton, J. L., Hayward, C., Rudan, I., Wild, S. H., Wilson, J. F., Campbell, H., Morris, A. & Price, J. F., Nov 2013, In: Nature Genetics. 45, 11, p. 1274-83 10 p.

    Research output: Contribution to journalArticlepeer-review

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  • Disentangling the genetics of lean mass

    Karasik, D., Zillikens, M. C., Hsu, Y-H., Aghdassi, A., Akesson, K., Amin, N., Barroso, I., Bennett, D. A., Bertram, L., Bochud, M., Borecki, I. B., Broer, L., Buchman, A. S., Byberg, L., Campbell, H., Campos-Obando, N., Cauley, J. A., Cawthon, P. M., Chambers, J. C., Chen, Z. & 137 others, Cho, N. H., Choi, H. J., Chou, W-C., Cummings, S. R., de Groot, L. C. P. G. M., De Jager, P. L., Demuth, I., Diatchenko, L., Econs, M. J., Eiriksdottir, G., Enneman, A. W., Eriksson, J., Eriksson, J. G., Estrada, K., Evans, D. S., Feitosa, M. F., Fu, M., Gieger, C., Grallert, H., Gudnason, V., Lenore, L. J., Hayward, C., Hofman, A., Homuth, G., Huffman, K. M., Husted, L. B., Illig, T., Ingelsson, E., Ittermann, T., Jansson, J-O., Johnson, T., Biffar, R., Jordan, J. M., Jula, A., Karlsson, M., Khaw, K-T., Kilpeläinen, T. O., Klopp, N., Kloth, J. S. L., Koller, D. L., Kooner, J. S., Kraus, W. E., Kritchevsky, S., Kutalik, Z., Kuulasmaa, T., Kuusisto, J., Laakso, M., Lahti, J., Lang, T., Langdahl, B. L., Lerch, M. M., Lewis, J. R., Lill, C., Lind, L., Lindgren, C., Liu, Y., Livshits, G., Ljunggren, Ö., Loos, R. J. F., Lorentzon, M., Luan, J., Luben, R. N., Malkin, I., McGuigan, F. E., Medina-Gomez, C., Meitinger, T., Melhus, H., Mellström, D., Michaëlsson, K., Mitchell, B. D., Morris, A. P., Mosekilde, L., Nethander, M., Newman, A. B., O'Connell, J. R., Oostra, B. A., Orwoll, E. S., Palotie, A., Peacock, M., Perola, M., Peters, A., Prince, R. L., Psaty, B. M., Räikkönen, K., Ralston, S. H., Ripatti, S., Rivadeneira, F., Robbins, J. A., Rotter, J. I., Rudan, I., Salomaa, V., Satterfield, S., Schipf, S., Shin, C. S., Smith, A. V., Smith, S. B., Soranzo, N., Spector, T. D., Stancáková, A., Stefansson, K., Steinhagen-Thiessen, E., Stolk, L., Streeten, E. A., Styrkarsdottir, U., Swart, K. M. A., Thompson, P., Thomson, C. A., Thorleifsson, G., Thorsteinsdottir, U., Tikkanen, E., Tranah, G. J., Uitterlinden, A. G., van Duijn, C. M., van Schoor, N. M., Vandenput, L., Vollenweider, P., Völzke, H., Wactawski-Wende, J., Walker, M., J Wareham, N., Waterworth, D., Weedon, M. N., Wichmann, H-E., Widen, E., Williams, F. M. K., Wilson, J. F., Wright, N. C., Yerges-Armstrong, L. M., Yu, L., Zhang, W., Zhao, J. H., Zhou, Y., Nielson, C. M., Harris, T. B., Demissie, S., Kiel, D. P. & Ohlsson, C., 5 Feb 2019, (E-pub ahead of print) In: American Journal of Clinical Nutrition.

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  • DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

    kConFab investigators, Perry, J. R. B., Hsu, Y-H., Chasman, D. I., Johnson, A. D., Elks, C., Albrecht, E., Andrulis, I. L., Beesley, J., Berenson, G. S., Bergmann, S., Bojesen, S. E., Bolla, M. K., Brown, J., Buring, J. E., Campbell, H., Chang-Claude, J., Chenevix-Trench, G., Corre, T., Couch, F. J. & 31 others, Cox, A., Czene, K., D'adamo, A. P., Davies, G., Deary, I. J., Dennis, J., Easton, D. F., Engelhardt, E. G., Eriksson, J. G., Esko, T., Fasching, P. A., Figueroa, J. D., Flyger, H., Fraser, A., Garcia-Closas, M., Gasparini, P., Gieger, C., Giles, G., Guenel, P., Hägg, S., Hall, P., Hayward, C., Hopper, J., Ingelsson, E., Kardia, S. L. R., Polasek, O., Rudan, I., Wild, S., Wilson, J. F., Wright, A. F. & Zgaga, L., May 2014, In: Human Molecular Genetics. 23, 9, p. 2490-2497 8 p.

    Research output: Contribution to journalArticlepeer-review

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  • Does inbreeding affect N-glycosylation of human plasma proteins?

    Polasek, O., Leutenegger, A-L., Gornik, O., Zgaga, L., Kolcic, I., McQuillan, R., Wilson, J. F., Hayward, C., Wright, A., Lauc, G., Campbell, H. & Rudan, I., May 2011, In: Molecular genetics and genomics. 285, 5, p. 427-432 6 p.

    Research output: Contribution to journalArticlepeer-review

  • Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals.

    Noordam, R., Young, W. J., Salman, R., Kanters, J. K., van den Berg, M. E., van Heemst, D., Lin, H. J., Barreto, S. M., Biggs, M. L., Biino, G., Repetto, L., Joshi, P., Shen, X. & Wilson, J., 25 Jun 2019, In: Journal of the American College of Cardiology.

    Research output: Contribution to journalArticlepeer-review

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  • Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations

    Xue, Y., Mezzavilla, M., Haber, M., McCarthy, S., Chen, Y., Narasimhan, V., Gilly, A., Ayub, Q., Colonna, V., Southam, L., Finan, C., Massaia, A., Chheda, H., Palta, P., Ritchie, G., Asimit, J., Dedoussis, G., Gasparini, P., Palotie, A., Ripatti, S. & 6 others, Soranzo, N., Daniela, T., Wilson, J., Durbin, R., Tyler-Smith, C. & Zeggini, E., 23 Jun 2017, (E-pub ahead of print) In: Nature Communications.

    Research output: Contribution to journalArticlepeer-review

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  • Erratum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

    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., Langenberg, C., Hofmann, O. M. & 138 others, Dupuis, J., Qi, L., Segŕ, A. V., Van Hoek, M., Navarro, P., Ardlie, K., Balkau, B., Benediktsson, R., Bennett, A. J., Blagieva, R., Boerwinkle, E., Bonnycastle, L. L., Bostrám, K. B., Bravenboer, B., Bumpstead, S., Burtt, N. P., Charpentier, G., Chines, P. S., Cornelis, M., Couper, D. J., Crawford, G., Doney, A. S. F., Elliott, K. S., Elliott, A. L., Erdos, M. R., Fox, C. S., Franklin, C. S., Ganser, M., Gieger, C., Grarup, N., Green, T., Griffin, S., Groves, C. J., Guiducci, C., Hadjadj, S., Hassanali, N., Herder, C., Isomaa, B., Jackson, A. U., Johnson, P. R. V., J́rgensen, T., Kao, W. H. L., Klopp, N., Kong, A., Kraft, P., Kuusisto, J., Lauritzen, T., Li, M., Lieverse, A., Lindgren, C. M., Lyssenko, V., Marre, M., Meitinger, T., Midthjell, K., Morken, M. A., Narisu, N., Nilsson, P., Owen, K. R., Payne, F., Perry, J. R. B., Petersen, A. K., Platou, C., Proeńa, C., Prokopenko, I., Rathmann, W., Rayner, N. W., Robertson, N. R., Rocheleau, G., Roden, M., Sampson, M. J., Saxena, R., Shields, B. M., Shrader, P., Sigurdsson, G., Sparsa̧, T., Strassburger, K., Stringham, H. M., Sun, Q., Swift, A. J., Thorand, B., Tichet, J., Tuomi, T., Van Dam, R. M., Van Haeften, T. W., Van Herpt, T., Van Vliet-Ostaptchouk, J. V., Walters, G. B., Weedon, M. N., Wijmenga, C., Witteman, J., Bergman, R. N., Cauchi, S., Collins, F. S., Gloyn, A. L., Gyllensten, U., Hansen, T., Hide, W. A., Hitman, G. A., Hofman, A., Hunter, D. J., Hveem, K., Laakso, M., Mohlke, K. L., Morris, A. D., Palmer, C. N. A., Pramstaller, P. P., Rudan, I., Sijbrands, E., Stein, L. D., Tuomilehto, J., Uitterlinden, A., Walker, M., Wareham, N. J., Watanabe, R. M., Abecasis, G. R., Boehm, B. O., Campbell, H., Daly, M. J., Hattersley, A. T., Hu, F. B., Meigs, J. B., Pankow, J. S., Pedersen, O., Wichmann, H. E., Barroso, I., Florez, J. C., Frayling, T. M., Groop, L., Sladek, R., Thorsteinsdottir, U., Wilson, J. F., Illig, T., Froguel, P., Van Duijn, C. M., Stefansson, K., Altshuler, D., Boehnke, M. & McCarthy, M. I., 29 Mar 2011, In: Nature Genetics. 43, 4

    Research output: Contribution to journalArticlepeer-review

  • 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 others, 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., 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

    Research output: Contribution to journalArticlepeer-review

  • Estrogens regulate glycosylation of immunoglobulin G in women and men

    Ercan, A., Kohrt, W., Cui, J., Deane, K., Pezer, M., Yu, M., Hausmann, J., Campbell, H., Kaiser, U., Rudd, P. M., Lauc, G., Wilson, J., Finkelstein, J. & Nigrovic, P., 23 Feb 2017, In: JCI Insight.

    Research output: Contribution to journalArticlepeer-review

    Open Access
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  • Evaluation of Bioelectrical Impedance Analysis for Identifying Overweight Individuals at Increased Cardiometabolic Risk: A Cross-Sectional Study

    Lamb, M. J. E., Byrne, C. D., Wilson, J. F. & Wild, S. H., 22 Sep 2014, In: PLoS ONE. 9, 9, p. e106134

    Research output: Contribution to journalArticlepeer-review

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  • Evidence for large-scale gene-by-smoking interaction effects on pulmonary function

    Aschard, H., Tobin, M. D., Hancock, D. B., Skurnik, D., Sood, A., James, A., Smith, A. V., Manichaikul, A., Campbell, A., Prins, B. P., Hayward, C., Loth, D. W., Porteous, D., Strachan, D. P., Zeggini, E., O'Connor, G. T., Brusselle, G. G., Boezen, H. M., Schulz, H., Deary, I. J. & 30 others, Hall, I. P., Rudan, I., Kaprio, J., Wilson, J., Wilk, J. B., Huffman, J., Zhao, J. H., de Jong, K., Lyytikäinen, L-P., Wain, L. V., Jarvelin, M-R., Kahonen, M., Fornage, M., Polasek, O., Cassano, P. A., Barr, R. G., Rawal, R., Harris, S., Gharib, S. A., Enroth, S., Heckbert, S. R., Lehtimaki, T., Gyllensten, U., Jackson, V. E., Gudnason, V., Tang, W., Dupuis, J., Artigas, M. S., Joshi, A. D. & Kraft, P., 12 Jan 2017, (E-pub ahead of print) In: International Journal of Epidemiology.

    Research output: Contribution to journalArticlepeer-review

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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 others, Ulivi, 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.

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  • ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

    Bihlmeyer, N. A., Brody, J. A., Smith, A. V., Warren, H. R., Lin, H., Isaacs, A., Liu, C-T., Marten, J., Radmanesh, F., Hall, L. M., Grarup, N., Mei, H., Müller-Nurasyid, M., Huffman, J. E., Verweij, N., Guo, X., Yao, J., Li-Gao, R., van den Berg, M., Weiss, S. & 80 others, Prins, B. P., van Setten, J., Haessler, J., Lyytikäinen, L-P., Li, M., Alonso, A., Soliman, E. Z., Bis, J. C., Austin, T., Chen, Y-D. I., Psaty, B. M., Harrris, T. B., Launer, L. J., Padmanabhan, S., Dominiczak, A., Huang, P. L., Xie, Z., Ellinor, P. T., Kors, J. A., Campbell, A., Murray, A. D., Nelson, C. P., Tobin, M. D., Bork-Jensen, J., Hansen, T., Pedersen, O., Linneberg, A., Sinner, M. F., Peters, A., Waldenberger, M., Meitinger, T., Perz, S., Kolcic, I., Rudan, I., de Boer, R. A., van der Meer, P., Lin, H. J., Taylor, K. D., de Mutsert, R., Trompet, S., Jukema, J. W., Maan, A. C., Stricker, B. H. C., Rivadeneira, F., Uitterlinden, A., Völker, U., Homuth, G., Völzke, H., Felix, S. B., Mangino, M., Spector, T. D., Bots, M. L., Perez, M., Raitakari, O. T., Kähönen, M., Mononen, N., Gudnason, V., Munroe, P. B., Lubitz, S. A., van Duijn, C. M., Newton-Cheh, C. H., Hayward, C., Rosand, J., Samani, N. J., Kanters, J. K., Wilson, J. G., Kääb, S., Polasek, O., van der Harst, P., Heckbert, S. R., Rotter, J. I., Mook-Kanamori, D. O., Eijgelsheim, M., Dörr, M., Jamshidi, Y., Asselbergs, F. W., Kooperberg, C., Lehtimäki, T., Arking, D. E. & Sotoodehnia, N., 11 Jan 2018, In: Circulation: Genomic and Precision Medicine. 11, 1, p. e001758 65 p.

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  • Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

    Chami, N., Chen, M-H., Slater, A. J., Eicher, J. D., Evangelou, E., Tajuddin, S. M., Love-Gregory, L., Kacprowski, T., Schick, U. M., Nomura, A., Giri, A., Lessard, S., Brody, J. A., Schurmann, C., Pankratz, N., Yanek, L. R., Manichaikul, A., Pazoki, R., Mihailov, E., Hill, W. D. & 93 others, Raffield, L. M., Burt, A., Bartz, T. M., Becker, D. M., Becker, L. C., Boerwinkle, E., Bork-Jensen, J., Bottinger, E. P., O'Donoghue, M. L., Crosslin, D. R., de Denus, S., Dubé, M-P., Elliott, P., Engström, G., Evans, M. K., Floyd, J. S., Fornage, M., Gao, H., Greinacher, A., Gudnason, V., Hansen, T., Harris, T. B., Hayward, C., Hernesniemi, J., Highland, H. M., Hirschhorn, J. N., Hofman, A., Irvin, M. R., Kähönen, M., Lange, E., Launer, L. J., Lehtimäki, T., Li, J., Liewald, D. C. M., Linneberg, A., Liu, Y., Lu, Y., Lyytikäinen, L-P., Mägi, R., Mathias, R. A., Melander, O., Metspalu, A., Mononen, N., Nalls, M. A., Nickerson, D. A., Nikus, K., O'Donnell, C. J., Orho-Melander, M., Pedersen, O., Petersmann, A., Polfus, L., Psaty, B. M., Raitakari, O. T., Raitoharju, E., Richard, M., Rice, K. M., Rivadeneira, F., Rotter, J. I., Schmidt, F., Smith, A. V., Starr, J. M., Taylor, K. D., Teumer, A., Thuesen, B. H., Torstenson, E. S., Tracy, R. P., Tzoulaki, I., Zakai, N. A., Vacchi-Suzzi, C., van Duijn, C. M., van Rooij, F. J. A., Cushman, M., Deary, I. J., Velez Edwards, D. R., Vergnaud, A-C., Wallentin, L., Waterworth, D. M., White, H. D., Wilson, J. G., Zonderman, A. B., Kathiresan, S., Grarup, N., Esko, T., Loos, R. J. F., Lange, L. A., Faraday, N., Abumrad, N. A., Edwards, T. L., Ganesh, S. K., Auer, P. L., Johnson, A. D., Reiner, A. P. & Lettre, G., 7 Jul 2016, In: American Journal of Human Genetics. 99, 1, p. 8-21 14 p.

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  • Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

    Nagy, R., Boutin, T. S., Marten, J., Huffman, J. E., Kerr, S. M., Campbell, A., Evenden, L., Gibson, J., Amador, C., Howard, D. M., Navarro, P., Morris, A., Deary, I. J., Hocking, L. J., Padmanabhan, S., Smith, B. H., Joshi, P., Wilson, J. F., Hastie, N. D., Wright, A. F. & 5 others, McIntosh, A. M., Porteous, D. J., Haley, C. S., Vitart, V. & Hayward, C., 7 Mar 2017, In: Genome Medicine. 9, 14 p., 23.

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  • Extensive female-mediated gene flow from sub-Saharan Africa into near eastern Arab populations

    Richards, M., Rengo, C., Cruciani, F., Gratrix, F., Wilson, J. F., Scozzari, R., Macaulay, V. & Torroni, A., 2003, In: American Journal of Human Genetics. 72, 4, p. 1058-64 7 p.

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  • Farming, foreign holidays, and vitamin D in Orkney

    Weiss, E., Zgaga, L., Read, S., Wild, S., Dunlop, M., Campbell, H., McQuillan, R. & Wilson, J., 17 May 2016, In: PLoS ONE. e0155633.

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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.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • Founding mothers of Jewish communities: geographically separated Jewish groups were independently founded by very few female ancestors

    Thomas, M. G., Weale, M. E., Jones, A. L., Richards, M., Smith, A., Redhead, N., Torroni, A., Scozzari, R., Gratrix, F., Tarekegn, A., Wilson, J. F., Capelli, C., Bradman, N. & Goldstein, D. B., 2002, In: American Journal of Human Genetics. 70, 6, p. 1411-20 10 p.

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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 others, Wang, 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.

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  • Gene-based whole genome sequencing meta-analysis of 250 circulating proteins in three isolated European populations

    Gilly, A., Klaric, L., Park, Y-C., Png, G., Barysenka, A., Marsh, J. A., Tsafantakis, E., Karaleftheri, M., Dedoussis, G., Wilson, J. F. & Zeggini, E., 30 Apr 2022, (E-pub ahead of print) In: Molecular Metabolism. p. 101509

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    Open Access
  • Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

    23Me Res Team, COGENT Cognitive Genomics Consorti & Social Sci Genetic Assoc Consortiu, Aug 2018, In: Nature Genetics. 50, 8, p. 1112-+ 16 p.

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  • Genes predict village of origin in rural Europe

    O'Dushlaine, C., McQuillan, R., Weale, M. E., Crouch, D. J. M., Johansson, A., Aulchenko, Y., Franklin, C. S., Polasek, O., Fuchsberger, C., Corvin, A., Hicks, A. A., Vitart, V., Hayward, C., Wild, S. H., Meitinger, T., van Duijn, C. M., Gyllensten, U., Wright, A., Campbell, H., Pramstaller, P. P. & 2 others, Rudan, I. & Wilson, J. F., Nov 2010, In: European Journal of Human Genetics. 18, 11, p. 1269-1270 2 p.

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  • Genetic adaptation of fatty-acid metabolism: A human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids

    Ameur, A., Enroth, S., Johansson, A., Zaboli, G., Igl, W., Johansson, A. C. V., Rivas, M. A., Daly, M. J., Schmitz, G., Hicks, A. A., Meitinger, T., Feuk, L., van Duijn, C., Oostra, B., Pramstaller, P. P., Rudan, I., Wright, A. F., Wilson, J. F., Campbell, H. & Gyllensten, U., 4 May 2012, In: American Journal of Human Genetics. 90, 5, p. 809-820 12 p.

    Research output: Contribution to journalArticlepeer-review

  • Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits

    Evangelou, E., Warren, H. R., Mosen-Ansorena, D., Mifsud, B., Pazoki, R., Gao, H., Ntritsos, G., Dimou, N., Cabrera-Cardenas, C., Karaman, I., Liang Ng, F., Evangelou, M., Witkowska, K., Tzanis, E., Hellwege, J. N., Giri, A., Velez Edwards, D. R., Sun, Y. V., Cho, K., Gaziano, J. M. & 260 others, Wilson, P. W. F., Tsao, P. S., Kovesdy, C. P., Esko, T., Mägi, R., Milani, L., Almgren, P., Boutin, T., Debette, S., Ding, J., Giulianini, F., Holliday, E. G., Jackson, A. U., Li-Gao, R., Lin, W-Y., Luan, J., Mangino, M., Oldmeadow, C., Prins, B. P., Qian, Y., Sargurupremraj, M., Shah, N., Surendran, P., Theriault, S., Verweij, N., Willems, S. M., Zhao, J. H., Amouyel, P., Connell, J. M. C., de Mutsert, R., Doney, A. S. F., Farrall, M., Menni, C., Morris, A., Noordam, R., Paré, G., Poulter, N. R., Shields, D. C., Stanton, A. V., Thom, S., Abecasis, G. R., Amin, N., Arking, D. E., Ayers, K. L., Barbieri, C. M., Batini, C., Bis, J. C., Blake, T., Bochud, M., Boehnke, M., Boerwinkle, E., Boomsma, D. I., Bottinger, E. P., Braund, P. S., Brumat, M., Campbell, A., Campbell, H., Chakravarti, A., Chambers, J. C., Chauhan, G., Ciullo, M., Cocca, M., Collins, F. S., Cordell, H. J., Davies, G., de Borst, M. H., Geus, E. J. C., Deary, I., Deelen, J., Del Greco, F. M., Demirkale, Y., Dörr, M., Ehret, G. B., Elosua, R., Enroth, S., Erzurumluoglu, A. M., Ferreira, T., Frånberg, M., Franco, O. H., Gandin, I., Gasparini, P., Giedraitis, V., Gieger, C., Girotto, G., Goel, A., Gow, A. J., Gudnason, V., Guo, X., Gyllensten, U., Hamsten, A., Harris, T. B., Harris, S., Hartman, C. A., Havulinna, A. S., Hicks, A. A., Hofer, E., Hofman, A., Hottenga, J-J., Huffman, J. E., Hwang, S-J., Ingelsson, E., James, A. L., Jansen, R., Jarvelin, M-R., Joehanes, R., Johansson, Å., Johnson, A. D., Joshi, P., Jousilahti, P., Jukema, J. W., Jula, A., Kähönen, M., Kathiresan, S., Keavney, B. D., Khaw, K. T., Knekt, P., Knight, J., Kolcic, I., Kooner, J. S., Koskinen, S., Kristiansson, K., Kutalik, Z., Laan, M., Larson, M., Launer, L. J., Lehne, B., Lehtimäki, T., Liewald, D., Lin, L., Lind, L., Lindgren, C. M., Liu, Y., Loos, R. J., Lopez, L., Lu, Y., Lyytikäinen, L-P., Mahajan, A., Mamasoula, C., Marrugat, J., Marten, J., Milaneschi, Y., Morgan, A., Morris, A. P., Morrison, A. C., Munson, P. J., Nalls, M. A., Nandakumar, P., Nelson, C. P., Niiranen, T., Nolte, I. M., Nutile, T., Oldehinkel, A. J., Oostra, B. A., O'Reilly, P. F., Org, E., Padmanabhan, S., Palmas, W., Palotie, A., Pattie, A., Penninx, B. W. J. H., Perola, M., Peters, A., Polasek, O., Pramstaller, P. P., Tri Nguyen, Q., Raitakari, O. T., Ren, M., Rettig, R., Rice, K. M., Ridker, P. M., Ried, J. S., Riese, H., Ripatti, S., Robino, A., Rose, L. M., Rotter, J. I., Rudan, I., Ruggiero, D., Saba, Y., Sala, C. F., Salomaa, V., Samani, N. J., Sarin, A-P., Schmidt, R., Schmidt, H., Shrine, N. R. G., Siscovick, D. S., Smith, A. V., Snieder, H., Sõber, S., Sorice, R., Starr, J., Stott, D. J., Strachan, D. P., Strawbridge, R. J., Sundstrom, J., Swertz, M. A., Taylor, K. D., Teumer, A., Tobin, M. D., Tomaszewski, M., Toniolo, D., Traglia, M., Trompet, S., Tuomilehto, J., Tzourio, C., Uitterlinden, A. G., Vaez, A., van der Most, P. J., van Duijn, C. M., Vergnaud, A-C., Verwoert, G. C., Vitart, V., Völker, U., Vollenweider, P., Vuckovic, D., Watkins, H., Wild, S., Willemsen, G., Wilson, J., Wrightl, A. F., Yao, J., Zemunik, T., Zhang, W., Attia, J., Butterworth, A. S., Chasman, D. I., Conen, D., Cucca, F., Danesh, J., Hayward, C., Howson, J. MM., Laakso, M., Lakatta, E. G., Langenberg, C., Melander, O., Mook-Kanamori, D. O., Palmer, C. N. A., Risch, L., Scott, R. A., Scott, R. J., Sever, P., Spector, T. D., van der Harst, P., Wareham, N. J., Zeggini, E., Levy, D., Munroe, P. B., Newton-Cheh, C., Brown, M. J., Metspalu, A., Hung, A. M., O'Donnell, C. J., Edwards, T. L., Psaty, B. M., Tzoulaki, I., Barnes, M. R., Wain, L. V., Elliott, P. & Caulfield, M. J., 17 Sep 2018, In: Nature Genetics. 50, p. 1412–1425

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  • Genetic and phenotypic links between obesity and extracellular vesicles

    Zhai, R., Pan, L., Yang, Z., Li, T., Ning, Z., Pawitan, Y., Wilson, J. F., Wu, D. & Shen, X., 31 Mar 2022, (E-pub ahead of print) In: Human Molecular Genetics.

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  • Genetic architecture of circulating lipid levels

    ENGAGE CONSORTIUM, Demirkan, A., Amin, N., Isaacs, A., Jarvelin, M-R., Whitfield, J. B., Wichmann, H-E., Kyvik, K. O. H. M., Rudan, I., Gieger, C., Hicks, A. A., Johansson, Å., Hottenga, J-J., Smith, J. J., Wild, S. H., Pedersen, N. L., Willemsen, G., Mangino, M., Hayward, C., Uitterlinden, A. G. & 27 others, Hofman, A., Witteman, J., Montgomery, G. W., Pietiläinen, K. H., Rantanen, T., Kaprio, J., Döring, A., Pramstaller, P. P., Gyllensten, U., de Geus, E. J. C., Penninx, B. W., Wilson, J. F., Rivadeneria, F., Magnusson, P. K. E., Boomsma, D. I., Spector, T., Campbell, H., Hoehne, B., Martin, N. G., Oostra, B. A., McCarthy, M., Peltonen-Palotie, L., Aulchenko, Y., Visscher, P. M., Ripatti, S., Janssens, A. C. J. W. & van Duijn, C. M., 2011, In: European Journal of Human Genetics. 19, 7, p. 813-9 7 p.

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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 others, Tayo, 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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  • Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

    CARe Consortium, Arking, D. E., Pulit, S. L., Crotti, L., van der Harst, P., Munroe, P. B., Koopmann, T. T., Sotoodehnia, N., Rossin, E. J., Morley, M., Wang, X., Johnson, A. D., Lundby, A., Gudbjartsson, D. F., Noseworthy, P. A., Eijgelsheim, M., Bradford, Y., Tarasov, K. V., Dörr, M., Müller-Nurasyid, M. & 31 others, Lahtinen, A. M., Nolte, I. M., Smith, A. V., Bis, J. C., Isaacs, A., Newhouse, S. J., Evans, D. S., Post, W. S., Waggott, D., Lyytikäinen, L-P., Hicks, A. A., Eisele, L., Ellinghaus, D., Hayward, C., Navarro, P., Ulivi, S., Tanaka, T., Tester, D. J., Chatel, S., Gustafsson, S., Kumari, M., Morris, R. W., Naluai, A. T., Padmanabhan, S., Kluttig, A., Strohmer, B., Wright, A. F., Campbell, H., Wild, S. H., Wilson, J. F. & Rudan, I., 22 Jun 2014, In: Nature Genetics. 46, 8, p. 826-836

    Research output: Contribution to journalArticlepeer-review

  • 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 others, Vitart, 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.

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  • Genetic correlations between diabetes and glaucoma: an analysis of continuous and dichotomous phenotypes

    UK Biobank, International Glaucoma Genetics Consortium, Laville, V., Kang, J. H., Cousins, C., Iglesias, A. I., Nagy, R., Cooke Bailey, J. N., Igo, R. P., Song, Y. E., Chasman, D. I., Christen, W., Kraft, P., Wilson, J. F. & Vitart, V., 20 May 2019, (E-pub ahead of print) In: American journal of ophthalmology.

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