학술논문


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'학술논문' 에서 검색결과 4,013건 | 목록 1~20
Academic Journal
Mahajan, AnubhaWessel, JenniferWillems, Sara MZhao, WeiRobertson, Neil RChu, Audrey YGan, WeiKitajima, HidetoshiTaliun, DanielRayner, N WilliamGuo, XiuqingLu, YingchangLi, ManJensen, Richard AHu, YaoHuo, ShaofengLohman, Kurt KZhang, WeihuaCook, James PPrins, Bram PeterFlannick, JasonGrarup, NielsTrubetskoy, Vassily VladimirovichKravic, JasminaKim, Young JinRybin, Denis VYaghootkar, HaniehMueller-Nurasyid, MartinaMeidtner, KarinaLi-Gao, RuifangVarga, Tibor VMarten, JonathanLi, JinSmith, Albert VernonAn, PingLigthart, SymenGustafsson, StefanMalerba, GiovanniDemirkan, AyseTajes, Juan FernandezSteinthorsdottir, ValgerdurWuttke, MatthiasLecoeur, CecilePreuss, MichaelBielak, Lawrence FGraff, MarielisaHighland, Heather MJustice, Anne ELiu, Dajiang JMarouli, EiriniPeloso, Gina MarieWarren, Helen RAfaq, SaimaAfzal, ShoaibAhlqvist, EmmaAlmgren, PeterAmin, NajafBang, Lia BBertoni, Alain GBombieri, CristinaBork-Jensen, JetteBrandslund, IvanBrody, Jennifer ABurtt, Noel PCanouil, MickaelChen, Yii-Der IdaCho, Yoon ShinChristensen, CramerEastwood, Sophie VEckardt, Kai-UweFischer, KristaGambaro, GiovanniGiedraitis, VilmantasGrove, Megan Lde Haan, Hugoline GHackinger, SophieHai, YangHan, SoheeTybjaerg-Hansen, AnneHivert, Marie-FranceIsomaa, BoJager, SusanneJorgensen, Marit EJorgensen, TorbenKarajamaki, AnnemariKim, Bong-JoKim, Sung SooKoistinen, Heikki AKovacs, PeterKriebel, JenniferKronenberg, FlorianLall, KristiLange, Leslie ALee, Jung-JinLehne, BenjaminLi, HuaixingLin, Keng-HungLinneberg, AllanLiu, Ching-TiLiu, JunLoh, MarieMagi, ReedikMamakou, VasilikiMcKean-Cowdin, RobertaNadkarni, GirishNeville, MattNielsen, Sune FNtalla, IoannaPeyser, Patricia ARathmann, WolfgangRice, KennethRich, Stephen SRode, LineRolandsson, OlovSchonherr, SebastianSelvin, ElizabethSmall, Kerrin SStancakova, AlenaSurendran, PraveenTaylor, Kent DTeslovich, Tanya MThorand, BarbaraThorleifsson, GudmarTin, AdrienneTonjes, AnkeVarbo, AnetteWitte, Daniel RWood, Andrew RYajnik, PranavYao, JieYengo, LoicYoung, RobinAmouyel, PhilippeBoeing, HeinerBoerwinkle, EricBottinger, Erwin PChowdhury, RajivCollins, Francis SDedoussis, GeorgeDehghan, AbbasDeloukas, PanosFerrario, Marco MFerrieres, JeanFlorez, Jose CFrossard, PhilippeGudnason, VilmundurHarris, Tamara BHeckbert, Susan RHowson, Joanna MMIngelsson, MartinKathiresan, SekarKee, FrankKuusisto, JohannaLangenberg, ClaudiaLauner, Lenore JLindgren, Cecilia MMannisto, SatuMeitinger, ThomasMelander, OlleMohlke, Karen LMoitry, MarieMorris, Andrew DMurray, Alison Dde Mutsert, ReneeOrho-Melander, MarjuOwen, Katharine RPerola, MarkusPeters, AnnetteProvince, Michael ARasheed, AsifRidker, Paul MRivadineira, FernandoRosendaal, Frits RRosengren, Anders HSalomaa, VeikkoSheu, Wayne H-HSladek, RobSmith, Blair HStrauch, KonstantinUitterlinden, Andre GVarma, RohitWiller, Cristen JBluher, MatthiasButterworth, Adam SChambers, John CampbellChasman, Daniel IDanesh, Johnvan Duijn, CorneliaDupuis, JoseeFranco, Oscar HFranks, Paul WFroguel, PhilippeGrallert, HaraldGroop, LeifHan, Bok-GheeHansen, TorbenHattersley, Andrew THayward, CarolineIngelsson, ErikKardia, Sharon LRKarpe, FredrikKooner, Jaspal SinghKottgen, AnnaKuulasmaa, KariLaakso, MarkkuLin, XuLind, LarsLiu, YongmeiLoos, Ruth JFMarchini, JonathanMetspalu, AndresMook-Kanamori, DennisNordestgaard, Borge GPalmer, Colin NAPankow, James SPedersen, OlufPsaty, Bruce MRauramaa, RainerSattar, NaveedSchulze, Matthias BSoranzo, NicoleSpector, Timothy DStefansson, KariStumvoll, MichaelThorsteinsdottir, UnnurTuomi, TiinamaijaTuomilehto, JaakkoWareham, Nicholas JWilson, James GZeggini, EleftheriaScott, Robert ABarroso, InesFrayling, Timothy MGoodarzi, Mark OMeigs, James BBoehnke, MichaelSaleheen, DanishMorris, Andrew PRotter, Jerome IMcCarthy, Mark IConsortium, ExomeBPConsortium, MAGICConsortium, GIANT
Nat Genet
NATURE GENETICS
Mahajan, A, Wessel, J, Willems, S M, Zhao, W, Robertson, N R, Chu, A Y, Gan, W, Kitajima, H, Taliun, D, Rayner, N W, Guo, X, Lu, Y, Li, M, Jensen, R A, Hu, Y, Huo, S, Lohman, K K, Zhang, W, Cook, J P, Prins, B P, Flannick, J, Grarup, N, Trubetskoy, V V, Kravic, J, Kim, Y J, Rybin, D V, Yaghootkar, H, Müller-Nurasyid, M, Meidtner, K, Li-Gao, R, Varga, T V, Marten, J, Li, J, Smith, A V, An, P, Ligthart, S, Gustafsson, S, Malerba, G, Demirkan, A, Tajes, J F, Steinthorsdottir, V, Wuttke, M, Lecoeur, C, Preuss, M, Bielak, L F, Graff, M, Highland, H M, Justice, A E, Liu, D J, Marouli, E, Peloso, G M, Warren, H R, ExomeBP Consortium, MAGIC Consortium, GIANT Consortium, Afaq, S, Afzal, S, Ahlqvist, E, Almgren, P, Amin, N, Bang, L B, Bertoni, A G, Bombieri, C, Bork-Jensen, J, Brandslund, I, Brody, J A, Burtt, N P, Canouil, M, Chen, Y-D I, Cho, Y S, Christensen, C, Eastwood, S V, Eckardt, K-U, Fischer, K, Gambaro, G, Giedraitis, V, Grove, M L, de Haan, H G, Hackinger, S, Hai, Y, Han, S, Tybjærg-Hansen, A, Hivert, M-F, Isomaa, B, Jäger, S, Jørgensen, M E, Jørgensen, T, Käräjämäki, A, Kim, B-J, Kim, S S, Koistinen, H A, Kovacs, P, Kriebel, J, Kronenberg, F, Läll, K, Lange, L A, Lee, J-J, Lehne, B, Li, H, Lin, K-H, Linneberg, A, Liu, C-T, Liu, J, Loh, M, Mägi, R, Mamakou, V, McKean-Cowdin, R, Nadkarni, G, Neville, M, Nielsen, S F, Ntalla, I, Peyser, P A, Rathmann, W, Rice, K, Rich, S S, Rode, L, Rolandsson, O, Schönherr, S, Selvin, E, Small, K S, Stančáková, A, Surendran, P, Taylor, K D, Teslovich, T M, Thorand, B, Thorleifsson, G, Tin, A, Tönjes, A, Varbo, A, Witte, D R, Wood, A R, Yajnik, P, Yao, J, Yengo, L, Young, R, Amouyel, P, Boeing, H, Boerwinkle, E, Bottinger, E P, Chowdhury, R, Collins, F S, Dedoussis, G, Dehghan, A, Deloukas, P, Ferrario, M M, Ferrieres, J, Florez, J C, Frossard, P, Gudnason, V, Harris, T B, Heckbert, S R, Howson, J M M, Ingelsson, M, Kathiresan, S, Kee, F, Kuusisto, J, Langenberg, C, Launer, L J, Lindgren, C M, Männistö, S, Meitinger, T, Melander, O, Mohlke, K L, Moitry, M, Morris, A P, Murray, A D, de Mutsert, R, Orho-Melander, M, Owen, K R, Perola, M, Peters, A, Province, M A, Rasheed, A, Ridker, P M, Rivadineira, F, Rosendaal, F R, Rosengren, A H, Salomaa, V, Sheu, W H-H, Sladek, R, Willer, C J, Blüher, M, Butterworth, A S, Chambers, J C, Chasman, D I, Danesh, J, van Duijn, C M, Dupuis, J, Franco, O H, Franks, P W, Froguel, P, Grallert, H, Groop, L, Kardia, S L R, Karpe, F, Kooner, J S, Köttgen, A, Kuulasmaa, K, Laakso, M, Lin, X, Lind, L, Liu, Y, Loos, R J F, Marchini, J, Metspalu, A, Mook-Kanamori, D O, Nordestgaard, B G, Palmer, C N A, Pankow, J S, Pedersen, O, Psaty, B M, Rauramaa, R, Sattar, N, Schulze, M B, Soranzo, N, Spector, T D, Stefansson, K, Stumvoll, M, Thorsteinsdottir, U, Tuomi, T, Tuomilehto, J, Wareham, N J, Wilson, J G, Zeggini, E, Scott, R A, Barroso, I, Frayling, T M, Goodarzi, M O, Meigs, J B, Boehnke, M, Saleheen, D, Morris, A P, Rotter, J I & McCarthy, M I 2018, 'Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes', Nature Genetics, vol. 50, no. 4, pp. 559-571. https://doi.org/10.1038/s41588-018-0084-1
ExomeBP Consortium, MAGIC Consortium, GIANT Consortium, Witte, D R & Hansen, T 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Mahajan, A, Wessel, J, Willems, S M, Zhao, W, Robertson, N R, Chu, A Y, Gan, W, Kitajima, H, Taliun, D, Rayner, N W, Guo, X, Lu, Y, Li, M, Jensen, R A, Hu, Y, Huo, S, Lohman, K K, Zhang, W, Cook, J P, Prins, B P, Flannick, J, Grarup, N, Trubetskoy, V V, Kravic, J, Kim, Y J, Rybin, D V, Yaghootkar, H, Müller-Nurasyid, M, Meidtner, K, Li-Gao, R, Varga, T V, Marten, J, Li, J, Smith, A V, An, P, Ligthart, S, Gustafsson, S, Malerba, G, Demirkan, A, Tajes, J F, Steinthorsdottir, V, Wuttke, M, Lecoeur, C, Preuss, M, Bielak, L F, Graff, M, Highland, H M, Morris, A & Hayward, C & Morris, A P 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Nat. Genet. 50, 559-571 (2018)
ExomeBP Consortium 2018, 'Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes', Nature Genetics, vol. 50, no. 4, pp. 559-571. https://doi.org/10.1038/s41588-018-0084-1
Nature Genetics, vol 50, iss 4
Grarup, N, Jørgensen, M E, Witte, D R, Hansen, T, Pedersen, O, ExomeBP Consortium, MAGIC Consortium & GIANT Consortium 2018, 'Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article', Nature Genetics, vol. 50, no. 4, pp. 559-571. https://doi.org/10.1038/s41588-018-0084-1
Nature Genetics
Academic Journal
Surendran, PraveenDrenos, FotiosYoung, RobinWarren, HelenCook, James PManning, Alisa KGrarup, NielsSim, XuelingBarnes, Daniel RWitkowska, KateStaley, James RTragante, ViniciusTukiainen, TaruYaghootkar, HaniehMasca, NicholasFreitag, Daniel FFerreira, TeresaGiannakopoulou, OlgaTinker, AndrewHarakalova, MagdalenaMihailov, EvelinLiu, ChunyuKraja, Aldi TFallgaard Nielsen, SuneRasheed, AsifSamuel, MariaZhao, WeiBonnycastle, Lori LJackson, Anne UNarisu, NarisuSwift, Amy JSoutham, LorraineMarten, JonathanHuyghe, Jeroen RStančáková, AlenaFava, CristianoOhlsson, ThereseMatchan, AngelaStirrups, Kathleen EBork-Jensen, JetteGjesing, Anette PKontto, JukkaPerola, MarkusShaw-Hawkins, SusanHavulinna, Aki SZhang, HeDonnelly, Louise AGroves, Christopher JRayner, N WilliamNeville, Matt JRobertson, Neil RYiorkas, Andrianos MHerzig, Karl-HeinzKajantie, EeroZhang, WeihuaWillems, Sara MLannfelt, LarsMalerba, GiovanniSoranzo, NicoleTrabetti, ElisabettaVerweij, NiekEvangelou, EvangelosMoayyeri, AlirezaVergnaud, Anne-ClaireNelson, Christopher PPoveda, AlaitzVarga, Tibor VCaslake, Murielde Craen, Anton JmTrompet, StellaLuan, Jian'anScott, Robert AHarris, Sarah ELiewald, David CmMarioni, RiccardoMenni, CristinaFarmaki, Aliki-EleniHallmans, GöranRenström, FridaHuffman, Jennifer EHassinen, MaijaBurgess, StephenVasan, Ramachandran SFelix, Janine FCHARGE-Heart Failure ConsortiumUria-Nickelsen, MariaMalarstig, AndersReily, Dermot FHoek, MaartenVogt, ThomasLin, HonghuangLieb, WolfgangEchoGen ConsortiumTraylor, MatthewMarkus, Hugh FMETASTROKE ConsortiumHighland, Heather MJustice, Anne EMarouli, EiriniGIANT ConsortiumLindström, JaanaUusitupa, MattiKomulainen, PirjoLakka, Timo ARauramaa, RainerPolasek, OzrenRudan, IgorRolandsson, OlovFranks, Paul WDedoussis, GeorgeSpector, Timothy DEPIC-InterAct ConsortiumJousilahti, PekkaMännistö, SatuDeary, Ian JStarr, John MLangenberg, ClaudiaWareham, Nick JBrown, Morris JDominiczak, Anna FConnell, John MJukema, J WouterSattar, NaveedFord, IanPackard, Chris JEsko, TõnuMägi, ReedikMetspalu, Andresde Boer, Rudolf Avan der Meer, Petervan der Harst, PimLifelines Cohort StudyGambaro, GiovanniIngelsson, ErikLind, Larsde Bakker, Paul IwNumans, Mattijs EBrandslund, IvanChristensen, CramerPetersen, Eva RbKorpi-Hyövälti, EevaOksa, HeikkiChambers, John CKooner, Jaspal SBlakemore, Alexandra IfFranks, SteveJarvelin, Marjo-RiittaHusemoen, Lise LLinneberg, AllanSkaaby, TeaThuesen, BetinaKarpe, FredrikTuomilehto, JaakkoDoney, Alex SfMorris, Andrew DPalmer, Colin NaHolmen, Oddgeir LingaasHveem, KristianWiller, Cristen JTuomi, TiinamaijaGroop, LeifKäräjämäki, AnneMariPalotie, AarnoRipatti, SamuliSalomaa, VeikkoAlam, Dewan SShafi Majumder, Abdulla AlDi Angelantonio, EmanueleChowdhury, RajivMcCarthy, Mark IPoulter, NeilStanton, Alice VSever, PeterAmouyel, PhilippeArveiler, DominiqueBlankenberg, StefanFerrières, JeanKee, FrankKuulasmaa, KariMüller-Nurasyid, MartinaVeronesi, GiovanniVirtamo, JarmoDeloukas, PanosWellcome Trust Case Control ConsortiumElliott, PaulUnderstanding Society Scientific GroupZeggini, EleftheriaKathiresan, SekarMelander, OlleKuusisto, JohannaLaakso, MarkkuPadmanabhan, SandoshPorteous, DavidHayward, CarolineScotland, GenerationCollins, Francis SMohlke, Karen LHansen, TorbenPedersen, OlufBoehnke, MichaelStringham, Heather MEPIC-CVD ConsortiumFrossard, PhilippeNewton-Cheh, ChristopherCHARGE+ Exome Chip Blood Pressure ConsortiumTobin, Martin DNordestgaard, Børge GrønneT2D-GENES ConsortiumGoT2DGenes ConsortiumExomeBP ConsortiumCHD Exome+ ConsortiumCaulfield, Mark JMahajan, AnubhaMorris, Andrew PTomaszewski, MaciejSamani, Nilesh JSaleheen, DanishAsselbergs, Folkert WLindgren, Cecilia MDanesh, JohnWain, Louise VButterworth, Adam SHowson, Joanna MmMunroe, Patricia B
Nat Genet
NATURE GENETICS
Surendran, P, Drenos, F, Young, R, Warren, H, Cook, J P, Manning, A K, Grarup, N, Sim, X, Barnes, D R, Witkowska, K, Staley, J R, Tragante, V, Tukiainen, T, Yaghootkar, H, Masca, N, Freitag, D F, Ferreira, T, Giannakopoulou, O, Tinker, A, Harakalova, M, Mihailov, E, Liu, C, Kraja, A T, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Bonnycastle, L L, Jackson, A U, Narisu, N, Swift, A J, Southam, L, Marten, J, Huyghe, J R, Stančáková, A, Fava, C, Ohlsson, T, Matchan, A, Stirrups, K E, Bork-Jensen, J, Gjesing, A P, Kontto, J, Perola, M, Shaw-Hawkins, S, Havulinna, A S, Zhang, H, Donnelly, L A, Groves, C J, Rayner, N W, Neville, M J, Robertson, N R, Yiorkas, A M, Herzig, K H, Kajantie, E, Zhang, W, Willems, S M, Lannfelt, L, Malerba, G, Soranzo, N, Trabetti, E, Verweij, N, Evangelou, E, Moayyeri, A, Vergnaud, A C, Nelson, C P, Poveda, A, Varga, T V, Caslake, M, De Craen, A J M, Trompet, S, Luan, JA, Scott, R A, Harris, S E, Liewald, D C M, Marioni, R, Menni, C, Farmaki, A E, Hallmans, G, Renström, F, Huffman, J E, Hassinen, M, Burgess, S, Vasan, R S, Felix, J F, Uria-Nickelsen, M, Malarstig, A, Reilly, D F, Hoek, M, Vogt, T F, Lin, H, Lieb, W, Traylor, M, Markus, H S, Highland, H M, Justice, A E, Marouli, E, Lindström, J, Uusitupa, M, Komulainen, P, Lakka, T A, Rauramaa, R, Polasek, O, Rudan, I, Rolandsson, O, Franks, P W, Dedoussis, G, Spector, T D, Jousilahti, P, Männistö, S, Deary, I J, Starr, J M, Langenberg, C, Wareham, N J, Brown, M J, Dominiczak, A F, Connell, J M, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Esko, T, Mägi, R, Metspalu, A, De Boer, R A, Van Der Meer, P, Van Der Harst, P, Gambaro, G, Ingelsson, E, Lind, L, De Bakker, P I W, Numans, M E, Brandslund, I, Christensen, C, Petersen, E R B, Korpi-Hyövälti, E, Oksa, H, Chambers, J C, Kooner, J S, Blakemore, A I F, Franks, S, Jarvelin, M R, Husemoen, L L, Linneberg, A, Skaaby, T, Thuesen, B, Karpe, F, Tuomilehto, J, Doney, A S F, Morris, A D, Palmer, C N A, Holmen, O L, Hveem, K, Willer, C J, Tuomi, T, Groop, L, Käräjämäki, A, Palotie, A, Ripatti, S, Salomaa, V, Alam, D S, Majumder, A A S, Di Angelantonio, E, Chowdhury, R, McCarthy, M I, Poulter, N, Stanton, A V, Sever, P, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrières, J, Kee, F, Kuulasmaa, K, Müller-Nurasyid, M, Veronesi, G, Virtamo, J, Deloukas, P, Elliott, P, Zeggini, E, Kathiresan, S, Melander, O, Kuusisto, J, Laakso, M, Padmanabhan, S, Porteous, D J, Hayward, C, Scotland, G, Collins, F S, Mohlke, K L, Hansen, T, Pedersen, O, Boehnke, M, Stringham, H M, Frossard, P, Newton-Cheh, C, Tobin, M D, Nordestgaard, B G, Caulfield, M J, Mahajan, A, Morris, A P, Tomaszewski, M, Samani, N J, Saleheen, D, Asselbergs, F W, Lindgren, C M, Danesh, J, Wain, L V, Butterworth, A S, Howson, J M M & Munroe, P B 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics, vol. 48, no. 10, pp. 1151-1161 . https://doi.org/10.1038/ng.3654
CHARGE-Heart Failure Consortium, EchoGen Consortium, METASTROKE Consortium, GIANT Consortium, EPIC-InterAct Consortium, Lifelines Cohort Study, Wellcome Trust Case Control Consortium, Understanding Society Scientific Group, Generation Scotland, EPIC-CVD Consortium, CHARGE+ Exome Chip Blood Pressure Consortium, T2D-GENES Consortium, GoT2DGenes Consortium, ExomeBP Consortium & CHD Exome+ Consortium 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics, vol. 48, no. 10, pp. 1151-1161 . https://doi.org/10.1038/ng.3654
Surendran, P, Drenos, F, Young, R, Warren, H, Cook, J P, Manning, A K, Grarup, N, Sim, X, Barnes, D R, Witkowska, K, Staley, J R, Tragante, V, Tukiainen, T, Yaghootkar, H, Masca, N, Freitag, D F, Ferreira, T, Giannakopoulou, O, Tinker, A, Harakalova, M, Mihailov, E, Liu, C, Kraja, A T, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Bonnycastle, L L, Jackson, A U, Narisu, N, Swift, A J, Southam, L, Marten, J, Huyghe, J R, Stančáková, A, Fava, C, Ohlsson, T, Matchan, A, Stirrups, K E, Bork-Jensen, J, Harris, S E, Liewald, D C M, Marioni, R, Polasek, O, Rudan, I, Deary, I J, Starr, J M, Morris, A D & Porteous, D J & Hayward, C 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics . https://doi.org/10.1038/ng.3654
Nat. Genet. 48, 1151-1161 (2016)
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세계정치 / Journal of World Politics. Apr 30, 2018 28:91
Academic Journal
van der Valk, R. J.Kreiner-Moller, E.Kooijman, M. N.Guxens, M.Stergiakouli, E.Saaf, A.Bradfield, J. P.Geller, F.Hayes, M. G.Cousminer, D. L.Korner, A.Thiering, E.Curtin, J. A.Myhre, R.Huikari, V.Joro, R.Kerkhof, M.Warrington, N. M.Pitkanen, N.Ntalla, I.Horikoshi, M.Veijola, R.Freathy, Rachel M.Teo, Y. Y.Barton, S. J.Evans, D. M.Kemp, J. P.St Pourcain, B.Ring, S. M.Davey Smith, G.Bergstrom, A.Kull, I.Hakonarson, H.Mentch, F. D.Bisgaard, H.Chawes, B.Stokholm, J.Waage, J.Eriksen, P.Sevelsted, A.Melbye, M.Early, GeneticsLifecourse Epidemiology, Consortiumvan Duijn, C. M.Medina-Gomez, C.Hofman, A.de Jongste, J. C.Taal, H. R.Uitterlinden, A. G.Genetic Investigation of, ANthropometric Traits ConsortiumArmstrong, L. L.Eriksson, J.Palotie, A.Bustamante, M.Estivill, X.Gonzalez, J. R.Llop, S.Kiess, W.Mahajan, A.Flexeder, C.Tiesler, C. M.Murray, C. S.Simpson, A.Magnus, P.Sengpiel, V.Hartikainen, A. L.Keinanen-Kiukaanniemi, S.Lewin, A.Da Silva Couto Alves, A.Blakemore, A. I.Buxton, J. L.Kaakinen, M.Rodriguez, A.Sebert, S.Vaarasmaki, M.Lakka, T.Lindi, V.Gehring, U.Postma, D. S.Ang, W.Newnham, J. P.Lyytikainen, L. P.Pahkala, K.Raitakari, O. T.Panoutsopoulou, K.Zeggini, E.Boomsma, D. I.Groen-Blokhuis, M.Ilonen, J.Franke, L.Hirschhorn, J. N.Pers, T. H.Liang, L.Huang, J.Hocher, B.Knip, M.Saw, S. M.Holloway, J. W.Melen, E.Grant, S. F.Feenstra, B.Lowe, W. L.Widen, E.Sergeyev, E.Grallert, H.Custovic, A.Jacobsson, B.Jarvelin, M. R.Atalay, M.Koppelman, G. H.Pennell, C. E.Niinikoski, H.Dedoussis, G. V.McCarthy, M. I.Frayling, Timothy M.Sunyer, J.Timpson, N. J.Rivadeneira, F.Bonnelykke, K.Jaddoe, V. W.Early Growth Genetics, Consortium
Hum Mol Genet
Recercat. Dipósit de la Recerca de Catalunya
instname
HUMAN MOLECULAR GENETICS
r-FISABIO. Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
r-FISABIO: Repositorio Institucional de Producción Científica
Human Molecular Genetics
van der Valk, R J P, Kreiner-Møller, E, Kooijman, M N, Guxens, M, Stergiakouli, E, Sääf, A, Bradfield, J P, Geller, F, Hayes, M G, Cousminer, D L, Bisgaard, H, Chawes, B, Stokholm, J, Waage, J, Eriksen, P, Sevelsted, A, Melbye, M, Feenstra, B, Pers, T H & Bønnelykke, K 2015, ' A novel common variant in DCST2 is associated with length in early life and height in adulthood ', Human Molecular Genetics, vol. 24, no. 4, pp. 1155-1168 . https://doi.org/10.1093/hmg/ddu510
van der Valk, R J P, Kreiner-Møller, E, Kooijman, M N, Guxens, M, Stergiakouli, E, Sääf, A, Bradfield, J P, Geller, F, Hayes, M G, Cousminer, D L, Körner, A, Thiering, E, Curtin, J A, Myhre, R, Huikari, V, Joro, R, Kerkhof, M, Warrington, N M, Pitkänen, N, Ntalla, I, Horikoshi, M, Veijola, R, Freathy, R M, Teo, Y-Y, Barton, S J, Evans, D M, Kemp, J P, St Pourcain, B, Ring, S M, Davey Smith, G, Bergström, A, Kull, I, Hakonarson, H, Mentch, F D, Bisgaard, H, Chawes, B, Stokholm, J, Waage, J, Eriksen, P, Sevelsted, A, Melbye, M, van Duijn, C M, Medina-Gomez, C, Hofman, A, de Jongste, J C, Taal, H R, Uitterlinden, A G, Armstrong, L L, Eriksson, J, Palotie, A, Bustamante, M, Estivill, X, Gonzalez, J R, Llop, S, Kiess, W, Mahajan, A, Flexeder, C, Tiesler, C M T, Murray, C S, Simpson, A, Magnus, P, Sengpiel, V, Hartikainen, A-L, Keinanen-Kiukaanniemi, S, Lewin, A, Da Silva Couto Alves, A, Blakemore, A I, Buxton, J L, Kaakinen, M, Rodriguez, A, Sebert, S, Vaarasmaki, M, Lakka, T, Lindi, V, Gehring, U, Postma, D S, Ang, W, Newnham, J P, Lyytikäinen, L-P, Pahkala, K, Raitakari, O T, Panoutsopoulou, K, Zeggini, E, Boomsma, D I, Groen-Blokhuis, M, Ilonen, J, Franke, L, Hirschhorn, J N, Pers, T H, Liang, L, Huang, J, Hocher, B, Knip, M, Saw, S-M, Holloway, J W, Melén, E, Grant, S F A, Feenstra, B, Lowe, W L, Widén, E, Sergeyev, E, Grallert, H, Custovic, A, Jacobsson, B, Jarvelin, M-R, Atalay, M, Koppelman, G H, Pennell, C E, Niinikoski, H, Dedoussis, G V, Mccarthy, M I, Frayling, T M, Sunyer, J, Timpson, N J, Rivadeneira, F, Bønnelykke, K & Jaddoe, V W V 2014, 'A novel common variant in DCST2 is associated with length in early life and height in adulthood.', Human Molecular Genetics, vol. 24, no. 4, pp. 1155-68. https://doi.org/10.1093/hmg/ddu510
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