Aldose reductase polymorphisms, fasting blood glucose, and age-related cortical cataract

by Tan, A.G., Kifley, A., Holliday, E.G., Klein, B.E.K., Iyengar, S.K., Lee, K.E., Jun, G.R., Cumming, R.G., Zhao, W., Wong, T.Y., Cheng, C.-Y., Mitchell, P., Wang, J.J.
Published 2021

Genetic association of refractive error and axial length with 15q14 but not 15q25 in the blue mountains eye study cohort

by Schache, M., Richardson, A.J., Mitchell, P., Wang, J.J., Rochtchina, E., Viswanathan, A.C., Wong, T.Y., Saw, S.M., Topouzis, F., Xie, J., Sim, X., Holliday, E.G., Attia, J., Scott, R.J., Baird, P.N.
Published 2014

Five-year progression of unilateral age-related macular degeneration to bilateral involvement: the Three Continent AMD Consortium report

by Joachim, N., Colijn, J.M., Kifley, A., Lee, K.E., Buitendijk, G.H.S., Klein, B.E.K., Myers, C.E., Meuer, S.M., Tan, A.G., Holliday, E.G., Attia, J., Liew, G., Iyengar, S.K., Jong, P.T.V.M. de, Hofman, A., Vingerling, J.R., Mitchell, P., Klaver, C.C.W., Klein, R., Wang, J.J.
Published 2017

Prediction of Age-related Macular Degeneration in the General Population The Three Continent AMD Consortium

by Buitendijk, G.H.S., Rochtchina, E., Myers, C., Duijn, C.M. van, Lee, K.E., Klein, B.E.K., Meuer, S.M., Jong, P.T.V.M. de, Holliday, E.G., Tan, A.G., Uitterlinden, A.G., Sivakumaran, T.S., Attia, J., Hofman, A., Mitchell, P., Vingerling, J.R., Iyengar, S.K., Janssens, A.C.J.W., Wang, J.J., Klein, R., Klaver, C.C.W.
Published 2013

Genetic Susceptibility, Dietary Antioxidants, and Long-Term Incidence of Age-Related Macular Degeneration in Two Populations

by Wang, J.J., Buitendijk, G.H.S., Rochtchina, E., Lee, K.E., Klein, B.E.K., Duijn, C.M. van, Flood, V.M., Meuer, S.M., Attia, J., Myers, C., Holliday, E.G., Tan, A.G., Smith, W.T., Iyengar, S.K., Jong, P.T.V.M. de, Hofman, A., Vingerling, J.R., Mitchell, P., Klein, R., Klaver, C.C.W.
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

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

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

Polygenic Overlap Between Kidney Function and Large Artery Atherosclerotic Stroke

by Holliday, E.G., Traylor, M., Malik, R., Bevan, S., Maguire, J., Koblar, S.A., Sturm, J., Hankey, G.J., Oldmeadow, C., McEvoy, M., Sudlow, C., Rothwell, P.M., Coresh, J., Hamet, P., Tremblay, J., Turner, S.T., Andrade, M. de, Rao, M., Schmidt, R., Crick, P.A., Robino, A., Peralta, C.A., Jukema, J.W., Mitchell, P., Rosas, S.E., Wang, J.J., Scott, R.J., Dichgans, M., Mitchell, B.D., Kao, W.H.L., Fox, C.S., Levi, C., Attia, J., Markus, H.S., CKDGen Consortium, Int Stroke Genetics 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

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

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

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

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants

by Malik, R., Freilinger, T., Anttila, V., Vander Heiden, J., Traylor, M., Vries, B. de, Holliday, E.G., Terwindt, G.M., Sturm, J., Bis, J.C., Hopewell, J.C., Ferrari, M.D., Rannikmae, K., Wessman, M., Kallela, M., Kubisch, C., Fornage, M., Meschia, J.F., Lehtimaki, T., Sudlow, C., Clarke, R., Chasman, D.I., Mitchell, B.D., Maguire, J., Kaprio, J., Farrall, M., Raitakari, O.T., Kurth, T., Ikram, M.A., Reiner, A.P., Longstreth, W.T., Rothwell, P.M., Strachan, D.P., Sharma, P., Seshadri, S., Quaye, L., Cherkas, L., Schurks, M., Rosand, J., Ligthart, L., Boncoraglio, G.B., Smith, G.D., Duijn, C.M. van, Stefansson, K., Worrall, B.B., Nyholt, D.R., Markus, H.S., Maagdenberg, A.M.J.M. van den, Cotsapas, C., Zwart, J.A., Palotie, A., Dichgans, M., Int Headache Genetics Consortium, METASTROKE Collaboration Int Strok
Published 2015

Genetic Loci for Retinal Arteriolar Microcirculation

by Sim, X., Jensen, R.A., Ikram, M.K., Cotch, M.F., Li, X.H., 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., Jong, P.T.V.M. de, Hofman, A., Rivadeneira, F., Uitterlinden, A.G., Duijn, C.M. van, 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., Zuydam, N.R. van, 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., Wellcome Trust Case Control Consor, Global BPGen Consortium
Published 2013

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

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

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

by Vries, P.S. de, 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., Franberg, M., Yang, Q., Ligthart, S., Hottenga, J.J., Rumley, A., Mulas, A., Craen, A.J.M. de, 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., Maat, M.P.M. de, Draisma, H.H.M., Lowe, G.D., Zoledziewska, M., Sattar, N., Lackner, K.J., Volker, U., McKnight, B., Huang, J., Holliday, E.G., McEvoy, M.A., Starr, J.M., Hysi, P.G., Hernandez, D.G., Guan, W.H., Rivadeneira, F., McArdle, W.L., Slagboom, P.E., Zeller, T., Psaty, B.M., Uitterlinden, A.G., Geus, E.J.C. de, Stott, D.J., Binder, H., Hofman, A., Franco, O.H., Rotter, J.I., Ferrucci, L., Spector, T.D., Deary, I.J., Marz, W., Greinacher, A., Wild, P.S., Cucca, F., Boomsma, D.I., Watkins, H., Tang, W.H., 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 2017

Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function

by Wyss, A.B., Sofer, T., Lee, M.K., Terzikhan, N., Nguyen, J.N., Lahousse, L., Latourelle, J.C., Smith, A.V., Bartz, T.M., Feitosa, M.F., Gao, W., Ahluwalia, T.S., Tang, W.B., Oldmeadow, C., Duan, Q., Jong, K. de, Wojczynski, M.K., Wang, X.Q., Noordam, R., Hartwig, F.P., Jackson, V.E., Wang, T.Y., Obeidat, M., Hobbs, B.D., Huan, T.X., Gui, H.S., Parker, M.M., Hu, D.L., Mogil, L.S., Kichaev, G., Jin, J.P., Graff, M., Harris, T.B., Kalhan, R., Heckbert, S.R., Paternoster, L., Burkart, K.M., Liu, Y.M., Holliday, E.G., Wilson, J.G., Vonk, J.M., Sanders, J.L., Barr, R.G., Mutsert, R. de, Menezes, A.M.B., Adams, H.H.H., Berge, M. van den, Joehanes, R., Levin, A.M., Liberto, J., Launer, L.J., Morrison, A.C., Sitlani, C.M., Celedon, J.C., Kritchevsky, S.B., Scott, R.J., Christensen, K., Rotter, J.I., Bonten, T.N., Wehrmeister, F.C., Bosse, Y., Xiao, S.J., Oh, S., Franceschini, N., Brody, J.A., Kaplan, R.C., Lohman, K., McEvoy, M., Province, M.A., Rosendaal, F.R., Taylor, K.D., Nickle, D.C., Williams, L.K., Burchard, E.G., Wheeler, H.E., Sin, D.D., Gudnason, V., North, K.E., Fornage, M., Psaty, B.M., Myers, R.H., O'Connor, G., Hansen, T., Laurie, C.C., Cassano, P.A., Sung, J., Kim, W.J., Attia, J.R., Lange, L., Boezen, H.M., Thyagarajan, B., Rich, S.S., Mook-Kanamori, D.O., Horta, B.L., Uitterlinden, A.G., , H.K. im, Cho, M.H., Brusselle, G.G., Gharib, S.A., Dupuis, J., Manichaikul, A., London, S.J.
Published 2018

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

by Ibrahim-Verbaas, C.A., Bressler, J., Debette, S., Schuur, M., Smith, A.V., Bis, J.C., Davies, G., Trompet, S., Smith, J.A., Wolf, C., Chibnik, L.B., Liu, Y., Vitart, V., Kirin, M., Petrovic, K., Polasek, O., Zgaga, L., Fawns-Ritchie, C., Hoffmann, P., Karjalainen, J., Lahti, J., Llewellyn, D.J., Schmidt, C.O., Mather, K.A., Chouraki, V., Sun, Q., Resnick, S.M., Rose, L.M., Oldmeadow, C., Stewart, M., Smith, B.H., Gudnason, V., Yang, Q., Mirza, S.S., Jukema, J.W., Dejager, P.L., Harris, T.B., Liewald, D.C., Amin, N., Coker, L.H., Stegle, O., Lopez, O.L., Schmidt, R., Teumer, A., Ford, I., Karbalai, N., Becker, J.T., Jonsdottir, M.K., Au, R., Fehrmann, R.S.N., Herms, S., Nalls, M., Zhao, W., Turner, S.T., Yaffe, K., Lohman, K., Swieten, J.C. van, Kardia, S.L.R., Knopman, D.S., Meeks, W.M., Heiss, G., Holliday, E.G., Schofield, P.W., Tanaka, T., Stott, D.J., Wang, J., Ridker, P., Gow, A.J., Pattie, A., Starr, J.M., Hocking, L.J., Armstrong, N.J., McLachlan, S., Shulman, J.M., Pilling, L.C., Eiriksdottir, G., Scott, R.J., Kochan, N.A., Palotie, A., Hsieh, Y.C., Eriksson, J.G., Penman, A., Gottesman, R.F., Oostra, B.A., Yu, L., DeStefano, A.L., Beiser, A., Garcia, M., Rotter, J.I., Nothen, M.M., Hofman, A., Slagboom, P.E., Westendorp, R.G.J., Buckley, B.M., Wolf, P.A., Uitterlinden, A.G., Psaty, B.M., Grabe, H.J., Bandinelli, S., Chasman, D.I., Grodstein, F., Roikkonen, K., Lambert, J.C., Porteous, D.J., Price, J.F., Sachdev, P.S., Ferrucci, L., Attia, J.R., Rudan, I., Hayward, C., Wright, A.F., Wilson, J.F., Cichon, S., Franke, L., Schmidt, H., Ding, J., Craen, A.J.M. de, Fornage, M., Bennett, D.A., Deary, I.J., Ikram, M.A., Launer, L.J., Fitzpatrick, A.L., Seshadri, S., Duijn, C.M. van, Mosley, T.H., Generation Scotland
Published 2016