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
67
 
2010
74
 
2013
62
 
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
80
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS)
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
73
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
77
 
2011
70
 
Genetic studies of congenital gastrointestinal diseases
Proceeding/Conference:SCBA (Society of Chinese Bioscientists in America) International Symposium
2011
3
Genetic study of a fami segregating Waardenburg-Shah syndrome
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
32
 
2012
60
 
2012
175
Genome-wide copy number variation in anorectal malformations
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
65
 
2013
142
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
66