Challenges in elucidating the genetics of diabetic retinopathy

by Kuo, J.Z., Wong, T.Y., Rotter, J.I., Wiggs, J.L.
Published 2014

Associations of candidate genes to age-related macular degeneration among racial/ethnic groups in the multi-ethnic study of atherosclerosis

by Klein, R., Li, X., Kuo, J.Z., Klein, B.E.K., Cotch, M.F., Wong, T.Y., Taylor, K.D., Rotter, J.I.
Published 2014

Personalized medicine in ophthalmology: From pharmacogenetic biomarkers to therapeutic and dosage optimization

by Ong, F.S, Kuo, J.Z, Wu, W.-C, Cheng, C.-Y, Blackwell, W.-L.B, Taylor, B.L, Grody, W.W, Rotter, J.I, Lai, C.-C, Wong, T.Y
Published 2020

No association of 9p21 with arterial elasticity and retinal microvascular findings

by Folsom, A.R., Pankow, J.S., Li, X., Duprez, D.A., Jacobs, D.R., Klein, R., Klein, B., Tang, W., Wong, T.Y., Cotch, M.F., Taylor, K.D., Rich, S.S., Hall, J.L., Post, W.S., Rotter, J.I.
Published 2014

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: The candidate gene association resource (CARe)

by Sobrin, L., Green, T., Sim, X., Jensen, R.A., Shyong Tai, E., Tay, W.T., Wang, J.J., Mitchell, P., Sandholm, N., Liu, Y., Hietala, K., Iyengar, S.K., Brooks, M., Buraczynska, M., van Zuydam, N., Smith, A.V., Gudnason, V., Doney, A.S.F., Morris, A.D., Leese, G.P., Palmer, C.N.A., Swaroop, A., Taylor Jr., H.A., Wilson, J.G., Penman, A., Chen, C.J., Groop, P.-H., Saw, S.-M., Aung, T., Klein, B.E., Rotter, J.I., Siscovick, D.S., Cotch, M.F., Klein, R., Daly, M.J., Wong, T.Y.
Published 2014

Insights into the Genetic Architecture of Early Stage Age-Related Macular Degeneration: A Genome-Wide Association Study Meta-Analysis

by Holliday, E.G., Smith, A.V., Cornes, B.K., Buitendijk, G.H.S., Jensen, R.A., Sim, X., Aspelund, T., Aung, T., Baird, P.N., Boerwinkle, E., Cheng, C.Y., van Duijn, C.M., Eiriksdottir, G., Gudnason, V., Harris, T., Hewitt, A.W., Inouye, M., Jonasson, F., Klein, B.E.K., Launer, L., Li, X., Liew, G., Lumley, T., McElduff, P., McKnight, B., Mitchell, P., Psaty, B.M., Rochtchina, E., Rotter, J.I., Scott, R.J., Tay, W., Taylor, K., Teo, Y.Y., Uitterlinden, A.G., Viswanathan, A., Xie, S., Vingerling, J.R., Klaver, C.C.W., Tai, E.S., Siscovick, D., Klein, R., Cotch, M.F., Wong, T.Y., Attia, J., Wang, J.J.
Published 2014

A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

by Meng W., Shah K.P., Pollack S., Toppila I., Hebert H.L., McCarthy M.I., Groop L., Ahlqvist E., Lyssenko V., Agardh E., Daniell M., Kaidonis G., Craig J.E., Mitchell P., Liew G., Kifley A., Wang J.J., Christiansen M.W., Jensen R.A., Penman A., Hancock H.A., Chen C.J., Correa A., Kuo J.Z., Li X., Chen Y.-D.I., Rotter J.I., Klein R., Klein B., Wong T.Y., Morris A.D., Doney A.S.F., Colhoun H.M., Price A.L., Burdon K.P., Groop P.-H., Sandholm N., Grassi M.A., Sobrin L., Palmer C.N.A., Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group
Published 2019

Genome-Wide Association Study of Retinopathy in Individuals without Diabetes

by Jensen, R.A., Sim, X., Li, X., Cotch, M.F., Ikram, M.K., Holliday, E.G., Eiriksdottir, G., Harris, T.B., Jonasson, F., Klein, B.E.K., Launer, L.J., Smith, A.V., Boerwinkle, E., Cheung, N., Hewitt, A.W., Liew, G., Mitchell, P., Wang, J.J., Attia, J., Scott, R., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., Taylor, K., Hofman, A., de Jong, P.T.V.M., Rivadeneira, F., Uitterlinden, A.G., Tay, W.-T., Teo, Y.Y., Seielstad, M., Liu, J., Cheng, C.-Y., Saw, S.-M., Aung, T., Ganesh, S.K., O'Donnell, C.J., Nalls, M.A., Wiggins, K.L., Kuo, J.Z., van Duijn, C.M., Gudnason, V., Klein, R., Siscovick, D.S., Rotter, J.I., Tai, E.S., Vingerling, J., Wong, T.Y.
Published 2014

Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: A meta-analysis

by Thomson, G., Valdes, A.M., Noble, J.A., Kockum, I., Grote, M.N., Najman, J., Erlich, H.A., Cucca, F., Pugliese, A., Steenkiste, A., Dorman, J.S., Caillat-Zucman, S., Hermann, R., Ilonen, J., Lambert, A.P., Bingley, P.J., Gillespie, K.M., Lernmark, Å., Sanjeevi, C.B., Rønningen, K.S., Undlien, D.E., Thorsby, E., Petrone, A., Buzzetti, R., Koeleman, B.P.C., Roep, B.O., Saruhan-Direskeneli, G., Uyar, F.A., Günoz, H., Gorodezky, C., Alaez, C., Boehm, B.O., Mlynarski, W., Ikegami, H., Berrino, M., Fasano, M.E., Dametto, E., Israel, S., Brautbar, C., Santiago-Cortes, A., Frazer De Llado, T., She, J.-X., Bugawan, T.L., Rotter, J.I., Raffel, L., Zeidler, A., Leyva-Cobian, F., Hawkins, B.R., Chan, S.H., Castano, L., Pociot, F., Nerup, J.
Published 2014

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

by Jakobsdottir J., van der Lee S.J., Bis J.C., Chouraki V., Li-Kroeger D., Yamamoto S., Grove M.L., Naj A., Vronskaya M., Salazar J.L., DeStefano A.L., Brody J.A., Smith A.V., Amin N., Sims R., Ibrahim-Verbaas C.A., Choi S.-H., Satizabal C.L., Lopez O.L., Beiser A., Ikram M.A., Garcia M.E., Hayward C., Varga T.V., Ripatti S., Franks P.W., Hallmans G., Rolandsson O., Jansson J.-H., Porteous D.J., Salomaa V., Eiriksdottir G., Rice K.M., Bellen H.J., Levy D., Uitterlinden A.G., Emilsson V., Rotter J.I., Aspelund T., O?Donnell C.J., Fitzpatrick A.L., Launer L.J., Hofman A., Wang L.-S., Williams J., Schellenberg G.D., Boerwinkle E., Psaty B.M., Seshadri S.
Published 2019

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

by Simpson C.L., Wojciechowski R., Oexle K., Murgia F., Portas L., Li X., Virginie J.M.V., Vitart V., Schache M., Mohsen Hosseini S., 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 P., Saw S.M., Fossarello M., Wang J.J., Polašek O., Campbell H., Rudan I., Oostra B.A., Uitterlinden A.G., Hofman A., Rivadeneira F., Amin N., Karssen L.C., Vingerling J.R., Döring 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., Meitinger T., Bailey-Wilson J.E., Stambolian D.
Published 2018

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

by Stambolian, D., Wojciechowski, R., Oexle, K., Pirastu, M., Li, X., Raffe, 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., Saw, 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., Polašek, 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., Foster, P.J., Topouzis, F., McGuffin, P., Sim, X., Inouye, M., Holliday, E.G., Attia, J., Scott, R.J., Rotter, J.I., Meitinger, T., Bailey-Wilson, J.E.
Published 2014

Genetic Loci for Retinal Arteriolar Microcirculation

by Sim, X., Jensen, R.A., Ikram, M.K., Cotch, M.F., Li, X., MacGregor, S., Xie, J., Smith, A.V., Boerwinkle, E., Mitchell, P., Klein, R., Klein, B.E.K., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., de Jong, P.T.V.M., Hofman, A., Rivadeneira, F., Uitterlinden, A.G., van Duijn, C.M., Aspelund, T., Eiriksdottir, G., Harris, T.B., Jonasson, F., Launer, L.J., Attia, J., Baird, P.N., Harrap, S., Holliday, E.G., Inouye, M., Rochtchina, E., Scott, R.J., Viswanathan, A., Li, G., Smith, N.L., Wiggins, K.L., Kuo, J.Z., Taylor, K.D., Hewitt, A.W., Martin, N.G., Montgomery, G.W., Sun, C., Young, T.L., Mackey, D.A., van Zuydam, N.R., Doney, A.S.F., Palmer, C.N.A., Morris, A.D., Rotter, J.I., Tai, E.S., Gudnason, V., Vingerling, J.R., Siscovick, D.S., Wang, J.J., Wong, T.Y.
Published 2014

Four novel loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation In vivo

by Kamran Ikram, M., Xueling, S., Jensen, R.A., Cotch, M.F., Hewitt, A.W., Ikram, M.A., Wang, J.J., Klein, R., Klein, B.E.K., Breteler, M.M.B., Cheung, N., Liew, G., Mitchell, P., Uitterlinden, A.G., Rivadeneira, F., Hofman, A., de Jong, P.T.V.M., van Duijn, C.M., Kao, L., Cheng, C.-Y., Smith, A.V., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., Jonasson, F., Eiriksdottir, G., Aspelund, T., Harris, T.B., Launer, L.J., Taylor, K.D., Li, X., Iyengar, S.K., Xi, Q., Sivakumaran, T.A., MacKey, D.A., MacGregor, S., Martin, N.G., Young, T.L., Bis, J.C., Wiggins, K.L., Heckbert, S.R., Hammond, C.J., Andrew, T., Fahy, S., Attia, J., Holliday, E.G., Scott, R.J., Islam, F.M.A., Rotter, J.I., McAuley, A.K., Boerwinkle, E., Tai, E.S., Gudnason, V., Siscovick, D.S., Vingerling, J.R., Wong, T.Y.
Published 2014

Trans-Ethnic Fine-Mapping of Lipid Loci Identifies Population-Specific Signals and Allelic Heterogeneity That Increases the Trait Variance Explained

by Wu Y., Waite L.L., Jackson A.U., Sheu W.-H.H., Buyske S., Absher D., Arnett D.K., Boerwinkle E., Bonnycastle L.L., Carty C.L., Cheng I., Cochran B., Croteau-Chonka D.C., Dumitrescu L., Eaton C.B., Franceschini N., Guo X., Henderson B.E., Hindorff L.A., Kim E., Kinnunen L., Komulainen P., Lee W.-J., Le Marchand L., Lin Y., Lindström J., Lingaas-Holmen O., Mitchell S.L., Narisu N., Robinson J.G., Schumacher F., Stančáková A., Sundvall J., Sung Y.-J., Swift A.J., Wang W.-C., Wilkens L., Wilsgaard T., Young A.M., Adair L.S., Ballantyne C.M., Bůžková P., Chakravarti A., Collins F.S., Duggan D., Feranil A.B., Ho L.-T., Hung Y.-J., Hunt S.C., Hveem K., Juang J.-M.J., Kesäniemi A.Y., Kuusisto J., Laakso M., Lakka T.A., Lee I.-T., Leppert M.F., Matise T.C., Moilanen L., Njølstad I., Peters U., Quertermous T., Rauramaa R., Rotter J.I., Saramies J., Tuomilehto J., Uusitupa M., Wang T.-D., Boehnke M., Haiman C.A., Chen Y.-D.I., Kooperberg C., Assimes T.L., Crawford D.C., Hsiung C.A., North K.E., Mohlke K.L.
Published 2020

Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study

by De Vries P.S., Sabater-Lleal M., Chasman D.I., Trompet S., Ahluwalia T.S., Teumer A., Kleber M.E., Chen M.-H., Wang J.J., Attia J.R., Marioni R.E., Steri M., Weng L.-C., Pool R., Grossmann V., Brody J.A., Venturini C., Tanaka T., Rose L.M., Oldmeadow C., Mazur J., Basu S., Frånberg M., Yang Q., Ligthart S., Hottenga J.J., Rumley A., Mulas A., De Craen A.J.M., Grotevendt A., Taylor K.D., Delgado G.E., Kifley A., Lopez L.M., Berentzen T.L., Mangino M., Bandinelli S., Morrison A.C., Hamsten A., Tofler G., De Maat M.P.M., Draisma H.H.M., Lowe G.D., Zoledziewska M., Sattar N., Lackner K.J., Völker U., McKnight B., Huang J., Holliday E.G., McEvoy M.A., Starr J.M., Hysi P.G., Hernandez D.G., Guan W., Rivadeneira F., McArdle W.L., Slagboom P.E., Zeller T., Psaty B.M., Uitterlinden A.G., De Geus E.J.C., Stott D.J., Binder H., Hofman A., Franco O.H., Rotter J.I., Ferrucci L., Spector T.D., Deary I.J., März W., Greinacher A., Wild P.S., Cucca F., Boomsma D.I., Watkins H., Tang W., Ridker P.M., Jukema J.W., Scott R.J., Mitchell P., Hansen T., O'Donnell C.J., Smith N.L., Strachan D.P., Dehghan A.
Published 2019

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

Erratum to: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (Nature Communications, (2018), 9, 1, (...

by Iglesias, A.I., Mishra, A., Vitart, V., Bykhovskaya, Y., Höhn, R., Springelkamp, H., Cuellar-Partida, G., Gharahkhani, P., Bailey, J.N.C., Willoughby, C.E., Li, X., Budenz, D.L., Christen, W.G., Fingert, J., Friedman, D.S., Gaasterland, D., Gaasterland, T., Hauser, M.A., Kraft, P., Lee, R.K., Lichter, P.R., Yazar, S., Liu, Y., Loomis, S.J., Moroi, S.E., Pericak-Vance, M.A., Realini, A., Richards, J.E., Schuman, J.S., Scott, W.K., Singh, K., Sit, A.J., Nag, A., Vollrath, D., Weinreb, R.N., Wollstein, G., Zack, D.J., Zhang, K., Uitterlinden, A.G., Vithana, E.N., Foster, P.J., Hysi, P.G., Hewitt, A.W., Khawaja, A.P., 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., Polašek, O., Rabinowitz, Y.S., Wiggs, J.L., Burdon, K.P., van Duijn, C.M., MacGregor, S., Siscovick, D., Mitchell, P., Tham, Y.C., Haines, J.L., Kearns, L.S., Hayward, C., Shi, Y., van Leeuwen, E.M., Taylor, K.D., Wang, J.J., Rochtchina, E., Attia, J., Scott, R., Holliday, E.G., Wong, T.Y., Baird, P.N., Xie, J., Inouye, M., Viswanathan, A., Sim, X., Bonnemaijer, P., Rotter, J.I., Martin, N.G., Zeller, T., Mills, R.A., Souzeau, E., Staffieri, S.E., Jonas, J.B., Schmidtmann, I., Boutin, T., Kang, J.H., Lucas, S.E.M., Beutel, M.E., Wilson, J.F., Donnelly, P., Barroso, I., Blackwell, J.M., Bramon, E., Brown, M.A., Casas, J.P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H.S., Mathew, C.G., Palmer, C.N.A., Plomin, R., Rautanen, A., Sawcer, S.J., Trembath, R.C., Wood, N.W., Spencer, C.C.A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Langford, C., Hunt, S.E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S.J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., McCann, O.T., Liddle, J., Potter, S.C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Allingham, R.R., Brilliant, M.H.
Published 2022

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

by Hofer, E., Roshchupkin, G.V., Adams, H.H.H., Knol, M.J., Lin, H., Li, S., Zare, H., Ahmad, S., Armstrong, N.J., Satizabal, C.L., Bernard, M., Bis, J.C., Gillespie, N.A., Luciano, M., Mishra, A., Scholz, M., Teumer, A., Xia, R., Jian, X., Mosley, T.H., Saba, Y., Pirpamer, L., Seiler, S., Becker, J.T., Carmichael, O., Rotter, J.I., Psaty, B.M., Lopez, O.L., Amin, N., van der Lee, S.J., Yang, Q., Himali, J.J., Maillard, P., Beiser, A.S., Decarli, C., Karama, S., Lewis, L., Harris, M., Bastin, M.E., Deary, I.J., Witte, A.V., Beyer, F., Loeffler, M., Mather, K.A., Schofield, P.R., Thalamuthu, A., Kwok, J.B., Wright, M.J., Ames, D., Trollor, J., Jiang, J., Brodaty, H., Wen, W., Vernooij, M.W., Hofman, A., Uitterlinden, A.G., Niessen, W.J., Wittfeld, K., Bülow, R., Völker, U., Pausova, Z., Pike, G.B., Maingault, S., Crivello, F., Tzourio, C., Amouyel, P., Mazoyer, B., Neale, M.C., Franz, C.E., Lyons, M.J., Panizzon, M.S., Andreassen, O.A., Dale, A.M., Logue, M., Grasby, K.L., Jahanshad, N., Painter, J.N., Colodro-Conde, L., Bralten, J., Hibar, D.P., Lind, P.A., Pizzagalli, F., Stein, J.L., Thompson, P.M., Medland, S.E., Sachdev, P.S., Kremen, W.S., Wardlaw, J.M., Villringer, A., van Duijn, C.M., Grabe, H.J., Longstreth, W.T., Fornage, M., Paus, T., Debette, S., Ikram, M.A., Schmidt, H., Schmidt, R., Seshadri, S., Ching, C.R.K., McMahon, M.A.B., Shatokhina, N., Zsembik, L.C.P., Agartz, I., Alhusaini, S., Almeida, M.A.A., Alnæs, D., Amlien, I.K., Andersson, M., Ard, T., Ashley-Koch, A., Brouwer, R.M., Buimer, E.E.L., Bürger, C., Cannon, D.M., Chakravarty, M., Chen, Q., Cheung, J.W., Couvy-Duchesne, B., Dalvie, S., de Araujo, T.K., de Zubicaray, G.I., de Zwarte, S.M.C., Braber, A.D., Doan, N.T., Dohm, K., Ehrlich, S., Engelbrecht, H.-R., Erk, S., Fan, C.C., Fedko, I.O., Foley, S.F., Ford, J.M., Fukunaga, M., Garrett, M.E., Ge, T., Giddaluru, S., Goldman, A.L., Groenewold, N.A., Grotegerd, D., Gurholt, T.P., Gutman, B.A., Hansell, N.K., Harris, M.A., Harrison, M.B., Haswell, C.C., Hauser, M., Herms, S., Heslenfeld, D.J., Ho, N.F., Hoehn, D., Hoffmann, P., Holleran, L., Hoogman, M., Hottenga, J.-J., Ikeda, M., Janowitz, D., Jansen, I.E., Jia, T., Jockwitz, C., Kanai, R., Kasperaviciute, D., Kaufmann, T., Kelly, S., Kikuchi, M., Klein, M., Knapp, M., Knodt, A.R., Krämer, B., Lam, M., Lancaster, T.M., Lee, P.H., Lett, T.A., Lopes-Cendes, I., Macciardi, F., Marquand, A.F., Zhou J.
Published 2021

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

by Stolk, L., Perry, J.R.B., Chasman, D.I., He, C., Mangino, M., Sulem, P., Barbalic, M., Broer, L., Byrne, E.M., Ernst, F., Esko, T., Franceschini, N., Gudbjartsson, D.F., Hottenga, J.-J., Kraft, P., McArdle, P.F., Porcu, E., Shin, S.-Y., Smith, A.V., Van Wingerden, S., Zhai, G., Zhuang, W.V., Albrecht, E., Alizadeh, B.Z., Aspelund, T., Bandinelli, S., Lauc, L.B., Beckmann, J.S., Boban, M., Boerwinkle, E., Broekmans, F.J., Burri, A., Campbell, H., Chanock, S.J., Chen, C., Cornelis, M.C., Corre, T., Coviello, A.D., D'Adamo, P., Davies, G., De Faire, U., De Geus, E.J.C., Deary, I.J., Dedoussis, G.V.Z., Deloukas, P., Ebrahim, S., Eiriksdottir, G., Emilsson, V., Eriksson, J.G., Fauser, B.C.J.M., Ferreli, L., Ferrucci, L., Fischer, K., Folsom, A.R., Garcia, M.E., Gasparini, P., Gieger, C., Glazer, N., Grobbee, D.E., Hall, P., Haller, T., Hankinson, S.E., Hass, M., Hayward, C., Heath, A.C., Hofman, A., Ingelsson, E., Janssens, A.C.J.W., Johnson, A.D., Karasik, D., Kardia, S.L.R., Keyzer, J., Kiel, D.P., Kolcic, I., Kutalik, Z., Lahti, J., Lai, S., Laisk, T., Laven, J.S.E., Lawlor, D.A., Liu, J., Lopez, L.M., Louwers, Y.V., Magnusson, P.K.E., Marongiu, M., Martin, N.G., Klaric, I.M., Masciullo, C., McKnight, B., Medland, S.E., Melzer, D., Mooser, V., Navarro, P., Newman, A.B., Nyholt, D.R., Onland-Moret, N.C., Palotie, A., Paré, G., Parker, A.N., Pedersen, N.L., Peeters, P.H.M., Pistis, G., Plump, A.S., Polasek, O., Pop, V.J.M., Psaty, B.M., R Currency Signikkönen, K., Rehnberg, E., Rotter, J.I., Rudan, I., Sala, C., Salumets, A., Scuteri, A., Singleton, A., Smith, J.A., Snieder, H., Soranzo, N., Stacey, S.N., Starr, J.M., Stathopoulou, M.G., Stirrups, K., Stolk, R.P., Styrkarsdottir, U., Sun, Y.V., Tenesa, A., Thorand, B., Toniolo, D., Tryggvadottir, L., Tsui, K., Ulivi, S., Van Dam, R.M., Van Der Schouw, Y.T., Van Gils, C.H., Van Nierop, P., Vink, J.M., Visscher, P.M., Voorhuis, M., Waeber, G., Wallaschofski, H., Wichmann, H.E., Widen, E., Wijnands-Van Gent, C.J.M., Willemsen, G., Wilson, J.F., Wolffenbuttel, B.H.R., Wright, A.F., Yerges-Armstrong, L.M., Zemunik, T., Zgaga, L., Zillikens, M.C., Zygmunt, M., Arnold, A.M., Boomsma, D.I., Buring, J.E., Crisponi, L., Demerath, E.W., Gudnason, V., Harris, T.B., Hu, F.B., Hunter, D.J., Launer, L.J., Metspalu, A., Montgomery, G.W., Oostra, B.A., Ridker, P.M., Sanna, S., Schlessinger, D., Spector, T.D., Stefansson, K., Streeten, E.A., Thorsteinsdottir, U., Uda, M., Uitterlinden, A.G., Van Duijn, C.M., Völzke, H., Murray, A., Murabito, J.M., Visser, J.A., Lunetta, K.L.
Published 2014