Professor Jamie Craig

  • Source: Scopus
  • Calculated based on no. of publications stored in Pure and citations from Scopus
1992 …2021

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  • Elevation of serum asymmetrical and symmetrical dimethylarginine in patients with advanced glaucoma

    Javadiyan, S., Burdon, K., Whiting, M., Abhary, S., Straga, T., Hewitt, A., Mills, R. & Craig, J., Apr 2012, In: Investigative Ophthalmology and Visual Science. 53, 4, p. 1923-1927 5 p.

    Research output: Contribution to journalArticlepeer-review

    24 Citations (Scopus)
  • Epha2 genotype influences ultraviolet radiation induced cataract in mice

    Dave, A., Craig, J. E., Skrzypiec, K., Quinn, S., Barnes, M., Di Girolamo, N., Mackey, D. A., Burdon, K. P., de Iongh, R. U. & Sharma, S., Nov 2019, In: Experimental Eye Research. 188, 10 p., 107806.

    Research output: Contribution to journalArticlepeer-review

    2 Citations (Scopus)
  • Epha2 Mutations Contribute to Congenital Cataract through Diverse Mechanisms

    Dave, A., Martin, S., Kumar, R., Craig, J., Burdon, K. & Sharma, S., 2016, In: Molecular Vision. 22, p. 18-30 13 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    13 Citations (Scopus)
  • Ethical considerations for the return of incidental findings in ophthalmic genomic research

    Souzeau, E., Burdon, K. P., Mackey, D. A., Hewitt, A. W., Savarirayan, R., Otlowski, M. & Craig, J., 9 Feb 2016, In: Translational Vision Science & Technology. 5, 1, p. 1-11 11 p., 3.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    6 Citations (Scopus)
  • Ethnic and mouse strain differences in central corneal thickness and association with pigmentation phenotype

    Dimasi, D., Hewitt, A., Kagame, K., Ruvama, S., Tindyebwa, L., Llamas, B., Kirk, K., Mitchell, P., Burdon, K. & Craig, J., 2011, In: PLoS One. 6, 8, p. e22103 e22103.

    Research output: Contribution to journalArticlepeer-review

    14 Citations (Scopus)
  • Evaluation of optinueurin sequence variations in 1,048 patients with open-angle glaucoma

    Alward, W., Kwon, Y., Kawase, K., Craig, J., Hayreh, S., Johnson, A., Khanna, C., Yamamoto, T., Mackey, D., Roos, B., Affatigato, L., Sheffield, V. & Stone, E., 2003, In: American Journal of Ophthalmology. 136, 5, p. 904-910 7 p., CC.

    Research output: Contribution to journalArticlepeer-review

    153 Citations (Scopus)
  • Evaluation of the Myocilin (MYOC) Glaucoma Gene in Monkey and Human Steroid-Induced Ocular Hypertension

    Fingert, J., Clark, A., Craig, J., Alward, W., Snibson, G., McLaughlin, M., Tuttle, L., Mackey, D., Sheffield, V. & Stone, E., 2001, In: Investigative Ophthalmology and Visual Science. 42, 1, p. 145-152 8 p.

    Research output: Contribution to journalArticlepeer-review

    97 Citations (Scopus)
  • Evidence for a novel glaucoma locus at chromosome 3p21-22

    Baird, P., Foote, S., Mackey, D., Craig, J. & Speed, T., 2005, In: Human Genetics. 117, 2-3, p. 249-257 9 p.

    Research output: Contribution to journalArticlepeer-review

    54 Citations (Scopus)
  • Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier

    Craig, J. E., Baird, P. N., Healey, D. L., McNaught, A. I., McCartney, P. J., Rait, J. L., Dickinson, J. L., Roe, L., Fingert, J. H., Stone, E. M. & Mackey, D. A., Sep 2001, In: Ophthalmology. 108, 9, p. 1607-1620 14 p.

    Research output: Contribution to journalArticlepeer-review

    88 Citations (Scopus)
  • Familial transmission risk of infantile glaucoma in Australia

    Hewitt, A., MacKinnon, J., Giubilato, A., Elder, J., Craig, J. & Mackey, D., 2006, In: Ophthalmic Genetics. 27, 3, p. 93-97 5 p.

    Research output: Contribution to journalArticlepeer-review

    2 Citations (Scopus)
  • Family-based genome-wide association study of south Indian pedigrees supports WNT7B as a central corneal thickness locus

    Mexican American Glaucoma Genetic Study, Gao, X. R., International Glaucoma Genetics Consortium, Hammond, C. J., McGregor, S., NEIGHBORHOOD Consortium & Sit, A., 1 May 2018, In: Investigative Ophthalmology and Visual Science. 59, 6, p. 2495-2502 8 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    3 Citations (Scopus)
    2 Downloads (Pure)
  • Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndrome

    Yazar, S., Franchina, M., Craig, J., Burdon, K. & Mackey, D., 4 Mar 2017, In: Ophthalmic Genetics. 38, 2, p. 171-174 4 p.

    Research output: Contribution to journalArticlepeer-review

    2 Citations (Scopus)
  • Fetal hemoglobin levels in adults

    Rochette, J., Craig, J. E., Thein, S. L. & Rochette, J., Dec 1994, In: Blood Reviews. 8, 4, p. 213-224 12 p.

    Research output: Contribution to journalArticlepeer-review

    128 Citations (Scopus)
  • Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degeneration

    Ormsby, R., Ranganathan, S., Tong, J., Griggs, K., Dimasi, D., Hewitt, A., Burdon, K., Craig, J., Hoh, J. & Gordon, D., 2008, In: Investigative Ophthalmology and Visual Science. 49, 5, p. 1763-1770 8 p.

    Research output: Contribution to journalArticlepeer-review

    70 Citations (Scopus)
  • Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study

    Sobrin, L., Chong, Y. H., Fan, Q., Gan, A., Stanwyck, L., Kaidonis, G., Craig, J., Kim, J., Liao, W-L., Huang, Y-C., Lee, W-J., Hung, Y-J., Guo, X., Hai, Y., Ipp, E., Pollack, S., Hancock, H., Price, A., Penman, A., Mitchell, P. & 23 others, Liew, G., Smith, A., Gudnason, V., Tan, G., Klein, B., Kuo, J., Li, X., Christiansen, M., Psaty, B., Sandow, K., Jensen, R., Klein, R., Cotch, M., Wang, J. J., Jia, Y., Chen, C., Chen, Y-D., Rotter, J., Tsai, F-J., Hanis, C., Burdon, K., Wong, T. & Cheng, C-Y., 1 Dec 2017, In: Diabetes. 66, 12, p. 3130-3141 12 p.

    Research output: Contribution to journalArticlepeer-review

    5 Citations (Scopus)
  • Genetic analysis of the clusterin gene in pseudoexfoliation syndrome.

    Burdon, K., Sharma, S., Hewitt, A., McMellon, A., JJ, W., DA, M., P, M. & Craig, J., 2008, In: Molecular Vision. 14, p. 1727-1736 10 p.

    Research output: Contribution to journalArticlepeer-review

    29 Citations (Scopus)
  • Genetic association at the 9p21 glaucoma locus contributes to sex bias in normal-tension glaucoma

    Ng, S. K., Burdon, K. P., Fitzgerald, J. T., Zhou, T., Fogarty, R., Souzeau, E., Landers, J., Mills, R. A., Casson, R. J., Ridge, B., Graham, S. L., Hewitt, A. W., Mackey, D. A., Healey, P. R., Wang, J. J., Mitchell, P., MacGregor, S. & Craig, J., 2016, In: Investigative Ophthalmology and Visual Science. 57, 7, p. 3416-3421 6 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    14 Citations (Scopus)
  • Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

    Aung, T., Ozaki, M., Lee, M., Schloetzer-Schrehardt, U., Thorleifsson, G., Mizoguchi, T., Igo, R., Haripriya, A., Williams, S., Astakhov, Y., Orr, A., Burdon, K., Nakano, S., Mori, K., Abu-Amero, K., Hauser, M., Li, Z., Prakadeeswari, G., Bailey, J., Cherecheanu, A. & 269 others, Kang, J., Nelson, S., Hayashi, K., Manabe, S., Kazama, S., Zarnowski, T., Inoue, K., Irkec, M., Coca-Prados, M., Sugiyama, K., Jarvela, I., Schlottmann, P., Lerner, F., Lamari, H., Nilgun, Y., Bikbov, M., Park, K-H., Cha, S., Yamashiro, K., Zenteno, J., Jonas, J., Kumar, R., Perera, S., Chan, A., Kobakhidze, N., George, R., Vijaya, L., Do, T., Edward, D., de Juan Marcos, L., Pakravan, M., Moghimi, S., Ideta, R., Bach-Holme, D., Kappelgaard, P., Wirostko, B., Thomas, S., Gaston, D., Bedard, K., Greer, W., Yang, Z., Chen, X., Huang, L., Sang, J., Jia, H., Jia, L., Qiao, C., Zhang, H., Liu, X., Zhao, B., Wang, Y., Xu, L., Leruez, S., Reynier, P., Chichua, G., Tabagari, S., Uebe, S., Zenkel, M., Berner, D., Mossbock, G., Weisschuh, N., Hoja, U., Welge-Luessen, U-C., Mardin, C., Founti, P., Chatzikyriakidou, A., Pappas, T., Anastasopoulos, E., Lambropoulos, A., Ghosh, A., Shetty, R., Porporato, N., Saravanan, V., Venkatesh, R., Shivkumar, C., Kalpana, N., Sarangapani, S., Kanavi, M., Beni, A., Yazdani, S., Lashay, A., Naderifar, H., Khatibi, N., Fea, A., Lavia, C., Dallorto, L., Rolle, T., Frezzotti, P., Paoli, D., Salvi, E., Manunta, P., Mori, Y., Miyata, K., Higashide, T., Chihara, E., Ishiko, S., Yoshida, A., Kiuchi, Y., Yanagi, M., Ohashi, T., Sakurai, T., Sugimoto, T., Chuman, H., Aihara, M., Inatani, M., Miyake, M., Gotoh, N., Matsuda, F., Yoshimura, N., Ikeda, Y., Ueno, M., Sotozono, C., Jeoung, J., Sagong, M., Park, K., Ahn, J., Cruz-Aguilar, M., Ezzouhairi, S., Rafei, A., Chong, Y., Ng, X., Goh, S., Chen, Y., Yong, V., Khan, M., Olawoye, O., Ashaye, A., Ugbede, I., Onakoya, A., Kizor-Akaraiwe, N., Teekhasaenee, C., Suwan, Y., Supakontanasan, W., Okeke, S., Uche, N., Asimadu, I., Ayub, H., Akhtar, F., Kosior-Jarecka, E., Lukasik, U., Lischinsky, I., Castro, V., Perez-Grossmann, R., Sunaric Megevand, G., Roy, S., Dervan, E., Silke, E., Rao, A., Sahay, P., Fornero, P., Cuello, O., Sivori, D., Zompa, T., Mills, R., Souzeau, E., Mitchell, P., Wang, J. J., Hewitt, A., Coote, M., Crowston, J., Astakhov, S., Akopov, E., Emelyanov, A., Vysochinskaya, V., Kazakbaeva, G., Fayzrakhmanov, R., Al-Obeidan, S., Owaidhah, O., Aljasim, L., Chowbay, B., Foo, J-N., Soh, R., Sim, K-S., Xie, Z., Cheong, A., Mok, S., Soo, H., Chen, X., Peh, S. Q., Heng, K., Husain, R., Ho, S-L., Hillmer, A., Cheng, C-Y., Escudero-Domínguez, F., González-Sarmiento, R., Martinon-Torres, F., Salas, A., Pathanapitoon, K., Hansapinyo, L., Wanichwecharugruang, B., Kitnarong, N., Sakuntabhai, A., Nguyn, H., Nguyn, G., Nguyn, T., Zenz, W., Binder, A., Klobassa, D., Hibberd, M., Davila, S., Herms, S., Nothen, M., Moebus, S., Rautenbach, R., Ziskind, A., Carmichael, T., Ramsay, M., Alvarez, L., Garcia, M., González-Iglesias, H., Rodríguez-Calvo, P., Fernández-Vega Cueto, L., Oguz, C., Tamcelik, N., Atalay, E., Batu, B., Aktas, D., Kasim, B., Wilson, R., Coleman, A., Liu, Y., Challa, P., Herndon, L., Kuchtey, R., Kuchtey, J., Curtin, K., Chaya, C., Crandall, A., Zangwill, L., Wong, T., Nakano, M., Kinoshita, S., den Hollander, A., Vesti, E., Fingert, J., Lee, R., Sit, A., Shingleton, B., Wang, N., Cusi, D., Qamar, R., Kraft, P., Pericak-Vance, M., Raychaudhuri, S., Heegaard, S., Kivela, T., Reis, A., Kruse, F., Weinreb, R., Pasquale, L., Haines, J., Thorsteinsdottir, U., Jonasson, F., Allingham, R., Milea, D., Ritch, R., Kubota, T., Tashiro, K., Vithana, E., Michael, S., Topouzis, F., Craig, J., Dubina, M., Sundaresan, P., Stefansson, K., Wiggs, J., Pasutto, F. & Khor, C-C., 1 Jul 2017, In: Nature Genetics. 49, 7, p. 993-1004 12 p.

    Research output: Contribution to journalArticlepeer-review

    47 Citations (Scopus)
  • Genetic Dissection of Acute Anterior Uveitis Reveals Similarities and Differences in Associations Observed With Ankylosing Spondylitis

    Robinson, P., Claushuis, T., Cortes, A., Martin, T., Evans, D., Leo, P., Mukhopadhyay, P., Bradbury, L., Cremin, K., Harris, J., Maksymowych, W., Inman, R., Rahman, P., Haroon, N., Gensler, L., Powell, J., Van Der Horst-Bruinsma, I., Hewitt, A., Craig, J., Lim, L. & 11 others, Wakefield, D., McCluskey, P., Voigt, V., Fleming, P., Degli-Esposti, M., Pointon, J., Weisman, M., Wordsworth, B., Reveille, J., Rosenbaum, J. & Brown, M., 1 Jan 2015, In: Arthritis & Rheumatology. 67, 1, p. 140-151 12 p.

    Research output: Contribution to journalArticlepeer-review

    62 Citations (Scopus)
  • Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q

    Zhu, G., Hewitt, A., Ruddle, J., Kearns, L., Brown, S., MacKinnon, J., Chen, C., Hammond, C., Craig, J., Montgomery, G., Martin, N. & Mackey, D., 2008, In: Ophthalmology. 115, 6, p. 1053-1057.e2 5 p.

    Research output: Contribution to journalArticlepeer-review

    42 Citations (Scopus)
  • Genetic heterogeneity in heterocellular hereditary persistence of fetal hemoglobin

    Craig, J. E., Rochette, J., Sampietro, M., Wilkie, A. O. M., Barnetson, R., Hatton, C. S. R., Demenais, F. & Thein, S. L., 1 Jul 1997, In: Blood. 90, 1, p. 428-434 7 p.

    Research output: Contribution to journalArticlepeer-review

    31 Citations (Scopus)
  • Genetic Investigation into the Endophenotypic Status of Central Corneal Thickness and Optic Disc Parameters in Relation to Open-Angle Glaucoma

    Dimasi, D., Burdon, K., Hewitt, A., Fitzgerald, J., Wang, J., Healey, P., Mitchell, P., Mackey, D. & Craig, J., Nov 2012, In: American Journal of Ophthalmology. 154, 5, p. 833-842.e2 10 p.

    Research output: Contribution to journalArticlepeer-review

    23 Citations (Scopus)
  • Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits

    Grassmann, F., Kiel, C., Zimmermann, M., Gorski, M., Grassmann, V., Stark, K., International AMD Genomics Consortium (IAMDGC), Heid, I. & Weber, B., 27 Mar 2017, In: Genome Medicine: medicine in the post-genomic era. 9, 1, 13 p., 29.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    33 Citations (Scopus)
    4 Downloads (Pure)
  • Genetics of Hb F/F cell variance in adults and heterocellular hereditary persistence of fetal hemoglobin

    Thein, S. L. & Craig, J. E., 1998, In: Hemoglobin. 22, 5-6, p. 401-414 14 p.

    Research output: Contribution to journalArticlepeer-review

    60 Citations (Scopus)
  • Genetic study of diabetic retinopathy: recruitment methodology and analysis of baseline characteristics

    Kaidonis, G., Abhary, S., Daniell, M., Gillies, M., Fogarty, R., Petrovsky, N., Jenkins, A., Essex, R., Chang, J., Pal, B., Hewitt, A., Burdon, K. & Craig, J., Jul 2014, In: Clinical and Experimental Ophthalmology. 42, 5, p. 486-493 8 p.

    Research output: Contribution to journalArticlepeer-review

    11 Citations (Scopus)
  • Genetic variation near GRB2 and KCNB2 identified by a genome-wide association study are reproducibly associated with Diabetic Retinopathy

    Kaidonis, G., Craig, J., Fogarty, R., Gillies, M., Shen, W., Sharma, S., Appukuttan, B., Pal, B., Sundaresan, P. & Burdon, K., Apr 2014, In: Investigative Ophthalmology and Visual Science. 55, 13, p. 2237-2237 1 p., 2267560.

    Research output: Contribution to journalArticlepeer-review

    21 Citations (Scopus)
  • Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

    Hysi, P., Cheng, C-Y., Springelkamp, H., Macgregor, S., Bailey, J., Wojciechowski, R., Vitart, V., Nag, A., Hewitt, A. W., Hohn, R., Venturini, C., Mirshahi, A., Ramdas, W., Thorleifsson, G., Vithana, E., Khor, C-C., Stefansson, A., Liao, J., Haines, J., Amin, N. & 74 others, Wang, Y., Wild, P., Ozel, A., Li, J., Fleck, B., Zeller, T., Staffieri, S., Teo, Y-Y., Cuellar-Partida, G., Luo, X., Allingham, R., Richards, J., Senft, A., Karssen, L., Zheng, Y., Bellenguez, C., Xu, L., Iglesias, A., Wilson, J., Kang, J., Van Leeuwen, E., Jonsson, V., Thorsteinsdottir, U., Despriet, D., Ennis, S., Moroi, S., Martin, N., Jansonius, N., Yazar, S., Tai, E-S., Amouyel, P., Kirwan, J., van Koolwijk, L., Hauser, M., Jonasson, F., Leo, P., Loomis, S., Fogarty, R., Rivadeneira, F., Kearns, L., Lackner, K., De Jong, P., Simpson, C., Pennell, C., Oostra, B., Uitterlinden, A., Saw, S-M., Lotery, A., Bailey-Wilson, J., Hofman, A., Vingerling, J., Maubaret, C., Pfeiffer, N., Wolfs, R., Lemij, H., Young, T., Pasquale, L., Delcourt, C., Spector, T., Klaver, C., Small, K., Burdon, K., Stefansson, K., Wong, T-Y., BMES GWAS Group, NEIGHBORHOOD Consortium, Wellcome Trust Case Control Co, Viswanathan, A., Mackey, D., Craig, J., Wiggs, J., van Duijn, C., Hammond, C. & Aung, T., 1 Jan 2014, In: Nature Genetics. 46, 10, p. 1126-1130 5 p.

    Research output: Contribution to journalArticlepeer-review

    136 Citations (Scopus)
  • Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

    Lu, Y., Vitart, V., Burdon, K., Khor, C-C., Bykhovskaya, Y., Mirshahi, A., Hewitt, A., Koehn, D., Hysi, P., Ramdas, W., Zeller, T., Vithana, E., Cornes, B., Tay, W-T., Tai, E-S., Cheng, C-Y., Liu, J., Foo, J-N., Saw, S-M., Thorleifsson, G. & 70 others, Stefansson, K., Dimasi, D., Mills, R., Mountain, J., Ang, W., Hoehn, R., Verhoeven, V., Grus, F., Wolfs, R., Castagne, R., Lackner, K., Springelkamp, H., Yang, J., Jonasson, F., Leung, D., Chen, L., Tham, C., Rudan, I., Vatavuk, Z., Hayward, C., Gibson, J., Cree, A., Macleod, A., Ennis, S., Polasek, O., Campbell, H., Wilson, J., Viswanathan, A., Fleck, B., Li, X., Siscovick, D., Taylor, K., Rotter, J., Yazar, S., Ulmer, M., Li, J., Yaspan, B., Ozel, A., Richards, J., Moroi, S., Haines, J., Kang, J., Pasquale, L., Allingham, R., Ashely-Koch, A., Mitchell, P., Wang, J. J., Wright, A., Pennell, C., Spector, T., Young, T., Klaver, C., Martin, N., Montgomery, G., Anderson, M., Aung, T., Willoughby, C., Wiggs, J., Pang, C. P., Thorsteinsdottir, U., Lotery, A., Hammond, C., van Duijn, C., Hauser, M., Rabinowitz, Y., Pfeiffer, N., Mackey, D., Craig, J., Macgregor, S. & Wong, T., 1 Feb 2013, In: Nature Genetics. 45, 2, p. 155-163 9 p.

    Research output: Contribution to journalArticlepeer-review

    172 Citations (Scopus)
  • Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

    EPIC-Norfolk Eye Study, Broadway, D., Chan, M., Garway-Heath, D., Hayat, S., Kerrison, N., Khaw, K-T., Langenberg, C., Luan, J., Luben, R., Scott, R., Wareham, N., Yip, J., Zhao, J. H., ANZRAG Consortium, Sharma, S., Martin, S., Zhou, T., Souzeau, E., Landers, J. & 18 others, Fitzgerald, J., Mills, R., Fogarty, R., Graham, S., Casson, R., Chehade, M., Klebe, S., Ruddle, J., Goldberg, I., White, A., Healey, P., Montgomery, G. W., Martin, N. G., Radford-Smith, G., Whiteman, D., Law, M. H., Brown, M. & Cremin, K., 11 Jan 2016, In: Nature Genetics. 48, 2, p. 189-194 6 p.

    Research output: Contribution to journalArticlepeer-review

    113 Citations (Scopus)
  • Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology

    Han, X., Qassim, A., An, J., Marshall, H., Zhou, T., Ong, J. S., Hassall, M. M., Hysi, P. G., Foster, P. J., Khaw, P. T., Mackey, D. A., Gharahkhani, P., Khawaja, A. P., Hewitt, A. W., Craig, J. E. & MacGregor, S., 6 Nov 2019, In: Human Molecular Genetics. 28, 21, p. 3680-3690 11 p.

    Research output: Contribution to journalArticlepeer-review

    5 Citations (Scopus)
  • Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

    Macgregor, S., Hewitt, A., Hysi, P., Ruddle, J., Medland, S., Henders, A., Gordon, S., Andrew, T., McEvoy, B., Sanfilippo, P., Carbonaro, F., Tah, V., Li, Y., Bennett, S., Craig, J., Montgomery, G., Tran-Viet, K-N., Brown, N., Spector, T., Martin, N. & 3 others, Young, T., Hammond, C. & Mackey, D., 15 Apr 2010, In: Human Molecular Genetics. 19, 13, p. 2716-2724 9 p., ddq144.

    Research output: Contribution to journalArticlepeer-review

    109 Citations (Scopus)
  • Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

    Landi, M. T., Bishop, D. T., MacGregor, S., Machiela, M. J., Stratigos, A. J., Ghiorzo, P., Brossard, M., Calista, D., Choi, J., Fargnoli, M. C., Zhang, T., Rodolfo, M., Trower, A. J., Menin, C., Martinez, J., Hadjisavvas, A., Song, L., Stefanaki, I., Scolyer, R., Yang, R. & 133 others, Goldstein, A. M., Potrony, M., Kypreou, K. P., Pastorino, L., Queirolo, P., Pellegrini, C., Cattaneo, L., Zawistowski, M., Gimenez-Xavier, P., Rodriguez, A., Elefanti, L., Manoukian, S., Rivoltini, L., Smith, B. H., Loizidou, M. A., Del Regno, L., Massi, D., Mandala, M., Khosrotehrani, K., Akslen, L. A., Amos, C. I., Andresen, P. A., Avril, M. F., Azizi, E., Soyer, H. P., Bataille, V., Dalmasso, B., Bowdler, L. M., Burdon, K. P., Chen, W. V., Codd, V., Craig, J. E., Dębniak, T., Falchi, M., Fang, S., Friedman, E., Simi, S., Galan, P., Garcia-Casado, Z., Gillanders, E. M., Gordon, S., Green, A., Gruis, N. A., Hansson, J., Harland, M., Harris, J., Helsing, P., Henders, A., Hočevar, M., Höiom, V., Hunter, D., Ingvar, C., Kumar, R., Lang, J., Lathrop, G. M., Lee, J. E., Li, X., Lubiński, J., Mackie, R. M., Malt, M., Malvehy, J., McAloney, K., Mohamdi, H., Molven, A., Moses, E. K., Neale, R. E., Novaković, S., Nyholt, D. R., Olsson, H., Orr, N., Fritsche, L. G., Puig-Butille, J. A., Qureshi, A. A., Radford-Smith, G. L., Randerson-Moor, J., Requena, C., Rowe, C., Samani, N. J., Sanna, M., Schadendorf, D., Schulze, H. J., Simms, L. A., Smithers, M., Song, F., Swerdlow, A. J., van der Stoep, N., Kukutsch, N. A., Visconti, A., Wallace, L., Ward, S. V., Wheeler, L., Sturm, R. A., Hutchinson, A., Jones, K., Malasky, M., Vogt, A., Zhou, W., Pooley, K. A., Elder, D. E., Han, J., Hicks, B., Hayward, N. K., Kanetsky, P. A., Brummett, C., Montgomery, G. W., Olsen, C. M., Hayward, C., Dunning, A. M., Martin, N. G., Evangelou, E., Mann, G. J., Long, G., Pharoah, P. D. P., Easton, D. F., Barrett, J. H., Cust, A. E., Abecasis, G., Duffy, D. L., Whiteman, D. C., Gogas, H., De Nicolo, A., Tucker, M. A., Newton-Bishop, J. A., GenoMEL Consortium, Q-MEGA and QTWIN Investigators, ATHENS Melanoma Study Group, 23andMe, The SDH Study Group, IBD Investigators, Essen-Heidelberg Investigators, AMFS Investigators, MelaNostrum Consortium & Law, M. H., May 2020, In: Nature Genetics. 52, 5, p. 494-504 11 p.

    Research output: Contribution to journalArticlepeer-review

    4 Citations (Scopus)
  • Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy

    Graham, P. S., Kaidonis, G., Abhary, S., Gillies, M. C., Daniell, M., Essex, R. W., Chang, J. H., Lake, S. R., Pal, B., Jenkins, A. J., Hewitt, A. W., Lamoureux, E. L., Hykin, P. G., Petrovsky, N., Brown, M. A., Craig, J. E. & Burdon, K., 8 May 2018, In: BMC Medical Genetics. 19, 1, 8 p., 71.

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

    Li, Q., Wojciechowski, R., Simpson, C. L., Hysi, P. G., Verhoeven, V. J. M., Ikram, M. K., Höhn, R., Vitart, V., Hewitt, A. W., Oexle, K., Mäkelä, K. M., MacGregor, S., Pirastu, M., Fan, Q., Cheng, C. Y., St Pourcain, B., McMahon, G., Kemp, J. P., Northstone, K., Rahi, J. S. & 73 others, Cumberland, P. M., Martin, N. G., Sanfilippo, P. G., Lu, Y., Wang, Y. X., Hayward, C., Polasek, O., Campbell, H., Bencic, G., Wright, A. F., Wedenoja, J., Zeller, T., Schillert, A., Mirshahi, A., Lackner, K., Yip, S. P., Yap, M. K. H., Ried, J. S., Gieger, C., Murgia, F., Wilson, J. F., Fleck, B., Yazar, S., Vingerling, J. R., Hofman, A., Uitterlinden, A., Rivadeneira, F., Amin, N., Karssen, L., Oostra, B. A., Zhou, X., Teo, Y. Y., Tai, E. S., Vithana, E., Barathi, V., Zheng, Y., Siantar, R. G., Neelam, K., Shin, Y., Lam, J., Yonova-Doing, E., Venturini, C., Hosseini, S. M., Wong, H. S., Lehtimäki, T., Kähönen, M., Raitakari, O., Timpson, N. J., Evans, D. M., Khor, C. C., Aung, T., Young, T. L., Mitchell, P., Klein, B. E., van Duijn, C. M., Meitinger, T., Jonas, J. B., Baird, P. N., Mackey, D. A., Wong, T. Y., Saw, S. M., Pärssinen, O., Stambolian, D., Hammond, C. J., Klaver, C. C. W., Williams, C., Paterson, A. D., Bailey Wilson, J. E., Guggenheim, J. A., The CREAM Consortium , Craig, J. E., Burdon, K. P. & Fogarty, R. D., Feb 2015, In: Human Genetics. 134, 2, p. 131-146 16 p.

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  • Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene

    Burdon, K., Fogarty, R., Shen, W., Abhary, S., Kaidonis, G., Appukuttan, B., Hewitt, A., Sharma, S., Daniell, M., Essex, R., Chang, J., Klebe, S., Lake, S., Pal, B., Jenkins, A., Govindarjan, G., Sundaresan, P., Lamoureux, E., Ramasamy, K., Pefkianaki, M. & 5 others, Hykin, P., Petrovsky, N., Brown, M., Gillies, M. & Craig, J., 24 Oct 2015, In: Diabetologia. 58, 10, p. 2288-2297 10 p.

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    37 Citations (Scopus)
  • Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

    Khor, C., Do, T., Jia, H., Nakano, M., George, R., Abu-Amero, K., Duvesh, R., Chen, L., Li, Z., Nongpiur, M., Perera, S., Qiao, C., Wong, H-T., Sakai, H., de Melo, M., Lee, M., Chan, A., Yakub, A., Dao, T., Ikeda, Y. & 208 others, Perez-Grossmann, R., Zarnowski, T., Day, A., Jonas, J., Tam, P., Tran, T., Ayub, H., Akhtar, F., Michael, S., Chew, P., Aljasim, L., Dada, T., Luu, T., Awadalla, M., Kitnarong, N., Wanichwecharungruang, B., Aung, Y. Y., Mohamed-Noor, J., Vijayan, S., Sripriya, S., Husain, R., Jap, A., Mani, B., Goh, D., Su, D., Wang, H., Yong, V., Yip, L., Trinh, T., Makornwattana, M., Nguyen, T., Leuenberger, E., Park, K-H., Wiyogo, W., Kumar, R., Tello, C., Kurimoto, Y., Thapa, S., Pathanapitoon, K., Salmon, J., Sohn, Y. H., Fea, A., Mineo, O., Lai, J., Tantisevi, V., Khaing, C. C., Mizoguchi, T., Nakano, S., Kim, C-Y., Tang, G., Fan, S., Wu, R., Meng, H., Nguyen, T., Tran, T., Ueno, M., Martinez, J., Ramli, N., Aung, Y., Reyes, R., Vernon, S., Fang, S., Xie, Z., Chen, X., Sim, K-S., Wong, T., Quek, D., Venkatesh, R., Kavitha, S., Krishnadas, S., Soumittra, N., Shantha, B., Lim, B-A., Ogle, J., de Vasconcellos, J., Costa, V., Abe, R., de Souza, B., Sng, C., Aquino, M., Kosior-Jarecka, E., Fong, G., Tamanaja, V., Fujita, R., Jiang, Y., Waseem, N., Low, S., Pham, H., Al Shahwan, S., Craven, E., Khan, M., Dada, R., Mohanty, K., Faiq, M., Hewitt, A., Burdon, K., Gan, E., Prutthipongsit, A., Patthanathamrongkasem, T., Catacutan, M. A., Felarca, I., Liao, C., Rusmayani, E., Istiantoro, V., Consolandi, G., Pignata, G., Lavia, C., Rojanapongpun, P., Mangkornkanokpong, L., Chansangpetch, S., Chan, J., Choy, B., Shum, J., Than, H., Oo, K., Han, A., Yong, V., Ng, X., Goh, S., Chong, Y., Hibberd, M., Seielstad, M., Png, E., Dunstan, S., van Vinh Chau, N., Bei, J-X., Zeng, Y-X., Karkey, A., Basnyat, B., Pasutto, F., Paoli, D., Frezzotti, P., Wang, J., Mitchell, P., Fingert, J., Allingham, R., Hauser, M., Lim, S., Chew, S., Ebstein, R., Sakuntabhai, A., Park, K., Ahn, J., Boland, G., Snippe, H., Stead, R., Quino, R., Zaw, S., Lukasik, U., Shetty, R., Zahari, M., Bae, H., Oo, N. L., Kubota, T., Manassakorn, A., Ho, W., Dallorto, L., Hwang, Y., Kiire, C., Kuroda, M., Djamal, Z., Peregrino, J., Ghosh, A., Jeoung, J., Hoang, T., Srisamran, N., Sandragasu, T., Set, S., Doan, V., Bhattacharya, S., Ho, C-L., Tan, D., Sihota, R., Loon, S-C., Mori, K., Kinoshita, S., den Hollander, A., Qamar, R., Wang, Y. X., Teo, Y. Y., Tai, E-S., Hartleben-Matkin, C., Lozano-Giral, D., Saw, S. M., Cheng, C. Y., Zenteno, J., Pang, C. P., Bui, H., Hee, O., Craig, J., Edward, D., Yonahara, M., Neto, J., Guevara-Fujita, M., Xu, L., Ritch, R., Tajudin, L-S., Wong, T., Al-Obeidan, S., Hon, D., Sundaresan, P., Tham, C., Foster, P., Vijaya, L., Tashiro, K., Vithana, E., Wang, N. & Aung, T., 4 Apr 2016, In: Nature Genetics. 48, 5, p. 556-562 7 p.

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  • Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma

    Shiga, Y., Akiyama, M., Nishiguchi, K. M., Sato, K., Shimozawa, N., Takahashi, A., Momozawa, Y., Hirata, M., Matsuda, K., Yamaji, T., Iwasaki, M., Tsugane, S., Oze, I., Mikami, H., Naito, M., Wakai, K., Yoshikawa, M., Miyake, M., Yamashiro, K., Japan Glaucoma Society Omics Group (JSG-OG) & 49 others, Kashiwagi, K., Iwata, T., Mabuchi, F., Takamoto, M., Ozaki, M., Kawase, K., Aihara, M., Araie, M., Yamamoto, T., Kiuchi, Y., Nakamura, M., Ikeda, Y., Sonoda, K-H., Ishibashi, T., Nitta, K., Iwase, A., Shirato, S., Oka, Y., Satoh, M., Sasaki, M., Fuse, N., Suzuki, Y., Cheng, C-Y., Khor, C. C., Baskaran, M., Perera, S., Aung, T., Vithana, E., Cooke Bailey, J. N., Kang, J. H., Pasquale, L. R., Haines, J. L., NEIGHBORHOOD Consortium, Wiggs, J. L., Burdon, K. P., Gharahkhani, P., Hewitt, A. W., Mackey, D. A., Macgregor, S., Craig, J. E., Allingham, R. R., Hauser, M., Ashaye, A., Budenz, D. L., Akafo, S., Williams, S. E. I., Kamatani, Y., Nakazawa, T. & Kubo, M., 15 Apr 2018, In: Human Molecular Genetics. 27, 8, p. 1486-1496 11 p.

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    38 Citations (Scopus)
  • Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

    Burdon, K., Macgregor, S., Hewitt, A., Sharma, S., Chidlow, G., Mills, R., Danoy, P., Casson, R., Viswanathan, A., Liu, J., Landers, J., Henders, A., Wood, J., Souzeau, E., Crawford, A., Leo, P., Wang, J., Rochtchina, E., Nyholt, D., Martin, N. & 5 others, Montgomery, G., Mitchell, P., Brown, M., Mackey, D. & Craig, J., Jun 2011, In: Nature Genetics. 43, 6, p. 574-578 5 p.

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    291 Citations (Scopus)
  • Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy

    Afshari, N., Igo, R., Morris, N., Stambolian, D., Sharma, S., V, L., Dunn, S., Stamler, J., Truitt, B., Rimmler, J., Kuot, A., Qin, X., Croasdale, C., Burdon, K., Riazuddin, S., Mills, R., Klebe, S., Minear, M., Zhao, J., Balajonda, E. & 16 others, Rosenwasser, G., Baratz, K., Mootha, V., Patel, S., Gregory, S., Bailey-Wilson, J., Price, M., Price, F., Craig, J., Fingert, J., Gottsch, J., Aldave, A., Klintworth, G., Lass, J., Li, Y. & Iyengar, S., 30 Mar 2017, In: Nature Communications. 8, 8 p., 14898.

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    51 Citations (Scopus)
  • Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos

    International Glaucoma Genetics Consortium, 15 Nov 2016, In: Human Molecular Genetics. 25, 22, p. 5035-5045 11 p.

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

    Verhoeven, V., Hysi, P., Wojciechowski, R., Fan, Q., Guggenheim, J., Höhn, R., MacGregor, S., Hewitt, A., Nag, A., Cheng, C., Yonova-Doing, C., Zhou, X., Ikram, M., Buitendijk, G., McMahon, G., Kemp, J., St Pourcain, B., Simpson, C., Mäkelä, K-M., Lehtimäki, T. & 82 others, Kähönen, M., Paterson, A., Hosseini, S., Wong, H., Xu, L., Jonas, J., Pärssinen, O., Wedenoja, J., Yip, S., Ho, D., Pang, C. P., Chen, L., Burdon, K., Craig, J., Klein, B., Klein, R., Haller, T., Matspalu, A., Khor, C-C., Tai, E-S., Aung, T., Vithana, E., Tay, W-T., Barathi, V., Evans, D., Timpson, N., Verkerk, A., Meitinger, T., Raitakari, O., Hawthorne, F., Spector, T., Karssen, L., Pirastu, M., Murgia, F., Ang, W., Mishra, A., Montgomery, G., Pennell, C., Cumberland, P., Cotlarciuc, I., Mitchell, P., Wang, J., Schache, M., Janmahasatian, S., Igo, R., Lass, J., Chew, E., Iyengar, S., Gorgels, T., Rudan, I., Hayward, C., Wright, A., Polasek, O., Vatavuk, Z., Wilson, J., Fleck, B., Zeller, T., Mirshahi, A., Müller, C., Uitterlinden, A., Rivadeneira, Vingerling, J., Hofman, A., Oostra, B., Amin, N., Bergen, A., Teo, Y-Y., Rahi, J., Vitart, V., Williams, C., Baird, P., Wong, T., Oexle, K., Pfeiffer, N., Mackey, D., Young, T., van Duijn, C., Saw, S-M., Bailey-Wilson, J., Stambolian, D., Klaver, C. & Hammond, C., 1 Mar 2013, In: Nature Genetics. 45, 3, p. 314-318 5 p.

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    251 Citations (Scopus)
  • Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

    Law, M., Bishop, D., Lee, J., Brossard, M., Martin, N., Moses, E., Song, F., Barrett, J., Kumar, R., Easton, D., Pharoah, P., Swerdlow, A., Kypreou, K., Taylor, J., Harland, M., Randerson-Moor, J., Akslen, L., Andresen, P., Avril, M-F., Azizi, E. & 55 others, Scarra, G., Brown, K., Debniak, T., Duffy, D., Elder, D., Fang, S., Friedman, E., Galan, P., Ghiorzo, P., Gillanders, E., Goldstein, A., Gruis, N., Hansson, J., Helsing, P., Hocevar, M., Hoiom, V., Ingvar, C., Kanetsky, P., Chen, W., Landi, M., Lang, J., Lathrop, M., Lubinski, J., Mackie, R., Mann, G., Molven, A., Montgomery, G., Novakovic, S., Olsson, H., Puig, S., Puig-Butille, J., Qureshi, A., Radford-Smith, G., Van Der Stoep, N., Van Doorn, R., Whiteman, D., Craig, J., Schadendorf, D., Simms, L., Burdon, K., Nyholt, D., Pooley, K., Orr, N., Stratigos, A., Cust, A., Ward, S., Hayward, N., Han, J., Schulze, H-J., Dunning, A., Newton Bishop, J., Demenais, F., Amos, C., Macgregor, S. & Iles, M., 27 Aug 2015, In: Nature Genetics. 47, 9, p. 987-995 9 p.

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  • Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma

    International Glaucoma Genetics Consortium, NEIGHBORHOOD Consortium & Pascale, L. R., 25 Jan 2018, In: PloS Genetics. 14, 1, e1007145.

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  • Glaucoma genetics: Where are we? Where will we go?

    Craig, J. & Mackey, D., 1999, In: Current Opinion in Ophthalmology. 10, 2, p. 126-134 9 p.

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    37 Citations (Scopus)
  • Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation

    Mackey, D., Healey, D., Fingert, J., Coote, M., Wong, T., Wilkinson, C., Mccartney, P., Rait, J., De Graaf, A., Stone, E. & Craig, J., 2003, In: Archives of Ophthalmology. 121, 8, p. 1172-1180 9 p., CC.

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    43 Citations (Scopus)
  • Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal-tension glaucoma, and advanced glaucoma

    Burdon, K., Crawford, A., Casson, R., Hewitt, A., Landers, J., Danoy, P., Mackey, D., Mitchell, P., Healey, P. & Craig, J., Aug 2012, In: Ophthalmology. 119, 8, p. 1539-1545 7 p.

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    53 Citations (Scopus)
  • Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

    Souzeau, E., Siggs, O., Zhou, T., Galanopoulos, A., Hodson, T., Taranath, D., Mills, R., Landers, J., Pater, J., Smith, J. E., Elder, J., Rait, J., Giles, P., Phakey, V., Staffieri, S., Kearns, L., Dubowsky, A., Mackey, D., Hewitt, A., Ruddle, J. & 2 others, Burdon, K. & Craig, J., 1 Jun 2017, In: European Journal of Human Genetics. 25, 7, p. 839-847 9 p.

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  • Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations

    Craig, J., Clark, J., Mcleod, J., Kirkland, M., Grant, G., Elder, J., Toohey, M., Kowal, L., Savoia, H., Chen, C., Roberts, S., Wirth, M. & Mackey, D., 2003, In: Archives of Ophthalmology. 121, 12, p. 1753-1761 9 p., CC.

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    52 Citations (Scopus)
  • Heritability of central corneal thickness in nuclear families

    Landers, J., Hewitt, A., Dimasi, D., Charlesworth, J., Straga, T., Mills, R., Savarirayan, R., Mackey, D., Burdon, K. & Craig, J., 2009, In: Investigative Ophthalmology and Visual Science. 50, 9, p. 4087-4090 4 p.

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    33 Citations (Scopus)
  • Heritable features of the optic disc: a novel twin method for determining genetic significance

    Hewitt, A., Poulsen, J., Alward, W., Bennett, S., Budde, W., Cooper, R., Craig, J., Fingert, J., Foster, P., Garway-Heath, D., Green, C., Hammond, C., Hayreh, S., Jonas, J., Kaufman, P., Miller, N., Morgan, W., Newman, N., Quigley, H., Samples, J. & 3 others, Spaeth, G., Pesudovs, K. & Mackey, D., 2007, In: Investigative Ophthalmology and Visual Science. 48, 6, p. 2469-2475 7 p.

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    18 Citations (Scopus)