Publications

Results 1-20 of 58 (Search time: 0.013 seconds).

Issue DateTitleAuthor(s)
131-Aug-2021A comprehensive risk score for effective risk stratification and screening of nasopharyngeal carcinomaZhou, Xiang; Cao, Su-Mei; Cai, Yong-Lin; Zhang, Xiao; Zhang, Shanshan; Feng, Guo-Fei; Chen, Yufeng; Feng, Qi-Sheng; Chen, Yijun; Chang, Ellen T.; Liu, Zhonghua; Adami, Hans-Olov; Liu, Jianjun ; Ye, Weimin; Zhang, Zhe; Zeng, Yi-Xin; Xu, Miao
22014A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosisRafiq S.; Khan S.; Tapper W.; Collins A.; Upstill-Goddard R.; Gerty S.; Blomqvist C.; Aittomäki K.; Couch F.J.; Liu J. ; Nevanlinna H.; Eccles D.
3Oct-2013Absence of A673T amyloid-β precursor protein variant in alzheimer's disease and other neurological diseasesTing, S.K.S.; Chong, M.-S.; Kandiah, N.; Hameed, S.; Tan, L.; Au, W.-L.; Prakash, K.M.; Pavanni, R.; Lee, T.-S. ; Foo, J.-N.; Bei, J.-X.; Yu, X.-Q.; Liu, J.-J. ; Zhao, Y.; Lee, W.-L.; Tan, E.-K.
42018Age at first birth in women is genetically associated with increased risk of schizophreniaNi, G.; Gratten, J.; Wray, N.R.; Lee, S.H.; Ripke, S.; Neale, B.M.; Corvin, A.; Walters, J.T.R.; Farh, K.-H.; Holmans, P.A.; Lee, P.; Bulik-Sullivan, B.; Collier, D.A.; Huang, H.; Pers, T.H.; Agartz, I.; Agerbo, E.; Albus, M.; Alexander, M.; Amin, F.; Bacanu, S.A.; Begemann, M.; Belliveau, R.A.; Bene, J.; Bergen, S.E.; Bevilacqua, E.; Bigdeli, T.B.; Black, D.W.; Bruggeman, R.; Buccola, N.G.; Buckner, R.L.; Byerley, W.; Cahn, W.; Cai, G.; Campion, D.; Cantor, R.M.; Carr, V.J.; Carrera, N.; Catts, S.V.; Chambert, K.D.; Chan, R.C.K.; Chen, R.Y.L.; Chen, E.Y.H.; Cheng, W.; Cheung, E.F.C.; Chong, S.A.; Cloninger, C.R.; Cohen, D.; Cohen, N.; Cormican, P.; Craddock, N.; Crowley, J.J.; Curtis, D.; Davidson, M.; Davis, K.L.; Degenhardt, F.; Del Favero, J.; Demontis, D.; Dikeos, D.; Dinan, T.; Djurovic, S.; Donohoe, G.; Drapeau, E.; Duan, J.; Dudbridge, F.; Durmishi, N.; Eichhammer, P.; Eriksson, J.; Escott-Price, V.; Essioux, L.; Fanous, A.H.; Farrell, M.S.; Frank, J.; Franke, L.; Freedman, R.; Freimer, N.B.; Friedl, M.; Friedman, J.I.; Fromer, M.; Genovese, G.; Georgieva, L.; Giegling, I.; Giusti-Rodríguez, P.; Godard, S.; Goldstein, J.I.; Golimbet, V.; Gopal, S.; Haan, L.D.; Hammer, C.; Hamshere, M.L.; Hansen, M.; Hansen, T.; Haroutunian, V.; Hartmann, A.M.; Henskens, F.A.; Herms, S.; Hirschhorn, J.N.; Hoffmann, P.; Hofman, A.; Hollegaard, M.V.; Hougaard, D.M.; Ikeda, M.; Joa, I.; Juliá, A.; Kahn, R.S.; Kalaydjieva, L.; Karachanak-Yankova, S.; Karjalainen, J.; Kavanagh, D.; Keller, M.C.; Kennedy, J.L.; Khrunin, A.; Kim, Y.; Klovins, J.; Knowles, J.A.; Konte, B.; Kucinskas, V.; Kucinskiene, Z.A.; Kuzelova-Ptackova, H.; Kähler, A.K.; Laurent, C.; Keong, J.L.C.; Legge, S.E.; Lerer, B.; Li, M.; Li, T.; Liang, K.-Y.; Lieberman, J.; Limborska, S.; Liu, J. ; Loughland, C.M.; Lubinski, J.; Lönnqvist, J.; Macek, M.; Magnusson, P.K.E.; Maher, B.S.; Maier, W.; Mallet, J.; Marsal, S.; Mattheisen, M.; Mattingsdal, M.; McCarley, R.W.; McDonald, C.; McIntosh, A.M.; Meier, S.; Meijer, C.J.; Melegh, B.; Melle, I.; Mesholam-Gately, R.I.; Metspalu, A.; Michie, P.T.; Milani, L.; Milanova, V.; Mokrab, Y.; Morris, D.W.; Mors, O.; Murphy, K.C.; Murray, R.M.; Myin-Germeys, I.; Müller-Myhsok, B.; Nelis, M.; Nenadic, I.; Nertney, D.A.; Nestadt, G.; Nicodemus, K.K.; Nikitina-Zake, L.; Nisenbaum, L.; Nordin, A.; O'callaghan, E.; O'dushlaine, C.; O'neill, F.A.; Oh, S.-Y.; Olincy, A.; Olsen, L.; Os, J.V.; Pantelis, C.; Papadimitriou, G.N.; Papiol, S.; Parkhomenko, E.; Pato, M.T.; Paunio, T.; Pejovic-Milovancevic, M.; Perkins, D.O.; Pietiläinen, O.; Pimm, J.; Pocklington, A.J.; Powell, J.; Price, A.; Pulver, A.E.; Purcell, S.M.; Quested, D.; Rasmussen, H.B.; Reichenberg, A.; Reimers, M.A.; Richards, A.L.
52005Analysis of LRRK2 functional domains in nondominant Parkinson diseaseSkipper L.; Shen H.; Chua E.; Bonnard C.; Kolatkar P. ; Tan L.C.S. ; Jamora R.D.; Puvan K. ; Puong K.Y.; Zhao Y.; Pavanni R. ; Wong M.C. ; Yuen Y. ; Farrer M.; Liu J.J. ; Tan E.K. 
62014Analysis of non-synonymous-coding variants of parkinson's disease-related pathogenic and susceptibility genes in East Asian populationsFoo 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. 
7Nov-2013Anassociation study of TOLL and CARD with leprosy susceptibility in Chinese populationLiu, H.; Bao, F.; Irwanto, A.; Fu, X.; Lu, N.; Yu, G.; Yu, Y.; Sun, Y.; Low, H.; Li, Y.; Liany, H.; Yuan, C.; Li, J.; Liu, J.; Chen, M.; Liu, H.; Wang, N.; You, J.; Ma, S.; Niu, G.; Zhou, Y.; Chu, T.; Tian, H.; Chen, S.; Zhang, X.; Liu, J. ; Zhang, F.
82019Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization StudyHuang, 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.
9Mar-2020Association of G6PD variants with hemoglobin A1c and impact on diabetes diagnosis in East Asian individualsLeong, A.; Lim, V.J.Y. ; Wang, C.; Chai, J.-F. ; Dorajoo, R.; Heng, C.-K. ; Van Dam, R.M. ; Koh, W.-P. ; Yuan, J.-M.; Jonas, J.B.; Wang, Y.X.; Wei, W.-B.; Liu, J. ; Reilly, D.F.; Wong, T.-Y. ; Cheng, C.-Y. ; Sim, X. 
102014Breast cancer risk assessment using genetic variants and risk factors in a Singapore Chinese populationLee C.P.L.; Irwanto A. ; Salim A.; Yuan J.-M.; Liu J. ; Koh W.P. ; Hartman M. 
112014Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutationsTan L.C.S. ; Methawasin K.; Teng E.W.L.; Ng A.R.J.; Seah S.H.; Au W.L. ; Liu J.J. ; Foo J.N.; Zhao Y.; Tan E.K. 
1211-Jul-2013Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma riskFoo, 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. 
132005Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's diseaseSkipper L.; Li Y.; Bonnard C.; Pavanni R. ; Yih Y.; Chua E.; Sung W.-K. ; Tan L. ; Wong M.-C. ; Tan E.-K. ; Liu J. 
142005CYP17 gene polymorphism in relation to breast cancer risk: a case-control studyEinarsdóttir, K; Rylander-Rudqvist, T; Humphreys, K; Ahlberg, S; Jonasdottir, G; Weiderpass, E; Chia, K.S ; Ingelman-Sundberg, M; Persson, I; Liu, J ; Hall, P; Wedrén, S
152010Deletion of the WD40 domain of LRRK2 in zebrafish causes parkinsonism-like loss of neurons and locomotive defectSheng, D.; Qu, D.; Kwok, K.H.H.; Ng, S.S.; Aw, S.S.; Liu, J. ; Lim, A.Y.M.; Lufkin, T.; Sinnakaruppan, M.; Lee, C.W.H.; Sung, W.K. ; Tan, E.K. ; Jesuthasan, S. 
169-Jun-2021Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomesGoodrich, Julia K.; Singer-Berk, Moriel; Son, Rachel; Sveden, Abigail; Wood, Jordan; England, Eleina; Cole, Joanne B.; Weisburd, Ben; Watts, Nick; Caulkins, Lizz; Dornbos, Peter; Koesterer, Ryan; Zappala, Zachary; Zhang, Haichen; Maloney, Kristin A.; Dahl, Andy; Aguilar-Salinas, Carlos A.; Atzmon, Gil; Barajas-Olmos, Francisco; Barzilai, Nir; Blangero, John; Boerwinkle, Eric; Bonnycastle, Lori L.; Bottinger, Erwin; Bowden, Donald W.; Centeno-Cruz, Federico; Chambers, John C.; Chami, Nathalie; Chan, Edmund ; Chan, Juliana; Cheng, Ching-Yu ; Cho, Yoon Shin; Contreras-Cubas, Cecilia; Córdova, Emilio; Correa, Adolfo; DeFronzo, Ralph A.; Duggirala, Ravindranath; Dupuis, Josee; Eugenia Garay-Sevilla, Ma; García-Ortiz, Humberto; Gieger, Christian; Glaser, Benjamin; González-Villalpando, Clicerio; Elena Gonzalez, Ma; Grarup, Niels; Groop, Leif; Gross, Myron; Haiman, Christopher; Han, Sohee; Hanis, Craig L.; Hansen, Torben; Heard-Costa, Nancy L.; Henderson, Brian E.; Hernandez, Juan Manuel Malacara; Hwang, Mi Yeong; Islas-Andrade, Sergio; Jørgensen, Marit E.; Kang, Hyun Min; Kim, Bong-Jo; Kim, Young Jin; Koistinen, Heikki A.; Kooner, Jaspal Singh; Kuusisto, Johanna; Kwak, Soo-Heon; Laakso, Markku; Lange, Leslie; Lee, Jong-Young; Lee, Juyoung; Lehman, Donna M.; Linneberg, Allan; Liu, Jianjun ; Loos, Ruth J. F.; Lyssenko, Valeriya; Ma, Ronald C. W.; Martínez-Hernández, Angélica; Meigs, James B.; Meitinger, Thomas; Mendoza-Caamal, Elvia; Mohlke, Karen L.; Morris, Andrew D.; Morrison, Alanna C.; Ng, Maggie C. Y.; Nilsson, Peter M.; O’Donnell, Christopher J.; Orozco, Lorena; Palmer, Colin N. A.; Park, Kyong Soo; Post, Wendy S.; Pedersen, Oluf; Preuss, Michael; Psaty, Bruce M.; Reiner, Alexander P.; Revilla-Monsalve, Cristina; Rich, Stephen S.; Rotter, Jerome I.; Saleheen, Danish; Schurmann, Claudia; Sim, Xueling ; Sladek, Rob; Small, Kerrin S.; So, Wing Yee; Spector, Timothy D.; Strauch, Konstantin; Strom, Tim M.; Tai, E. Shyong ; Tam, Claudia H. T.; Teo, Yik Ying ; Thameem, Farook; Tomlinson, Brian; Tracy, Russell P.; Tuomi, Tiinamaija; Tuomilehto, Jaakko; Tusié-Luna, Teresa; van Dam, Rob M. ; Vasan, Ramachandran S.; Wilson, James G.; Witte, Daniel R.; Wong, Tien-Yin ; Burtt, Noel P.; Zaitlen, Noah; McCarthy, Mark I.; Boehnke, Michael; Pollin, Toni I.; Flannick, Jason; Mercader, Josep M.; O’Donnell-Luria, Anne; Baxter, Samantha; Florez, Jose C.; MacArthur, Daniel G.; Udler, Miriam S.
1720-Aug-2021Discovery of Novel Genetic Risk Loci for Acute Central Serous Chorioretinopathy and Genetic Pleiotropic Effect With Age-Related Macular DegenerationFeng, Lei; Chen, Si; Dai, Huatuo; Dorajoo, Rajkumar; Liu, Jianjun ; Kong, Jinfeng; Yin, Xianyong; Ren, Yunqing
182020Effect of plasma polyunsaturated fatty acid levels on leukocyte telomere lengths in the Singaporean Chinese populationChang, X.; Dorajoo, R.; Sun, Y.; Wang, L.; Ong, C.N. ; Liu, J. ; Khor, C.C. ; Yuan, J.-M.; Koh, W.P. ; Friedlander, Y.; Heng, C.-K. 
192018Erratum to: Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians (Scientific Reports, (2018), 8, 1, (5109), 10.1038/s41598-018-23407-1)Gurung R.L.; Dorajoo R.; Liu S.; M Y.; Liu J.-J. ; Wang L.; Guo L.; Yu X.; Liu J.-J.; Lim S.C. 
202017Estimation of kinship coefficient in structured and admixed populations using sparse sequencing dataDou J.; Sun B. ; Sim X. ; Hughes J.D.; Reilly D.F.; Tai E.S. ; Liu J. ; Wang C.