Results 1 to 12 of 12
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TypeTitleAuthor(s)YearViews
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; Agartz, I; Agerbo, E; Albus, M; Alexander, M; Amin, F; Bacanu, SA; Begemann, M; Belliveau Jr, RA; Bene, J; Bergen, SE; Bevilacqua, E; Bigdeli, TB; Black, DW; Bruggeman, R; Buccola, NG; Buckner, RL; Byerley, W; Cahn, W; Cai, GQ; Campion, D; 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; Julia, A; Kahn, RS; Kalaydjieva, L; Karachanak-Yankova, S; Karjalainen, J; Kavanagh, D; Keller, MC; Kennedy, JL; Khrunin, A; Kim, YJ; Klovins, J; Knowles, JA; Konte, B; Kucinskas, V; Kucinskiene, ZA; Kuzelova-Ptackova, H; Kahler, AK; Laurent, C; Lee, CKJ; Lee, SH; Legge, SE; Lerer, B; Li, M; Li, T; Liang, KY; Lieberman, J; Limborska, S; Loughland, CM; Lubinski, J; Lonnqvist, J; Macek Jr, M; Magnusson, PKE; Maher, BS; Maler, W; Mallet, J; Marsal, S; Mattheisen, M; Mattingsdal, M; McCarley, RW; McDonald, C; Mclntosh, AM; Meier, S; Meijer, CJ; Melegh, B; Melle, I; Mesholam-Gately, RI; Metspalu, A; Michie, PT; Milani, L; Milanova, V; Mokrab, Y; Morris, DW; Mors, O; Murphy, KC; Murray, RM; Myin-Germeys, I; Muller-Myhsok, B; Melis, M; Nenadic, I; Nertney, DA; Nestadt, G; Nicodemus, KK; Nikitina-Zake, L; Nisenbaum, L; Nordin, A; O'Callaghan, E; O'Dushlaine, C; O'Neill, FA; Oh, SY; Olincy, A; Olsen, L; Van Os, J; Psychosis Endophenotypes International Consortium, '; Pantelis, C; Papadimitriou, GN; Papiol, S; Parkhomenko, E; Pato, MT; Paunio, T; Pejovic-Milovancevic, M; Perkins, DO; Pietilainen, O; Pimm, J; Pocklington, AJ; Powell, J; Price, A; Pulver, AE; Purcell, SM; Quested, D; Rasmussen, HB; Reichenberg, A; Reimers, MA; Richards, AL; Roffman, JL; Roussos, P; Ruderier, DM; Salomaa, V; Sanders, AR; Schall, U; Schubert, CR; Schulze, TG; Schwab, SG; Scolnick, EM; Scott, RJ; Seidman, LJ; Shi, JX; Sigurdsson, E; Silagadze, T; Silverman, JM; Sim, K; Slominsky, P; Smoller, JW; SO, HC; Spencer, CCA; Stahl, EA; Stefansson, H; Steinberg, S; Stogmann, E; Straub, RE; Strengman, E; Strohmaier, J; Stroup, TS; Subramaniam, M; Suvisaan, J; Svrakic, DM; Szatkiewicz, JP; Soderman, E; Thirumalai, S; Toncheva, D; Tosato, S; Veijola, J; Waddington, J; Walsh, D; Wang, D; Wang, Q; Webb, BT; Weiser, M; Wildenauer, DB; Williams, NM; Williams, S; Witt, SH; Wolen, AR; Wong, EHM; Wormley, BK; Xi, HS; Zai, CC; Zheng, XB; Zimprich, F; Wray, NR; Stefansson, K; Visscher, PM; Wellcome Trust Case-Control Consortium 2, '; Adolfsson, R; Andreassen, OA; Blackwood, DHR; Bramon, E; Buxbaum, JD; Borglum, AD; Cichon, S; Darvasi, A; Domenici, E; Ehrenreich, H; Esko, T; Gejman, PV; Gill, M; Gurling, H; Hultman, CM; Lwata, N; Jablensky, AV; Jonsson, EG; Kendler, KS; Kirov, G; Knight, J; Lencz, T; Levinson, D; Li, QGS; Liu, JJ; Malhotra, AK; McCarroll, SA; McQuillin, A; Moran, JL; Mortensen, PB; Mowry, BJ; Nothen, MM; Ophoff, RA; Owen, MJ; Palotie, A; Pato, CN; Petryshen, TL; Posthuma, D; Rietschel, M; Riley, BP; Rujescu, D; Sham, PC; Sklar, P; St Clair, D; Weinberger, DR; Wendland, JR; Werge, T; Daly, MJ; Sullivan, PF; O'Donovan, MC201419
 
Genome-wide copy number variation study in anorectal malformations
Journal:
Human Molecular Genetics
Publisher:
Oxford University Press. The Journal's web site is located at http://hmg.oxfordjournals.org/
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, MM2013223
 
Comprehensive comparison of copy number variations detection using Illumina Omni 2.5M and Affymetrix CytoScan® arrays
Proceedings/Conference:
63rd ASHG Annual Meeting Poster Abstracts 2013
Publisher:
American Society of Human Genetics (ASHG).
Tang, SM; Wong, EHM; Gui, H; Cherny, SS; Sham, PC; Tam, PKH; Garcia-Barcelo, MM201330
 
Fine mapping on chromosome 10q24.2 implicates ADD3 in biliary atresia
Proceedings/Conference:
Annual Meeting of American Society of Human Genetics, ASHG 2012
Publisher:
American Society of Human Genetics
Garcia-Barcelo, MM; Cheng, G; Tang, CSM; Liu, X; Zhang, R; So, MT; Wong, EHM; Chung, PHY; Chan, IHY; Liu, J; Zhong, W; Xia, H; Yu, J; Wong, KKY; Cherny, SS; Sham, PC; Tam, PKH2012117
 
Genome-wide copy number variation in anorectal malformations
Proceedings/Conference:
Annual Meeting of American Society of Human Genetics, ASHG 2012
Publisher:
American Society of Human Genetics.
Cherny, SS; Wong, EHM; Cui, L; Ng, CL; Tang, CSM; So, MT; Yip, BHK; Cheng, G; Lui, VCH; Sham, PC; Tam, PKH; Garcia-Barcelo, MM201298
 
Genetic study of a family segregating Shah-Waardenburg syndrome
Proceedings/Conference:
International Symposium on Development of the Enteric Nervous System: Cells, Signals and Genes
Cui, L; Wong, EHM; Zhu, J; Firmato de, AM; Tam, PKH; Garcia-Barcelo, MM201290
 
Genome-wide copy number analysis uncovers a new HSCR gene: NRG3
Journal:
PLoS Genetics
Publisher:
Public Library of Science. The Journal's web site is located at http://www.plosgenetics.org/
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, PHY; Liu, XL; Wong, KKY; Marshall, CR; Scherer, S; Cherny, SS; Sham, PC; Tam, PKH; GarciaBarceló, MM2012300
 
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS)
Proceedings/Conference:
Annual Meeting of American Society of Human Genetics, ASHG 2012
Publisher:
American Society of Human Genetics.
Cheng, G; Wong, EHM; Sham, PC; Cherny, SS; Maas, S; Scherer, SW; Marshall, CR; Pereira, SL; Tam, PKH; Garcia-Barcelo, MM2012160
 
Genetic study of a fami segregating Waardenburg-Shah syndrome
Proceedings/Conference:
Annual Meeting of American Society of Human Genetics, ASHG 2012
Publisher:
American Society of Human Genetics.
Cui, L; Wong, EHM; Zhu, J; de Almeida, MF; Tam, PKH; Garcia-Barcelo, M201281
 
Functional characterisation reveals PTPN21 as a positive mediator of NRG3, a potential risk factor in Schizophrenia
Proceedings/Conference:
Research Postgraduate Symposium, the University of Hong Kong
Lam, HC; Cherny, SS; Wong, EHM; Sham, PC; Jin, D; Song, Y2011138
 
Genomi-wide association study on anorectal malformations in the Chinese population
Proceedings/Conference:
Annual Meeting of the American Society of Human Genetics, ASHG 2010
Publisher:
The American Society of Human Genetics.
Wong, EHM; Tang, CSM; Barcelo, MG; Zhang, XJ; Liu, JJ; Cherny, SS; Sham, PC; Tam, PKH2010177
 
Codon usage bias and the evolution of influenza A viruses. Codon Usage Biases of Influenza Virus
Journal:
BMC Evolutionary Biology
Publisher:
BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcevolbiol/
Wong, EHM; Smith, DK; Rabadan, R; Peiris, M; Poon, LLM2010180
 
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