Differences in the Surgical Outcomes of Glaucoma Surgery in Patients of African Caribbean Descent by Nagar, A. M., Maghsoudlou, P., Wormald, R., Barton, K., Hysi, P., Lim, K. S.

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Germline Genetic Contributions to Risk for Esophageal Adenocarcinoma, Barrett's Esophagus, and Gastroesophageal Reflux by EK, Weronica E, LEVINE, David M, ROMERO, Yvonne, CHOW, Wong-Ho, MURRAY, Liam J, GAMMON, Marilie D, LIU, Geoffrey, BERNSTEIN, Leslie, CASSON, Alan G, RISCH, Harvey A, SHAHEEN, Nicholas J, BIRD, Nigel C, D'AMATO, Mauro, REID, Brian J, CORLEY, Douglas A, HARDIE, Laura J, WEIMIN YE, WU, Anna H, ZUCCHELLI, Marco, SPECTOR, Tim D, HYSI, Pirro, VAUGHAN, Thomas L, WHITEMAN, David C, PEDERSEN, Nancy L, MACGREGOR, Stuart, MAGNUSSON, Patrik K. E, BRESSO, Francesca, ONSTAD, Lynn E, SCHMIDT, Peter T, TÖRNBLOM, Hans, NORDENSTEDT, Helena

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UK Biobank retinal imaging grading: methodology, baseline characteristics and findings for common ocular diseases by Warwick, Alasdair N., Curran, Katie, Hamill, Barbra, Stuart, Kelsey, Khawaja, Anthony P., Foster, Paul J., Lotery, Andrew J., Quinn, Michael, Madhusudhan, Savita, Balaskas, Konstantinos, Peto, Tunde

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A meta‐analysis of reflux genome‐wide association studies in 6750 Northern Europeans from the general population by Bonfiglio, F., Hysi, P. G., Ek, W., Karhunen, V., Rivera, N. V., Männikkö, M., Nordenstedt, H., Zucchelli, M., Bresso, F., Williams, F., Tornblom, H., Magnusson, P. K., Pedersen, N. L., Ronkainen, J., Schmidt, P. T., D'Amato, M.

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Correction: UK Biobank retinal imaging grading: methodology, baseline characteristics and findings for common ocular diseases by Warwick, Alasdair N., Curran, Katie, Hamill, Barbra, Stuart, Kelsey, Khawaja, Anthony P., Foster, Paul J., Lotery, Andrew J., Quinn, Michael, Madhusudhan, Savita, Balaskas, Konstantinos, Peto, Tunde

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A GWAS meta‐analysis from 5 population‐based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome by Bonfiglio, F., Henström, M., Nag, A., Hadizadeh, F., Zheng, T., Cenit, M. C., Tigchelaar, E., Williams, F., Reznichenko, A., Ek, W. E., Rivera, N. V., Homuth, G., Aghdassi, A. A., Kacprowski, T., Männikkö, M., Karhunen, V., Bujanda, L., Rafter, J., Wijmenga, C., Ronkainen, J., Hysi, P., Zhernakova, A., D'Amato, M.

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Validation of printed and computerised crowded Kay picture logMAR tests against gold standard ETDRS acuity test chart measurements in adult and amblyopic paediatric subjects by Shah, N, Laidlaw, D A H, Rashid, S, Hysi, P

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Genome‐wide association studies for the identification of keratoconus susceptibility regions by HYSI, P

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Association between a complex insertion/deletion polymorphism in NOD1 (CARD4) and susceptibility to inflammatory bowel disease by McGovern, Dermot P.B., Hysi, Pirro, Ahmad, Tariq, van Heel, David A., Moffatt, Miriam F., Carey, Alisoun, Cookson, William O.C., Jewell, Derek P.

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NOD1 variation, immunoglobulin E and asthma by Hysi, Pirro, Kabesch, Michael, Moffatt, Miriam F., Schedel, Michaela, Carr, David, Zhang, Youming, Boardman, Brenda, von Mutius, Erika, Weiland, Stephan K., Leupold, Wolfgang, Fritzsch, Christian, Klopp, Norman, Musk, A. William, James, Alan, Nunez, Gabriel, Inohara, Naohiro, Cookson, William O.C.

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Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation by Artigas, María Soler, Wain, Louise V., Miller, Suzanne, Kheirallah, Abdul Kader, Huffman, Jennifer E., Ntalla, Ioanna, Shrine, Nick, Obeidat, Ma’en, Trochet, Holly, McArdle, Wendy L., Alves, Alexessander Couto, Hui, Jennie, Zhao, Jing Hua, Joshi, Peter K., Teumer, Alexander, Albrecht, Eva, Imboden, Medea, Rawal, Rajesh, Lopez, Lorna M., Marten, Jonathan, Enroth, Stefan, Surakka, Ida, Polasek, Ozren, Lyytikäinen, Leo-Pekka, Granell, Raquel, Hysi, Pirro G., Flexeder, Claudia, Mahajan, Anubha, Beilby, John, Bossé, Yohan, Brandsma, Corry-Anke, Campbell, Harry, Gieger, Christian, Gläser, Sven, González, Juan R., Grallert, Harald, Hammond, Chris J., Harris, Sarah E., Hartikainen, Anna-Liisa, Heliövaara, Markku, Henderson, John, Hocking, Lynne, Horikoshi, Momoko, Hutri-Kähönen, Nina, Ingelsson, Erik, Johansson, Åsa, Kemp, John P., Kolcic, Ivana, Kumar, Ashish, Lind, Lars, Melén, Erik, Musk, Arthur W., Navarro, Pau, Nickle, David C., Padmanabhan, Sandosh, Raitakari, Olli T., Ried, Janina S., Ripatti, Samuli, Schulz, Holger, Scott, Robert A., Sin, Don D., Starr, John M., Viñuela, Ana, Völzke, Henry, Wild, Sarah H., Wright, Alan F., Zemunik, Tatijana, Jarvis, Deborah L., Spector, Tim D., Evans, David M., Lehtimäki, Terho, Vitart, Veronique, Kähönen, Mika, Gyllensten, Ulf, Rudan, Igor, Deary, Ian J., Karrasch, Stefan, Probst-Hensch, Nicole M., Heinrich, Joachim, Stubbe, Beate, Wilson, James F., Wareham, Nicholas J., James, Alan L., Morris, Andrew P., Jarvelin, Marjo-Riitta, Hayward, Caroline, Sayers, Ian, Strachan, David P., Hall, Ian P., Tobin, Martin D.

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Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 by Grosche, Sarah, Marenholz, Ingo, Esparza-Gordillo, Jorge, Arnau-Soler, Aleix, Pairo-Castineira, Erola, Rüschendorf, Franz, Ahluwalia, Tarunveer S., Almqvist, Catarina, Arnold, Andreas, Baurecht, Hansjörg, Bisgaard, Hans, Bønnelykke, Klaus, Brown, Sara J., Bustamante, Mariona, Curtin, John A., Custovic, Adnan, Dharmage, Shyamali C., Esplugues, Ana, Falchi, Mario, Fernandez-Orth, Dietmar, Ferreira, Manuel A. R., Franke, Andre, Gerdes, Sascha, Gieger, Christian, Hakonarson, Hakon, Holt, Patrick G., Homuth, Georg, Hubner, Norbert, Hysi, Pirro G., Jarvelin, Marjo-Riitta, Karlsson, Robert, Koppelman, Gerard H., Lau, Susanne, Lutz, Manuel, Magnusson, Patrik K. E., Marks, Guy B., Müller-Nurasyid, Martina, Nöthen, Markus M., Paternoster, Lavinia, Pennell, Craig E., Peters, Annette, Rawlik, Konrad, Robertson, Colin F., Rodriguez, Elke, Sebert, Sylvain, Simpson, Angela, Sleiman, Patrick M. A., Standl, Marie, Stölzl, Dora, Strauch, Konstantin, Szwajda, Agnieszka, Tenesa, Albert, Thompson, Philip J., Ullemar, Vilhelmina, Visconti, Alessia, Vonk, Judith M., Wang, Carol A., Weidinger, Stephan, Wielscher, Matthias, Worth, Catherine L., Xu, Chen-Jian, Lee, Young-Ae

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A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration by de Vries, Paul S, Chasman, Daniel I, Sabater-Lleal, Maria, Chen, Ming-Huei, Huffman, Jennifer E, Steri, Maristella, Tang, Weihong, Teumer, Alexander, Marioni, Riccardo E, Grossmann, Vera, Hottenga, Jouke J, Trompet, Stella, Müller-Nurasyid, Martina, Zhao, Jing Hua, Brody, Jennifer A, Kleber, Marcus E, Guo, Xiuqing, Wang, Jie Jin, Auer, Paul L, Attia, John R, Yanek, Lisa R, Ahluwalia, Tarunveer S, Lahti, Jari, Venturini, Cristina, Tanaka, Toshiko, Bielak, Lawrence F, Joshi, Peter K, Rocanin-Arjo, Ares, Kolcic, Ivana, Navarro, Pau, Rose, Lynda M, Oldmeadow, Christopher, Riess, Helene, Mazur, Johanna, Basu, Saonli, Goel, Anuj, Yang, Qiong, Ghanbari, Mohsen, Willemsen, Gonneke, Rumley, Ann, Fiorillo, Edoardo, de Craen, Anton J M, Grotevendt, Anne, Scott, Robert, Taylor, Kent D, Delgado, Graciela E, Yao, Jie, Kifley, Annette, Kooperberg, Charles, Qayyum, Rehan, Lopez, Lorna M, Berentzen, Tina L, Räikkönen, Katri, Mangino, Massimo, Bandinelli, Stefania, Peyser, Patricia A, Wild, Sarah, Trégouët, David-Alexandre, Wright, Alan F, Marten, Jonathan, Zemunik, Tatijana, Morrison, Alanna C, Sennblad, Bengt, Tofler, Geoffrey, de Maat, Moniek P M, de Geus, Eco J C, Lowe, Gordon D, Zoledziewska, Magdalena, Sattar, Naveed, Binder, Harald, Völker, Uwe, Waldenberger, Melanie, Khaw, Kay-Tee, Mcknight, Barbara, Huang, Jie, Jenny, Nancy S, Holliday, Elizabeth G, Qi, Lihong, Mcevoy, Mark G, Becker, Diane M, Starr, John M, Sarin, Antti-Pekka, Hysi, Pirro G, Hernandez, Dena G, Jhun, Min A, Campbell, Harry, Hamsten, Anders, Rivadeneira, Fernando, Mcardle, Wendy L, Slagboom, P Eline, Zeller, Tanja, Koenig, Wolfgang, Psaty, Bruce M, Haritunians, Talin, Liu, Jingmin, Palotie, Aarno, Uitterlinden, André G, Stott, David J, Hofman, Albert, Franco, Oscar H

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Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study by de Vries, Paul S, Sabater-Lleal, Maria, Chasman, Daniel I, Trompet, Stella, Ahluwalia, Tarunveer S, Teumer, Alexander, Kleber, Marcus E, Chen, Ming-Huei, Wang, Jie Jin, Attia, John R, Marioni, Riccardo E, Steri, Maristella, Weng, Lu-Chen, Pool, Rene, Grossmann, Vera, Brody, Jennifer A, Venturini, Cristina, Tanaka, Toshiko, Rose, Lynda M, Oldmeadow, Christopher, Mazur, Johanna, Basu, Saonli, Frånberg, Mattias, Yang, Qiong, Ligthart, Symen, Hottenga, Jouke J, Rumley, Ann, Mulas, Antonella, de Craen, Anton J M, Grotevendt, Anne, Taylor, Kent D, Delgado, Graciela E, Kifley, Annette, Lopez, Lorna M, Berentzen, Tina L, Mangino, Massimo, Bandinelli, Stefania, Morrison, Alanna C, Hamsten, Anders, Tofler, Geoffrey, de Maat, Moniek P M, Draisma, Harmen H M, Lowe, Gordon D, Zoledziewska, Magdalena, Sattar, Naveed, Lackner, Karl J, Völker, Uwe, McKnight, Barbara, Huang, Jie, Holliday, Elizabeth G, McEvoy, Mark A, Starr, John M, Hysi, Pirro G, Hernandez, Dena G, Guan, Weihua, Rivadeneira, Fernando, McArdle, Wendy L, Slagboom, P Eline, Zeller, Tanja, Psaty, Bruce M, Uitterlinden, André G, de Geus, Eco J C, Stott, David J, Binder, Harald, Hofman, Albert, Franco, Oscar H, Rotter, Jerome I, Ferrucci, Luigi, Spector, Tim D, Deary, Ian J, März, Winfried, Greinacher, Andreas, Wild, Philipp S, Cucca, Francesco, Boomsma, Dorret I, Watkins, Hugh, Tang, Weihong, Ridker, Paul M, Jukema, Jan W, Scott, Rodney J, Mitchell, Paul, Hansen, Torben, O'Donnell, Christopher J, Smith, Nicholas L, Strachan, David P, Dehghan, Abbas

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D101 INFLAMMATION IN THE TRANSPLANTED LUNG AND FIBROSIS: Targeted Sequencing Identified Novel Common Genetic Variants Of Tollip Associated With Idiopathic Pulmonary Fibrosis Suscep... by Ma, S-F, Acosta-Herrera, M, Huang, Y, Barreto-Luis, A, Vij, R, Oldham, J, Hysi, P, Flores, C, Noth, I

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Validation of printed and computerised crowded Kay picture IogMAR tests against gold standard ETDRS acuity test chart measurements in adult and amblyopic paediatric subjects by SHAH, N, LAIDLAW, Dah, RASHID, S, HYSI, P

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A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort by Nag, Abhishek, Venturini, Cristina, Small, Kerrin S, Young, Terri L, Viswanathan, Ananth C, Mackey, David A, Hysi, Pirro G, Hammond, Christopher

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Haplotypes and asthma by Moffatt, Miriam, Hysi, Pirro, Cookson, William

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Genome-wide association studies of gastroesophageal reflux symptoms in 25 000 individuals from Swedish, Finnish and UK population-based cohorts by D'Amato, M, Bonfiglio, F, Hysi, P, Ek, W, Rivera, NV, Nordenstedt, H, Bresso, F, Schmidt, PT, Williams, F, Tornblom, H, Magnusson, P, Pedersen, NL, Mannikko, M, Karhunen, V, Ronkainen, J

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LD mapping of maternally and non-maternally derived alleles and atopy in Fc[varepsilon]RI- beta by Traherne, JA, Hill, M R, Hysi, P, D'Amato, M, Broxholme, J, Mott, R, Moffatt, M F, Cookson, WOCM

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