Identification of sequence variants influencing immunoglobulin levels

by Jonsson, S., Sveinbjornsson, G., Portilla, A.L.D., Swaminathan, B., Plomp, R., Dekkers, G., Ajore, R., Ali, M., Bentlage, A.E.H., Elmer, E., Eyjolfsson, G.I., Gudjonsson, S.A., Gullberg, U., Gylfason, A., Halldorsson, B.V., Hansson, M., Holm, H., Johansson, A., Johnsson, E., Jonasdottir, A., Ludviksson, B.R., Oddsson, A., Olafsson, I., Olafsson, S., Sigurdardottir, O., Sigurdsson, A., Stefansdottir, L., Masson, G., Sulem, P., Wuhrer, M., Wihlborg, A.K., Thorleifsson, G., Gudbjartsson, D.F., Thorsteinsdottir, U., Vidarsson, G., Jonsdottir, I., Nilsson, B., Stefansson, K.
Published 2017

A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

by Helgason, H., Sulem, P., Duvvari, M.R., Luo, H.R., Thorleifsson, G., Stefansson, H., Jonsdottir, I., Masson, G., Gudbjartsson, D.F., Walters, G.B., Magnusson, O.T., Kong, A., Rafnar, T., Kiemeney, L.A., Schoenmaker-Koller, F.E., Zhao, L., Boon, C.J.F., Song, Y.J., Fauser, S., Pei, M., Ristau, T., Patel, S., Liakopoulos, S., Ven, J.P.H. van de, Hoyng, C.B., Ferreyra, H., Duan, Y., Bernstein, P.S., Geirsdottir, A., Helgadottir, G., Stefansson, E., Hollander, A.I. den, Zhang, K., Jonasson, F., Sigurdsson, H., Thorsteinsdottir, U., Stefansson, K.
Published 2013

Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31

by Styrkarsdottir, U., Thorleifsson, G., Helgadottir, H.T., Bomer, N., Metrustry, S., Bierma-Zeinstra, S., Strijbosch, A.M., Evangelou, E., Hart, D., Beekman, M., Jonasdottir, A., Sigurdsson, A., Eiriksson, F.F., Thorsteinsdottir, M., Frigge, M.L., Kong, A., Gudjonsson, S.A., Magnusson, O.T., Masson, G., Hofman, A., Arden, N.K., Ingvarsson, T., Lohmander, S., Kloppenburg, M., Rivadeneira, F., Nelissen, R.G.H.H., Spector, T., Uitterlinden, A., Slagboom, P.E., Thorsteinsdottir, U., Jonsdottir, I., Valdes, A.M., Meulenbelt, I., Meurs, J. van, Jonsson, H., Stefansson, K., TREAT OA Consortium, arcOGEN Consortium
Published 2014

Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12

by Kilarski, L.L., Achterberg, S., Devan, W.J., Traylor, M., Malik, R., Lindgren, A., Pare, G., Sharma, P., Slowik, A., Thijs, V., Walters, M., Worrall, B.B., Sale, M.M., Algra, A., Kappelle, L.J., Wijmenga, C., Norrving, B., Sandling, J.K., Ronnblom, L., Goris, A., Franke, A., Sudlow, C., Rothwell, P.M., Levi, C., Holliday, E.G., Fornage, M., Psaty, B., Gretarsdottir, S., Thorsteinsdottir, U., Seshadri, S., Mitchell, B.D., Kittner, S., Clarke, R., Hopewell, J.C., Bis, J.C., Boncoraglio, G.B., Meschia, J., Ikram, M.A., Hansen, B.M., Montaner, J., Thorleifsson, G., Stefanson, K., Rosand, J., Bakker, P.I.W. de, Farrall, M., Dichgans, M., Markus, H.S., Bevan, S., Garnet Collaborative Res Grp, Wellcome Trust Case, Australian Stroke, Metastroke Consortium, Int Stroke Genetics Consortium
Published 2014

A genome-wide association study of early menopause and the combined impact of identified variants

by Perry, J.R.B., Corre, T., Esko, T., Chasman, D.I., Fischer, K., Franceschini, N., He, C., Kutalik, Z., Mangino, M., Rose, L.M., Vernon smith, A., Stolk, L., Sulem, P., Weedon, M.N., Zhuang, W.V., Arnold, A., Ashworth, A., Bergmann, S., Buring, J.E., Burri, A., Chen, C., Cornelis, M.C., Couper, D.J., Goodarzi, M.O., Gudnason, V., Harris, T., Hofman, A., Jones, M., Kraft, P., Launer, L., Laven, J.S.E., Li, G., Mcknight, B., Masciullo, C., Milani, L., Orr, N., Psaty, B.M., Ridker, P.M., Rivadeneira, F., Sala, C., Salumets, A., Schoemaker, M., Traglia, M., Waeber, G., Chanock, S.J., Demerath, E.W., Garcia, M., Hankinson, S.E., Hu, F.B., Hunter, D.J., Lunetta, K.L., Metspalu, A., Montgomery, G.W., Murabito, J.M., Newman, A.B., Ong, K.K., Spector, T.D., Stefansson, K., Swerdlow, A.J., Thorsteinsdottir, U., Van dam, R.M., Uitterlinden, A.G., Visser, J.A., Vollenweider, P., Toniolo, D., Murray, A.
Published 2014

No additional prognostic value of genetic information in the prediction of vascular events after cerebral ischemia of arterial origin: The PROMISe study

by Achterberg S., Kappelle L.J., De Bakker P.I.W., Traylor M., Algra A., Van Der Graaf Y., Grobbee D.E., Rutten G.E.H.M., Visseren F.L.J., Moll F.L., Mali W.P.T.M., Doevendans P.A., Martin F., Holliday E.G., Sudlow C., Hopewell J.C., Cheng Y.-C., Fornage M., Ikram M.A., Malik R., Bevan S., Thorsteinsdottir U., DeStefano A.L., Worrall B.B., Reiner A.P., Mitchell B.D., Clarke R., Levi C., Seshadri S., Boncoraglio G.B., Sharma P., Bis J.C., Gretarsdottir S., Psaty B.M., Rothwell P.M., Rosand J., Meschia J.F., Stefansson K., Dichgans M., Markus H.S.
Published 2020

Assessment of Osteoarthritis Candidate Genes in a Meta-Analysis of Nine Genome-Wide Association Studies

by Rodriguez-Fontenla, C., Calaza, M., Evangelou, E., Valdes, A.M., Arden, N., Blanco, F.J., Carr, A., Chapman, K., Deloukas, P., Doherty, M., Esko, T., Aleta, C.M.G., Carnota, J.J.G.R., Helgadottir, H., Hofman, A., Jonsdottir, I., Kerkhof, H.J.M., Kloppenburg, M., McCaskie, A., Ntzani, E.E., Ollier, W.E.R., Oreiro, N., Panoutsopoulou, K., Ralston, S.H., Ramos, Y.F., Riancho, J.A., Rivadeneira, F., Slagboom, P.E., Styrkarsdottir, U., Thorsteinsdottir, U., Thorleifsson, G., Tsezou, A., Uitterlinden, A.G., Wallis, G.A., Wilkinson, J.M., Zhai, G.J., Zhu, Y.Y., Felson, D.T., Ioannidis, J.P.A., Loughlin, J., Metspalu, A., Meulenbelt, I., Stefansson, K., Meurs, J.B. van, Zeggini, E., Spector, T.D., Gonzalez, A., arcOGEN Consortium
Published 2014

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

by Evangelou, E., Kerkhof, H.J., Styrkarsdottir, U., Ntzani, E.E., Bos, S.D., Esko, T., Evans, D.S., Metrustry, S., Panoutsopoulou, K., Ramos, Y.F.M., Thorleifsson, G., Tsilidis, K.K., Arden, N., Aslam, N., Bellamy, N., Birrell, F., Blanco, F.J., Carr, A., Chapman, K., Day-Williams, A.G., Deloukas, P., Doherty, M., Engstrom, G., Helgadottir, H.T., Hofman, A., Ingvarsson, T., Jonsson, H., Keis, A., Keurentjes, J.C., Kloppenburg, M., Lind, P.A., McCaskie, A., Martin, N.G., Milani, L., Montgomery, G.W., Nelissen, R.G.H.H., Nevitt, M.C., Nilsson, P.M., Ollier, W.E.R., Parimi, N., Rai, A., Ralston, S.H., Reed, M.R., Riancho, J.A., Rivadeneira, F., Rodriguez-Fontenla, C., Southam, L., Thorsteinsdottir, U., Tsezou, A., AWallis, G., Wilkinson, J.M., Gonzalez, A., Lane, N.E., Lohmander, L.S., Loughlin, J., Metspalu, A., Uitterlinden, A.G., Jonsdottir, I., Stefansson, K., Slagboom, P.E., Zeggini, E., Meulenbelt, I., Ioannidis, J.P.A., Spector, T.D., Meurs, J.B.J. van, Valdes, A.M., arcOGEN Consortium
Published 2014

Physical and neurobehavioral determinants of reproductive onset and success.

by Day, FR, Helgason, H, Chasman, DI, Rose, LM, Loh, P-R, Scott, RA, Helgason, A, Kong, A, Masson, G, Magnusson, OT, Gudbjartsson, D, Thorsteinsdottir, U, Buring, JE, Ridker, PM, Sulem, P, Stefansson, K, Ong, KK, Perry, JRB
Published 2016

A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus

by Oei, L., Hsu, Y.H., Styrkarsdottir, U., Eussen, B.H., Klein, A. de, Peters, M.J., Halldorsson, B., Liu, C.T., Alonso, N., Kaptoge, S.K., Thorleifsson, G., Hallmans, G., Hocking, L.J., Husted, L.B., Jameson, K.A., Kruk, M., Lewis, J.R., Patel, M.S., Scollen, S., Svensson, O., Trompet, S., Schoor, N.M. van, Zhu, K., Buckley, B.M., Cooper, C., Ford, I., Goltzman, D., Gonzalez-Macias, J., Langdahl, B.L., Leslie, W.D., Lips, P., Lorenc, R.S., Olmos, J.M., Pettersson-Kymmer, U., Reid, D.M., Riancho, J.A., Slagboom, P.E., Garcia-Ibarbia, C., Ingvarsson, T., Johannsdottir, H., Luben, R., Medina-Gomez, C., Arp, P., Nandakumar, K., Palsson, S.T., Sigurdsson, G., Meurs, J.B.J. van, Zhou, Y.H., Hofman, A., Jukema, J.W., Pols, H.A.P., Prince, R.L., Cupples, L.A., Marshall, C.R., Pinto, D., Sato, D., Scherer, S.W., Reeve, J., Thorsteinsdottir, U., Karasik, D., Richards, J.B., Stefansson, K., Uitterlinden, A.G., Ralston, S.H., Ioannidis, J.P.A., Kiel, D.P., Rivadeneira, F., Estrada, K.
Published 2014

Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility

by Chintalapudi, S.R, Maria, D, Di Wang, X, Bailey, J.N.C, Allingham, R, Brilliant, M, Budenz, D, Fingert, J, Gaasterland, D, Gaasterland, T, Haines, J.L, Hark, L, Hauser, M, Igo, R, Hee Kang, J, Kraft, P, Lee, R, Lichter, P, Liu, Y, Moroi, S, Pasquale, L.R, Pericak-Vance, M, Realini, A, Rhee, D, Richards, J.R, Ritch, R, Schuman, J, Scott, W.K, Singh, K, Sit, A, Vollrath, D, Wollstein, G, Zack, D, Aung, T, Bonnemaijer, P, Cheng, C.-Y, Craig, J, Van Duijn, C, Gharahkhani, P, Iglesias Gonzalez, A, Hammond, C.J, Hewitt, A, Hoehn, R, Jonansson, F, Khawaja, A, Chuen Khor, C, Klaver, C.C.W, Lotery, A, MacKey, D, MacGregor, S, Pang, C, Pasutto, F, Stefansson, K, Thorleifsson, G, Thorsteinsdottir, U, Vitart, V, Vithana, E, Young, T, Zeller, T, Hysi, P.G, Wiggs, J.L, Williams, R.W, Jablonski, M.M
Published 2020

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

by 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., Thorleifsson, 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., Li, X., Siscovick, D., Taylor, K.D., Rotter, J.I., Yazar, S., Ulmer, M., Li, J., Yaspan, B.L., Ozel, A.B., Richards, J.E., Moroi, S.E., Haines, J.L., Kang, J.H., Pasquale, L.R., Allingham, R.R., Ashley-Koch, A., Mitchell, P., Wang, J.J., Wright, A.F., Pennell, C., Spector, T.D., Young, T.L., Klaver, C.C.W., Martin, N.G., Montgomery, G.W., Anderson, M.G., Aung, T., Willoughby, C.E., Wiggs, J.L., Pang, C.P., Thorsteinsdottir, U., Lotery, A.J., Hammond, C.J., Van Duijn, C.M., Hauser, M.A., Rabinowitz, Y.S., Pfeiffer, N., MacKey, D.A., Craig, J.E., MacGregor, S., Wong, T.Y.
Published 2014

Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation

by Horikoshi, M., Magi, R., Bunt, M. van de, Surakka, I., Sarin, A.P., Mahajan, A., Marullo, L., Thorleifsson, G., Hagg, S., Hottenga, J.J., Ladenvall, C., Ried, J.S., Winkler, T.W., Willems, S.M., Pervjakova, N., Esko, T., Beekman, M., Nelson, C.P., Willenborg, C., Wiltshire, S., Ferreira, T., Fernandez, J., Gaulton, K.J., Steinthorsdottir, V., Hamsten, A., Magnusson, P.K.E., Willemsen, G., Milaneschi, Y., Robertson, N.R., Groves, C.J., Bennett, A.J., Lehtimaki, T., Viikari, J.S., Rung, J., Lyssenko, V., Perola, M., Heid, I.M., Herder, C., Grallert, H., Muller-Nurasyid, M., Roden, M., Hypponen, E., Isaacs, A., Leeuwen, E.M. van, Karssen, L.C., Mihailov, E., Houwing-Duistermaat, J.J., Craen, A.J.M. de, Deelen, J., Havulinna, A.S., Blades, M., Hengstenberg, C., Erdmann, J., Schunkert, H., Kaprio, J., Tobin, M.D., Samani, N.J., Lind, L., Salomaa, V., Lindgren, C.M., Slagboom, P.E., Metspalu, A., Duijn, C.M. van, Eriksson, J.G., Peters, A., Gieger, C., Jula, A., Groop, L., Raitakari, O.T., Power, C., Penninx, B.W.J.H., Geus, E. de, Smit, J.H., Boomsma, D.I., Pedersen, N.L., Ingelsson, E., Thorsteinsdottir, U., Stefansson, K., Ripatti, S., Prokopenko, I., McCarthy, M.I., Morris, A.P., Engage Consortium
Published 2015

The impact of low-frequency and rare variants on lipid levels

by Surakka, I., Horikoshi, M., Magi, R., Sarin, A.P., Mahajan, A., Lagou, V., Marullo, L., Ferreira, T., Miraglio, B., Timonen, S., Kettunen, J., Pirinen, M., Karjalainen, J., Thorleifsson, G., Hagg, S., Hottenga, J.J., Isaacs, A., Ladenvall, C., Beekman, M., Esko, T., Ried, J.S., Nelson, C.P., Willenborg, C., Gustafsson, S., Westra, H.J., Blades, M., Craen, A.J.M. de, Geus, E.J. de, Deelen, J., Grallert, H., Hamsten, A., Havulinna, A.S., Hengstenberg, C., Houwing-Duistermaat, J.J., Hypponen, E., Karssen, L.C., Lehtimaki, T., Lyssenko, V., Magnusson, P.K.E., Mihailov, E., Muller-Nurasyid, M., Mpindi, J.P., Pedersen, N.L., Penninx, B.W.J.H., Perola, M., Pers, T.H., Peters, A., Rung, J., Smit, J.H., Steinthorsdottir, V., Tobin, M.D., Tsernikova, N., Leeuwen, E.M. van, Viikari, J.S., Willems, S.M., Willemsen, G., Schunkert, H., Erdmann, J., Samani, N.J., Kaprio, J., Lind, L., Gieger, C., Metspalu, A., Slagboom, P.E., Groop, L., Duijn, C.M. van, Eriksson, J.G., Jula, A., Salomaa, V., Boomsma, D.I., Power, C., Raitakari, O.T., Ingelsson, E., Jarvelin, M.R., Thorsteinsdottir, U., Franke, L., Ikonen, E., Kallioniemi, O., Pietiainen, V., Lindgren, C.M., Stefansson, K., Palotie, A., McCarthy, M.I., Morris, A.P., Prokopenko, I., Ripatti, S., ENGAGE Consortium
Published 2015

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

by Traylor, M., Farrall, M., Holliday, E.G., Sudlow, C., Hopewell, J.C., Cheng, Y.C., Fomage, M., Ikram, M.A., Malik, R., Bevan, S., Thorsteinsdottir, U., Nalls, M.A., Longstreth, W.T., Wiggins, K.L., Yadav, S., Parati, E.A., DeStefano, A.L., Worrall, B.B., Kittner, S., Khan, M.S., Reiner, A.P., Helgadottir, A., Achterberg, S., Fernandez-Cadenas, I., Abboud, S., Schmidt, R., Walters, M., Chen, W.M., Ringelstein, E.B., O'Donnell, M., Ho, W.K., Pera, J., Lemmens, R., Norrving, B., Higgins, P., Benn, M., Sale, M., Kuhlenbaumer, G., Doney, A.S.F., Vicente, A.M., Delavaran, H., Algra, A., Davies, G., Oliveira, S.A., Palmer, C.N.A., Deary, I., Schmidt, H., Pandolfo, M., Montaner, J., Carty, C., Bakker, P.I.W. de, Kostulas, K., Ferro, J.M., Zuydam, N.R. van, Valdimarsson, E., Nordestgaard, B.G., Lindgren, A., Thijs, V., Slowik, A., Saleheen, D., Pare, G., Berger, K., Thorleifsson, G., Hofman, A., Mosley, T.H., Mitchell, B.D., Furie, K., Clarke, R., Levi, C., Seshadri, S., Gschwendtner, A., Boncoraglio, G.B., Sharma, P., Bis, J.C., Gretarsdottir, S., Psaty, B.M., Rothwell, P.M., Rosand, J., Meschia, J.F., Stefansson, K., Dichgans, M., Markus, H.S., Australian Stroke Genetics Collabo, WTCCC 2, Int Stroke Genetics Consortium
Published 2012

Functional characterization of GWAS loci associated with fracture risk

by Oei, L., Reppe, S., Ntzani, E., Hibbs, M., Choi, K., Zheng, H.F., Estrada, K., Peppel, J. van de, Nielson, C., Styrkarsdottir, U., Ridker, P., Hsu, Y.H., Garcia, M., Aragaki, A., Duncan, E., Enneman, A., Lehtimaki, T., Esko, T., Trompet, S., Kaptoge, S., Eriksson, J., Amin, N., Kung, A., Medina-Gomez, C., Tsilidis, K., Thorleifsson, G., Rose, L., Zmuda, J., Liu, C.T., Vernon-Smith, A., Srikanth, P., Wilson, S., Clark, G., Viikari, J., Mihailov, E., Moayyeri, A., Li, G., Kammerer, C., Lorentzon, M., Rivera, N., Xiao, S.M., Yang, J., Visscher, P., Tranah, G., Evans, D., Karasik, D., Siggeirsdottir, K., Oei, E., Stefansson, K., Aalto, V., Willner, D., Wareham, N., Minster, R., Bis, J., Duijn, C. van, Boyle, A., Snyder, M., Herrera, L., Cupples, L.A., Aspelund, T., Raitakari, O., Leo, P., Khaw, K.T., Robbins, J., Liu, Y.M., Breda, S., Luben, R., Cauley, J., Arnold, A., Stolk, L., Pols, H., Hofman, A., Shen, J., Meurs, J. van, Sham, P., Zillikens, M., Ohlsson, C., Psaty, B., Harris, T., Reeve, J., Jukema, J.W., Metspalu, A., Kahonen, M., Velde, N. van der, Brown, M., Gudnason, V., Ioannidis, J., Uitterlinden, A., Cummings, S., Spector, T., Kiel, D., Jackson, R., Thorsteinsdottir, U., Chasman, D., Orwoll, E., Yadav, V., Leeuwen, J. van, Evangelou, E., Grundberg, E., Richards, B., Gautvik, K., Rivadeneira, F., Ackert-Bicknell, C., GEFOS Consortium
Published 2013

The genetic basis of cross-phenotype correlation with bone fracture risk: the GEFOS consortium

by Oei, L., Nordstrom, P., Ntzani, E., Zheng, H.F., Estrada, K., Duncan, E., Medina-Gomez, C., Kaptoge, S., Hsu, Y.H., Yang, J., Nielson, C., Styrkarsdottir, U., Ridker, P., Garcia, M., Aragaki, A., Enneman, A., Lehtimaki, T., Esko, T., Trompet, S., Eriksson, J., Amin, N., Kung, A., Tsilidis, K., Thorleifsson, G., Rose, L., Zmuda, J., Liu, C.T., Vernon-Smith, A., Srikanth, P., Wilson, S., Clark, G., Viikari, J., Mihailov, E., Moayyeri, A., Li, G., Kammerer, C., Lorentzon, M., Rivera, N., Xiao, S.M., Tranah, G., Evans, D., Siggeirsdottir, K., Oei, E., Stefansson, K., Aalto, V., Willner, D., Wareham, N., Minster, R., Bis, J., Duijn, C. van, Boyle, A., Snyder, M., Herrera, L., Cupples, L.A., Aspelund, T., Raitakari, O., Leo, P., Khaw, K.T., Robbins, J., Liu, Y.M., Breda, S., Luben, R., Cauley, J., Arnold, A., Reppe, S., Hibbs, M., Stolk, L., Pasco, J., Grundberg, E., Gautvik, K., Ackert-Bicknell, C., Yadav, V., Choi, K., Peppel, J. van de, Leeuwen, J. van, Pols, H., Hofman, A., Shen, J., Meurs, J. van, Atanasovska, B., Sham, P., Ohlsson, C., Psaty, B., Harris, T., Reeve, J., Jukema, J.W., Metspalu, A., Kahonen, M., Velde, N. van der, Brown, M., Gudnason, V., Ioannidis, J., Uitterlinden, A., Cummings, S., Spector, T., Kiel, D., Jackson, R., Thorsteinsdottir, U., Chasman, D., Orwoll, E., Karasik, D., Zillikens, M., Evangelou, E., Richards, B., Visscher, P., Michaelsson, K., Rivadeneira, F.
Published 2013

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

by Springelkamp, H., Hohn, R., Mishra, A., Hysi, P.G., Khor, C.C., Loomis, S.J., Bailey, J.N.C., Gibson, J., Thorleifsson, G., Janssen, S.F., Luo, X.Y., Ramdas, W.D., Vithana, E., Nongpiur, M.E., Montgomery, G., Xu, L., Mountain, J.E., Gharahkhani, P., Lu, Y., Amin, N., Karssen, L.C., Sim, K.S., Leeuwen, E.M. van, Iglesias, A.I., Verhoeven, V.J.M., Hauser, M.A., Loon, S.C., Despriet, D.D.G., Nag, A., Venturini, C., Sanfilippo, P.G., Schillert, A., Kang, J.H., Landers, J., Jonasson, F., Cree, A.J., Koolwijk, L.M.E. van, Rivadeneira, F., Souzeau, E., Jonsson, V., Menon, G., Weinreb, R.N., Jong, P.T.V.M. de, Oostra, B.A., Uitterlinden, A.G., Hofman, A., Ennis, S., Thorsteinsdottir, U., Burdon, K.P., Spector, T.D., Mirshahi, A., Saw, S.M., Vingerling, J.R., Teo, Y.Y., Haines, J.L., Wolfs, R.C.W., Lemij, H.G., Tai, E.S., Jansonius, N.M., Jonas, J.B., Cheng, C.Y., Aung, T., Viswanathan, A.C., Klaver, C.C.W., Craig, J.E., Macgregor, S., Mackey, D.A., Lotery, A.J., Stefansson, K., Bergen, A.A.B., Young, T.L., Wiggs, J.L., Pfeiffer, N., Wong, T.Y., Pasquale, L.R., Hewitt, A.W., Duijn, C.M. van, Hammond, C.J., Blue Mt Eye Study GWAS Grp, NEIGHBORHOOD Consortium, Wellcome Trust Case Control Consor
Published 2014

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

by Hysi, P.G., Cheng, C.Y., Springelkamp, H., Macgregor, S., Bailey, J.N.C., Wojciechowski, R., Vitart, V., Nag, A., Hewitt, A.W., Hohn, R., Venturini, C., Mirshahi, A., Ramdas, W.D., Thorleifsson, G., Vithana, E., Khor, C.C., Stefansson, A.B., Liao, J.M., Haines, J.L., Amin, 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.Y., Allingham, R.R., Richards, J.E., Senft, A., Karssen, L.C., Zheng, Y.F., Bellenguez, C., Xu, L., Iglesias, A.I., Wilson, J.F., Kang, J.H., Leeuwen, E.M. van, Jonsson, V., Thorsteinsdottir, U., Despriet, D.D.G., Ennis, S., Moroi, S.E., Martin, N.G., Jansonius, N.M., Yazar, S., Tai, E.S., Amouyel, P., Kirwan, J., Koolwijk, L.M.E. van, Hauser, M.A., Jonasson, F., Leo, P., Loomis, S.J., Fogarty, R., Rivadeneira, F., Kearns, L., Lackner, K.J., Jong, P.T.V.M. de, Simpson, C.L., Pennell, C.E., Oostra, B.A., Uitterlinden, A.G., Saw, S.M., Lotery, A.J., Bailey-Wilson, J.E., Hofman, A., Vingerling, J.R., Maubaret, C., Pfeiffer, N., Wolfs, R.C.W., Lemij, H.G., Young, T.L., Pasquale, L.R., Delcourt, C., Spector, T.D., Klaver, C.C.W., Small, K.S., Burdon, K.P., Stefansson, K., Wong, T.Y., Viswanathan, A., Mackey, D.A., Craig, J.E., Wiggs, J.L., Duijn, C.M. van, Hammond, C.J., Aung, T., BMES GWAS Grp, NEIGHBORHOOD Consortium, Wellcome Trust Case Control Conso
Published 2014

The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis

by Fall T., Hägg S., Mägi R., Ploner A., Fischer K., Horikoshi M., Sarin A.-P., Thorleifsson G., Ladenvall C., Kals M., Kuningas M., Draisma H.H.M., Ried J.S., van Zuydam N.R., Huikari V., Mangino M., Sonestedt E., Benyamin B., Nelson C.P., Rivera N.V., Kristiansson K., Shen H.-y., Havulinna A.S., Dehghan A., Donnelly L.A., Kaakinen M., Nuotio M.-L., Robertson N., de Bruijn R.F.A.G., Ikram M.A., Amin N., Balmforth A.J., Braund P.S., Doney A.S.F., Döring A., Elliott P., Esko T., Franco O.H., Gretarsdottir S., Hartikainen A.-L., Heikkilä K., Herzig K.-H., Holm H., Hottenga J.J., Hyppönen E., Illig T., Isaacs A., Isomaa B., Karssen L.C., Kettunen J., Koenig W., Kuulasmaa K., Laatikainen T., Laitinen J., Lindgren C., Lyssenko V., Läärä E., Rayner N.W., Männistö S., Pouta A., Rathmann W., Rivadeneira F., Ruokonen A., Savolainen M.J., Sijbrands E.J.G., Small K.S., Smit J.H., Steinthorsdottir V., Syvänen A.-C., Taanila A., Tobin M.D., Uitterlinden A.G., Willems S.M., Willemsen G., Witteman J., Perola M., Evans A., Ferrières J., Virtamo J., Kee F., Tregouet D.-A., Arveiler D., Amouyel P., Ferrario M.M., Brambilla P., Hall A.S., Heath A.C., Madden P.A.F., Martin N.G., Montgomery G.W., Whitfield J.B., Jula A., Knekt P., Oostra B., van Duijn C.M., Penninx B.W.J.H., Davey Smith G., Kaprio J., Samani N.J., Gieger C., Peters A., Wichmann H.-E., Boomsma D.I., de Geus E.J.C., Tuomi T.M., Power C., Hammond C.J., Spector T.D., Lind L., Orho-Melander M., Palmer C.N.A., Morris A.D., Groop L., Järvelin M.-R., Salomaa V., Vartiainen E., Hofman A., Ripatti S., Metspalu A., Thorsteinsdottir U., Stefansson K., Pedersen N.L., McCarthy M.I., Ingelsson E., Prokopenko I.
Published 2019