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Showing results 1305 to 1324 of 2925 < previous next >

Title	Author(s)	Issue Date
Hypomanic symptoms in early pregnancy: prevalence and associated factors Journal:Archives of Women's Mental Health	Chan, CY Lee, AM Chung, KF Koh, YW Lam, SK Lee, CP Leung, KY Tang, CSK	2020
HYST: A hybrid set-based test for genome-wide association studies, with application to protein-protein interaction-based association analysis Journal:American Journal of Human Genetics	Li, MX Kwan, JSH Sham, PC	2012
"I can put the medicine in his soup, Doctor!" Journal:Journal of Medical Ethics	Wong, JGWS Poon, Y Hui, EC	2005
iCartiGD: the Integrated Cartilage Gene Database Proceeding/Conference:Asia-Pacific Bioinformatics Conference, APBC 2007	Yeung, MY Smith, DK Chan, SY Wong, BCW Cheung, KMC Cheah, KSE Sham, PC Chan, D Song, Y	2007
iCartiGD: The Integrated Cartilage Gene Database Journal:BMC Genetics	Yeung, MY Smith, DK Chan, MSY Li, CM Wong, BC Cheung, KMC Luk, KDK Cheah, KSE Sham, P Chan, D Song, YQ	2007
Ideas/delusions of reference: development and validation of a new rating scale Proceeding/Conference:Schizophrenia Research	Wong, GHY Chiu, CPY Law, CW Chen, EYH	2008
Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups Journal:Nature Communications	Wang, YF Zhang, Y Lin, Z ZHANG, H Wang, TY CAO, Y Morris, DL Sheng, Y Yin, X Zhong, SL Gu, X LEI, Y He, J Wu, Q SHEN, J Yang, J Lam, TH Lin, JH Mai, Z GUO, M Tang, Y Chen, Y Song, Q Ban, B Mok, CC Cui, Y Lu, L Shen, N Sham, PC Lau, CS Smith, DK Vyse, TJ Zhang, X Lau, YL Yang, W	2021
Identification of a functional variant in CHST3 associated with the susceptibility for lumbar disc degeneration Proceeding/Conference:Symposium of the Hong Kong Society for Developmental Biology, HKSDB 2012	Song, Y Karasugi, T Cheung, KMC Chiba, K Ho, DWH Miyake, A Kao, PYP Sze, KL Yee, AFY Takahashi, A Kawaguchi, Y Mikami, Y Matsumoto, M Togawa, D Kanayama, M Shi, D Dai, J Jiang, Q Wu, C Tian, W Wang, NA Leong, JCY Luk, KDK Yip, SP Cherny, SS Wang, JJ Mundlos, S Kelempisioti, A Eskola, PJ Mannikko, M Makela, P Karppinen, J Jarvelin, MR O Reilly, PF Kubo, M Kimura, T Kubo, T Toyama, Y Mizuta, H Cheah, KSE Tsunoda, T Sham, PC Ikegawa, S Chan, D	2012
Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism Journal:EBioMedicine	Lam, WY Tang, SM So, MT Yue, H HSU, SJ Chung, HY Nicholls, JM Yeung, F Lee, DCW Ngo, DN Nguyen, PAH Mitchison, HM Jenkins, D O'Callaghan, C Garcia-Barcelo, MM Lee, SL Sham, PC Lui, VCH Tam, PKH	2021
Identification of Chinese medicine syndromes in persistent insomnia associated with major depressive disorder: a latent tree analysis Journal:Chinese Medicine	Yeung, WF Chung, KF Zhang, NLW Zhang, SP Yung, KP Chen, PX Ho, YYF	2016
Identification of common and rare genetic risk factors for lumbar disc degeneration	Li, Yan 李艳 Advisor(s):Sham, PC Cheah, KSE	2016
Identification of disease genes: technology and strategies Proceeding/Conference:Colloquium on Genome Research	Sham, PC	2010
Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in Southern Chinese Journal:PLoS ONE	Li, Y Fu, L Wong, AMG Fan, YH Li, MX Bei, JX Jia, WH Zeng, YX Chan, D Cheung, KMC Sham, P Chua, D Guan, XY Song, YQ	2011
Identification of GLI Mutations in Patients with Hirschsprung Disease That Disrupt Enteric Nervous System Development in Mice Journal:Gastroenterology	Liu, AJ Lai, FPL Gui, HS Sham, MH Tam, PKH Garcia-Barcelo, MM Hui, CC Ngan, ESW	2015
Identification of igf1, slc4a4, wwox, and sfmbt1 as hypertension susceptibility genes in han chinese with a genome-wide gene-based association study Journal:PLoS ONE	Yang, HC Liang, YJ Chen, JW Chiang, KM Chung, CM Ho, HY Ting, CT Lin, TH Sheu, SH Tsai, WC Chen, JH Leu, HB Yin, WH Chiu, TY Chern, CI Lin, SJ Tomlinson, B Guo, Y Sham, PC Cherny, SS Lam, TH Thomas, G Pan, WH	2012
Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population Journal:American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	So, HC Fong, PY Chen, RYL Hui, TCK Ng, MYM Cherny, SS Mak, WWM Cheung, EFC Chan, RCK Chen, EYH Li, T Sham, PC	2010
Identification of novel rare coding variants contributing to schizophrenia and antipsychotic treatment response	Wu, Hei-man 胡希文	2016
Identification of rare variants in the NRG1 gene of Hirschsprung's patients Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009	Garcia-Barcelo, MM Tang, WK Miao, XP Tang, CSM So, MT Leon, YY Sham, PC Cherny, SS Tam, PKH	2009
Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders	Ying, Dingge 应鼎阁	2013
Identification of the CACNA2D2 gene on chromosome 3p21 as a novel susceptibility gene for osteoporosis Proceeding/Conference:Journal of Bone and Mineral Research	Huang, Q Cheung, CL Fong, P Ng, M Mak, W Chan, VNY Sham, PC Kung, AWC	2007

Showing results 1305 to 1324 of 2925 < previous next >