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
84
 
2010
91
 
2013
79
 
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
88
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS)
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
82
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
86
 
2011
79
 
Genetic studies of congenital gastrointestinal diseases
Proceeding/Conference:SCBA (Society of Chinese Bioscientists in America) International Symposium
2011
6
Genetic study of a fami segregating Waardenburg-Shah syndrome
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
39
 
2012
67
 
2012
190
Genome-wide copy number variation in anorectal malformations
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
87
 
2013
148
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
74