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| | Issue Date | Title | Author(s) |
| 1 | 2015 | A highly efficient CMOS nanoplasmonic crystal enhanced slow-wave thermal emitter improves infrared gas-sensing devices | Saw, W.-Y ; Liu, X ; Khor, C.-C ; Takeuchi, F; Katsuya, T; Kimura, R; Nabika, T; Ohkubo, T; Tabara, Y; Yamamoto, K; Yokota, M; Akiyama, K; Asano, H; Asayama, K; Haga, T; Hara, A; Hirose, T; Hosaka, M; Ichihara, S; Imai, Y; Inoue, R; Ishiguro, A; Isomura, M; Isono, M; Kamide, K; Kato, N; Kikuya, M; Kohara, K; Matsubara, T; Matsuda, A; Metoki, H; Miki, T; Murakami, K; Nakatochi, M; Ogihara, T; Ohnaka, K; Rakugi, H; Satoh, M; Shiwaku, K; Sugimoto, K; Takami, Y; Takayanagi, R; Tsubota-Utsugi, M; Yamamoto, K; Yamasaki, M; Yasui, D; Teo, Y.-Y ; Japanese Genome Variation Consortium; Pusch, A; De Luca, A; Oh, S.S; Wuestner, S; Roschuk, T; Chen, Y ; Boual, S; Ali, Z; Phillips, C.C; Hong, M ; Maier, S.A; Udrea, F; Hopper, R.H; Hess, O |
| 2 | 2017 | A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy | Seco, C.Z; Castells-Noba A.; Joo, S.-H; Schraders, M.; Foo, J.N.; Van Der Voet, M.; Velan, S.S ; Nijhof, B.; Oostrik, J.; De Vrieze, E.; Katana, R.; Mansoor, A.; Huynen, M.; Szklarczyk, R.; Oti, M.; Tranebjarg, L.; Van Wijk, E.; Scheffer-De Gooyert, J.M.; Siddique, S.; Baets, J.; De Jonghe, P.; Kazmi, S.A.R.; Sadananthan, S.A ; Van De Warrenburg, B.P.; Khor, C.C ; Göpfert, M.C.; Qamar, R.; Schenck, A.; Kremer, H.; Siddiqi, S. |
| 3 | 2011 | A hybrid framework for genome wide epistasis discovery | Tan, Z.; Zhang, Z.; Liu, J.; Kwoh, C.K.; Ong, S.H. ; Teo, Y.Y. ; Khor, C.C. ; Tai, E.S.; Aung, T.; Vithana, E.; Wong, T.Y. |
| 4 | 2014 | A novel splice-site mutation in ALS establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias | Siddiqi S.; Foo J.N.; Vu A.; Azim S.; Silver D.L. ; Mansoor A.; Tay S.K.H. ; Abbasi S.; Hashmi A.H.; Janjua J.; Khalid S.; Tai E.S. ; Yeo G.W.; Khor C.C. |
| 5 | 7-Nov-2013 | A study assessing the association of glycated hemoglobin a1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of asian ancestry | Chen, P.; Ong, R.T.-H. ; Tay, W.-T.; Sim, X. ; Ali, M.; Xu, H. ; Suo, C. ; Liu, J.; Chia, K.-S. ; Vithana, E.; Young, T.L.; Aung, T.; Lim, W.-Y. ; Khor, C.-C. ; Cheng, C.-Y. ; Wong, T.-Y. ; Teo, Y.-Y. ; Tai, E.-S. |
| 6 | 2014 | ABCC5, a Gene That Influences the Anterior Chamber Depth, Is Associated with Primary Angle Closure Glaucoma | Nongpiur M.E.; Khor C.C. ; Jia H.; Cornes B.K.; Chen L.-J.; Qiao C.; Nair K.S.; Cheng C.-Y. ; Xu L.; George R.; Tan D.; Abu-Amero K.; Perera S.A.; Ozaki M.; Mizoguchi T.; Kurimoto Y.; Low S.; Tajudin L.-S.A.; Ho C.-L.; Tham C.C.Y.; Soto I.; Chew P.T.K. ; Wong H.-T.; Shantha B.; Kuroda M.; Osman E.A.; Tang G.; Fan S.; Meng H.; Wang H.; Feng B.; Yong V.H.K.; Ting S.M.L.; Li Y.; Wang Y.-X.; Li Z.; Lavanya R.; Wu R.-Y.; Zheng Y.-F.; Su D.H.; Loon S.-C.; Allingham R.R.; Hauser M.A.; Soumittra N.; Ramprasad V.L.; Waseem N.; Yaakub A.; Chia K.-S. ; Kumaramanickavel G.; Wong T.T.; How A.C.; Chau T.N.B.; Simmons C.P.; Bei J.-X.; Zeng Y.-X.; Bhattacharya S.S.; Zhang M.; Tan D.T.; Teo Y.-Y. ; Al-Obeidan S.A.; Hon D.N.; Tai E.-S. ; Saw S.-M. ; Foster P.J.; Vijaya L.; Jonas J.B.; Wong T.-Y. ; John S.W.M.; Pang C.-P.; Vithana E.N.; Wang N.; Aung T. |
| 7 | 2014 | Analysis of non-synonymous-coding variants of parkinson's disease-related pathogenic and susceptibility genes in East Asian populations | Foo J.N.; Tan L.C. ; Liany H.; Koh T.H.; Irwan I.D.; Ng Y.Y.; Ahmad-Annuar A.; Au W.-L. ; Aung T. ; Chan A.Y.Y.; Chong S.-A.; Chung S.J.; Jung Y.; Khor C.C. ; Kim J.; Lee J. ; Lim S.-Y.; Mok V.; Prakash K.-M. ; Song K.; Tai E.-S. ; Vithana E.N. ; Wong T.-Y. ; Tan E.-K. ; Liu J. |
| 8 | 2019 | Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study | Huang, T.; Wang, T.; Zheng, Y.; Ellervik, C.; Li, X.; Gao, M.; Fang, Z.; Chai, J.-F. ; Ahluwalia, T.V.S.; Wang, Y.; Voortman, T.; Noordam, R.; Frazier-Wood, A.; Scholz, M.; Sonestedt, E.; Akiyama, M.; Dorajoo, R. ; Zhou, A.; Kilpeläinen, T.O.; Kleber, M.E.; Crozier, S.R.; Godfrey, K.M.; Lemaitre, R.; Felix, J.F.; Shi, Y. ; Gupta, P. ; Khor, C.-C. ; Lehtimäki, T.; Wang, C.A.; Tiesler, C.M.T.; Thiering, E.; Standl, M.; Rzehak, P.; Marouli, E.; He, M.; Lecoeur, C.; Corella, D.; Lai, C.-Q.; Moreno, L.A.; Pitkänen, N.; Boreham, C.A.; Zhang, T.; Saw, S.M. ; Ridker, P.M.; Graff, M.; van Rooij, F.J.A.; Uitterlinden, A.G.; Hofman, A.; van Heemst, D.; Rosendaal, F.R.; de Mutsert, R.; Burkhardt, R.; Schulz, C.-A.; Ericson, U.; Kamatani, Y.; Yuan, J.-M.; Power, C.; Hansen, T.; Sørensen, T.I.A.; Tjønneland, A.; Overvad, K.; Delgado, G.; Cooper, C.; Djousse, L.; Rivadeneira, F.; Jameson, K.; Zhao, W.; Liu, J. ; Lee, N.R.; Raitakari, O.; Kähönen, M.; Viikari, J.; Grote, V.; Langhendries, J.-P.; Koletzko, B.; Escribano, J.; Verduci, E.; Dedoussis, G.; Yu, C.; Tham, Y.C.; Lim, B.; Lim, S.H.; Froguel, P.; Balkau, B.; Fink, N.R.; Vinding, R.K.; Sevelsted, A.; Bisgaard, H.; Coltell, O.; Dallongeville, J.; Gottrand, F.; Pahkala, K.; Niinikoski, H.; Hyppönen, E.; Pedersen, O.; März, W.; Inskip, H.; Jaddoe, V.W.V.; Dennison, E.; Wong, T.Y.; Sabanayagam, C.; Tai, E.-S. ; Mohlke, K.L.; Mackey, D.A.; Gruszfeld, D.; Deloukas, P.; Tucker, K.L.; Fumeron, F.; Bønnelykke, K.; Rossing, P.; Estruch, R.; Ordovas, J.M.; Arnett, D.K.; Meirhaeghe, A.; Amouyel, P.; Cheng, C.-Y. ; Sim, X. ; Teo, Y.Y. ; van Dam, R.M. ; Koh, W.-P. ; Orho-Melander, M.; Loeffler, M.; Kubo, M.; Thiery, J.; Mook-Kanamori, D.O.; Mozaffarian, D.; Psaty, B.M.; Franco, O.H.; Wu, T.; North, K.E.; Davey Smith, G.; Chavarro, J.E.; Chasman, D.I.; Qi, L.; BIRTH-GENE (BIG) Study Working Group. |
| 9 | Jul-2011 | Association of TCF4 gene polymorphisms with Fuchs' corneal dystrophy in the Chinese | Thalamuthu, A.; Khor, C.C. ; Venkataraman, D.; Koh, L.W.; Tan, D.T.H.; Aung, T.; Mehta, J.S. ; Vithana, E.N. |
| 10 | 2016 | Branched peptide, B2088, disrupts the supramolecular organization of lipopolysaccharides and sensitizes the gram-negative bacteria | Fan, Q ; Guo, X; Tideman, J.W.L; Williams, K.M; Yazar, S; Hosseini, S.M; Howe, L.D; Pourcain, B.S; Evans, D.M; Timpson, N.J; McMahon, G; Hysi, P.G; Krapohl, E; Wang, Y.X; Jonas, J.B; Baird, P.N; Wang, J.J ; Cheng, C.-Y ; Teo, Y.-Y ; Wong, T.-Y ; Ding, X; Wojciechowski, R; Young, T.L ; Pärssinen, O; Oexle, K; Pfeiffer, N; Bailey-Wilson, J.E; Paterson, A.D; Klaver, C.C.W; Plomin, R; Hammond, C.J; He, M; Saw, S.-M ; Guggenheim, J.A; Meguro, A; Wright, A.F; Hewitt, A.W; Young, A.L; Veluchamy, A.B ; Metspalu, A; Döring, A; Khawaja, A.P; Klein, B.E; St Pourcain, B; Fleck, B; Klaver, C.C.W; Hayward, C; Williams, C; Delcourt, C; Pang, C.P; Khor, C.-C ; Gieger, C; Simpson, C.L; Van Duijn, C.M; Mackey, D.A; Stambolian, D; Chew, E; Tai, E.-S ; Mihailov, E; Smith, G.D; Biino, G; Campbell, H; Rudan, I; Seppälä, I; Kaprio, J; Wilson, J.F; Craig, J.E; Ried, J.S; Korobelnik, J.-F; Fondran, J.R; Liao, J ; Zhao, J.H; Xie, J; Kemp, J.P; Lass, J.H; Rahi, J.S; Wedenoja, J; Mäkelä, K.-M; Burdon, K.P; Khaw, K.-T; Yamashiro, K; Chen, L.J; Xu, L; Farrer, L; Ikram, M.K ; Deangelis, M.M; Morrison, M; Schache, M; Pirastu, M; Miyake, M; Yap, M.K.H; Fossarello, M; Kähönen, M; Tedja, M.S; Yoshimura, N; Martin, N.G; Wareham, N.J; Mizuki, N; Raitakari, O; Polasek, O; Tam, P.O; Foster, P.J; Mitchell, P; Chen, P ; Cumberland, P; Gharahkhani, P; Höhn, R; Fogarty, R.D; Luben, R.N; Igo, R.P; Klein, R; Janmahasatian, S; Yip, S.P; Feng, S; Vaccargiu, S; Panda-Jonas, S; MacGregor, S; Iyengar, S.K; Rantanen, T; Lehtimäki, T; Meitinger, T; Aung, T ; Haller, T; Vitart, V; Nangia, V; Verhoeven, V.J.M; Jhanji, V; Zhao, W; Chen, W; Zhou, X; Lu, Y; Vatavuk, Z; The CREAM Consortium; Lakshminarayanan, R ; Tan, W.X; Aung, T.T; Goh, E.T.L; Muruganantham, N; Li, J ; Chang, J.Y.T; Dikshit, N ; Saraswathi, P; Lim, R.R; Kang, T.S ; Balamuralidhar, V ; Sukumaran, B ; Verma, C.S ; Sivaraman, J ; Chaurasia, S.S; Liu, S ; Beuerman, R.W |
| 11 | 2008 | CD209 genetic polymorphism and tuberculosis disease | Vannberg F.O.; Chapman S.J.; Khor C.C. ; Tosh K.; Floyd S.; Jackson-Sillah D.; Crampin A.; Sichali L.; Bah B.; Gustafson P.; Aaby P.; McAdam K.P.W.J.; Bah-Sow O.; Lienhardt C.; Sirugo G.; Fine P.; Hill A.V.S. |
| 12 | 2014 | Characterizing the genetic differences between two distinct migrant groups from Indo-European and Dravidian speaking populations in India | Ali M.; Liu X. ; Pillai E.N. ; Chen P. ; Khor C.-C. ; Ong R.T.H. ; Teo Y.-Y. |
| 13 | 2016 | Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium | Fan, Q ; Guo, X; Tideman, J.W.L; Williams, K.M; Yazar, S; Hosseini, S.M; Howe, L.D; Pourcain, B.S; Evans, D.M; Timpson, N.J; McMahon, G; Hysi, P.G; Krapohl, E; Wang, Y.X; Jonas, J.B; Baird, P.N; Wang, J.J ; Cheng, C.-Y ; Teo, Y.-Y ; Wong, T.-Y ; Ding, X; Wojciechowski, R; Young, T.L ; Pärssinen, O; Oexle, K; Pfeiffer, N; Bailey-Wilson, J.E; Paterson, A.D; Klaver, C.C.W; Plomin, R; Hammond, C.J; He, M; Saw, S.-M ; Guggenheim, J.A; Meguro, A; Wright, A.F; Hewitt, A.W; Young, A.L; Veluchamy, A.B ; Metspalu, A; Döring, A; Khawaja, A.P; Klein, B.E; St Pourcain, B; Fleck, B; Klaver, C.C.W; Hayward, C; Williams, C; Delcourt, C; Pang, C.P; Khor, C.-C ; Gieger, C; Simpson, C.L; Van Duijn, C.M; Mackey, D.A; Stambolian, D; Chew, E; Tai, E.-S ; Mihailov, E; Smith, G.D; Biino, G; Campbell, H; Rudan, I; Seppälä, I; Kaprio, J; Wilson, J.F; Craig, J.E; Ried, J.S; Korobelnik, J.-F; Fondran, J.R; Liao, J ; Zhao, J.H; Xie, J; Kemp, J.P; Lass, J.H; Rahi, J.S; Wedenoja, J; Mäkelä, K.-M; Burdon, K.P; Khaw, K.-T; Yamashiro, K; Chen, L.J; Xu, L; Farrer, L; Ikram, M.K ; Deangelis, M.M; Morrison, M; Schache, M; Pirastu, M; Miyake, M; Yap, M.K.H; Fossarello, M; Kähönen, M; Tedja, M.S; Yoshimura, N; Martin, N.G; Wareham, N.J; Mizuki, N; Raitakari, O; Polasek, O; Tam, P.O; Foster, P.J; Mitchell, P; Chen, P ; Cumberland, P; Gharahkhani, P; Höhn, R; Fogarty, R.D; Luben, R.N; Igo, R.P; Klein, R; Janmahasatian, S; Yip, S.P; Feng, S; Vaccargiu, S; Panda-Jonas, S; MacGregor, S; Iyengar, S.K; Rantanen, T; Lehtimäki, T; Meitinger, T; Aung, T ; Haller, T; Vitart, V; Nangia, V; Verhoeven, V.J.M; Jhanji, V; Zhao, W; Chen, W; Zhou, X; Lu, Y; Vatavuk, Z; The CREAM Consortium |
| 14 | 11-Jul-2013 | Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma risk | Foo, J.N.; Smedby, K.E.; Akers, N.K.; Berglund, M.; Irwan, I.D.; Jia, X.; Li, Y.; Conde, L.; Darabi, H.; Bracci, P.M.; Melbye, M.; Adami, H.-O.; Glimelius, B.; Khor, C.C. ; Hjalgrim, H.; Padyukov, L.; Humphreys, K.; Enblad, G.; Skibola, C.F.; De Bakker, P.I.W.; Liu, J. |
| 15 | Feb-2011 | Collagen-related genes influence the glaucoma risk factor, central corneal thickness | Vithana, E.N.; Aung, T.; Khor, C.C. ; Cornes, B.K.; Tay, W.-T.; Sim, X. ; Lavanya, R.; Wu, R.; Zheng, Y.; Hibberd, M.L.; Chia, K.S. ; Seielstad, M.; Goh, L.K. ; Saw, S.-M. ; Tai, E.S.; Wong, T.Y. |
| 16 | 21-Aug-2013 | Combined genotype and haplotype tests for region-based association studies | Zakharov, S.; Wong, T.Y.; Aung, T.; Vithana, E.N.; Khor, C.C. ; Salim, A. ; Thalamuthu, A. |
| 17 | 2010 | Common NFKBIL2 polymorphisms and susceptibility to pneumococcal disease: A genetic association study | Chapman S.J.; Khor C.C. ; Vannberg F.O.; Rautanen A.; Walley A.; Segal S.; Moore C.E.; Davies R.J.O.; Day N.P.; Peshu N.; Crook D.W.; Berkley J.A.; Williams T.N.; Scott J.A.; Hill A.V.S. |
| 18 | 2013 | Coordinated genetic scaling of the human eye: Shared determination of axial eye length and corneal curvature | Guggenheim, J.A.; Zhou, X. ; Evans, D.M.; Timpson, N.J.; McMahon, G.; Kemp, J.P.; Pourcain, B.S.; Northstone, K.; Ring, S.M.; Fan, Q.; Wong, T.-Y. ; Cheng, C.Y. ; Khor, C.C. ; Aung, T.; Saw, S.M. ; Williams, C. |
| 19 | 10-Jan-2013 | Deep whole-genome sequencing of 100 southeast Asian malays | Wong, L.-P.; Ong, R.T.-H. ; Poh, W.-T. ; Liu, X.; Chen, P.; Li, R.; Lam, K.K.-Y.; Pillai, N.E.; Sim, K.-S.; Xu, H. ; Sim, N.-L.; Teo, S.-M. ; Foo, J.-N.; Tan, L.W.-L.; Lim, Y.; Koo, S.-H.; Gan, L.S.-H.; Cheng, C.-Y. ; Wee, S. ; Yap, E.P.-H.; Ng, P.C.; Lim, W.-Y. ; Soong, R. ; Wenk, M.R.; Aung, T.; Wong, T.-Y. ; Khor, C.-C. ; Little, P.; Chia, K.-S. ; Teo, Y.-Y. |
| 20 | 1-Apr-2014 | Different hereditary contribution of the CFH gene between polypoidal choroidal vasculopathy and age-related macular degeneration in Chinese Han people | Huang, L.; Li, Y.; Guo, S.; Sun, Y.; Zhang, C.; Bai, Y.; Li, S.; Yang, F.; Zhao, M.; Wang, B.; Yu, W.; Zhao, M.; Khor, C.C. ; Li, X. |
