Browsing by Author Wong, EHM

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TitleAuthor(s)Issue DateViews
 
Ripke, SNeale, BMCorvin, AWalters, JTRFarh, KHHolmans, PALee, PBulik-Sullivan, BCollier, DAHuang, HLPers, THJulia, AKahn, RSKalaydjieva, LKarachanak-Yankova, SKarjalainen, JKavanagh, DKeller, MCKennedy, JLKhrunin, AKim, YJAgartz, IKlovins, JKnowles, JAKonte, BKucinskas, VKucinskiene, ZAKuzelova-Ptackova, HKahler, AKLaurent, CLee, CKJLee, SHAgerbo, ELegge, SELerer, BLi, MLi, TLiang, KYLieberman, JLimborska, SLoughland, CMLubinski, JLonnqvist, JAlbus, MMacek Jr, MMagnusson, PKEMaher, BSMaler, WMallet, JMarsal, SMattheisen, MMattingsdal, MMcCarley, RWMcDonald, CAlexander, MMclntosh, AMMeier, SMeijer, CJMelegh, BMelle, IMesholam-Gately, RIMetspalu, AMichie, PTMilani, LMilanova, VAmin, FMokrab, YMorris, DWMors, OMurphy, KCMurray, RMMyin-Germeys, IMuller-Myhsok, BMelis, MNenadic, INertney, DABacanu, SANestadt, GNicodemus, KKNikitina-Zake, LNisenbaum, LNordin, AO'Callaghan, EO'Dushlaine, CO'Neill, FAOh, SYOlincy, ABegemann, MOlsen, LVan Os, JPsychosis Endophenotypes International Consortium, 'Pantelis, CPapadimitriou, GNPapiol, SParkhomenko, EPato, MTPaunio, TPejovic-Milovancevic, MBelliveau Jr, RAPerkins, DOPietilainen, OPimm, JPocklington, AJPowell, JPrice, APulver, AEPurcell, SMQuested, DRasmussen, HBBene, JReichenberg, AReimers, MARichards, ALRoffman, JLRoussos, PRuderier, DMSalomaa, VSanders, ARSchall, USchubert, CRBergen, SESchulze, TGSchwab, SGScolnick, EMScott, RJSeidman, LJShi, JXSigurdsson, ESilagadze, TSilverman, JMSim, KBevilacqua, ESlominsky, PSmoller, JWSO, HCSpencer, CCAStahl, EAStefansson, HSteinberg, SStogmann, EStraub, REStrengman, EBigdeli, TBStrohmaier, JStroup, TSSubramaniam, MSuvisaan, JSvrakic, DMSzatkiewicz, JPSoderman, EThirumalai, SToncheva, DTosato, SBlack, DWVeijola, JWaddington, JWalsh, DWang, DWang, QWebb, BTWeiser, MWildenauer, DBWilliams, NMWilliams, SBruggeman, RWitt, SHWolen, ARWong, EHMWormley, BKXi, HSZai, CCZheng, XBZimprich, FWray, NRStefansson, KBuccola, NGVisscher, PMWellcome Trust Case-Control Consortium 2, 'Adolfsson, RAndreassen, OABlackwood, DHRBramon, EBuxbaum, JDBorglum, ADCichon, SDarvasi, ABuckner, RLDomenici, EEhrenreich, HEsko, TGejman, PVGill, MGurling, HHultman, CMLwata, NJablensky, AVJonsson, EGByerley, WKendler, KSKirov, GKnight, JLencz, TLevinson, DLi, QGSLiu, JJMalhotra, AKMcCarroll, SAMcQuillin, ACahn, WMoran, JLMortensen, PBMowry, BJNothen, MMOphoff, RAOwen, MJPalotie, APato, CNPetryshen, TLPosthuma, DCai, GQRietschel, MRiley, BPRujescu, DSham, PCSklar, PSt Clair, DWeinberger, DRWendland, JRWerge, TDaly, MJCampion, DSullivan, PFO'Donovan, MCCantor, RMCarr, VJCarrera, NCatts, SVChambert, KDChan, RCKChen, RYLChen, EYHCheng, WCheung, EFCChong, SACloninger, CRCohen, DCohen, NCormican, PCraddock, NCrowley, JJCirtis, DDavidson, MDavis, KLDegenhardt, FDel Favero, JDemontis, DDikeos, DDinan, TDjurovic, SDonohoe, GDrapeau, EDuan, JDudbridge, FDurmishi, NEichhammer, PEriksson, JEscott-Price, VEssioux, LFanous, AHFarrell, MSFrank, JFranke, LFreedman, RFreimer, NBFriedl, MFriedman, JLFromer, MGenovese, GGeorgieva, LGiegling, LGiusti-Rodriguez, PGodard, SGoldstein, JLGolimbet, VGopal, SGratten, JHaan, LDHammer, CHamshere, MLHansen, MHansen, THaroutunian, VHartmann, AMHenskens, FAHerms, SHirschhorn, JNHoffmann, PHofman, AHollegaard, MVHougaard, DMIkeda, MJoa, L
2014
94
 
2010
240
 
2013
27
 
2013
56
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS)
Proceeding/Conference:Annual Meeting of American Society of Human Genetics, ASHG 2012
2012
210
Fine mapping on chromosome 10q24.2 implicates ADD3 in biliary atresia
Proceeding/Conference:Annual Meeting of American Society of Human Genetics, ASHG 2012
2012
164
 
Functional characterisation reveals PTPN21 as a positive mediator of NRG3, a potential risk factor in Schizophrenia
Proceeding/Conference:Research Postgraduate Symposium, the University of Hong Kong
2011
170
Genetic study of a fami segregating Waardenburg-Shah syndrome
Proceeding/Conference:Annual Meeting of American Society of Human Genetics, ASHG 2012
2012
123
 
Genetic study of a family segregating Shah-Waardenburg syndrome
Proceeding/Conference:International Symposium on Development of the Enteric Nervous System: Cells, Signals and Genes
2012
134
 
2012
390
Genome-wide copy number variation in anorectal malformations
Proceeding/Conference:Annual Meeting of American Society of Human Genetics, ASHG 2012
2012
137
 
2013
278
Genomi-wide association study on anorectal malformations in the Chinese population
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010
2010
210