Improved Prediction of Endoxifen Metabolism by CYP2D6 Genotype in Breast Cancer Patients Treated with Tamoxifen von 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 von 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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Leprosy and the adaptation of human toll-like receptor 1 von 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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CD209 genetic polymorphism and tuberculosis disease von 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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Prediction of Susceptibility to First-Line Tuberculosis Drugs by DNA Sequencing von Allix-Béguec, Caroline, Arandjelovic, Irena, Bi, Lijun, Beckert, Patrick, Bonnet, Maryline, Bradley, Phelim, Cabibbe, Andrea M, Cancino-Muñoz, Irving, Caulfield, Mark J, Chaiprasert, Angkana, Cirillo, Daniela M, Clifton, David A, Comas, Iñaki, Crook, Derrick W, De Filippo, Maria R, de Neeling, Han, Diel, Roland, Drobniewski, Francis A, Faksri, Kiatichai, Farhat, Maha R, Fleming, Joy, Fowler, Philip, Fowler, Tom A, Gao, Qian, Gardy, Jennifer, Gascoyne-Binzi, Deborah, Gibertoni-Cruz, Ana-Luiza, Gil-Brusola, Ana, Golubchik, Tanya, Gonzalo, Ximena, Grandjean, Louis, He, Guangxue, Guthrie, Jennifer L, Hoosdally, Sarah, Hunt, Martin, Iqbal, Zamin, Ismail, Nazir, Johnston, James, Khanzada, Faisal M, Khor, Chiea C, Kohl, Thomas A, Kong, Clare, Lipworth, Sam, Liu, Qingyun, Maphalala, Gugu, Martinez, Elena, Mathys, Vanessa, Merker, Matthias, Miotto, Paolo, Mistry, Nerges, Moore, David A J, Murray, Megan, Niemann, Stefan, Omar, Shaheed V, Ong, Rick T-H, Peto, Tim E A, Posey, James E, Prammananan, Therdsak, Pym, Alexander, Rodrigues, Camilla, Rodrigues, Mabel, Rodwell, Timothy, Rossolini, Gian M, Sánchez Padilla, Elisabeth, Schito, Marco, Shen, Xin, Shendure, Jay, Sintchenko, Vitali, Sloutsky, Alex, Smith, E Grace, Snyder, Matthew, Soetaert, Karine, Starks, Angela M, Supply, Philip, Suriyapol, Prapat, Tahseen, Sabira, Tang, Patrick, Teo, Yik-Ying, Thuong, Thuong N T, Thwaites, Guy, Tortoli, Enrico, van Soolingen, Dick, Walker, A Sarah, Walker, Timothy M, Wilcox, Mark, Wilson, Daniel J, Wyllie, David, Yang, Yang, Zhang, Hongtai, Zhao, Yanlin, Zhu, Baoli

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X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development von 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 Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis von Khan, Amir, Sow, Oumou Y, Lienhardt, Christian, Day, Nicholas P, Grignani, Robert T, Maitland, Kathryn, Vannberg, Fredrik O, Williams, Thomas N, Crook, Derrick W, Aucan, Christophe, Segal, Shelley, Peshu, Nobert, Aaby, Peter, O'Neill, Luke A J, Kyrieleis, Otto, Moore, Catrin E, Sillah, Jackson, Chapman, Stephen J, Walley, Andrew J, Khor, Chiea C, Dunne, Aisling, Scott, Anthony, Campbell, Sarah J, Murphy, Caroline, Yala, Djamel, Berkley, James A, Ling, Edmund Y, Frodsham, Angela J, Knox, Kyle, Davies, Robert J O, Marsh, Kevin, Hill, Adrian V S, Kwiatkowski, Dominic P, Sirugo, Giorgio

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

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cMET and Refractive Error Progression in Children von Khor, Chiea C., MBBS, DPhil, Grignani, Robert, MBBS, DPhil, Ng, Daniel P.K., PhD, Toh, Kai Yee, BSc, Chia, Kee-Seng, MPH, PhD, Tan, Donald, FRCOpth, Goh, Denise L.M., MD, MRCPCH, Saw, Seang-Mei, MPH, PhD

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CISH and Susceptibility to Infectious Diseases von Khor, Chiea C, Vannberg, Fredrik O, Chapman, Stephen J, Guo, Haiyan, Wong, Sunny H, Walley, Andrew J, Vukcevic, Damjan, Rautanen, Anna, Mills, Tara C, Chang, Kwok-Chiu, Kam, Kai-Man, Crampin, Amelia C, Ngwira, Bagrey, Leung, Chi-Chiu, Tam, Cheuk-Ming, Chan, Chiu-Yeung, Sung, Joseph J.Y, Yew, Wing-Wai, Toh, Kai-Yee, Tay, Stacey K.H, Kwiatkowski, Dominic, Lienhardt, Christian, Hien, Tran-Tinh, Day, Nicholas P, Peshu, Nobert, Marsh, Kevin, Maitland, Kathryn, Scott, J. Anthony, Williams, Thomas N, Berkley, James A, Floyd, Sian, Tang, Nelson L.S, Fine, Paul E.M, Goh, Denise L.M, Hill, Adrian V.S

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Hepatocyte Growth Factor and Retinal Arteriolar Diameter in Singapore Chinese von Khor, Chiea C., MBBS, DPhil, Fan, Qiao, PhD, Goh, Liang-Kee, PhD, Wong, Tien Y., MD, PhD, Li, Yi-Ju, PhD, Cheung, Ning, MD, Seielstad, Mark, PhD, Goh, Denise L.M., MD, Young, Terri L., MD, Tai, E.-Shyong, MD, Saw, Seang-Mei, MD, PhD

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Mannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema von 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 von 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 von 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? von Khor, Chiea C, Hibberd, Martin L

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PTPN22 and invasive bacterial disease von Chapman, Stephen J, Khor, Chiea C, Vannberg, Fredrik O, Maskell, Nicholas A, Davies, Christopher WH, Hedley, Emma L, Segal, Shelley, Moore, Catrin E, Knox, Kyle, Day, Nicholas P, Gillespie, Stephen H, Crook, Derrick W, Davies, Robert JO, Hill, Adrian VS

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Functional polymorphisms in the FCN2 gene are not associated with invasive pneumococcal disease von 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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Reply to "Analysis of association of the TIRAP (MAL) S180L variant and tuberculosis in three populations" von Hill, Andrian VS, Khor, Chiea C, Chapman, Stephen J, Vannberg, Fredrik O, O'Neill, Luke AJ

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SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function von 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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Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome von 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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