Improved Prediction of Endoxifen Metabolism by CYP2D6 Genotype in Breast Cancer Patients Treated with Tamoxifen by Schroth, Werner, Winter, Stefan, Mürdter, Thomas, Schaeffeler, Elke, Eccles, Diana, Eccles, Bryony, Chowbay, Balram, Khor, Chiea C, Tfayli, Arafat, Zgheib, Nathalie K, Eichelbaum, Michel, Schwab, Matthias, Brauch, Hiltrud

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Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome by Hirbo, Jibril B, Pasutto, Francesca, Gamazon, Eric R, Evans, Patrick, Pawar, Priyanka, Berner, Daniel, Sealock, Julia, Tao, Ran, Straub, Peter S, Konkashbaev, Anuar I, Breyer, Max A, Schlötzer-Schrehardt, Ursula, Reis, André, Brantley, Jr, Milam A, Khor, Chiea C, Joos, Karen M, Cox, Nancy J

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CD209 genetic polymorphism and tuberculosis disease by Vannberg, Fredrik O, Chapman, Stephen J, Khor, Chiea C, Tosh, Kerrie, Floyd, Sian, Jackson-Sillah, Dolly, Crampin, Amelia, Sichali, Lifted, Bah, Boubacar, Gustafson, Per, Aaby, Peter, McAdam, Keith P W J, Bah-Sow, Oumou, Lienhardt, Christian, Sirugo, Giorgio, Fine, Paul, Hill, Adrian V S

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Leprosy and the adaptation of human toll-like receptor 1 by Wong, Sunny H, Gochhait, Sailesh, Malhotra, Dheeraj, Pettersson, Fredrik H, Teo, Yik Y, Khor, Chiea C, Rautanen, Anna, Chapman, Stephen J, Mills, Tara C, Srivastava, Amit, Rudko, Aleksey, Freidin, Maxim B, Puzyrev, Valery P, Ali, Shafat, Aggarwal, Shweta, Chopra, Rupali, Reddy, Belum S N, Garg, Vijay K, Roy, Suchismita, Meisner, Sarah, Hazra, Sunil K, Saha, Bibhuti, Floyd, Sian, Keating, Brendan J, Kim, Cecilia, Fairfax, Benjamin P, Knight, Julian C, Hill, Philip C, Adegbola, Richard A, Hakonarson, Hakon, Fine, Paul E M, Pitchappan, Ramasamy M, Bamezai, Rameshwar N K, Hill, Adrian V S, Vannberg, Fredrik O

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X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development by Webb, Tom R., Matarin, Mar, Gardner, Jessica C., Kelberman, Dan, Hassan, Hala, Ang, Wei, Michaelides, Michel, Ruddle, Jonathan B., Pennell, Craig E., Yazar, Seyhan, Khor, Chiea C., Aung, Tin, Yogarajah, Mahinda, Robson, Anthony G., Holder, Graham E., Cheetham, Michael E., Traboulsi, Elias I., Moore, Anthony T., Sowden, Jane C., Sisodiya, Sanjay M., Mackey, David A., Tuft, Stephen J., Hardcastle, Alison J.

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A targeted approach to genome-wide studies reveals new genetic associations with central corneal thickness by Benson, Matthew D, Khor, Chiea C, Gage, Philip J, Lehmann, Ordan J

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Mannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema by Chapman, Stephen J, Vannberg, Fredrik O, Khor, Chiea C, Rautanen, Anna, Maskell, Nicholas A, Davies, Christopher W H, Moore, Catrin E, Day, Nicholas P, Crook, Derrick W, Davies, Robert J O, Hill, Adrian V S

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IκB genetic polymorphisms and invasive pneumococcal disease by CHAPMAN, Stephen J, KHOR, Chiea C, DENNY, Paul, DAY, Nicholas P, CROOK, Derrick W, DAVIES, Robert J. O, HILL, Adrian V. S, VANNBERG, Fredrik O, FRODSHAM, Angela, WALLEY, Andrew, MASKELL, Nicholas A, DAVIES, Christopher W. H, SEGAL, Shelley, MOORE, Catrin E, GILLESPIE, Stephen H

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Common NFKBIL2 polymorphisms and susceptibility to pneumococcal disease: a genetic association study by Chapman, Stephen J, Khor, Chiea C, Vannberg, Fredrik O, Rautanen, Anna, Walley, Andrew, Segal, Shelley, Moore, Catrin E, Davies, Robert J O, Day, Nicholas P, Peshu, Norbert, Crook, Derrick W, Berkley, James A, Williams, Thomas N, Scott, J Anthony, Hill, Adrian V S

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Shared pathways to infectious disease susceptibility? by Khor, Chiea C, Hibberd, Martin L

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Functional polymorphisms in the FCN2 gene are not associated with invasive pneumococcal disease by Chapman, Stephen J., Vannberg, Fredrik O., Khor, Chiea C., Segal, Shelley, Moore, Catrin E., Knox, Kyle, Day, Nicholas P., Davies, Robert J.O., Crook, Derrick W., Hill, Adrian V.S.

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Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome by Tadros, Rafik, Mizusawa, Yuka, Postema, Pieter G., Beekman, Leander, Walsh, Roddy, Hasegawa, Kanae, Barc, Julien, Ernsting, Marko, Turkowski, Kari L., Mazzanti, Andrea, Beckmann, Britt M., Shimamoto, Keiko, Diamant, Ulla-Britt, Wijeyeratne, Yanushi D., Kucho, Yu, Robyns, Tomas, Ishikawa, Taisuke, Arbelo, Elena, Christiansen, Michael, Winbo, Annika, Jabbari, Reza, Steinfurt, Johannes, Rudic, Boris, Loeys, Bart, Shoemaker, M. Ben, Weeke, Peter E., Pfeiffer, Ryan, Davies, Brianna, Andorin, Antoine, Hofman, Nynke, Dagradi, Federica, Pedrazzini, Matteo, Tester, David J., Bos, J. Martijn, Sarquella-Brugada, Georgia, Campuzano, Óscar, Platonov, Pyotr G., Stallmeyer, Birgit, Zumhagen, Sven, Nannenberg, Eline A., Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Shaw, Christopher E., Shaw, Pamela J., Morrison, Karen E., Andersen, Peter M., Müller-Nurasyid, Martina, Cusi, Daniele, Barlassina, Cristina, Galan, Pilar, Munter, Markus, Werge, Thomas, Ribasés, Marta, Aung, Tin, Khor, Chiea C., Ozaki, Mineo, Lichtner, Peter, Meitinger, Thomas, van Tintelen, J. Peter, Hoedemaekers, Yvonne, Denjoy, Isabelle, Leenhardt, Antoine, Napolitano, Carlo, Shimizu, Wataru, Schott, Jean-Jacques, Gourraud, Jean-Baptiste, Makiyama, Takeru, Ohno, Seiko, Itoh, Hideki, Krahn, Andrew D., Antzelevitch, Charles, Roden, Dan M., Saenen, Johan, Borggrefe, Martin, Odening, Katja E., Ellinor, Patrick T., Tfelt-Hansen, Jacob, Skinner, Jonathan R., van den Berg, Maarten P., Olesen, Morten Salling, Brugada, Josep, Brugada, Ramón, Breckpot, Jeroen, Yoshinaga, Masao, Behr, Elijah R., Rydberg, Annika, Aiba, Takeshi, Kääb, Stefan, Priori, Silvia G., Guicheney, Pascale, Tan, Hanno L., Newton-Cheh, Christopher, Ackerman, Michael J., Schwartz, Peter J., Schulze-Bahr, Eric, Horie, Minoru, Wilde, Arthur A., Tanck, Michael W.T., Bezzina, Connie R.

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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility by Wessel, Jennifer, Chu, Audrey Y, Willems, Sara M, Dauriz, Marco, Raghavan, Sridharan, Hidalgo, Bertha, An, Ping, Lu, Yingchang, Ehm, Margaret G, Baldridge, Abigail S, Freitag, Daniel F, Garcia, Melissa E, Hara, Kazuo, Jakobsdottir, Johanna, Lange, Leslie A, Layton, Jill C, Li, Man, Morrison, Alanna C, Peters, Marjolein J, Southam, Lorraine, Stoiber, Marcus H, Strawbridge, Rona J, Varga, Tibor V, Barbieri, Caterina, Bombieri, Cristina, Bowden, Donald W, Burns, Sean M, Chen, Yuning, Chen, Yii-DerI, Cheng, Ching-Yu, Ehret, Georg B, Eiriksdottir, Gudny, Escher, Stefan A, Frånberg, Mattias, Gambaro, Giovanni, Goel, Anuj, Grove, Megan L, Karaleftheri, Maria, Kirkpatrick, Andrea, Kraja, Aldi T, Kuusisto, Johanna, Lange, Ethan M, Lee, I T, Lee, Wen-Jane, Leong, Aaron, Liao, Jiemin, Lindgren, Cecilia M, Malerba, Giovanni, Mamakou, Vasiliki, Maruthur, Nisa M, McLeod, Olga, Mohlke, Karen L, Muzny, Donna M, Renström, Frida, Rice, Ken, Sala, Cinzia F, Soranzo, Nicole, Speliotes, Elizabeth K, Stirrups, Kathleen, Thanopoulou, Anastasia, Traglia, Michela, Tsafantakis, Emmanouil, Javad, Sundas, Yanek, Lisa R, Becker, Diane M, Bis, Joshua C, Brown, James B, Ingelsson, Erik, Karter, Andrew J, Lorenzo, Carlos, Peloso, Gina M, Vaidya, Dhananjay, Varma, Rohit, Wagenknecht, Lynne E, Dedoussis, George, Deloukas, Panos, Franco, Oscar H, Gibbs, Richard A, Gudnason, Vilmundur, Hofman, Albert, Jansson, Jan-Håkan, Langenberg, Claudia, Launer, Lenore J, Levy, Daniel, Oostra, Ben A, Padmanabhan, Sandosh, Pankow, James S, Rudan, Igor, Schulze, Matthias B, Smith, Blair H, Walker, Mark, Wong, Tien Y, Laakso, Markku, Borecki, Ingrid B, van Duijn, Cornelia M, Waterworth, Dawn M, Loos, Ruth J.F., Meigs, James B, Scott, Robert A, Goodarzi, Mark O

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SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function by Li, Man, Li, Yong, Weeks, Olivia, Mijatovic, Vladan, Teumer, Alexander, Huffman, Jennifer E, Tromp, Gerard, Fuchsberger, Christian, Gorski, Mathias, Lyytikäinen, Leo-Pekka, Nutile, Teresa, Sedaghat, Sanaz, Sorice, Rossella, Tin, Adrienne, Yang, Qiong, Ahluwalia, Tarunveer S, Arking, Dan E, Bihlmeyer, Nathan A, Böger, Carsten A, Carroll, Robert J, Chasman, Daniel I, Cornelis, Marilyn C, Dehghan, Abbas, Faul, Jessica D, Feitosa, Mary F, Gambaro, Giovanni, Gasparini, Paolo, Giulianini, Franco, Heid, Iris, Huang, Jinyan, Imboden, Medea, Jackson, Anne U, Jeff, Janina, Jhun, Min A, Katz, Ronit, Kifley, Annette, Kilpeläinen, Tuomas O, Kumar, Ashish, Laakso, Markku, Li-Gao, Ruifang, Lohman, Kurt, Lu, Yingchang, Mägi, Reedik, Malerba, Giovanni, Mihailov, Evelin, Mohlke, Karen L, Mook-Kanamori, Dennis O, Robino, Antonietta, Ruderfer, Douglas, Salvi, Erika, Schick, Ursula M, Schulz, Christina-Alexandra, Smith, Albert V, Smith, Jennifer A, Traglia, Michela, Yerges-Armstrong, Laura M, Zhao, Wei, Goodarzi, Mark O, Kraja, Aldi T, Liu, Chunyu, Wessel, Jennifer, Boerwinkle, Eric, Borecki, Ingrid B, Bork-Jensen, Jette, Bottinger, Erwin P, Braga, Daniele, Brandslund, Ivan, Brody, Jennifer A, Campbell, Archie, Carey, David J, Christensen, Cramer, Coresh, Josef, Crook, Errol, Curhan, Gary C, Cusi, Daniele, de Boer, Ian H, de Vries, Aiko P J, Denny, Joshua C, Devuyst, Olivier, Dreisbach, Albert W, Endlich, Karlhans, Esko, Tõnu, Franco, Oscar H, Fulop, Tibor, Gerhard, Glenn S, Glümer, Charlotte, Gottesman, Omri, Grarup, Niels, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hayward, Caroline, Hocking, Lynne, Hofman, Albert, Hu, Frank B, Husemoen, Lise Lotte N, Jackson, Rebecca D, Jørgensen, Torben, Jørgensen, Marit E, Kähönen, Mika

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Combined genotype and haplotype tests for region-based association studies by Zakharov, Sergii, Wong, Tien Yin, Aung, Tin, Vithana, Eranga Nishanthie, Khor, Chiea Chuen, Salim, Agus, Thalamuthu, Anbupalam

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Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome by Lahrouchi, Najim, Tadros, Rafik, Crotti, Lia, Mizusawa, Yuka, Postema, Pieter G, Beekman, Leander, Walsh, Roddy, Hasegawa, Kanae, Barc, Julien, Ernsting, Marko, Turkowski, Kari L, Mazzanti, Andrea, Beckmann, Britt M, Shimamoto, Keiko, Diamant, Ulla-Britt, Wijeyeratne, Yanushi D, Kucho, Yu, Robyns, Tomas, Ishikawa, Taisuke, Arbelo, Elena, Christiansen, Michael, Winbo, Annika, Jabbari, Reza, Lubitz, Steven A, Steinfurt, Johannes, Rudic, Boris, Loeys, Bart, Shoemaker, M Ben, Weeke, Peter E, Pfeiffer, Ryan, Davies, Brianna, Andorin, Antoine, Hofman, Nynke, Dagradi, Federica, Pedrazzini, Matteo, Tester, David J, Bos, J Martijn, Sarquella-Brugada, Georgia, Campuzano, Óscar, Platonov, Pyotr G, Stallmeyer, Birgit, Zumhagen, Sven, Nannenberg, Eline A, Veldink, Jan H, van den Berg, Leonard H, Al-Chalabi, Ammar, Shaw, Christopher E, Shaw, Pamela J, Morrison, Karen E, Andersen, Peter M, Müller-Nurasyid, Martina, Cusi, Daniele, Barlassina, Cristina, Galan, Pilar, Lathrop, Mark, Munter, Markus, Werge, Thomas, Ribasés, Marta, Aung, Tin, Khor, Chiea C, Ozaki, Mineo, Lichtner, Peter, Meitinger, Thomas, van Tintelen, J Peter, Hoedemaekers, Yvonne, Denjoy, Isabelle, Leenhardt, Antoine, Napolitano, Carlo, Shimizu, Wataru, Schott, Jean-Jacques, Gourraud, Jean-Baptiste, Makiyama, Takeru, Ohno, Seiko, Itoh, Hideki, Krahn, Andrew D, Antzelevitch, Charles, Roden, Dan M, Saenen, Johan, Borggrefe, Martin, Odening, Katja E, Ellinor, Patrick T, Tfelt-Hansen, Jacob, Skinner, Jonathan R, van den Berg, Maarten P, Olesen, Morten Salling, Brugada, Josep, Brugada, Ramón, Makita, Naomasa, Breckpot, Jeroen, Yoshinaga, Masao, Behr, Elijah R, Rydberg, Annika, Aiba, Takeshi, Kääb, Stefan, Priori, Silvia G, Guicheney, Pascale, Tan, Hanno L, Newton-Cheh, Christopher, Ackerman, Michael J, Schwartz, Peter J

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Abstract O.17: Whole Genome Sequencing of a six-member African American family with two Kawasaki disease-affected siblings identifies novel susceptibility variants by Kim, Jihoon, Shimizu, Chisato, Yang, Hai, Harismendy, Olivier, Truong Hoang, Long, Levy, Eric, Cimaz, Rolando, Burgner, David, Yeung, Rae S, Khor, Chiea C, Davila, Sonia, Levin, Michael, Kuijpers, Taco W, Hibberd, Martin L, Ohno-Machado, Lucila, Burns, Jane C

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Abstract O.16: Comprehensive Genotyping Of The FCGR2/3 Locus Reveals A Novel Association Of FCGR2C-ORF With Susceptibility To Kawasaki Disease by Kuijpers, Taco W, Tacke, Carline E, Nagelkerke, Sietse Q, Breunis, Willemijn B, Hoang, Long T, Png, Eileen, Geissler, Judy, Tanck, Michael W, Ellis, Justine A, Ponsonby, Anne L, Davila, Sonia, Khor, Chiea C, de Boer, Martin, van der Heijden, Joris, Fijnvandraat, Karin, van der Schoot, E., van den Berg, Timo K, Yeung, Rae S, Levin, Michael L, Burgner, David, Shimizu, Chisato, Burns, Jane C, Hibberd, Martin L

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Leprosy and the Adaptation of Human Toll-Like Receptor 1: e1000979 by Wong, Sunny H, Gochhait, Sailesh, Malhotra, Dheeraj, Pettersson, Fredrik H, Teo, Yik Y, Khor, Chiea C, Rautanen, Anna, Chapman, Stephen J, Mills, Tara C, Srivastava, Amit, Rudko, Aleksey, Freidin, Maxim B, Puzyrev, Valery P, Ali, Shafat, Aggarwal, Shweta, Chopra, Rupali, Reddy, Belum SN, Garg, Vijay K, Roy, Suchismita, Meisner, Sarah, Hazra, Sunil K, Saha, Bibhuti, Floyd, Sian, Keating, Brendan J, Kim, Cecilia, Fairfax, Benjamin P, Knight, Julian C, Hill, Philip C, Adegbola, Richard A, Hakonarson, Hakon, Fine, Paul EM, Pitchappan, Ramasamy M, Bamezai, Rameshwar NK, Hill, Adrian VS, Vannberg, Fredrik O

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IkappaB genetic polymorphisms and invasive pneumococcal disease by Chapman, Stephen J, Khor, Chiea C, Vannberg, Fredrik O, Frodsham, Angela, Walley, Andrew, Maskell, Nicholas A, Davies, Christopher W H, Segal, Shelley, Moore, Catrin E, Gillespie, Stephen H, Denny, Paul, Day, Nicholas P, Crook, Derrick W, Davies, Robert J O, Hill, Adrian V S

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