학술논문

발행년
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(예 : 2010-2015)
'학술논문' 에서 검색결과 167건 | 목록 160~170
Academic Journal
Hehir-Kwa, J. Y., T. Marschall, W. P. Kloosterman, L. C. Francioli, J. A. Baaijens, L. J. Dijkstra, A. Abdellaoui, et al. 2016. “A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.” Nature Communications 7 (1): 12989. doi:10.1038/ncomms12989. http://dx.doi.org/10.1038/ncomms12989.
Academic Journal
Francioli, Laurent CCretu-Stancu, MirceaGarimella, Kiran VFromer, MenachemKloosterman, Wigard PWijmenga, CiscaInvestigator, PrincipalSwertz, Morris Avan Duijn, Cornelia MBoomsma, Dorret ISlagboom, PElinevan Ommen, Gertjan Bde Bakker, Paul IWvan Dijk, FreerkMenelaou, AndronikiNeerincx, Pieter BTPulit, Sara LDeelen, PatrickElbers, Clara CFrancesco Palamara, PierPe'er, ItsikAbdellaoui, Abdelvan Oven, MannisVermaat, MartijnLi, MingkunLaros, Jeroen FJStoneking, Markde Knijff, PeterKayser, ManfredVeldink, Jan Hvan den Berg, Leonard HByelas, Heorhiyden Dunnen, Johan TDijkstra, MartijnAmin, Najafvan der Velde, K JoeriHottenga, Jouke Janvan Setten, Jessicavan Leeuwen, Elisabeth MKanterakis, AlexandrosKattenberg, MathijsKarssen, Lennart Cvan Schaik, Barbera DCBot, JanNijman, Isaäc JRenkens, Ivovan Enckevort, DavidMei, HailiangKoval, VyacheslavEstrada, KarolMedina-Gomez, CarolinaYe, KaiLameijer, Eric-WubboMoed, Matthijs HHehir-Kwa, Jayne YHandsaker, Robert EMcCarroll, Steven ASunyaev, Shamil RPolak, PazVuzman, DanaSohail, MashaalHormozdiari, FereydounMarschall, TobiasSchönhuth, AlexanderGuryev, VictorSlagboom, P ElineBeekman, Marian Bde Craen, Anton JMSuchiman, H Eka DHofman, AlbertOostra, BenIsaacs, AaronRivadeneira, FernandoUitterlinden, André GWillemsen, GonnekePlatteel, MathieuPitts, Steven JPotluri, ShobhaSundar, PurnimaCox, David RLi, QibinLi, YingruiDu, YuanpingChen, RuoyanCao, HongzhiLi, NingCao, SujieWang, JunBovenberg, Jasper ABrandsma, MargreetSamocha, Kaitlin ENeale, Benjamin MDaly, Mark JBanks, EricDePristo, Mark A
Francioli, L. C., M. Cretu-Stancu, K. V. Garimella, M. Fromer, W. P. Kloosterman, C. Wijmenga, P. Investigator, et al. 2016. “A framework for the detection of de novo mutations in family-based sequencing data.” European Journal of Human Genetics 25 (2): 227-233. doi:10.1038/ejhg.2016.147. http://dx.doi.org/10.1038/ejhg.2016.147.
Academic Journal
van Leeuwen, Elisabeth M.Karssen, Lennart C.Deelen, JorisIsaacs, AaronMedina-Gomez, CarolinaMbarek, HamdiKanterakis, AlexandrosTrompet, StellaPostmus, IrisVerweij, Niekvan Enckevort, David J.Huffman, Jennifer E.White, Charles C.Feitosa, Mary F.Bartz, Traci M.Manichaikul, AniJoshi, Peter K.Peloso, Gina M.Deelen, Patrickvan Dijk, FreerkWillemsen, Gonnekede Geus, Eco J.Milaneschi, YuriPenninx, Brenda W.J.H.Francioli, Laurent C.Menelaou, AndronikiPulit, Sara L.Rivadeneira, FernandoHofman, AlbertOostra, Ben A.Franco, Oscar H.Leach, Irene MateoBeekman, Mariande Craen, Anton J.M.Uh, Hae-WonTrochet, HollyHocking, Lynne J.Porteous, David J.Sattar, NaveedPackard, Chris J.Buckley, Brendan M.Brody, Jennifer A.Bis, Joshua C.Rotter, Jerome I.Mychaleckyj, Josyf C.Campbell, HarryDuan, QingLange, Leslie A.Wilson, James F.Hayward, CarolinePolasek, OzrenVitart, VeroniqueRudan, IgorWright, Alan F.Rich, Stephen S.Psaty, Bruce M.Borecki, Ingrid B.Kearney, Patricia M.Stott, David J.Adrienne Cupples, L.Neerincx, Pieter B.T.Elbers, Clara C.Francesco Palamara, PierPe'er, ItsikAbdellaoui, AbdelKloosterman, Wigard P.van Oven, MannisVermaat, MartijnLi, MingkunLaros, Jeroen F.J.Stoneking, Markde Knijff, PeterKayser, ManfredVeldink, Jan H.van den Berg, Leonard H.Byelas, Heorhiyden Dunnen, Johan T.Dijkstra, MartijnAmin, NajafJoeri van der Velde, K.van Setten, JessicaKattenberg, Mathijsvan Schaik, Barbera D.C.Bot, JanNijman, Isaäc J.Mei, HailiangKoval, VyacheslavYe, KaiLameijer, Eric-WubboMoed, Matthijs H.Hehir-Kwa, Jayne Y.Handsaker, Robert E.Sunyaev, Shamil R.Sohail, MashaalHormozdiari, FereydounMarschall, TobiasSchönhuth, AlexanderGuryev, VictorSuchiman, H. Eka D.Wolffenbuttel, Bruce H.Platteel, MathieuPitts, Steven J.Potluri, ShobhaCox, David R.Li, QibinLi, YingruiDu, YuanpingChen, RuoyanCao, HongzhiLi, NingCao, SujieWang, JunBovenberg, Jasper A.Jukema, J. Woutervan der Harst, PimSijbrands, Eric J.Hottenga, Jouke-JanUitterlinden, Andre G.Swertz, Morris A.van Ommen, Gert-Jan B.de Bakker, Paul I.W.Eline Slagboom, P.Boomsma, Dorret I.Wijmenga, Ciscavan Duijn, Cornelia M.
van Leeuwen, E. M., L. C. Karssen, J. Deelen, A. Isaacs, C. Medina-Gomez, H. Mbarek, A. Kanterakis, et al. 2015. “Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels.” Nature Communications 6 (1): 6065. doi:10.1038/ncomms7065. http://dx.doi.org/10.1038/ncomms7065.
Academic Journal
Deelen, PatrickMenelaou, Andronikivan Leeuwen, Elisabeth MKanterakis, Alexandrosvan Dijk, FreerkMedina-Gomez, CarolinaFrancioli, Laurent CHottenga, Jouke JanKarssen, Lennart CEstrada, KarolKreiner-Møller, EskilRivadeneira, Fernandovan Setten, JessicaGutierrez-Achury, JavierWestra, Harm-JanFranke, Ludevan Enckevort, DavidDijkstra, MartijnByelas, Heorhiyvan Duijn, Cornelia MSwertz, Morris ANeerincx, Pieter B TPulit, Sara LElbers, Clara CFrancesco Palamara, PierPe'er, ItsikAbdellaoui, AbdelKloosterman, Wigard Pvan Oven, MannisVermaat, MartijnLi, MingkunLaros, Jeroen F JStoneking, Markde Knijff, PeterKayser, ManfredVeldink, Jan Hvan den Berg, Leonard Hden Dunnen, Johan TAmin, Najafvan der Velde, K JoeriJan Hottenga, JoukeKattenberg, Mathijsvan Schaik, Barbera D CBot, JanNijman, Isaäuc JMei, HailiangKoval, VyacheslavYe, KaiLameijer, Eric-WubboMoed, Matthijs HHehir-Kwa, Jayne YHandsaker, Robert ESunyaev, Shamil RSohail, MashaalHormozdiari, FereydounMarschall, TobiasMarschall, SchönhuthGuryev, Victorde Bakker, Paul I WSlagboom, P ElineBeekman, Marian Bde Craen, Anton J MSuchiman, H Eka DHofman, Albertvan Duijn, CorneliaBoomsma, Dorret IWillemsen, GonnekeWolffenbuttel, Bruce HPlatteel, MathieuPitts, Steven JPotluri, ShobhaCox, David RLi, QibinLi, YingruiDu, YuanpingChen, RuoyanCao, HongzhiLi, NingCao, SujieWang, JunBovenberg, Jasper Acommittee, SteeringWijmenga, Ciscavan Ommen, Gertjan B
Deelen, P., A. Menelaou, E. M. van Leeuwen, A. Kanterakis, F. van Dijk, C. Medina-Gomez, L. C. Francioli, et al. 2014. “Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands'.” European Journal of Human Genetics 22 (11): 1321-1326. doi:10.1038/ejhg.2014.19. http://dx.doi.org/10.1038/ejhg.2014.19.
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[AR] Mei, Hailiang
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