HKU Scholars Hub: Browsing DSpace

Browsing "Genome Research Centre" by Title

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 110 to 129 of 286 < previous next >

Title	Author(s)	Issue Date
Gamma-glutamyl transferase level predicts the development of hypertension in Hong Kong Chinese Proceeding/Conference:Hong Kong Medical Journal	Cheung, BMY Ong, KL Tso, AWK Cherny, SS Sham, PC Lam, TH Lam, KSL	2011
Gamma-glutamyl transferase level predicts the development of hypertension in Hong Kong Chinese Journal:Clinica Chimica Acta	Cheung, BMY Ong, KL Tso, AWK Cherny, SS Sham, PC Lam, TH Lam, KSL	2011
GATES: A rapid and powerful gene-based association test using extended Simes procedure Journal:American Journal of Human Genetics	Li, MX Gui, HS Kwan, JSH Sham, PC	2011
GC content increased at CpG flanking positions of fish genes compared with sea squirt orthologs as a mechanism for reducing impact of DNA methylation Journal:PLoS ONE	Wang, Y Leung, FCC	2008
Genetic analysis of recently identified osteoporosis susceptibility genes in southern Chinese Journal:Journal of Clinical Endocrinology and Metabolism	Xiao, SM Kung, AWC Sham, PC Tan, KCB	2013
Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene Journal:Frontiers in Neuroscience	Ma, SL Chen, LH Lee, CC Lai, KYC Hung, SF Tang, CP Ho, TP Shea, C Mo, F Mak, TSH Sham, PC Leung, PWL	2021
Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population Journal:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics	Gui, H Li, M Sham, PC Baum, LW International League Against Epilepsy Consortium on Complex Epilepsies Kwan, P Cherny, SS	2018
Genetic regulation of Pigment Epithelium-Derived Factor (PEDF): An exome-chip association analysis in Chinese subjects with Type 2 Diabetes Journal:Diabetes	Cheung, CYY Lee, CH Tang, CS Xu, A Au, KW Fong, CHY Ng, KKK Kwok, KHM Chow, WS Woo, YC Yuen, MMA Hai, J Tan, KCB Lam, TH Tse, HF Sham, PC Lam, KSL	2019
Genetic risks for chronic periodontitis: preliminary data of a genome-wide association study Proceeding/Conference:IADR / PER 2014 Congress	Zhang, Y Song, Y Samartzis, D Bow, C Cheah, KSE Cheung, MCH Sham, PC Chan, D Leung, KKH	2014
Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese Journal:Journal of Human Genetics	Cheung, CL Lau, KS Sham, PC Tan, KCB Kung, AWC	2013
Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: a report from the female lung cancer consortium in Asia Journal:International Journal of Cancer	Lee, VHF Wang, JJ Sihoe, DLA Wong, MP	2015
Genetic variants associated with persistent central obesity and the metabolic syndrome in a 12-year longitudinal study Journal:European Journal of Endocrinology	Cheung, CYY Tso, AWK Cheung, BMY Xu, A Ong, KL Law, LSC Wat, NMS Janus, ED Sham, PC Lam, KSL	2011
Genetic variants in GREM2 are associated with bone mineral density in a southern Chinese population Journal:Journal of Clinical Endocrinology and Metabolism	Cheung, CL Lau, KS Sham, PC Tan, KCB Kung, AWC	2013
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients Journal:Neurology	Baum, LW	2018
Genome-wide detection and characterization of positive selection in human populations Journal:Nature	Sabeti, PC Varilly, P Fry, B Lohmueller, J Hostetter, E Cotsapas, C Xie, X Byrne, EH McCarroll, SA Gaudet, R Schaffner, SF Lander, ES Frazer, KA Ballinger, DG Cox, DR Hinds, DA Stuve, LL Gibbs, RA Belmont, JW Boudreau, A Hardenbol, P Leal, SM Pasternak, S Wheeler, DA Willis, TD Yu, F Yang, H Zeng, C Gao, Y Hu, H Hu, W Li, C Lin, W Liu, S Pan, H Tang, X Wang, J Wang, W Yu, J Zhang, B Zhang, Q Zhao, H Zhao, H Zhou, J Gabriel, SB Barry, R Blumenstiel, B Camargo, A Defelice, M Faggart, M Goyette, M Gupta, S Moore, J Nguyen, H Onofrio, RC Parkin, M Roy, J Stahl, E Winchester, E Ziaugra, L Altshuler, D Shen, Y Yao, Z Huang, W Chu, X He, Y Jin, L Liu, Y Shen, Y Sun, W Wang, H Wang, Y Wang, Y Xiong, X Xu, L Waye, MMY Tsui, SKW Xue, H Wong, JTF Galver, LM Fan, JB Gunderson, K Murray, SS Oliphant, AR Chee, MS Montpetit, A Chagnon, F Ferretti, V Leboeuf, M Olivier, JF Phillips, MS Roumy, S Sallée, C Verner, A Hudson, TJ Kwok, PY Cai, D Koboldt, DC Miller, RD Pawlikowska, L TaillonMiller, P Xiao, M Tsui, LC Mak, W You, QS Tam, PKH Nakamura, Y Kawaguchi, T Kitamoto, T Morizono, T Nagashima, A Ohnishi, Y Sekine, A Tanaka, T Tsunoda, T Deloukas, P Bird, CP Delgado, M Dermitzakis, ET Gwilliam, R Hunt, S Morrison, J Powell, D Stranger, BE Whittaker, P Bentley, DR Daly, MJ De Bakker, PIW Barrett, J Chretien, YR Maller, J McCarroll, S Patterson, N Pe'Er, I Price, A Purcell, S Richter, DJ Saxena, R Sham, PC Stein, LD Krishnan, L Smith, AV TelloRuiz, MK Thorisson, GA Chakravarti, A Chen, PE Cutler, DJ Kashuk, CS Lin, S Abecasis, GR Guan, W Li, Y Munro, HM Qin, ZS Thomas, DJ McVean, G Auton, A Bottolo, L Cardin, N Eyheramendy, S Freeman, C Marchini, J Myers, S Spencer, C Stephens, M Donnelly, P Cardon, LR Clarke, G Evans, DM Morris, AP Weir, BS Johnson, TA Mullikin, JC Sherry, ST Feolo, M Skol, A Zhang, H Matsuda, I Fukushima, Y MacEr, DR Suda, E Rotimi, CN Adebamowo, CA Ajayi, I Aniagwu, T Marshall, PA Nkwodimmah, C Royal, CDM Leppert, MF Dixon, M Peiffer, A Qiu, R Kent, A Kato, K Niikawa, N Adewole, IF Knoppers, BM Foster, MW Clayton, EW Watkin, J Muzny, D Nazareth, L Sodergren, E Weinstock, GM Yakub, I Birren, BW Wilson, RK Fulton, LL Rogers, J Burton, J Carter, NP Clee, CM Griffiths, M Jones, MC McLay, K Plumb, RW Ross, MT Sims, SK Willey, DL Chen, Z Han, H Kang, L Godbout, M Wallenburg, JC L'Archevêque, P Bellemare, G Saeki, K Wang, H An, D Fu, H Li, Q Wang, Z Wang, R Holden, AL Brooks, LD McEwen, JE Guyer, MS Wang, VO Peterson, JL Shi, M Spiegel, J Sung, LM Zacharia, LF Collins, FS Kennedy, K Jamieson, R Stewart, J	2007
Genome-wide gene-set analysis identifies different patterns of genetic sharing across complex phenotypes Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2015	Gui, H Kwan, J Sham, PC Cherny, SS Li, M	2015
Genome-wide identification of active enhancers in the developing mouse nucleus pulposus Proceeding/Conference:Hong Kong Inter-University Postgraduate Symposium in Biochemical Sciences, 2017	Qin, Y Ng, RK Ng, TW Tong, KK Au, TYK Niu, B Tan, Z Yip, MS Wang, JJ Sham, PC Cheah, KSE	2017
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Journal:Nature Communications	International League Against Epilepsy Consortium on Complex Epilepsies Baum, L Cherny, SS Lau, Y-L	2018
Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations Journal:Annals of the Rheumatic Diseases	Zhang, Y Yang, J Zhang, J Sun, L Hirankarn, N Pan, HF Lau, WCS Chan, DTM Lee, TL Leung, AMH Mok, CC Zhang, L Wang, Y Shen, JJ Wong, SN Lee, KW Ho, MHK Lee, PPW Chung, BHY Chong, CY Wong, RWS Mok, TMY Wong, WHS Tong, KL Tse, NKC Li, XP Avihingsanon, Y Rianthavorn, P Deekajorndej, T Suphapeetiporn, K Shotelersuk, V Ying, SKY Fung, SKS Lai, WM Wong, CM Ng, IOL Garcia-Barcelo, MM Cherny, SS Cui, Y Sham, PC Yang, S Ye, DQ Zhang, XJ Lau, YL Yang, W	2015
Genomic diversity of Epstein-Barr Virus genomes isolated from primary nasopharyngeal carcinoma biopsies Proceeding/Conference:Hong Kong International Cancer Congress, HKICC 2014	Kwok, H Wu, CW Palser, AL Kellam, P Sham, PC Kwong, DLW Chiang, AKS	2014

Showing results 110 to 129 of 286 < previous next >