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
62
 
2010
78
 
2013
55
 
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
72
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS)
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
68
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
75
 
2011
73
Genetic study of a fami segregating Waardenburg-Shah syndrome
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
28
 
2012
59
 
2012
170
Genome-wide copy number variation in anorectal malformations
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
63
 
2013
139
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
96