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Title	Author(s)	Issue Date	Views
The -1997 G/T polymorphism in the COLIA1 upstream regulatory region is associated with hip bone mineral density (BMD) in Chinese nuclear families Journal:Calcified Tissue International	Zhang, YY Lei, SF Mo, XY Wang, YB Li, MX Deng, HW	2005	63
-459C>T point mutation in 5′ non-coding region of human GJB1 gene is linked to X-linked Charcot-Marie-Tooth neuropathy Journal:Journal of the Peripheral Nervous System	Li, M Cheng, TS Ho, PWL Chan, KH Mak, W Cheung, RTF Ramsden, DB Sham, PC Song, Y Ho, SL	2009	197
A powerful conditional gene-based association approach implicated functionally important genes for schizophrenia Journal:Bioinformatics	Li, M Jiang, L Mak, SHT Kwan, SH Xue, C Chen, P Leung, HCM Cui, L Li, T Sham, PC	2019	165
Allele and genotype frequencies of polymorphic FMO3 gene in two genetically distinct populations Journal:Cell Biochemistry and Function	Hao, D Sun, J Furnes, B Schlenk, D Li, M Yang, S Yang, L	2007	116
Alpha2-HS glycoprotein gene is associated with bone size at the hip in Chinese Journal:Acta Genetica Sinica	Liu, YJ Liu, XH Lei, SF Li, MX Deng, HW	2005	53
Association and linkage analyses of interleukin-6 gene 634C/G polymorphism and bone phenotypes in Chinese Journal:Journal of Bone and Mineral Metabolism	Lei, SF Liu, YZ Deng, FY Li, YM Li, MX Deng, HW	2005	53
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
Bone mineral density in elderly Chinese: Effects of age, sex, weight, height, and body mass index Journal:Journal of Bone and Mineral Metabolism	Lei, SF Deng, FY Li, MX Dvornyk, V Deng, HW	2004	149
Burden of rare variants in ALS genes influences survival in familial and sporadic ALS Journal:Neurobiology of Aging	Pang, SYY HSU, SJ Teo, KC LI, Y Kung, MHW Cheah, KSE Chan, D Cheung, KMC Li, M Sham, PC Ho, SL	2017
The (CA) n polymorphism of the TNFR2 gene is associated with peak bone density in Chinese nuclear families Journal:Journal of Human Genetics	Xu, H Zhao, LJ Lei, SF Li, MX Sun, X Deng, FY Jiang, DK Deng, HW	2005	82
Cancer gene mutations in congenital pulmonary airway malformation patients Journal:ERJ Open Research	HSU, SJ ZHANG, R Yeung, F Tang, SM WONG, KL So, MT Xia, H Sham, PC Tam, PKH Li, M Wong, KKY Garcia-Barcelo, MM	2019
Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese Journal:Schizophrenia Bulletin	Wong, HME SO, HC Li, M Wang, Q Butler, WL BASIL, P WU, HM Hui, TCK CHOI, SC So, MT Garcia-Barcelo, MM McAlonan, GM Chen, EYH Cheung, EFC Chan, RCK Purcell, SM Cherny, SS Chen, RYL Li, T Sham, PC	2014	86
Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset Journal:BMC Research Notes	Gui, H Li, M Sham, PC Cherny, SS	2011
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases Journal:Nucleic Acids Research	Li, MX Gui, HS Kwan, JSH Bao, SY Sham, PC	2012	181
De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca Journal:Human Molecular Genetics	HSU, SJ So, MT Tang, SM Karim, A Porsch, RM Wong, CWY Yu, MON Yeung, F Xia, H ZHANG, R Cherny, SS Chung, HY Wong, KKY Sham, PC Ngo, ND Li, M Tam, PKH Lui, VCH Garcia-Barcelo, MM	2018	32
DEPD: A novel database for differentially expressed proteins Journal:Bioinformatics	He, QY Cao, J Liu, XH Li, MX Liu, YS Xie, JY Liang, SP	2005	115
Development of a bioinformatics and statistical framework to integratebiological resources for genome-wide genetic mapping and itsapplications	Li, Miaoxin.李淼新. Advisor(s):Song, Y Sham, PC	2009
Erratum: Tests of linkage and association of the COL1A2 gene with bone phenotypes' variation in Chinese nuclear families (Bone (2003) 33 (614-619) DOI: 10.1016/S8756-3282(03)00234-5) Journal:Bone	Deng, FY Liu, MY Li, MX Lei, SF Qin, YJ Zhou, Q Liu, YJ Deng, HW	2004	57
Estrogen Receptor α Gene Polymorphisms and Peak Bone Density in Chinese Nuclear Families Journal:Journal of Bone and Mineral Research	Qin, YJ Shen, H Huang, QR Zhao, LJ Zhou, Q Li, MX He, JW Mo, XY Lu, JH Recker, RR Deng, HW	2003	76
Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets Journal:Human Genetics	Li, MX Yeung, JMY Cherny, SS Sham, PC	2012	154

Showing results 1 to 20 of 77 next >