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
95
 
2010
96
 
2013
86
 
Comprehensive comparison of copy number variations detection using Illumina Omni 2.5M and Affymetrix CytoScan® arrays
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013
2013
104
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS)
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
95
Fine mapping on chromosome 10q24.2 implicates ADD3 in biliary atresia
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
89
 
2011
66
 
Genetic studies of congenital gastrointestinal diseases
Proceeding/Conference:SCBA (Society of Chinese Bioscientists in America) International Symposium
2011
8
Genetic study of a fami segregating Waardenburg-Shah syndrome
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
48
 
2012
71
 
2012
156
Genome-wide copy number variation in anorectal malformations
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
109
 
2013
144
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
64