학술논문

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학술논문
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'학술논문' 에서의 검색결과 12건 | 목록 1~10

  • 7 .
    Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
    저자
    by Andlauer, Till F M; Guzman-Parra, Jose; Orozco Diaz, Guillermo; Freimer, Nelson B; Frisén, Louise, et al. 
    소스
    Molecular Psychiatry, 26(4), 1286-1298. Nature Publishing Group
    Andlauer, T F M, Rietschel, M, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Abdellaoui, A, Derks, E M, Dolan, C V, Hottenga, J J, Mbarek, H, Middeldorp, C M, Milaneschi, Y, Nivard, M G, Peyrot, W J, Posthuma, D, Willemsen, G, Boomsma, D I, de Geus, E J C, W J H Penninx, B & Sullivan, P 2021, ' Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders ', Molecular Psychiatry, vol. 26, no. 4, pp. 1286-1298 . https://doi.org/10.1038/s41380-019-0558-2
    Molecular Psychiatry
    Molecular psychiatry 26, 1286–1298 (2021). doi:10.1038/s41380-019-0558-2
    Andlauer, T F M, Guzman-Parra, J, Streit, F, Strohmaier, J, González, M J, Gil Flores, S, Cabaleiro Fabeiro, F J, del Río Noriega, F, Perez, F P, Haro González, J, Orozco Diaz, G, de Diego-Otero, Y, Moreno-Küstner, B, Auburger, G, Degenhardt, F, Heilmann-Heimbach, S, Herms, S, Hoffmann, P, Frank, J, Foo, J C, Treutlein, J, Witt, S H, Cichon, S, Kogevinas, M, Stahl, E A, Breen, G, Forstner, A J, McQuillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H A, de Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Pers, T H, Holmans, P A, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-Rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-Hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B, Bøen, E, Boks, M, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-Grauholm, J, Byerley, W, Casas, M, Cerrato, F, Cervantes, P, Chambert, K, Charney, A W, Chen, D, Churchhouse, C, Clarke, T K, Coryell, W, Craig, D W, Cruceanu, C, Czerski, P M, Dale, A M, de Jong, S, Degenhardt, F, Del-Favero, J, DePaulo, J R, Djurovic, S, Dobbyn, A L, Dumont, A, Elvsåshagen, T, Escott-Price, V, Fan, C C, Fischer, S B, Flickinger, M, Foroud, T M, Forty, L, Frank, J, Fraser, C, Freimer, N B, Frisén, L, Gade, K, Gage, D, Garnham, J, Giambartolomei, C, Pedersen, M G, Goldstein, J, Gordon, S D, Gordon-Smith, K, Green, E K, Green, M J, Greenwood, T A, Grove, J, Guan, W, Parra, J G, Hamshere, M L, Hautzinger, M, Heilbronner, U, Herms, S, Hipolito, M, Hoffmann, P, Holland, D, Huckins, L, Jamain, S, Johnson, J S, Juréus, A, Kandaswamy, R, Karlsson, R, Kennedy, J L, Kittel-Schneider, S, Knowles, J A, Kogevinas, M, Koller, A C, Kupka, R, Lavebratt, C, Lawrence, J, Lawson, W B, Leber, M, Lee, P H, Levy, S E, Li, J Z, Liu, C, Lucae, S, Maaser, A, MacIntyre, D J, Mahon, P B, Maier, W, Martinsson, L, McCarroll, S, McGuffin, P, McInnis, M G, McKay, J D, Medeiros, H, Medland, S E, Meng, F, Milani, L, Montgomery, G W, Morris, D W, Mühleisen, T W, Mullins, N, Nguyen, H, Nievergelt, C M, Adolfsson, A N, Nwulia, E A, O’Donovan, C, Loohuis, L M O, Ori, A P S, Oruc, L, Ösby, U, Perlis, R H, Perry, A, Pfennig, A, Potash, J B, Purcell, S M, Regeer, E J, Reif, A, Reinbold, C S, Rice, J P, Richards, A L, Rivas, F, Rivera, M, Roussos, P, Ruderfer, D M, Ryu, E, Sánchez-Mora, C, Schatzberg, A F, Scheftner, W A, Schork, N J, Weickert, C S, Shehktman, T, Shilling, P D, Sigurdsson, E, Slaney, C, Smeland, O B, Sobell, J L, Hansen, C S, Spijker, A T, Clair, D S, Steffens, M, Strauss, J S, Streit, F, Strohmaier, J, Szelinger, S, Thompson, R C, EThorgeirsson, T, Treutlein, J, Vedde, H, Wang, W, Watson, S J, Weickert, T W, Witt, S H, Xi, S, Xu, W, Young, A H, Zandi, P, Zhang, P, Zollner, S, Adolfsson, R, Agartz, I, Alda, M, Backlund, L, Baune, B T, Bellivier, F, Berrettini, W H, Biernacka, J M, Blackwood, D H R, Boehnke, M, Børglum, A D, Corvin, A, Craddock, N, Daly, M J, Dannlowski, U, Esko, T, Etain, B, Frye, M, Fullerton, J M, Gershon, E S, Gill, M, Goes, F S, Grigoroiu-Serbanescu, M, Hauser, J, Hougaard, D M, Hultman, C M, Jones, I, Jones, L A, Kahn, R S, Kirov, G, Landén, M, Leboyer, M, Lewis, C M, Li, Q S, Lissowska, J, Martin, N G, Mayoral, F, McElroy, S L, McIntosh, A M, McMahon, F J, Melle, I, Metspalu, A, Mitchell, P B, Morken, G, Mors, O, Mortensen, P B, Müller-Myhsok, B, Myers, R M, Neale, B M, Nimgaonkar, V, Nordentoft, M, Nöthen, M M, O’Donovan, M C, Oedegaard, K J, Owen, M J, Paciga, S A, Pato, C, Pato, M T, Posthuma, D, Ramos-Quiroga, J A, Ribasés, M, Rietschel, M, Rouleau, G A, Schalling, M, Schofield, P R, Schulze, T G, Serretti, A, Smoller, J W, Stefansson, H, Stefansson, K, Stordal, E, Sullivan, P F, Turecki, G, Vaaler, A E, Vieta, E, Vincent, J B, Werge, T, Nurnberger, J I, Wray, N R, Florio, A D, Edenberg, H J, Cichon, S, Ophoff, R A, Scott, L J, Andreassen, O A, Kelsoe, J, Sklar, P, Ripke, S, Mattheisen, M, Trzaskowski, M, Byrne, E M, Abdellaoui, A, Adams, M J, Agerbo, E, Air, T M, Bacanu, S A, Bækvad-Hansen, M, Beekman, A T F, Bigdeli, T B, Binder, E B, Bryois, J, Buttenschøn, H N, Bybjerg-Grauholm, J, Cai, N, Castelao, E, Christensen, J H, Clarke, T K, Coleman, J R I, Colodro-Conde, L, Couvy-Duchesne, B, Craddock, N, Crawford, G E, Davies, G, Deary, I J, Degenhardt, F, Derks, E M, Direk, N, Dolan, C V, Dunn, E C, Eley, T C, Escott-Price, V, Kiadeh, F F H, Finucane, H K, Foo, J C, Forstner, A J, Frank, J, Gaspar, H A, Gill, M, Goes, F S, Gordon, S D, Grove, J, Hall, L S, Hansen, C S, Hansen, T F, Herms, S, Hickie, I B, Hoffmann, P, Homuth, G, Horn, C, Hottenga, J J, Hougaard, D M, Howard, D M, Ising, M, Jansen, R, Jorgenson, E, Knowles, J A, Kohane, I S, Hill, Kraft, J, Kretzschmar, W W, Kutalik, Z, Li, Y, Lind, P A, MacIntyre, D J, MacKinnon, D F, Maier, R M, Maier, W, Marchini, J, Mbarek, H, McGrath, P, McGuffin, P, Mehta, D, Middeldorp, C M, Mihailov, E, Milaneschi, Y, Milani, L, Mondimore, F M, Montgomery, G W, Mostafavi, S, Mullins, N, Nauck, M, Ng, B, Nivard, M G, Nyholt, D R, O’Reilly, P F, Oskarsson, H, Painter, J N, Pedersen, C B, Pedersen, M G, Peterson, R E, Pettersson, E, Peyrot, W J, Pistis, G, Posthuma, D, Quiroz, J A, Qvist, P, Rice, J P, Riley, B P, Rivera, M, Mirza, S S, Schoevers, R, Schulte, E C, Shen, L, Shi, J, Shyn, S I, Sigurdsson, E, Sinnamon, G C B, Smit, J H, Smith, D J, Steinberg, S, Streit, F, Strohmaier, J, Tansey, K E, Teismann, H, Teumer, A, Thompson, W, Thomson, P A, Thorgeirsson, T E, Traylor, M, Treutlein, J, Trubetskoy, V, Uitterlinden, A G, Umbricht, D, Van der Auwera, S, van Hemert, A M, Viktorin, A, Visscher, P M, Wang, Y, Webb, B T, Weinsheimer, S M, Wellmann, J, Willemsen, G, Witt, S H, Wu, Y, Xi, H S, Yang, J, Zhang, F, Arolt, V, Baune, B T, Berger, K, Boomsma, D I, Cichon, S, de Geus, E J C, DePaulo, J R, Domenici, E, Domschke, K, Esko, T, Grabe, H J, Hamilton, S P, Hayward, C, Heath, A C, Kendler, K S, Kloiber, S, Lewis, G, Li, Q S, Lucae, S, Madden, P A F, Magnusson, P K, Martin, N G, McIntosh, A M, Metspalu, A, Mors, O, Müller-Myhsok, B, Nordentoft, M, Nöthen, M M, O’Donovan, M C, Paciga, S A, Pedersen, N L, Penninx, B W J H, Perlis, R H, Porteous, D J, Potash, J B, Preisig, M, Rietschel, M, Schaefer, C, Schulze, T G, Smoller, J W, Tiemeier, H, Uher, R, Völzke, H, Weissman, M M, Werge, T, Levinson, D F, Børglum, A D, Sullivan, P F, Rivas, F, Mayoral, F, Müller-Myhsok, B, Forstner, A J, Nöthen, M M, Rietschel, M, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2021, ' Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders ', Molecular Psychiatry, vol. 26, no. 4, pp. 1286-1298 . https://doi.org/10.1038/s41380-019-0558-2
    Andlauer, T F M, Guzman-Parra, J, Streit, F, Strohmaier, J, González, M J, Gil Flores, S, Cabaleiro Fabeiro, F J, Del Río Noriega, F, Perez, F P, Haro González, J, Orozco Diaz, G, de Diego-Otero, Y, Moreno-Küstner, B, Auburger, G, Degenhardt, F, Heilmann-Heimbach, S, Herms, S, Hoffmann, P, Frank, J, Foo, J C, Treutlein, J, Witt, S H, Cichon, S, Kogevinas, M, Rivas, F, Mayoral, F, Müller-Myhsok, B, Forstner, A J, Nöthen, M M, Rietschel, M & Bipolar Disorder Working Group of the Psychiatric Genomics Consortium 2021, ' Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders ', Molecular Psychiatry, vol. 26, no. 4, pp. 1286-1298 . https://doi.org/10.1038/s41380-019-0558-2
    Print: 1359-4184
    Andlauer, T F M, Guzman-Parra, J, Streit, F, Strohmaier, J, González, M J, Gil Flores, S, Cabaleiro Fabeiro, F J, del Río Noriega, F, Perez, F P, Haro González, J, Orozco Diaz, G, de Diego-Otero, Y, Moreno-Küstner, B, Auburger, G, Degenhardt, F, Heilmann-Heimbach, S, Herms, S, Hoffmann, P, Frank, J, Foo, J C, Treutlein, J, Witt, S H, Cichon, S, Kogevinas, M, Stahl, E A, Breen, G, Forstner, A J, McQuillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H A, de Leeuw, C A, Steinberg, S, Pers, T H, Bækvad-Hansen, M, Pedersen, C B, Pedersen, M G, Hansen, C S, Nordentoft, M, Werge, T, Hansen, T F, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2021, ' Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders ', Molecular Psychiatry, vol. 26, no. 4, pp. 1286-1298 . https://doi.org/10.1038/s41380-019-0558-2
    Molecular psychiatry, 26(4), 1286-1298. Nature Publishing Group
    Deary, I & Davies, G 2019, ' Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders ', Molecular Psychiatry, vol. 26, no. 1, pp. 1286–1298 . https://doi.org/10.1038/s41380-019-0558-2
  • 7 .
    Complement genes contribute sex-biased vulnerability in diverse disorders
    저자
    by Kamitaki, Nolan; Sekar, Aswin; Consortium, Schizophrenia Working Group of the Psychiatric Genomics; Friedman, Joseph I; Fromer, Menachem, et al. 
    소스
    Nature, 582, 577-581. Nature Publishing Group
    Nature, 582(7813), 577-581. Nature Publishing Group
    Nature 582(7813), 577-581 (2020). doi:10.1038/s41586-020-2277-x
    Nature
    Schizophrenia Working Group of the Psychiatric Genomics Consortium, Psychosis Endophenotypes International Consortium & Wellcome Trust Case–Control Consortium 2 2020, ' Complement genes contribute sex-biased vulnerability in diverse disorders ', Nature, vol. 582, no. 7813, pp. 577-581 . https://doi.org/10.1038/s41586-020-2277-x
    Nature, vol 582, iss 7813
    Nature. Nature Publishing Group
    Kamitaki, N, Sekar, A, Handsaker, R E, de Rivera, H, Tooley, K, Morris, D L, Taylor, K E, Whelan, C W, Tombleson, P, Loohuis, L M O, Psychosis Endophenotypes International Consortium, Wellcome Trust Case–Control Consortium 2, Psychosis Endophenotype International Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Boehnke, M, Kimberly, R P, Kaufman, K M, Harley, J B, Langefeld, C D, Seidman, C E, Pato, M T, Pato, C N, Ophoff, R A, Graham, R R, Criswell, L A, Vyse, T J & McCarroll, S A 2020, ' Complement genes contribute sex-biased vulnerability in diverse disorders ', Nature . https://doi.org/10.1038/s41586-020-2277-x
    Kamitaki, N, Sekar, A, Handsaker, R E, de Rivera, H, Tooley, K, Morris, D L, Taylor, K E, Whelan, C W, Tombleson, P, Loohuis, L M O, Boehnke, M, Kimberly, R P, Kaufman, K M, Harley, J B, Langefeld, C D, Seidman, C E, Pato, M T, Pato, C N, Ophoff, R A, Graham, R R, Criswell, L A & Vyse, T J & McCarroll, S A 2020, ' Complement genes contribute sex-biased vulnerability in diverse disorders ', Nature, vol. 582, no. 7813, pp. 577-581 . https://doi.org/10.1038/s41586-020-2277-x
    Kamitaki, N, Sekar, A, Handsaker, R E, de Rivera, H, Tooley, K, Morris, D L, Taylor, K E, Whelan, C W, Tombleson, P, Loohuis, L M O, Boehnke, M, Kimberly, R P, Kaufman, K M, Harley, J B, Langefeld, C D, Seidman, C E, Pato, M T, Pato, C N, Ophoff, R A, Graham, R R, Criswell, L A, Vyse, T J, McCarroll, S A & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2020, ' Complement genes contribute sex-biased vulnerability in diverse disorders ', Nature, vol. 582, no. 7813, pp. 577-581 . https://doi.org/10.1038/s41586-020-2277-x
  • 7 .
    Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa
    저자
    by Walton, E; Hibar, D; Yilmaz, Z; Jahanshad, N; Cheung, J, et al. 
    소스
    Molecular neurobiology 56(7), 5146-5156 (2019). doi:10.1007/s12035-018-1439-4
    Molecular neurobiology, vol 56, iss 7
    Dipòsit Digital de la UB
    Universidad de Barcelona
    PGC-ED, ENIGMA Genetics Working Group & Milaneschi, Y 2019, ' Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa ', Molecular Neurobiology, vol. 56, no. 7, pp. 5146-5156 . https://doi.org/10.1007/s12035-018-1439-4
    Molecular Neurobiology, 56(7), 5146. Humana Press
    Walton, E, Hibar, D, Yilmaz, Z, Jahanshad, N, Batury, V-L, Seitz, J, Bulik, C M & Thompson, P M & Ehrlich, S 2019, ' Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa ', Molecular Neurobiology, vol. 56, no. 7, pp. 5146-5156 . https://doi.org/10.1007/s12035-018-1439-4
    MOLECULAR NEUROBIOLOGY
    Molecular neurobiology, 56(7), 5146-5156. Humana Press
    Molecular Neurobiology
    Molecular Neurobiology, 56(7), 5146-5156. Humana Press
  • 7 .
    Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
    저자
    by Franke, Barbara; Stein, Jason L; McIntosh, Andrew M; Eichhammer, Peter; Eriksson, Johan, et al. 
    소스
    Nature Neuroscience
    Nature Neuroscience, Nature Publishing Group, 2016, 19 (3), pp.420-431. ⟨10.1038/nn.4228⟩
    Nature neuroscience, 19(3), 420-431. NATURE AMERICA INC
    Nature neuroscience
    Nature Neuroscience, 19(3), 420. Nature Publishing Group
    Franke, B, Stein, J L, Ripke, S, Anttila, V, Hibar, D P, van Hulzen, K J E, Arias-Vasquez, A, Smoller, J W, Nichols, T E, Neale, M C, McIntosh, A M, Lee, P, McMahon, F J, Meyer-Lindenberg, A, Mattheisen, M, Andreassen, O A, Gruber, O, Sachdev, P S, Roiz-Santiañez, R, Saykin, A J, Ehrlich, S, Mather, K A, Turner, J A, Schwarz, E, Thalamuthu, A, Yao, Y, Ho, Y Y W, Martin, N G, Wright, M J, O'Donovan, M C, Thompson, P M & Neale, B M & Medland, S E & Sullivan, P F 2016, ' Genetic influences on schizophrenia and subcortical brain volumes : Large-scale proof of concept ', Nature Neuroscience, vol. 19, no. 3, pp. 420–431 . https://doi.org/10.1038/nn.4228
    Nature Neuroscience, 2016, 19 (3), pp.420-431. ⟨10.1038/nn.4228⟩
    Nature neuroscience, vol 19, iss 3
    Nature Neuroscience, 19, 420-31
    Franke, B, Stein, J L, Ripke, S, Anttila, V, Hibar, D P, van Hulzen, K J E, Arias-Vasquez, A, Smoller, J W, Nichols, T E, Neale, M C, McIntosh, A M, Lee, P, McMahon, F J, Meyer-Lindenberg, A, Mattheisen, M, Andreassen, O A, Gruber, O, Sachdev, P S, Roiz-Santiañez, R, Saykin, A J, Ehrlich, S, Mather, K A, Turner, J A, Schwarz, E, Thalamuthu, A, Yao, Y, Ho, Y Y W, Martin, N G, Wright, M J, O'Donovan, M C, Thompson, P M, Neale, B M, Medland, S E, Sullivan, P F & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2016, ' Genetic influences on schizophrenia and subcortical brain volumes : large-scale proof of concept ', Nature Neuroscience, vol. 19, no. 3, pp. 420-31 . https://doi.org/10.1038/nn.4228
    Franke, Barbara; Franke, Barbara; Stein, Jason L; Ripke, Stephan; Anttila, Verneri; Hibar, Derrek P; et al.(2016). Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept.. Nature neuroscience, 19(3), 420-431. doi: 10.1038/nn.4228. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/96n5p3jc
    Nature Neuroscience, 19, 3, pp. 420-31
    Nature reviews / Neuroscience 19(3), 420-431 (2016). doi:10.1038/nn.4228
    Nature Neuroscience, 19(3), 420-431. Nature Publishing Group
    Nature neuroscience, 19(3), 420-+. Nature Publishing Group
    Franke, B, Stein, J L, Ripke, S, Anttila, V, Hibar, D P, van Hulzen, K J E, Arias-Vasquez, A, Smoller, J W, Nichols, T E, Neale, M C, McIntosh, A M, Lee, P, McMahon, F J, Meyer-Lindenberg, A, Mattheisen, M, Andreassen, O A, Gruber, O, Sachdev, P S, Roiz-Santiañez, R, Saykin, A J, Ehrlich, S, Mather, K A, Turner, J A, Schwarz, E, Thalamuthu, A, Yao, Y, Ho, Y Y W, Martin, N G, Wright, M J, den Braber, A, Fedko, I O, Hottenga, J J, van t Ent, D, Boomsma, D I, de Geus, E J C, O'Donovan, M C, Thompson, P M, Neale, B M, Medland, S E & Sullivan, P F 2016, ' Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept ', Nature Neuroscience, vol. 19, no. 3, pp. 420-431 . https://doi.org/10.1038/nn.4228
  • 7 .
    Rare and low-frequency coding variants alter human adult height
    저자
    by Marouli, Eirini; Graff, Mariaelisa; Medina-Gomez, Carolina; Lo, Ken Sin; Wood, Andrew R, et al. 
    소스
    Nature, 542, 186-190
    Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Li, J, Posthuma, D, van Schoor, N M & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
    Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjær, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Jørgensen, T & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
    Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Posthuma, D & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
    NATURE
    Nature, 542(7640), 186-190. Nature Publishing Group
    Nature 542, 186-190 (2017)
    Nature
    Nature, vol 542, iss 7640
    Marouli, E, Graff, M, Medina-Gómez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V R, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Brandslund, I, Christensen, C, Hansen, T, Jensen, G B, Jørgensen, M E & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
    Marouli, E, Graff, M, Medina-Gómez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S M, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Oxvig, C & EPIC InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
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    Nature, 542(7640), 186-190
    Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Lophatananon, A & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
    Nature, 542, 7640, pp. 186-190
    Nature, 542(7640), 186. Nature Research
    Nature, vol. 542, no. 7640, pp. 186-190
    Marouli, E; Graff, M; Medina-Gomez, C; Lo, KS; Wood, AR; Kjaer, TR; et al.(2017). Rare and low-frequency coding variants alter human adult height. Nature, 542(7640), 186-190. doi: 10.1038/nature21039. UCLA: Retrieved from: http://www.escholarship.org/uc/item/1sq5r8fb
    Nature, 542, 186. Nature Publishing Group
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