학술논문

발행년
-
(예 : 2010-2015)
'학술논문' 에서 검색결과 81건 | 목록 1~10
Academic Journal
Smedley, DamianSmith, Katherine R.Martin, AntonioThomas, Ellen A.McDonagh, Ellen M.Cipriani, ValentinaEllingford, Jamie M.Arno, GavinTucci, AriannaVandrovcova, JanaChan, GeorgiaWilliams, Hywel J.Ratnaike, ThilokaWei, WeiStirrups, KathleenIbanez, KristinaMoutsianas, LoukasWielscher, MatthiasNeed, AnnaBarnes, Michael R.Vestito, LetiziaBuchanan, JamesWordsworth, SarahAshford, SofieRehmstrom, KarolaLi, EmilyFuller, GavinTwiss, PhilipSpasic-Boskovic, OliveraHalsall, SallyFloto, R. AndresPoole, KennethWagner, AnnetteMehta, Sarju G.Gurnell, MarkBurrows, NigelJames, RogerPenkett, ChristopherDewhurst, EleanorGraf, StefanMapeta, RutendoKasanicki, MaryHaworth, AndreaSavage, HelenBabcock, MelanieReese, Martin G.Bale, MarkBaple, EmmaBoustred, ChristopherBrittain, Helende Burca, AnnaBleda, MartaDevereau, AndrewHalai, DinaHaraldsdottir, EikHyder, ZerinKasperaviciute, DaliaPatch, ChristinePolychronopoulos, DimitrisMatchan, AngelaSultana, RazvanRyten, MinaTavares, Ana L. T.Tregidgo, CarolynTurnbull, ClareWelland, MatthewWood, SuzanneSnow, CatherineWilliams, EleanorLeigh, SarahFoulger, Rebecca E.Daugherty, Louise C.Niblock, OliviaLeong, Ivone U. S.Wright, Caroline F.Davies, JimCrichton, CharlesWelch, JamesWoods, KerrieAbulhoul, LaraAurora, PaulBockenhauer, DetlefBroomfield, AlexanderCleary, Maureen A.Lam, TanyaDattani, MehulFootitt, EmmaGanesan, VijeyaGrunewald, StephanieCompeyrot-Lacassagne, SandrineMuntoni, FrancescoPilkington, ClarissaQuinlivan, RosalineThapar, NikhilWallis, ColinWedderburn, Lucy R.Worth, AustenBueser, TeofilaCompton, CeciliaDeshpande, CharuFassihi, HivaHaque, EshikaIzatt, LouiseJosifova, DraganaMohammed, ShehlaRobert, LeemaRose, SarahRuddy, DeborahSarkany, RobertSay, GenevieveShaw, Adam C.Wolejko, AgataHabib, BishoyBurns, GavinHunter, SarahGrocock, Russell J.Humphray, Sean J.Robinson, Peter N.Haendel, MelissaSimpson, Michael A.Banka, SiddharthClayton-Smith, JillDouzgou, SofiaHall, GeorginaThomas, Huw B.O'Keefe, Raymond T.Michaelides, MichelMoore, Anthony T.Malka, SamPontikos, NikolasBrowning, Andrew C.Straub, VolkerGorman, Grainne S.Horvath, RitaQuinton, RichardSchaefer, Andrew M.Yu-Wai-Man, PatrickTurnbull, Doug M.McFarland, RobertTaylor, Robert W.O'Connor, EmerYip, JaniceNewland, KatrinaMorris, Huw R.Polke, JamesWood, Nicholas W.Campbell, CarolynCamps, CarmeGibson, KateKoelling, NilsLester, TracyNemeth, Andrea H.Palles, ClaireRoy, Noemi B. A.Sen, ArjuneTaylor, JohnCacheiro, PilarJacobsen, Julius O.Seaby, Eleanor G.Davison, ValChitty, LynDouglas, AngelaNaresh, KikkeriMcMullan, DomEllard, SianTemple, I. KarenMumford, Andrew D.Wilson, GillBeales, PhilBitner-Glindzicz, MariaBlack, GraemeBradley, John R.Brennan, PaulBurn, JohnChinnery, Patrick F.Elliott, PerryFlinter, FrancesHoulden, HenryIrving, MelitaNewman, WilliamRahman, ShamimaSayer, John A.Taylor, Jenny C.Webster, Andrew R.Wilkie, Andrew O. M.Ouwehand, Willem H.Raymond, F. LucyChisholm, JohnHill, SueBentley, DavidScott, Richard H.Fowler, TomRendon, AugustoCaulfield, Mark10000 Genomes Project Pilot
NEW ENGLAND JOURNAL OF MEDICINE; NOV 11 2021, 385 20, p1868-p1880, 13p.
Academic Journal
Walter, KlaudiaMin, Josine L.Huang, JieCrooks, LucyMemari, YasinPerry, John R. B.Xu, ChangJiangFutema, MartaLawson, DanielIotchkova, ValentinaSchiffels, StephanHendricks, Audrey E.Danecek, PetrLi, RuiFloyd, JamesWain, Louise V.Humphries, Steve E.Barrett, Jeffrey C.Bala, SenduranClapham, PeterCoates, GuyCox, TonyDaly, AllanDu, YuanpingEdkins, SarahEllis, PeterFlicek, PaulGuo, XiaosenGuo, XueqinHuang, LirenJackson, David K.Joyce, ChrisKeane, ThomasKolb-Kokocinski, AnjaLangford, CordeliaLi, YingruiLiang, JieqinLin, HongLiu, RyanMaslen, JohnMcCarthy, Shane, (co-chair); Muddyman, DawnQuail, Michael A.Stalker, Jim, (co-chair); Sun, JianpingTian, JingWang, GuangbiaoWang, JunWang, YuWong, KimZhang, PingboBirney, EwanBoustred, ChrisChen, LuClement, GailCocca, MassimilianoSmith, George DaveyDay, Ian N. M.Day-Williams, AaronDown, ThomasDunham, IanEvans, David M.Gaunt, Tom R.Geihs, MatthiasHart, DeborahHowie, BryanHubbard, TimHysi, PirroJamshidi, YaldaKarczewski, Konrad J.Kemp, John P.Lachance, GenevieveLek, MonkolLopes, MargaridaMacArthur, Daniel G.Marchini, JonathanMangino, MassimoMathieson, IainMetrustry, SarahMoayyeri, AlirezaNorthstone, KatePanoutsopoulou, KalliopePaternoster, LaviniaQuaye, LydiaRichards, Brent J., (co-chair); Ring, SusanRitchie, Graham R. S.Shihab, Hashem A.Shin, So-YounSmall, Kerrin S.Artigas, María SolerSoranzo, Nicole, (co-chair); Southam, LorraineSpector, Timothy D.St Pourcain, BeateSurdulescu, GabrielaTachmazidou, IoannaTimpson, Nicholas J., (co-chair); Tobin, Martin D.Valdes, Ana M.Visscher, Peter M.Ward, KirstenWilson, Scott G.Yang, JianZhang, FengZheng, Hou-FengAnney, RichardAyub, MuhammadBlackwood, DouglasBolton, Patrick F.Breen, GeromeCollier, David A.Craddock, NickCurran, SarahCurtis, DavidGallagher, LouiseGeschwind, DanielGurling, HughHolmans, PeterLee, IreneLönnqvist, JoukoMcGuffin, PeterMcIntosh, Andrew M.McKechanie, Andrew G.McQuillin, AndrewMorris, JamesOʼDonovan, Michael C.Owen, Michael J., (co-chair); Palotie, Aarno, (co-chair); Parr, Jeremy R.Paunio, TiinaPietilainen, OlliRehnström, KarolaSharp, Sally I.Skuse, DavidSt Clair, DavidSuvisaari, JaanaWalters, James T. R.Williams, Hywel J.Barroso, Inês, (co-chair); Bochukova, ElenaBounds, RebeccaDominiczak, AnnaFarooqi, Sadaf I., (co-chair); Keogh, JuliaMarenne, GaëlleMorris, AndrewOʼRahilly, StephenPorteous, David J.Smith, Blair H.Wheeler, EleanorAl Turki, SaeedAnderson, Carl A.Antony, DinuBeales, PhilBentham, JamieBhattacharya, ShoumoCalissano, MattiaCarss, KerenChatterjee, KrishnaCirak, SebahattinCosgrove, CatherineFitzpatrick, David R., (co-chair); Foley, Reghan A.Franklin, Christopher S.Grozeva, DetelinaHurles, Matthew E., (co-chair); Mitchison, Hannah M.Muntoni, FrancescoOnoufriadis, AlexandrosParker, VictoriaPayne, FelicityRaymond, Lucy F.Roberts, NicolaSavage, David B.Scambler, PeterSchmidts, MiriamSchoenmakers, NadiaSemple, Robert K.Serra, EvaSpasic-Boskovic, OliveraStevens, Elizabethvan Kogelenberg, MargrietVijayarangakannan, ParthibanWilliamson, Kathleen A.Wilson, CrispianWhyte, TamiekaCiampi, AntonioGreenwood, Celia M. T., (co-chair); Oualkacha, KarimZeggini, Eleftheria, (co-chair); Bobrow, MartinGriffin, HeatherKaye, Jane, (co-chair); Kennedy, KarenKent, AlastairSmee, CarolCharlton, RuthEkong, RosemaryKhawaja, FarrahLopes, Luis R.Migone, NicolaPayne, Stewart J.Plagnol, Vincent, (chair); Pollitt, Rebecca C.Povey, SueRidout, Cheryl K.Robinson, Rachel L.Scott, Richard H.Shaw, AdamSyrris, PetrosTaylor, RohanVandersteen, Anthony M.Durbin, Richard, (chair); Amuzu, AntoinetteCasas, Juan PabloChambers, John C.Dedoussis, GeorgeGambaro, GiovanniGasparini, PaoloIsaacs, AaronJohnson, JonKleber, Marcus E.Kooner, Jaspal S.Langenberg, ClaudiaLuan, JianʼanMalerba, GiovanniMärz, WinfriedMatchan, AngelaMorris, RichardNordestgaard, Børge G.Benn, MarianneScott, Robert A.Toniolo, DanielaTraglia, MichelaTybjaerg-Hansen, Annevan Duijn, Cornelia M.van Leeuwen, Elisabeth M.Varbo, AnetteWhincup, PeterZaza, GianluigiZhang, Weihua
Nature. Oct 01, 2015 526(7571):82-90
Review
Wong-Spracklen VMY; Department of Paediatric Neurology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Kolesnik A; MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.; Eck J; MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.; Sabanathan S; Department of Paediatric Neurosciences, Evelina Childrens Hospital, London, UK.; Spasic-Boskovic O; East Genomic Laboratory Hub, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Maw A; Department of Paediatric Neurology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Baker K; MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.; Department of Medical Genetics, University of Cambridge, Cambridge, UK.
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Academic Journal
Wei, WeiTuna, SalihKeogh, Michael J.Smith, Katherine R.Aitman, Timothy J.Beales, Phil L.Bennett, David L.Gale, Daniel P.Bitner-Glindzicz, Maria A. K.Black, Graeme C.Brennan, PaulElliott, PerryFlinter, Frances A.Floto, R. AndresHoulden, HenryIrving, MelitaKoziell, AniaMaher, Eamonn R.Markus, Hugh S.Morrell, Nicholas W.Newman, William G.Roberts, IreneSayer, John A.Smith, Kenneth G. C.Taylor, Jenny C.Watkins, HughWebster, Andrew R.Wilkie, Andrew O. M.Williamson, CatherineAttwood, AnthonyBrown, MatthewBrod, Naomi ClementsCrisp-Hihn, AbigailDavis, JohnDeevi, Sri V. V.Dewhurst, Eleanor F.Edwards, KarenErwood, MarieFox, JamesFrary, Amy J.Hu, FengyuanJolley, JenniferKingston, NathalieLinger, RachelMapeta, RutendoMartin, JenniferMeacham, StuartPapadia, SofiaRayner-Matthews, Paula J.Samarghitean, CrinaShamardina, OlgaSimeoni, IleniaStaines, SimonStaples, EmilyStark, HannahStephens, JonathanTitterton, Catherinevon Ziegenweidt, JulieWatt, ChristopherWhitehorn, DeborahWood, YvetteYates, KatherineYu, PingJames, RogerAshford, SofiePenkett, Christopher J.Stirrups, Kathleen E.Bariana, TadbirLentaigne, ClaireSivapalaratnam, SutheshWestbury, Sarah K.Allsup, David J.Bakchoul, TamamBiss, TinaBoyce, SaraCollins, JanineCollins, Peter W.Curry, Nicola S.Downes, KateDutt, TinaErber, Wendy N.Evans, GillianEverington, TamaraFavier, RemiGomez, KeithGreene, DanielGresele, PaoloHart, DanielKazmi, RashidKelly, Anne M.Lambert, MicheleMadan, BellaMangles, SarahMathias, MaryMillar, CarolynObaji, SamyaPeerlinck, KathelijneRoughley, CatherineSchulman, SolScully, MarieShapiro, Susan E.Sibson, KeithSims, Matthew C.Tait, R. CampbellTalks, KateThys, ChantalToh, Cheng-HockVan Geet, ChrisWestwood, John-PaulMumford, Andrew D.Ouwehand, Willem H.Freson, KathleenLaffan, Michael A.Tan, Rhea Y. Y.Harkness, KirstyMehta, SarjuMuir, Keith W.Hassan, AhamadTraylor, MatthewDrazyk, Anna M.Parry, DavidAhmed, MunazaKazkaz, HanadiVandersteen, Anthony M.Ormondroyd, ElizabethThomson, KateDent, TimothyBuchan, Rachel J.Bueser, TeofilaCarr-White, GeraldCook, StuartDaniels, Matthew J.Harper, Andrew R.Ware, James S.Dixon, Peter H.Chambers, JennyCheng, FloriaEstiu, Maria C.Hague, William M.Marschall, Hanns-UlrichVazquez-Lopez, MartaArno, GavinFrench, Courtney E.Michaelides, MichelMoore, Anthony T.Sanchis-Juan, AlbaCarss, KerenRaymond, F. LucyChinnery, Patrick F.Griffiths, PhilipHorvath, RitaHudson, GavinJurkute, NeringaPyle, AngelaYu-Wai-Man, PatrickWhitworth, JamesAdlard, JulianArmstrong, RuthBrewer, CaroleCasey, RuthCole, Trevor R. P.Evans, Dafydd GarethGreenhalgh, LynnHanson, Helen L.Hoffman, JonathanIzatt, LouiseKumar, AjithLalloo, FionaOng, Kai RenPark, Soo-MiSearle, ClaireSide, LucySnape, KatieWoodward, EmmaTischkowitz, MarcGrozeva, DetelinaKurian, Manju A.Themistocleous, Andreas C.Gosal, DavidMarshall, AndrewMatthews, EmmaMcCarthy, Mark I.Renton, TaraRice, Andrew S. C.Vale, TomWalker, Suellen M.Woods, Christopher GeoffreyThaventhiran, James E.Allen, Hana LangoSavic, SinisaAlachkar, HanaAntrobus, RichardBaxendale, Helen E.Browning, Michael J.Buckland, Matthew S.Cooper, NicholaEdgar, J. David M.Egner, WilliamGilmour, Kimberly C.Goddard, SarahGordins, PavelsGrigoriadou, SofiaHackett, ScottHague, RosieHayman, GrantHerwadkar, ArchanaHuissoon, Aarnoud P.Jolles, StephenKelleher, PeterKumararatne, DinakanthaLonghurst, HilaryLorenzo, Lorena E.Lyons, Paul A.Maimaris, JesmeenNoorani, SadiaRichter, AlexSargur, Ravishankar B.Sewell, W. A. CarrockThomas, DavidThomas, Moira J.Worth, AustenYong, Patrick F. K.Kuijpers, Taco W.Thrasher, Adrian J.Levine, Adam P.Sadeghi-Alavijeh, OmidWong, Edwin K. S.Cook, H. TerenceChan, Melanie M. Y.Hall, MatthewHarris, ClaireMcAlinden, PaulMarchbank, Kevin J.Marks, StephenMaxwell, HeatherMozere, MonikaWessels, JulieJohnson, Sally A.Bleda, MartaHadinnapola, CharakaHaimel, MatthiasSwietlik, EmiliaBogaard, HarmChurch, ColinCoghlan, GerryCondliffe, RobinCorris, PaulDanesino, CesareEyries, MelanieGall, HenningGhofrani, Hossein-ArdeschirGibbs, J. Simon R.Girerd, BarbaraHolden, SimonHouweling, ArjanHoward, Luke S.Humbert, MarcKiely, David G.Kovacs, GaborLawrie, AllanRoss, Robert V. MacKenzieMoledina, ShahinMontani, DavidNewnham, MichaelOlschewski, AndreaOlschewski, HorstPeacock, AndrewPepke-Zaba, JoannaScelsi, LauraSeeger, WernerSoubrier, FlorentSuntharalingam, JayToshner, MarkTreacy, CarmenTrembath, RichardNoordegraaf, Anton VonkWaisfisz, QuintenWharton, JohnWilkins, Martin R.Wort, Stephen J.Graf, StefanLouka, EleniRoy, Noemi B.Rao, AnupamaAncliff, PhilipBabbs, ChristianLayton, D. MarkMead, Adam J.O'Sullivan, JenniferOkoli, StevenSaleem, MoinBierzynska, AgnieszkaDiz, Carmen BugarinColby, ElizabethEkani, Melanie N.Satchell, SimonFowler, TomRendon, AugustoScott, RichardSmedley, DamianThomas, EllenCaulfield, MarkAbbs, StephenBurrows, NigelChitre, ManaliGattens, MichaelGurnell, MarkKelsall, WilfPoole, Ken E. S.Ross-Russell, RobertSpasic-Boskovic, OliveraTwiss, PhilipWagner, AnnetteBanka, SiddharthClayton-Smith, JillDouzgou, SofiaAbulhoul, LaraAurora, PaulBockenhauer, DetlefCleary, MaureenDattani, MehulGanesan, VijeyaPilkington, ClarissaRahman, ShamimaShah, NeilWedderburn, LucyCompton, Cecilia J.Deshpande, CharuFassihi, HivaHaque, EshikaJosifova, DraganaMohammed, Shehla N.Robert, LeemaRose, Sarah J.Ruddy, Deborah M.Sarkany, Robert N.Sayer, GenevieveShaw, Adam C.Campbell, CarolynGibson, KateKoelling, NilsLester, TracyNemeth, Andrea H.Palles, ClairePatel, SmitaSen, ArjuneTaylor, JohnTomlinson, Ian P.Malka, SamanthaBrowning, Andrew C.Burn, JohnDe Soyza, AnthonyGraham, JodiePearce, SimonQuinton, RichardSchaefer, Andrew M.Wilson, Brian T.Wright, MichaelSimpson, MichaelSyrris, PetrosBradley, John R.Turro, ErnestNIHR BioResource-Rare Dis100000 Genomes Project-Rare Dis
SCIENCE; MAY 24 2019, 364 6442, p749-p+, 59p.
Academic Journal
Bengani H; MRC Human Genetics Unit, IGMM, University of Edinburgh (UoE), Edinburgh, United Kingdom.; Grozeva D; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.; Institute of Psychological Medicine & Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom.; Moyon L; Ecole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, France.; Bhatia S; MRC Human Genetics Unit, IGMM, University of Edinburgh (UoE), Edinburgh, United Kingdom.; Louros SR; Centre for Discovery Brain Sciences, Patrick Wild Centre, University of Edinburgh, Edinburgh, United Kingdom.; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, United Kingdom.; Hope J; Institute of Genomic and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.; Jackson A; Centre for Discovery Brain Sciences, Patrick Wild Centre, University of Edinburgh, Edinburgh, United Kingdom.; Prendergast JG; Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.; Owen LJ; MRC Human Genetics Unit, IGMM, University of Edinburgh (UoE), Edinburgh, United Kingdom.; Naville M; Ecole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, France.; Rainger J; MRC Human Genetics Unit, IGMM, University of Edinburgh (UoE), Edinburgh, United Kingdom.; Grimes G; Institute of Genomic and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.; Halachev M; Institute of Genomic and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.; Murphy LC; Institute of Genomic and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.; Spasic-Boskovic O; East Midlands and East of England NHS Genomic Laboratory Hub, Molecular Genetics, Adden brooke's Hospital, Cambridge University Hospitals NHS Foundation Trust Cambridge, Cambridge, United Kingdom.; van Heyningen V; MRC Human Genetics Unit, IGMM, University of Edinburgh (UoE), Edinburgh, United Kingdom.; Kind P; Centre for Discovery Brain Sciences, Patrick Wild Centre, University of Edinburgh, Edinburgh, United Kingdom.; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, United Kingdom.; Abbott CM; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, United Kingdom.; Institute of Genomic and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.; Osterweil E; Centre for Discovery Brain Sciences, Patrick Wild Centre, University of Edinburgh, Edinburgh, United Kingdom.; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, United Kingdom.; Raymond FL; Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.; Roest Crollius H; Ecole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, France.; FitzPatrick DR; MRC Human Genetics Unit, IGMM, University of Edinburgh (UoE), Edinburgh, United Kingdom.; Simons Initiative for the Developing Brain, University of Edinburgh, Edinburgh, United Kingdom.
Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
Academic Journal
Publisher: Dustri-Verlag Country of Publication: Germany NLM ID: 8214420 Publication Model: Print Cited Medium: Internet ISSN: 0722-5091 (Print) Linking ISSN: 07225091 NLM ISO Abbreviation: Clin Neuropathol Subsets: MEDLINE
Academic Journal
Haworth, S.Min, J.L.Evans, D.M.Gaunt, T.R.Kemp, J.P.Northstone, K.Paternoster, L.Shihab, H.A.Shin, S.-Y.Davey Smith, G.Timpson, N.St Pourcain, B.Shapland, C.Y.Fisher, S.E.Hayward, C.Jackson, A.Cleal, L.Huffmann, J.Fitzpatrick, D.R.Williamson, K.A.Wilson, J.F.Vitart, V.Prins, B.P.Tachmazidou, I.Walter, K.Iotchkova, V.Turki, S.A.Anderson, C.A.Bala, S.Barrett, J.C.Barroso, I.Carss, K.Chen, L.Clapham, P.Coates, G.Cox, T.Crooks, L.Daly, A.Danecek, P.Day-Williams, A.Down, T.Durbin, R.Edkins, S.Ellis, P.Flicek, P.Floyd, J.Franklin, C.S.Geihs, M.Hendricks, A.E.Huang, J.Hubbard, T.Hurles, M.E.Jackson, D.K.Joyce, C.Keane, T.Kennedy, K.van Kogelenberg, M.Kolb-Kokocinski, A.Langford, C.Lopes, M.Marenne, G.Maslen, J.McCarthy, S.Memari, Y.Morris, J.Muddyman, D.Palotie, A.Panoutsopoulou, K.Payne, F.Pietilainen, O.Quail, M.A.Rehnström, K.Ritchie, G.R.S.Schiffels, S.Serra, E.Smee, C.Soranzo, N.Southam, L.Stalker, J.Vijayarangakannan, P.Wheeler, E.Wong, K.Zeggini, E.Felix, J.F.Medina-Gomez, C.Rivadeneira, F.Jaddoe, V.W.V.Wang, C.Pennell, C.E.Ahluwalia, T.S.Sass, L.Bønnelykke, K.Bisgaard, H.Vrijheid, M.Guxens, M.Sunyer, J.Fernandez-Orth, D.Tian, J.Timmers, P.R.H.J.Morris, A.Cole, T.J.Dedoussis, G.Anney, R.Gallagher, L.Antony, D.Beales, P.Mitchison, H.M.Scambler, P.Schmidts, M.Scott, R.H.Artigas, M.S.Tobin, M.D.Wain, L.V.Ayub, M.Bochukova, E.Bounds, R.Chatterjee, K.Farooqi, I.S.Keogh, J.O’Rahilly, S.Parker, V.Savage, D.B.Schoenmakers, N.Semple, R.K.Bentham, J.Bhattacharya, S.Cosgrove, C.Birney, E.Dunham, I.Blackwood, D.McIntosh, A.M.McKechanie, A.G.Bobrow, M.Grozeva, D.Raymond, F.L.Roberts, N.Spasic-Boskovic, O.Wilson, C.Bolton, P.F.Curran, S.Breen, G.Collier, D.A.McGuffin, P.Boustred, C.Calissano, M.Cirak, S.Foley, A.R.Muntoni, F.Stevens, E.Whyte, T.Charlton, R.Robinson, R.L.Ciampi, A.Greenwood, C.M.T.Richards, J.B.Sun, J.Xu, C.J.Clement, G.Hart, D.Hysi, P.Lachance, G.Mangino, M.Metrustry, S.Moayyeri, A.Perry, J.R.B.Quaye, L.Small, K.S.Spector, T.D.Surdulescu, G.Valdes, A.M.Ward, K.Wilson, S.G.Zhang, F.Cocca, M.Craddock, N.Holmans, P.O’Donovan, M.C.Owen, M.J.Walters, J.T.R.Williams, H.J.Curtis, D.Day, I.N.M.Dominiczak, A.Onoufriadis, A.Du, Y.Guo, X.Guo, X.Huang, L.Li, Y.Liang, J.Lin, H.Wang, G.Wang, J.Wang, Y.Zhang, P.Ekong, R.Povey, S.Visscher, P.M.Yang, J.Futema, M.Humphries, S.E.Geschwind, D.Li, R.Zheng, H.-F.Griffin, H.Kaye, J.Gurling, H.McQuillin, A.Sharp, S.I.Howie, B.Jamshidi, Y.Karczewski, K.J.Lek, M.MacArthur, D.G.Kent, A.Khawaja, F.Taylor, R.Lawson, D.Lee, I.Skuse, D.Liu, R.Lönnqvist, J.Paunio, T.Suvisaari, J.Lopes, L.R.Syrris, P.Marchini, J.Mathieson, I.Migone, N.Oualkacha, K.Parr, J.R.Payne, S.J.Plagnol, V.Pollitt, R.C.Porteous, D.J.Ridout, C.K.Ring, S.Shaw, A.Smith, B.H.St Clair, D.Vandersteen, A.M.
In: Nature Communications. (Nature Communications, 1 December 2019, 10(1))
Academic Journal
Sanchis-Juan A; Department of Haematology, NHS Blood and Transplant Centre, University of Cambridge, Cambridge, United Kingdom.; Cambridge University Hospitals NHS Foundation Trust, NIHR BioResource, Cambridge, United Kingdom.; Bitsara C; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.; Low KY; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.; Carss KJ; Department of Haematology, NHS Blood and Transplant Centre, University of Cambridge, Cambridge, United Kingdom.; Cambridge University Hospitals NHS Foundation Trust, NIHR BioResource, Cambridge, United Kingdom.; French CE; Cambridge University Hospitals NHS Foundation Trust, NIHR BioResource, Cambridge, United Kingdom.; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.; Spasic-Boskovic O; East Anglian Medical Genetics Service, Cambridge University Hospital, Cambridge, United Kingdom.; Jarvis J; Clinical Genetics Unit, Birmingham Women's NHS Foundation Trust, Birmingham, United Kingdom.; Field M; Genetics of Learning Disability Service (Hunter Genetics), Waratah, NSW, Australia.; Raymond FL; Cambridge University Hospitals NHS Foundation Trust, NIHR BioResource, Cambridge, United Kingdom.; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.; Grozeva D; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.
Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Academic Journal
Grolleman JE; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; de Voer RM; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands. Electronic address: richarda.devoer@radboudumc.nl.; Elsayed FA; Department of Pathology, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.; Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.; Weren RDA; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Palles C; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.; Ligtenberg MJL; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands; Department of Pathology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Vos JR; Department of Human Genetics, Radboud Institute for Health Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Ten Broeke SW; Department of Clinical Genetics, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.; de Miranda NFCC; Department of Pathology, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.; Kuiper RA; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Kamping EJ; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Jansen EAM; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Vink-Börger ME; Department of Pathology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Popp I; Department of Human Genetics, University of Würzburg, 97074 Würzburg, Germany.; Lang A; Vorarlberg Cancer Registry, Agency for Preventive and Social Medicine, Bregenz 6900, Austria.; Spier I; Institute of Human Genetics, University of Bonn, 53127 Bonn, Germany; Center for Hereditary Tumor Syndromes, University of Bonn, 53127 Bonn, Germany.; Hüneburg R; Center for Hereditary Tumor Syndromes, University of Bonn, 53127 Bonn, Germany; Department of Internal Medicine I, University of Bonn, 53127 Bonn, Germany.; James PA; Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbournem, VIC 3000, Australia.; Li N; Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC 3000, Australia.; Staninova M; Center for Biomolecular Pharmaceutical Analyzes, UKIM Faculty of Pharmacy, 1000 Skopje, Republic of Macedonia.; Lindsay H; Leeds Genetics Laboratory, Leeds Teaching Hospitals NHS Trust, Leeds LS9 7TF, UK.; Cockburn D; Leeds Genetics Laboratory, Leeds Teaching Hospitals NHS Trust, Leeds LS9 7TF, UK.; Spasic-Boskovic O; East Anglian Medical Genetics Service, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.; Clendenning M; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, Parkville, VIC 3010, Australia; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Parkville, VIC 3010, Australia.; Sweet K; Division of Human Genetics, Ohio State University Medical Centre, Columbus, OH 43221, USA.; Capellá G; Hereditary Cancer Program, Catalan Institute of Oncology, IDIBELL, CIBERONC, Hospitalet de Llobregat, Barcelona 08908, Spain.; Sjursen W; Department of Medical Genetics, St Olavs University Hospital, 7030 Trondheim, Norway; Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), 7491, Trondheim, Norway.; Høberg-Vetti H; Western Norway Familial Cancer Center, Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, 5021 Bergen, Norway.; Jongmans MC; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Neveling K; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Geurts van Kessel A; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Morreau H; Department of Pathology, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.; Hes FJ; Department of Clinical Genetics, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.; Sijmons RH; Department of Genetics, University Medical Center Groningen, University of Groningen, 9700 RB Groningen, The Netherlands.; Schackert HK; Department of Surgical Research, Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany.; Ruiz-Ponte C; Fundación Pública Galega de Medicina Xenómica (FPGMX)-SERGAS, Grupo de Medicina Xenómica-USC, Instituto de Investigación Sanitaria de Santiago (IDIS), Santiago de Compostela, Galicia 15706, Spain.; Dymerska D; Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland.; Lubinski J; Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland.; Rivera B; Gerald Bronfman Department of Oncology, McGill University, Montreal, QC H3A 0G4, Canada.; Foulkes WD; Department of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.; Tomlinson IP; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK; Oxford National Institute for Health Research (NIHR) Comprehensive Biomedical Research Centre, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.; Valle L; Hereditary Cancer Program, Catalan Institute of Oncology, IDIBELL, CIBERONC, Hospitalet de Llobregat, Barcelona 08908, Spain.; Buchanan DD; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, Parkville, VIC 3010, Australia; University of Melbourne Centre for Cancer Research, Victorian Comprehensive Cancer Centre, Parkville, VIC 3010, Australia; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, VIC 3010, Australia; Genomic Medicine and Family Cancer Clinic, Royal Melbourne Hospital, Parkville, VIC 3010, Australia.; Kenwrick S; East Anglian Medical Genetics Service, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.; Adlard J; Yorkshire Regional Genetics Service and University of Leeds, Leeds LS7 4SA, UK.; Dimovski AJ; Center for Biomolecular Pharmaceutical Analyzes, UKIM Faculty of Pharmacy, 1000 Skopje, Republic of Macedonia.; Campbell IG; Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC 3000, Australia.; Aretz S; Institute of Human Genetics, University of Bonn, 53127 Bonn, Germany; Center for Hereditary Tumor Syndromes, University of Bonn, 53127 Bonn, Germany.; Schindler D; Department of Human Genetics, University of Würzburg, 97074 Würzburg, Germany.; van Wezel T; Department of Pathology, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.; Hoogerbrugge N; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.; Kuiper RP; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands; Princess Máxima Center for Pediatric Oncology, 3584 CT Utrecht, The Netherlands. Electronic address: r.kuiper@prinsesmaximacentrum.nl.
Publisher: Cell Press Country of Publication: United States NLM ID: 101130617 Publication Model: Print Cited Medium: Internet ISSN: 1878-3686 (Electronic) Linking ISSN: 15356108 NLM ISO Abbreviation: Cancer Cell Subsets: MEDLINE
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