학술논문
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'학술논문'
에서 검색결과 403건 | 목록
1~20
Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing
Academic Journal
Eisfeldt, J; Higginbotham, EJ; Lenner, F; Howe, J; Fernandez, BA; Lindstrand, A; Scherer, SW; Feuk, L
GENOME RESEARCH. 34(11):1763-1773
Academic Journal
Yoo, S; Garg, E; Elliott, LT; Hung, RJ; Halevy, AR; Brooks, JD; Bull, SB; Gagnon, F; Greenwood, CMT; Lawless, JF; Paterson, AD; Sun, L; Zawati, MH; Lerner-Ellis, J; Abraham, RJS; Birol, I; Bourque, G; Garant, J-M; Gosselin, C; Li, J; Whitney, J; Thiruvahindrapuram, B; Herbrick, J-A; Lorenti, M; Reuter, MS; Adeoye, OO; Liu, S; Allen, U; Bernier, FP; Biggs, CM; Cheung, AM; Cowan, J; Herridge, M; Maslove, DM; Modi, BP; Mooser, V; Morris, SK; Ostrowski, M; Parekh, RS; Pfeffer, G; Suchowersky, O; Taher, J; Upton, J; Warren, RL; Yeung, RSM; Aziz, N; Turvey, SE; Knoppers, BM; Lathrop, M; Jones, SJM; Scherer, SW; Strug, LJ
BMC Genomic Data. May 2, 2023, Vol. 24 Issue 1
Academic Journal
Maihofer, AX; Engchuan, W; Huguet, G; Klein, M; MacDonald, JR; Shanta, O; Thiruvahindrapuram, B; Jean-Louis, M; Saci, Z; Jacquemont, S; Scherer, SW; Ketema, E; Aiello, AE; Amstadter, AB; Avdibegović, E; Babic, D; Baker, DG; Bisson, JI; Boks, MP; Bolger, EA; Bryant, RA; Bustamante, AC; Caldas-de-Almeida, JM; Cardoso, G; Deckert, J; Delahanty, DL; Domschke, K; Dunlop, BW; Dzubur-Kulenovic, A; Evans, A; Feeny, NC; Franz, CE; Gautam, A; Geuze, E; Goci, A; Hammamieh, R; Jakovljevic, M; Jett, M; Jones, I; Kaufman, ML; Kessler, RC; King, AP; Kremen, WS; Lawford, BR; Lebois, LAM; Lewis, C; Liberzon, I; Linnstaedt, SD; Lugonja, B; Luykx, JJ; Lyons, MJ; Mavissakalian, MR; McLaughlin, KA; McLean, SA; Mehta, D; Mellor, R; Morris, CP; Muhie, S; Orcutt, HK; Peverill, M; Ratanatharathorn, A; Risbrough, VB; Rizzo, A; Roberts, AL; Rothbaum, AO; Rothbaum, BO; Roy-Byrne, P; Ruggiero, KJ; Rutten, BPF; Schijven, D; Seng, JS; Sheerin, CM; Sorenson, MA; Teicher, MH; Uddin, M; Ursano, RJ; Vinkers, CH; Voisey, J; Weber, H; Winternitz, S; Xavier, M; Yang, R; McD Young, R; Zoellner, LA; Psychiatric Genomics Consortium PTSD Working Group; Psychiatric Genomics Consortium CNV Working Group; Salem, RM; Shaffer, RA; Wu, T; Ressler, KJ; Stein, MB; Koenen, KC; Sebat, J; Nievergelt, CM
Mol Psychiatry
Psychiatric Genomics Consortium PTSD Working Group & Psychiatric Genomics Consortium CNV Working Group 2022, 'Rare copy number variation in posttraumatic stress disorder', Molecular Psychiatry, vol. 27, no. 12, pp. 5062-5069. https://doi.org/10.1038/s41380-022-01776-4
Molecular psychiatry, vol. 27, no. 12, pp. 5062-5069
Molecular Psychiatry, vol 27, iss 12
Psychiatric Genomics Consortium PTSD Working Group & Psychiatric Genomics Consortium CNV Working Group 2022, 'Rare copy number variation in posttraumatic stress disorder', Molecular Psychiatry, vol. 27, no. 12, pp. 5062-5069. https://doi.org/10.1038/s41380-022-01776-4
Molecular psychiatry, vol. 27, no. 12, pp. 5062-5069
Molecular Psychiatry, vol 27, iss 12
Academic Journal
Scherer, SW; Cheung, J; MacDonald, JR; Osborne, LR; Nakabayashi, K; Herbrick, JA; Carson, AR; Parker-Katiraee, L; Skaug, J; Khaja, R
SCIENCE. 300(5620):767-772
Academic Journal
Stamouli, S; Anderlid, B-M; Willfors, C; Thiruvahindrapuram, B; Wei, J; Berggren, S; Nordgren, A; Scherer, SW; Lichtenstein, P; Tammimies, K
TWIN RESEARCH AND HUMAN GENETICS. 21(1):1-11
Academic Journal
Loviglio, M. N; Leleu, M.; Männik, K.; Passeggeri, M.; Giannuzzi, G.; van der Werf, I.; Waszak, S. M.; Zazhytska, M.; Roberts Caldeira, I.; Gheldof, N.; Migliavacca, E.; Alfaiz, A. A.; Hippolyte, L.; Maillard, A. M.; van Dijck, A.; Kooy, R. F.; Sanlaville, D.; Rosenfeld, J. A.; Shaffer, L. G.; Andrieux, J.; Marshall, C.; Scherer, S. W.; Shen, Y.; Gusella, J. F.; Thorsteinsdottir, U.; Thorleifsson, G.; Dermitzakis, E. T.; Deplancke, B.; Beckmann, J. S.; Rougemont, J.; Jacquemont, S.; Reymond, A.; Collaborators: Loviglio MN; Männik K; van der Werf I; Giannuzzi G; Zazhytska M; Gheldof N; Migliavacca E; Alfaiz AA; Roberts Caldeira I; Hippolyte L; Maillard AM; Ferrarini A; Butschi FN; Conrad B; Addor MC; Belfiore M; Roetzer K; Dijck AV; Blaumeiser B; Kooy F; Roelens F; Dheedene A; Chiaie BD; Menten B; Oostra A; Caberg JH; Carter M; Kellam B; Stavropoulos DJ; Marshall C; Scherer SW; Weksberg R; Cytrynbaum C; Bassett A; Lowther C; Gillis J; MacKay S; Bache I; Ousager LB; Smerdel MP; Graakjaer J; Kjaergaard S; Metspalu A; Mathieu M; Bonneau D; Guichet A; Parent P; Férec C; Gerard M; Plessis G; Lespinasse J; Masurel A; Marle N; Faivre L; Callier P; Layet V; Meur NL; Le Goff C; Duban Bedu B; Sukno S; Boute O; Andrieux J; Blanchet P; Geneviève D; Puechberty J; Schneider A; Leheup B; Jonveaux P; Mercier S; David A; Le Caignec C; de Pontual L; Pipiras E; Jacquette A; Keren B; Gilbert Dussardier B; Bilan F; Goldenberg A; Chambon P; Toutain A; Till M; Sanlaville D; Leube B; Royer Pokora B; Grabe HJ; Schmidt CO; Schurmann C; Homuth G; Thorleifsson G; Thorsteinsdottir U; Bernardini L; Novelli A; Micale L; Merla G; Zollino M; MARI, FRANCESCA; Rizzo CL; RENIERI, ALESSANDRA; Silengo M; Vulto van Silfhout AT; Schouten M; Pfundt R; de Leeuw N; Vansenne F; Maas SM; Barge Schaapveld DQ; Knegt AC; Stadheim B; Rodningen O; Houge G; Price S; Hawkes L; Campbell C; Kini U; Vogt J; Walters R; Blakemore A; Gusella JF; Shen Y; Scott D; Bacino CA; Tsuchiya K; Ladda R; Sell S; Asamoah A; Hamati AI; Rosenfeld JA; Shaffer LG; Mitchell E; Hodge JC; Beckmann JS; Jacquemont S; Reymond A; Ewans LJ; Mowat D; Walker J; Amor DJ; Esch HV; Leroy P; Bamforth JS; Babu D; Isidor B; DiDonato N; Hackmann K; Passeggeri M; Haeringen AV; Smith R; Ellingwood S; Farber DM; Puri V; Zadeh N; Weaver DD; Miller M; Wilks T; Jorgez CJ; Lafayette D; Jacquemont S.
Mol Psychiatry
Molecular Psychiatry, 22, 6, pp. 836-849
Molecular Psychiatry, Vol. 22, No 6 (2017) pp. 836-849
Molecular Psychiatry, vol. 22, no. 6, pp. 836-849
Molecular psychiatry
Ousager, L B & 2p15 Consortium 2017, ' Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes ', Molecular Psychiatry, vol. 22, no. 6, pp. 836-849 . https://doi.org/10.1038/mp.2016.84
Molecular Psychiatry
Molecular Psychiatry, 22, 6, pp. 836-849
Molecular Psychiatry, Vol. 22, No 6 (2017) pp. 836-849
Molecular Psychiatry, vol. 22, no. 6, pp. 836-849
Molecular psychiatry
Ousager, L B & 2p15 Consortium 2017, ' Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes ', Molecular Psychiatry, vol. 22, no. 6, pp. 836-849 . https://doi.org/10.1038/mp.2016.84
Molecular Psychiatry
Academic Journal
Carter, MT; Nikkel, SM; Fernandez, BA; Marshall, CR; Noor, A; Lionel, AC; Prasad, A; Pinto, D; Joseph-George, AM; Noakes, C; Fairbrother-Davies, C; Roberts, W; Vincent, J; Weksberg, R; Scherer, SW
Clinical Genetics. Nov 01, 2011 80(5):435-443
Academic Journal
Periodical
Chan, EM; Bulman, DE; Paterson, AD; Turnbull, J; Andermann, E; Andermann, F; Rouleau, GA; Delgado-Escueta, AV; Scherer, SW; Minassian, BA
Journal of Medical Genetics. September, 2003, Vol. 40 Issue 9, p671, 5 p.
Academic Journal
D'Abate, L; Walker, S; Yuen, RKC; Tammimies, K; Buchanan, JA; Davies, RW; Thiruvahindrapuram, B; Wei, J; Brian, J; Bryson, SE; Dobkins, K; Howe, J; Landa, R; Leef, J; Messinger, D; Ozonoff, S; Smith, IM; Stone, WL; Warren, ZE; Young, G; Zwaigenbaum, L; Scherer, SW
Nat Commun
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
Nature Communications, vol 10, iss 1
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
Nature Communications, vol 10, iss 1
Academic Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 167(6):1381-1385
Academic Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 168(4):258-264
Academic Journal
Dyment, D; Filges, I; Helm, B; Hutchison, HT; Jeng, LJB; Laumonnier, F; Marshall, CR; Menzel, M; Parkash, S; Parker, MJ; The, DDD STUDY; Raymond, FL; Rideout, AL; Roberts, W; Rupps, R; Schanze, I; Schrander-Stumpel, CTRM; Speevak, MD; Stavropoulos, DJ; Stevens, SJC; Thomas, ERA; Toutain, A; Vergano, S; Weksberg, R; Scherer, SW; Vincent, JB; Chaudhry, A; Noor, A; Degagne, B; Baker, K; Bok, LA; Brady, AF; Chitayat, D; Chung, BHY; Cytrynbaum, C; Carter, MT
Clinical Genetics
Academic Journal
Arking, DE; Pulit, SL; Crotti, L; van der Harst, P; Munroe, PB; Koopmann, TT; Sotoodehnia, N; Rossin, EJ; Morley, M; Wang, X; Johnson, AD; Lundby, A; Gudbjartsson, DF; Noseworthy, PA; Eijgelsheim, M; Bradford, Y; Tarasov, KV; Dörr, M; Müller-Nurasyid, M; Lahtinen, AM; Nolte, IM; Smith, AV; Bis, JC; Isaacs, A; Newhouse, SJ; Evans, DS; Post, WS; Waggott, D; Lyytikäinen, LP; Hicks, AA; Eisele, L; Ellinghaus, D; Hayward, C; Navarro, P; Ulivi, S; Tanaka, T; Tester, DJ; Chatel, S; Gustafsson, S; Kumari, M; Morris, RW; Naluai, ÅT; Padmanabhan, S; Kluttig, A; Strohmer, B; Panayiotou, AG; Torres, M; Knoflach, M; Hubacek, JA; Slowikowski, K; Raychaudhuri, S; Kumar, RD; Harris, TB; Launer, LJ; Shuldiner, AR; Alonso, A; Bader, JS; Ehret, G; Huang, H; Kao, WH; Strait, JB; Macfarlane, PW; Brown, M; Caulfield, MJ; Samani, NJ; Kronenberg, F; Willeit, J; CARe Consortium; COGENT Consortium; Smith, JG; Greiser, KH; Meyer Zu Schwabedissen, H; Werdan, K; Carella, M; Zelante, L; Heckbert, SR; Psaty, BM; Rotter, JI; Kolcic, I; Polašek, O; Wright, AF; Griffin, M; Daly, MJ; DCCT/EDIC; Arnar, DO; Hólm, H; Thorsteinsdottir, U; eMERGE Consortium; Denny, JC; Roden, DM; Zuvich, RL; Emilsson, V; Plump, AS; Larson, MG; O'Donnell, CJ; Yin, X; Bobbo, M; D'Adamo, AP; Iorio, A; Sinagra, G; Carracedo, A; Cummings, SR; Nalls, MA; Jula, A; Kontula, KK; Marjamaa, A; Oikarinen, L; Perola, M; Porthan, K; Erbel, R; Hoffmann, P; Jöckel, KH; Kälsch, H; Nöthen, MM; HRGEN Consortium; den Hoed, M; Loos, RJ; Thelle, DS; Gieger, C; Meitinger, T; Perz, S; Peters, A; Prucha, H; Sinner, MF; Waldenberger, M; de Boer, RA; Franke, L; van der Vleuten, PA; Beckmann, BM; Martens, E; Bardai, A; Hofman, N; Wilde, AA; Behr, ER; Dalageorgou, C; Giudicessi, JR; Medeiros-Domingo, A; Barc, J; Kyndt, F; Probst, V; Ghidoni, A; Insolia, R; Hamilton, RM; Scherer, SW; Brandimarto, J; Margulies, K; Moravec, CE; del Greco M, F; Fuchsberger, C; O'Connell, JR; Lee, WK; Watt, GC; Campbell, H; Wild, SH; El Mokhtari, NE; Frey, N; Asselbergs, FW; Mateo Leach, I; Navis, G; van den Berg, MP; van Veldhuisen, DJ; Kellis, M; Krijthe, BP; Franco, OH; Hofman, A; Kors, JA; Uitterlinden, AG; Witteman, JC; Kedenko, L; Lamina, C; Oostra, BA; Abecasis, GR; Lakatta, EG; Mulas, A; Orrú, M; Schlessinger, D; Uda, M; Markus, MR; Völker, U; Snieder, H; Spector, TD; Ärnlöv, J; Lind, L; Sundström, J; Syvänen, AC; Kivimaki, M; Kähönen, M; Mononen, N; Raitakari, OT; Viikari, JS; Adamkova, V; Kiechl, S; Brion, M; Nicolaides, AN; Paulweber, B; Haerting, J; Dominiczak, AF; Nyberg, F; Whincup, PH; Hingorani, AD; Schott, JJ; Bezzina, CR; Ingelsson, E; Ferrucci, L; Gasparini, P; Wilson, JF; Rudan, I; Franke, A; Mühleisen, TW; Pramstaller, PP; Lehtimäki, TJ; Paterson, AD; Parsa, A; Liu, Y; van Duijn, CM; Siscovick, DS; Gudnason, V; Jamshidi, Y; Salomaa, V; Felix, SB; Sanna, S; Ritchie, MD; Stricker, BH; Stefansson, K; Boyer, LA; Cappola, TP; Olsen, JV; Lage, K; Schwartz, PJ; Kääb, S; Chakravarti, A; Ackerman, MJ; Pfeufer, A; de Bakker, PI; Newton-Cheh, C
Nat Genet
Nature Genetics, Vol. 46, No 8 (2014) pp. 826-836
Arking, D E, Pulit, S L, Crotti, L, van der Harst, P, Munroe, P B, Koopmann, T T, Sotoodehnia, N, Rossin, E J, Morley, M, Wang, X, Johnson, A D, Lundby, A, Gudbjartsson, D F, Noseworthy, P A, Eijgelsheim, M, Bradford, Y, Tarasov, K V, Dörr, M, Müller-Nurasyid, M, Lahtinen, A M, Nolte, I M, Smith, A V, Bis, J C, Isaacs, A, Newhouse, S J, Evans, D S, Post, W S, Waggott, D, Lyytikäinen, L-P, Hicks, A A, Eisele, L, Ellinghaus, D, Hayward, C, Navarro, P, Ulivi, S, Tanaka, T, Tester, D J, Chatel, S, Gustafsson, S, Kumari, M, Morris, R W, Naluai, A T, Padmanabhan, S, Kluttig, A, Strohmer, B, Panayiotou, A G, Torres, M, Knoflach, M, Olsen, J V, Hansen, K L & CARe Consortium 2014, ' Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization ', Nature Genetics, vol. 46, no. 8, pp. 826-838 . https://doi.org/10.1038/ng.3014
Arking, D E, Pulit, S L, Crotti, L, Van Der Harst, P, Munroe, P B, Koopmann, T T, Sotoodehnia, N, Rossin, E J, Morley, M, Wang, X, Johnson, A D, Lundby, A, Gudbjartsson, D F, Noseworthy, P A, Eijgelsheim, M, Bradford, Y, Tarasov, K V, Dörr, M, Müller-Nurasyid, M, Lahtinen, A M, Nolte, I M, Smith, A V, Bis, J C, Isaacs, A, Newhouse, S J, Evans, D S, Post, W S, Waggott, D, Lyytikäinen, L P, Hicks, A A, Eisele, L, Ellinghaus, D, Hayward, C, Navarro, P, Ulivi, S, Tanaka, T, Tester, D J, Chatel, S, Gustafsson, S, Kumari, M, Morris, R W, Naluai, A T, Padmanabhan, S, Kluttig, A, Strohmer, B, Panayiotou, A G, Torres, M, Knoflach, M, Hubacek, J A, Slowikowski, K, Raychaudhuri, S, Kumar, R D, Harris, T B, Launer, L J, Shuldiner, A R, Alonso, A, Bader, J S, Ehret, G, Huang, H, Kao, W H L, Strait, J B, Macfarlane, P W, Brown, M, Caulfield, M J, Samani, N J, Kronenberg, F, Willeit, J, Smith, J G, Greiser, K H, Zu Schwabedissen, H M, Werdan, K, Carella, M, Zelante, L, Heckbert, S R, Psaty, B M, Rotter, J I, Kolcic, I, Polašek, O, Wright, A F, Griffin, M, Daly, M J, Arnar, D O, Hólm, H, Thorsteinsdottir, U, Denny, J C, Roden, D M, Zuvich, R L, Emilsson, V, Plump, A S, Larson, M G, O'Donnell, C J, Yin, X, Bobbo, M, D'Adamo, A P, Iorio, A, Sinagra, G, Carracedo, A, Cummings, S R, Nalls, M A, Jula, A, Kontula, K K, Marjamaa, A, Oikarinen, L, Perola, M, Porthan, K, Erbel, R, Hoffmann, P, Jöckel, K H, Kälsch, H, Nöthen, M M, Den Hoed, M, Loos, R J F, Thelle, D S, Gieger, C, Meitinger, T, Perz, S, Peters, A, Prucha, H, Sinner, M F, Waldenberger, M, De Boer, R A, Franke, L, Van Der Vleuten, P A, Beckmann, B M, Martens, E, Bardai, A, Hofman, N, Wilde, A A M, Behr, E R, Dalageorgou, C, Giudicessi, J R, Medeiros-Domingo, A, Barc, J, Kyndt, F, Probst, V, Ghidoni, A, Insolia, R, Hamilton, R M, Scherer, S W, Brandimarto, J, Margulies, K, Moravec, C E, Del Greco M, F, Fuchsberger, C, O'Connell, J R, Lee, W K, Watt, G C M, Campbell, H, Wild, S H, El Mokhtari, N E, Frey, N, Asselbergs, F W, Leach, I M, Navis, G, Van Den Berg, M P, Van Veldhuisen, D J, Kellis, M, Krijthe, B P, Franco, O H, Hofman, A, Kors, J A, Uitterlinden, A G, Witteman, J C M, Kedenko, L, Lamina, C, Oostra, B A, Abecasis, G R, Lakatta, E G, Mulas, A, Orrú, M, Schlessinger, D, Uda, M, Markus, M R P, Völker, U, Snieder, H, Spector, T D, Ärnlöv, J, Lind, L, Sundström, J, Syvänen, A C, Kivimaki, M, Kähönen, M, Mononen, N, Raitakari, O T, Viikari, J S, Adamkova, V, Kiechl, S, Brion, M, Nicolaides, A N, Paulweber, B, Haerting, J, Dominiczak, A F, Nyberg, F, Whincup, P H, Hingorani, A D, Schott, J J, Bezzina, C R, Ingelsson, E, Ferrucci, L, Gasparini, P, Wilson, J F, Rudan, I, Franke, A, Mühleisen, T W, Pramstaller, P P, Lehtimäki, T J, Paterson, A D, Parsa, A, Liu, Y, Van Duijn, C M, Siscovick, D S, Gudnason, V, Jamshidi, Y, Salomaa, V, Felix, S B, Sanna, S, Ritchie, M D, Stricker, B H, Stefansson, K, Boyer, L A, Cappola, T P, Olsen, J V, Lage, K, Schwartz, P J, Kääb, S, Chakravarti, A, Ackerman, M J, Pfeufer, A, De Bakker, P I W & Newton-Cheh, C 2014, 'Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization', Nature Genetics, vol. 46, no. 8, pp. 826-836. https://doi.org/10.1038/ng.3014
Nature Genetics, Vol. 46, No 8 (2014) pp. 826-836
Arking, D E, Pulit, S L, Crotti, L, van der Harst, P, Munroe, P B, Koopmann, T T, Sotoodehnia, N, Rossin, E J, Morley, M, Wang, X, Johnson, A D, Lundby, A, Gudbjartsson, D F, Noseworthy, P A, Eijgelsheim, M, Bradford, Y, Tarasov, K V, Dörr, M, Müller-Nurasyid, M, Lahtinen, A M, Nolte, I M, Smith, A V, Bis, J C, Isaacs, A, Newhouse, S J, Evans, D S, Post, W S, Waggott, D, Lyytikäinen, L-P, Hicks, A A, Eisele, L, Ellinghaus, D, Hayward, C, Navarro, P, Ulivi, S, Tanaka, T, Tester, D J, Chatel, S, Gustafsson, S, Kumari, M, Morris, R W, Naluai, A T, Padmanabhan, S, Kluttig, A, Strohmer, B, Panayiotou, A G, Torres, M, Knoflach, M, Olsen, J V, Hansen, K L & CARe Consortium 2014, ' Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization ', Nature Genetics, vol. 46, no. 8, pp. 826-838 . https://doi.org/10.1038/ng.3014
Arking, D E, Pulit, S L, Crotti, L, Van Der Harst, P, Munroe, P B, Koopmann, T T, Sotoodehnia, N, Rossin, E J, Morley, M, Wang, X, Johnson, A D, Lundby, A, Gudbjartsson, D F, Noseworthy, P A, Eijgelsheim, M, Bradford, Y, Tarasov, K V, Dörr, M, Müller-Nurasyid, M, Lahtinen, A M, Nolte, I M, Smith, A V, Bis, J C, Isaacs, A, Newhouse, S J, Evans, D S, Post, W S, Waggott, D, Lyytikäinen, L P, Hicks, A A, Eisele, L, Ellinghaus, D, Hayward, C, Navarro, P, Ulivi, S, Tanaka, T, Tester, D J, Chatel, S, Gustafsson, S, Kumari, M, Morris, R W, Naluai, A T, Padmanabhan, S, Kluttig, A, Strohmer, B, Panayiotou, A G, Torres, M, Knoflach, M, Hubacek, J A, Slowikowski, K, Raychaudhuri, S, Kumar, R D, Harris, T B, Launer, L J, Shuldiner, A R, Alonso, A, Bader, J S, Ehret, G, Huang, H, Kao, W H L, Strait, J B, Macfarlane, P W, Brown, M, Caulfield, M J, Samani, N J, Kronenberg, F, Willeit, J, Smith, J G, Greiser, K H, Zu Schwabedissen, H M, Werdan, K, Carella, M, Zelante, L, Heckbert, S R, Psaty, B M, Rotter, J I, Kolcic, I, Polašek, O, Wright, A F, Griffin, M, Daly, M J, Arnar, D O, Hólm, H, Thorsteinsdottir, U, Denny, J C, Roden, D M, Zuvich, R L, Emilsson, V, Plump, A S, Larson, M G, O'Donnell, C J, Yin, X, Bobbo, M, D'Adamo, A P, Iorio, A, Sinagra, G, Carracedo, A, Cummings, S R, Nalls, M A, Jula, A, Kontula, K K, Marjamaa, A, Oikarinen, L, Perola, M, Porthan, K, Erbel, R, Hoffmann, P, Jöckel, K H, Kälsch, H, Nöthen, M M, Den Hoed, M, Loos, R J F, Thelle, D S, Gieger, C, Meitinger, T, Perz, S, Peters, A, Prucha, H, Sinner, M F, Waldenberger, M, De Boer, R A, Franke, L, Van Der Vleuten, P A, Beckmann, B M, Martens, E, Bardai, A, Hofman, N, Wilde, A A M, Behr, E R, Dalageorgou, C, Giudicessi, J R, Medeiros-Domingo, A, Barc, J, Kyndt, F, Probst, V, Ghidoni, A, Insolia, R, Hamilton, R M, Scherer, S W, Brandimarto, J, Margulies, K, Moravec, C E, Del Greco M, F, Fuchsberger, C, O'Connell, J R, Lee, W K, Watt, G C M, Campbell, H, Wild, S H, El Mokhtari, N E, Frey, N, Asselbergs, F W, Leach, I M, Navis, G, Van Den Berg, M P, Van Veldhuisen, D J, Kellis, M, Krijthe, B P, Franco, O H, Hofman, A, Kors, J A, Uitterlinden, A G, Witteman, J C M, Kedenko, L, Lamina, C, Oostra, B A, Abecasis, G R, Lakatta, E G, Mulas, A, Orrú, M, Schlessinger, D, Uda, M, Markus, M R P, Völker, U, Snieder, H, Spector, T D, Ärnlöv, J, Lind, L, Sundström, J, Syvänen, A C, Kivimaki, M, Kähönen, M, Mononen, N, Raitakari, O T, Viikari, J S, Adamkova, V, Kiechl, S, Brion, M, Nicolaides, A N, Paulweber, B, Haerting, J, Dominiczak, A F, Nyberg, F, Whincup, P H, Hingorani, A D, Schott, J J, Bezzina, C R, Ingelsson, E, Ferrucci, L, Gasparini, P, Wilson, J F, Rudan, I, Franke, A, Mühleisen, T W, Pramstaller, P P, Lehtimäki, T J, Paterson, A D, Parsa, A, Liu, Y, Van Duijn, C M, Siscovick, D S, Gudnason, V, Jamshidi, Y, Salomaa, V, Felix, S B, Sanna, S, Ritchie, M D, Stricker, B H, Stefansson, K, Boyer, L A, Cappola, T P, Olsen, J V, Lage, K, Schwartz, P J, Kääb, S, Chakravarti, A, Ackerman, M J, Pfeufer, A, De Bakker, P I W & Newton-Cheh, C 2014, 'Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization', Nature Genetics, vol. 46, no. 8, pp. 826-836. https://doi.org/10.1038/ng.3014
Academic Journal
Lionel AC; Tammimies K; Vaags AK; Rosenfeld JA; Ahn JW; Merico D; Noor A; Runke CK; Pillalamarri VK; Carter MT; Gazzellone MJ; Thiruvahindrapuram B; Fagerberg C; Laulund LW; Pellecchia G; Lamoureux S; Deshpande C; Clayton Smith J; White AC; Leather S; Trounce J; Melanie Bedford H; Hatchwell E; Eis PS; Yuen RK; Walker S; Uddin M; Geraghty MT; Nikkel SM; Tomiak EM; Fernandez BA; Soreni N; Crosbie J; Arnold PD; Schachar RJ; Roberts W; Paterson AD; So J; Szatmari P; Chrysler C; Woodbury Smith M; Brian Lowry R; Zwaigenbaum L; Mandyam D; Wei J; Macdonald JR; Howe JL; Nalpathamkalam T; Wang Z; Tolson D; Cobb DS; Wilks TM; Sorensen MJ; Bader PI; An Y; Wu BL; Musumeci SA; Romano C; Postorivo D; Nardone AM; Monica MD; Scarano G; Zoccante L; Novara F; Zuffardi O; Ciccone R; Antona V; Carella M; Zelante L; Cavalli P; Poggiani C; Cavallari U; Argiropoulos B; Chernos J; Brasch Andersen C; Speevak M; FICHERA, Marco; Ogilvie CM; Shen Y; Hodge JC; Talkowski ME; Stavropoulos DJ; Marshall CR; Scherer SW
Lionel, A C, Tammimies, K, Vaags, A K, Rosenfeld, J A, Ahn, J W, Merico, D, Noor, A, Runke, C K, Pillalamarri, V K, Carter, M T, Gazzellone, M J, Thiruvahindrapuram, B, Fagerberg, C R, Laulund, L W, Pellecchia, G, Lamoureux, S, Deshpande, C, Clayton-Smith, J, White, A C, Leather, S, Trounce, J, Bedford, H M, Hatchwell, E, Eis, P S, Yuen, R K C, Walker, S, Uddin, M, Geraghty, M T, Nikkel, S M, Tomiak, E M, Fernandez, B A, Soreni, N, Crosbie, J, Arnold, P D, Schachar, R J, Roberts, W, Paterson, A D, So, J, Szatmari, P, Chrysler, C, Woodbury-Smith, M, Lowry, R B, Zwaigenbaum, L, Mandyam, D, Wei, J, Macdonald, J R, Howe, J L, Nalpathamkalam, T, Wang, Z, Tolson, D, Cobb, D S, Wilks, T M, Sorensen, M J, Bader, P I, An, Y, Wu, B-L, Musumeci, S A, Romano, C, Postorivo, D, Nardone, A M, Della Monica, M, Scarano, G, Zoccante, L, Novara, F, Zuffardi, O, Ciccone, R, Antona, V, Carella, M, Zelante, L, Cavalli, P, Poggiani, C, Cavallari, U, Argiropoulos, B, Chernos, J, Brasch-Andersen, C, Speevak, M, Fichera, M, Ogilvie, C M, Shen, Y, Hodge, J C, Talkowski, M E, Stavropoulos, D J, Marshall, C R & Scherer, S W 2014, ' Disruption of the ASTN2 / TRIM32 locus at 9q33.1 is a risk factor in males for Autism Spectrum Disorders, ADHD and other neurodevelopmental phenotypes ', Human Molecular Genetics, vol. 23, no. 10, ddt669, pp. 2752-2768 . https://doi.org/10.1093/hmg/ddt669
Human Molecular Genetics, vol 23, iss 10
Human Molecular Genetics, vol 23, iss 10
Academic Journal
Dubuc, AM; Morrissy, AS; Kloosterhof, Nanne; Northcott, PA; Yu, EPY; Shih, D; Peacock, J; Grajkowska, W; van Meter, T; Eberhart, CG; Pfister, S; Marra, MA; Weiss, WA; Scherer, SW; Rutka, JT; French, Pim; Taylor, MD
Acta Neuropathologica. 123:485-499
Academic Journal
Rucker, JJH; Breen, G; Pinto, D; Pedroso, I; Lewis, CM; Cohen-Woods, S; Uher, R; Schosser, A; Rivera, M; Aitchison, KJ; Craddock, N; Owen, MJ; Jones, L; Jones, I; Korszun, A; Muglia, P; Barnes, MR; Preisig, M; Mors, O; Gill, M; Maier, W; Rice, J; Rietschel, M; Holsboer, F; Farmer, AE; Craig, IW; Scherer, SW; McGuffin, P
Mol Psychiatry
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Rucker, J J H, Breen, G, Pinto, D, Pedroso, I, Lewis, C M, Cohen-Woods, S, Uher, R, Schosser, A, Rivera, M, Aitchison, K J, Craddock, N, Owen, M J, Jones, L, Jones, I, Korszun, A, Muglia, P, Barnes, M R, Preisig, M, Mors, O, Gill, M, Maier, W, Rice, J, Rietschel, M, Holsboer, F, Farmer, A E, Craig, I W, Scherer, S W & McGuffin, P 2013, 'Genome-wide association analysis of copy number variation in recurrent depressive disorder', Molecular Psychiatry, vol. 18, pp. 183–189. https://doi.org/10.1038/mp.2011.144
Molecular Psychiatry, vol. 18, no. 2, pp. 183-189
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Academic Journal
Grafodatskaya, D; Drmic, I; Chung, BHY; Carter, M; Fernandez, BA; Scherer, SW; Roberts, W; Weksberg, R; Marshall, CR
European Journal of Medical Genetics. 54:e516-e520
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