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Showing results 1 to 14 of 14

	Title	Author(s)	Issue Date
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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

Showing results 1 to 14 of 14