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Showing results 1 to 14 of 14

	Title	Author(s)	Issue Date	Views
	Biological insights from 108 schizophrenia-associated genetic loci Journal:Nature	Ripke, S Neale, BM Corvin, A Walters, JTR Farh, KH Holmans, PA Lee, P Bulik-Sullivan, B Collier, DA Huang, HL Pers, TH Julia, A Kahn, RS Kalaydjieva, L Karachanak-Yankova, S Karjalainen, J Kavanagh, D Keller, MC Kennedy, JL Khrunin, A Kim, YJ Agartz, I Klovins, J Knowles, JA Konte, B Kucinskas, V Kucinskiene, ZA Kuzelova-Ptackova, H Kahler, AK Laurent, C Lee, CKJ Lee, SH Agerbo, E Legge, SE Lerer, B Li, M Li, T Liang, KY Lieberman, J Limborska, S Loughland, CM Lubinski, J Lonnqvist, J Albus, M Macek Jr, M Magnusson, PKE Maher, BS Maler, W Mallet, J Marsal, S Mattheisen, M Mattingsdal, M McCarley, RW McDonald, C Alexander, M Mclntosh, AM Meier, S Meijer, CJ Melegh, B Melle, I Mesholam-Gately, RI Metspalu, A Michie, PT Milani, L Milanova, V Amin, F Mokrab, Y Morris, DW Mors, O Murphy, KC Murray, RM Myin-Germeys, I Muller-Myhsok, B Melis, M Nenadic, I Nertney, DA Bacanu, SA Nestadt, G Nicodemus, KK Nikitina-Zake, L Nisenbaum, L Nordin, A O'Callaghan, E O'Dushlaine, C O'Neill, FA Oh, SY Olincy, A Begemann, M Olsen, L Van Os, J Psychosis Endophenotypes International Consortium, 'Pantelis, C Papadimitriou, GN Papiol, S Parkhomenko, E Pato, MT Paunio, T Pejovic-Milovancevic, M Belliveau Jr, RA Perkins, DO Pietilainen, O Pimm, J Pocklington, AJ Powell, J Price, A Pulver, AE Purcell, SM Quested, D Rasmussen, HB Bene, J Reichenberg, A Reimers, MA Richards, AL Roffman, JL Roussos, P Ruderier, DM Salomaa, V Sanders, AR Schall, U Schubert, CR Bergen, SE Schulze, TG Schwab, SG Scolnick, EM Scott, RJ Seidman, LJ Shi, JX Sigurdsson, E Silagadze, T Silverman, JM Sim, K Bevilacqua, E Slominsky, P Smoller, JW SO, HC Spencer, CCA Stahl, EA Stefansson, H Steinberg, S Stogmann, E Straub, RE Strengman, E Bigdeli, TB Strohmaier, J Stroup, TS Subramaniam, M Suvisaan, J Svrakic, DM Szatkiewicz, JP Soderman, E Thirumalai, S Toncheva, D Tosato, S Black, DW Veijola, J Waddington, J Walsh, D Wang, D Wang, Q Webb, BT Weiser, M Wildenauer, DB Williams, NM Williams, S Bruggeman, R Witt, SH Wolen, AR Wong, EHM Wormley, BK Xi, HS Zai, CC Zheng, XB Zimprich, F Wray, NR Stefansson, K Buccola, NG Visscher, PM Wellcome Trust Case-Control Consortium 2, 'Adolfsson, R Andreassen, OA Blackwood, DHR Bramon, E Buxbaum, JD Borglum, AD Cichon, S Darvasi, A Buckner, RL Domenici, E Ehrenreich, H Esko, T Gejman, PV Gill, M Gurling, H Hultman, CM Lwata, N Jablensky, AV Jonsson, EG Byerley, W Kendler, KS Kirov, G Knight, J Lencz, T Levinson, D Li, QGS Liu, JJ Malhotra, AK McCarroll, SA McQuillin, A Cahn, W Moran, JL Mortensen, PB Mowry, BJ Nothen, MM Ophoff, RA Owen, MJ Palotie, A Pato, CN Petryshen, TL Posthuma, D Cai, GQ Rietschel, M Riley, BP Rujescu, D Sham, PC Sklar, P St Clair, D Weinberger, DR Wendland, JR Werge, T Daly, MJ Campion, D Sullivan, PF O'Donovan, MC Cantor, RM Carr, VJ Carrera, N Catts, SV Chambert, KD Chan, RCK Chen, RYL Chen, EYH Cheng, W Cheung, EFC Chong, SA Cloninger, CR Cohen, D Cohen, N Cormican, P Craddock, N Crowley, JJ Cirtis, D Davidson, M Davis, KL 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, AH Farrell, MS Frank, J Franke, L Freedman, R Freimer, NB Friedl, M Friedman, JL Fromer, M Genovese, G Georgieva, L Giegling, L Giusti-Rodriguez, P Godard, S Goldstein, JL Golimbet, V Gopal, S Gratten, J Haan, LD Hammer, C Hamshere, ML Hansen, M Hansen, T Haroutunian, V Hartmann, AM Henskens, FA Herms, S Hirschhorn, JN Hoffmann, P Hofman, A Hollegaard, MV Hougaard, DM Ikeda, M Joa, L	2014	154
	Codon usage bias and the evolution of influenza A viruses. Codon Usage Biases of Influenza Virus Journal:BMC Evolutionary Biology	Wong, EHM Smith, DK Rabadan, R Peiris, M Poon, LLM	2010	165
	Common genetic variants regulating ADD3 gene expression alter biliary atresia risk Journal:Journal of Hepatology	Cheng, G Tang, CSM Wong, EHM Cheng, WWC So, MT Miao, X Zhang, R Cui, L Liu, X Ngan, ESW Lui, VCH Chung, HY Chan, IHY Liu, J Zhong, W Xia, H Yu, J Qiu, X Wu, X Wang, B Dong, X Tou, J Huang, L Yi, B Ren, H Chan, EKW Ye, K O'Reilly, PF Wong, KKY Sham, PC Cherny, SS Tam, PKH García-Barceló, MM	2013	166
	Comprehensive comparison of copy number variations detection using Illumina Omni 2.5M and Affymetrix CytoScan® arrays Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Tang, SM Wong, EHM Gui, H Cherny, SS Sham, PC Tam, PKH Garcia-Barcelo, MM	2013	101
	Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS) Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012	Cheng, G Wong, EHM Sham, PC Cherny, SS Maas, S Scherer, SW Marshall, CR Pereira, SL Tam, PKH Garcia-Barcelo, MM	2012	99
	Fine mapping on chromosome 10q24.2 implicates ADD3 in biliary atresia Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012	Garcia-Barcelo, MM Cheng, G Tang, CSM Liu, X Zhang, R So, MT Wong, EHM Chung, HY Chan, IHY Liu, J Zhong, W Xia, H Yu, J Wong, KKY Cherny, SS Sham, PC Tam, PKH	2012	65
	Functional characterisation reveals PTPN21 as a positive mediator of NRG3, a potential risk factor in Schizophrenia Proceeding/Conference:Research Postgraduate Symposium, RPS 2011	Lam, HC Cherny, SS Wong, EHM Sham, PC Jin, D Song, Y	2011	122
	Genetic studies of congenital gastrointestinal diseases Proceeding/Conference:SCBA (Society of Chinese Bioscientists in America) International Symposium	Tam, PKH Garcia-Barcelo, MM Tang, SM Yeung, MY Cheng, G Wong, EHM Cui, L Cherny, SS Sham, PC	2011	39
	Genetic study of a fami segregating Waardenburg-Shah syndrome Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012	Cui, L Wong, EHM Zhu, J de Almeida, MF Tam, PKH Garcia-Barcelo, M	2012	71
	Genetic study of a family segregating Shah-Waardenburg syndrome Proceeding/Conference:ENS 2012 Meeting	Cui, L Wong, EHM Zhu, J Firmato de, AM Tam, PKH Garcia-Barcelo, MM	2012	46
	Genome-wide copy number analysis uncovers a new HSCR gene: NRG3 Journal:PLoS Genetics	Tang, CSM Cheng, G So, MT Yip, BHK Miao, XP Wong, EHM Ngan, ESW Lui, VCH Song, YQ Chan, D Cheung, K Yuan, ZW Lei, L Chung, HY Liu, XL Wong, KKY Marshall, CR Scherer, S Cherny, SS Sham, PC Tam, PKH GarciaBarceló, MM	2012	241
	Genome-wide copy number variation in anorectal malformations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012	Cherny, SS Wong, EHM Cui, L Ng, CL Tang, CSM So, MT Yip, BHK Cheng, G Lui, VCH Sham, PC Tam, PKH Garcia-Barcelo, MM	2012	90
	Genome-wide copy number variation study in anorectal malformations Journal:Human Molecular Genetics	Wong, EHM Cui, L Ng, CL Tang, CSM Liu, X So, MT Yip, BHK Cheng, G Zhang, R Tang, WK Yang, W Lau, YL Baum, L Kwan, P Sun, LD Zuo, XB Ren, YQ Yin, XY Miao, X Liu, JJ Lui, VCH Ngan, ESW Yuan, ZW Zhang, SW Xia, JL Wang, HL Sun, XB Wang, RY Chang, T Chan, IHY Chung, HY Zhang, XJ Wong, KKY Cherny, SS Sham, PC Tam, PKH Garcia-Barcelo, MM	2013	104
	Genomi-wide association study on anorectal malformations in the Chinese population Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010	Wong, EHM Tang, CSM Barcelo, MG Zhang, XJ Liu, JJ Cherny, SS Sham, PC Tam, PKH	2010	131

Showing results 1 to 14 of 14