Zobrazeno 1 - 10
of 210
pro vyhledávání: '"Windham, BG"'
Autor:
Shihua Li, Melissa J. Green, Nagata M, Miyamoto S, Le Grand Q, Pourcain Bs, Grabe Hj, Catherine Helmer, William R. Reay, Nele Friedrich, Mazoyer B, Seshadri S, Per Hoffmann, Simon Haworth, Veronica Witte A, Yang Q, Max Lam, Teunissen Mw, Fang-Chi Hsu, Debette S, Murray J. Cairns, Amod Ar, Setoh K, Windham Bg, Shareefa Dalvie, Georg Homuth, Charlie S. DeCarli, Gennady V. Roshchupkin, Céline S. Reinbold, Mühleisen Tw, Nakahara S, Van der Auwera S, Xueqiu Jian, Cecil Ca, Jean-François Dartigues, Alexa S. Beiser, Stein Jl, Houlden H, Christiane Jockwitz, Moebus S, Claudia L. Satizabal, Tavia E. Evans, Matsuda F, Cora E. Lewis, Wittfeld K, Calhoun Vd, van der Lugt A, Teumer A, Pausova Z, W. T. Longstreth, Aniket Mishra, Tomáš Paus, Vernooij Mw, Medland Se, Palmer Nd, Ahmad R. Hariri, Adrian Preda, Clifford R. Jack, van Erp Tg, Amaia Carrion-Castillo, Werring Dj, Gwénaëlle Catheline, Asta Håberg, Robin Bülow, Sven Cichon, Yann Quidé, Muetzel R, Tabara Y, Sidney S, Cheung C, Brunner Hg, Annchen R. Knodt, Mosley Th, van Dam-Nolen Dh, Hostettler Ic, Jean Shin, Shapland Cy, Reut Avinun, Crivello F, Mäkitie O, Fornage M, Yoshida K, Villringer A, Lim K, Schreiner Pj, Bowden Dw, Thompson Pm, Daniel Bos, Uhlmann A, Enlund-Cerullo M, Schmidt R, Hieab H.H. Adams, Neda Jahanshad, Frauke Beyer, Gloria H.Y. Li, Fabio Macciardi, Lamballais S, Kämpe A, Judith M. Ford, Poot Ra, J. C. Bis, Yoichiro Kamatani, Ami Tsuchida, Markus Scholz, Ikram Ma, Andersson S, Lenore J. Launer, Stein Dj, Koudstaal Pj, Barry I. Freedman, Barbara Franke, Ikram Mk, Sim K, Marie-Gabrielle Duperron, Bryan Rn, Svenja Caspers, Pawlak Ma, Tonya White, Maria J. Knol
Publikováno v:
bioRxiv
The size of the human head is determined by growth in the first years of life, while the rest of the body typically grows until early adulthood1. Such complex developmental processes are regulated by various genes and growth pathways2. Rare genetic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7257a6f2bd075e933a9651bd717040d3
https://doi.org/10.1101/2020.07.15.191114
https://doi.org/10.1101/2020.07.15.191114
Autor:
Davies, G, Lam, M, Harris, SE, Trampush, JW, Luciano, M, Hill, WD, Hagenaars, SP, Ritchie, SJ, Marioni, RE, Fawns-Ritchie, C, Liewald, DCM, Okely, JA, Ahola-Olli, AV, Barnes, CLK, Bertram, L, Bis, JC, Burdick, KE, Christoforou, A, Derosse, P, Djurovic, S, Espeseth, T, Giakoumaki, S, Giddaluru, S, Gustavson, DE, Hayward, C, Hofer, E, Ikram, MA, Karlsson, R, Knowles, E, Lahti, J, Leber, M, Li, S, Mather, KA, Melle, I, Morris, D, Oldmeadow, C, Palviainen, T, Payton, A, Pazoki, R, Petrovic, K, Reynolds, CA, Sargurupremraj, M, Scholz, M, Smith, JA, Smith, AV, Terzikhan, N, Thalamuthu, A, Trompet, S, Van Der Lee, SJ, Ware, EB, Windham, BG, Wright, MJ, Yang, J, Yu, J, Ames, D, Amin, N, Amouyel, P, Andreassen, OA, Armstrong, NJ, Assareh, AA, Attia, JR, Attix, D, Avramopoulos, D, Bennett, DA, Böhmer, AC, Boyle, PA, Brodaty, H
Publikováno v:
Davies, G; Lam, M; Harris, SE; Trampush, JW; Luciano, M; Hill, WD; et al.(2018). Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications, 9(1). doi: 10.1038/s41467-018-04362-x. UCLA: Retrieved from: http://www.escholarship.org/uc/item/13g1w2rc
© 2018 The Author(s). General cognitive function is a prominent and relatively stable human trait that is associated with many important life outcomes. We combine cognitive and genetic data from the CHARGE and COGENT consortia, and UK Biobank (total
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::6015d06c9226adc75509fd8642b513a0
http://www.escholarship.org/uc/item/13g1w2rc
http://www.escholarship.org/uc/item/13g1w2rc
Autor:
Davies, G, Armstrong, N, Bis, JC, Bressler, J, Chouraki, V, Giddaluru, S, Hofer, E, Ibrahim-Verbaas, CA, Kirin, M, Lahti, J, van der Lee, SJ, Le Hellard, S, Liu, T, Marioni, RE, Oldmeadow, C, Postmus, I, Smith, AV, Smith, JA, Thalamuthu, A, Thomson, R, Vitart, V, Wang, J, Yu, L, Zgaga, L, Zhao, W, Boxall, R, Harris, SE, Hill, WD, Liewald, DC, Luciano, M, Adams, H, Ames, D, Amin, N, Amouyel, P, Assareh, AA, Au, R, Becker, JT, Beiser, A, Berr, C, Bertram, L, Boerwinkle, E, Buckley, BM, Campbell, H, Corley, J, De Jager, PL, Dufouil, C, Eriksson, JG, Espeseth, T, Faul, JD, Ford, I, Generation Scotland, Gottesman, RF, Griswold, ME, Gudnason, V, Harris, TB, Heiss, G, Hofman, A, Holliday, EG, Huffman, J, Kardia, SLR, Kochan, N, Knopman, DS, Kwok, JB, Lambert, J-C, Lee, T, Li, G, Li, S-C, Loitfelder, M, Lopez, OL, Lundervold, AJ, Lundqvist, A, Mather, KA, Mirza, SS, Nyberg, L, Oostra, BA, Palotie, A, Papenberg, G, Pattie, A, Petrovic, K, Polasek, O, Psaty, BM, Redmond, P, Reppermund, S, Rotter, JI, Schmidt, H, Schuur, M, Schofield, PW, Scott, RJ, Steen, VM, Stott, DJ, van Swieten, JC, Taylor, KD, Trollor, J, Trompet, S, Uitterlinden, AG, Weinstein, G, Widen, E, Windham, BG, Jukema, JW, Wright, AF
Publikováno v:
Molecular psychiatry, vol 20, iss 2
General cognitive function is substantially heritable across the human life course from adolescence to old age. We investigated the genetic contribution to variation in this important, health- and well-being-related trait in middle-aged and older adu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e4faf92e84ee9c023cc8a4990e7362b0
https://escholarship.org/uc/item/1195r9dg
https://escholarship.org/uc/item/1195r9dg
Autor:
Davies, Gail, Armstrong, N, Bis, JC, Bressler, J, Chouraki, V, Giddaluru, Sudheer, Hofer, E, Ibrahim-Verbaas, CA, Kirin, M, Lahti, J, Van Der Lee, SJ, Le Hellard, Stephanie, Liu, T, Marioni, RE, Oldmeadow, C, Postmus, I, Smith, AV, Smith, JA, Thalamuthu, A, Thomson, R, Vitart, V, Wang, J, Yu, L, Zgaga, L, Zhao, W, Boxall, R, Harris, SE, Hill, WD, Liewald, DC, Luciano, M, Adams, H, Ames, D, Amin, N, Amouyel, P, Assareh, AA, Au, R, Becker, JT, Beiser, A, Berr, C, Bertram, L, Boerwinkle, E, Buckley, BM, Campbell, H, Corley, J, De Jager, PL, Dufouil, C, Eriksson, JG, Espeseth, Thomas, Faul, JD, Ford, I, Scotland, Generation, Gottesman, RF, Griswold, ME, Gudnason, V, Harris, TB, Heiss, G, Hofman, A, Holliday, EG, Huffman, J, Kardia, SLR, Kochan, N, Knopman, DS, Kwok, JB, Lambert, JC, Lee, T, Li, G, Li, SC, Loitfelder, M, Lopez, OL, Lundervold, Astri, Lundqvist, A, Mather, KA, Mirza, SS, Nyberg, L, Oostra, BA, Palotie, A, Papenberg, G, Pattie, A, Petrovic, K, Polasek, O, Psaty, BM, Redmond, P, Reppermund, S, Rotter, JI, Schmidt, H, Schuur, M, Schofield, PW, Scott, RJ, Steen, Vidar Martin, Stott, DJ, Van Swieten, JC, Taylor, KD, Trollor, J, Trompet, S, Uitterlinden, AG, Weinstein, G, Widen, E, Windham, BG, Jukema, JW, Wright, AF, Wright, MJ, Yang, Q, Amieva, H, Attia, JR, Bennett, DA, Brodaty, H, De Craen, AJM, Hayward, C, Ikram, MA, Lindenberger, U, Nilsson, LG, Porteous, DJ, Räikkönen, K, Rudan, I, Sachdev, PS, Schmidt, R, Schofield, PR, Srikanth, V, Starr, JM, Turner, ST, Weir, DR, Wilson, JF, Van Duijn, C, Launer, L, Fitzpatrick, AL, Seshadri, S, Mosley, TH, Deary, IJ, Reinvang, Ivar
Publikováno v:
Davies, Gail Armstrong, N Bis, JC Bressler, J Chouraki, V Giddaluru, Sudheer Hofer, E Ibrahim-Verbaas, CA Kirin, M Lahti, J Van Der Lee, SJ Le Hellard, Stephanie Liu, T Marioni, RE Oldmeadow, C Postmus, I Smith, AV Smith, JA Thalamuthu, A Thomson, R Vitart, V Wang, J Yu, L Zgaga, L Zhao, W Boxall, R Harris, SE Hill, WD Liewald, DC Luciano, M Adams, H Ames, D Amin, N Amouyel, P Assareh, AA Au, R Becker, JT Beiser, A Berr, C Bertram, L Boerwinkle, E Buckley, BM Campbell, H Corley, J De Jager, PL Dufouil, C Eriksson, JG Espeseth, Thomas Faul, JD Ford, I Scotland, Generation Gottesman, RF Griswold, ME Gudnason, V Harris, TB Heiss, G Hofman, A Holliday, EG Huffman, J Kardia, SLR Kochan, N Knopman, DS Kwok, JB Lambert, JC Lee, T Li, G Li, SC Loitfelder, M Lopez, OL Lundervold, Astri Lundqvist, A Mather, KA Mirza, SS Nyberg, L Oostra, BA Palotie, A Papenberg, G Pattie, A Petrovic, K Polasek, O Psaty, BM Redmond, P Reppermund, S Rotter, JI Schmidt, H Schuur, M Schofield, PW Scott, RJ Steen, Vidar Martin Stott, DJ Van Swieten, JC Taylor, KD Trollor, J Trompet, S Uitterlinden, AG Weinstein, G Widen, E Windham, BG Jukema, JW Wright, AF Wright, MJ Yang, Q Amieva, H Attia, JR Bennett, DA Brodaty, H De Craen, AJM Hayward, C Ikram, MA Lindenberger, U Nilsson, LG Porteous, DJ Räikkönen, K Rudan, I Sachdev, PS Schmidt, R Schofield, PR Srikanth, V Starr, JM T
Molecular Psychiatry
Molecular Psychiatry
Externí odkaz:
http://hdl.handle.net/10852/48372
https://www.duo.uio.no/bitstream/handle/10852/48372/2/mp2014188a.pdf
https://www.duo.uio.no/bitstream/handle/10852/48372/2/mp2014188a.pdf
Autor:
Verhaaren, BFJ, Debette, S, Bis, JC, Smith, JA, Ikram, MK, Adams, HH, Beecham, AH, Rajan, KB, Lopez, LM, Barral, S, Van Buchem, MA, Van Der Grond, J, Smith, AV, Hegenscheid, K, Aggarwal, NT, De Andrade, M, Atkinson, EJ, Beekman, M, Beiser, AS, Blanton, SH, Boerwinkle, E, Brickman, AM, Bryan, RN, Chauhan, G, Chen, CPLH, Chouraki, V, De Craen, AJM, Crivello, F, Deary, IJ, Deelen, J, De Jager, PL, Dufouil, C, Elkind, MSV, Evans, DA, Freudenberger, P, Gottesman, RF, Gunason, V, Habes, M, Heckbert, SR, Heiss, G, Hilal, S, Hofer, E, Hofman, A, Ibrahim-Verbaas, CA, Knopman, DS, Lewis, CE, Liao, J, Liewald, DCM, Luciano, M, Van Der Lugt, A, Martinez, OO, Mayeux, R, Mazoyer, B, Nalls, M, Nauck, M, Niessen, WJ, Oostra, BA, Psaty, BM, Rice, KM, Rotter, JI, Von Sarnowski, B, Schmidt, H, Schreiner, PJ, Schuur, M, Sidney, SS, Sigurdsson, S, Slagboom, PE, Stott, DJM, Van Swieten, JC, Teumer, A, Töglhofer, AM, Traylor, M, Trompet, S, Turner, ST, Tzourio, C, Uh, HW, Uitterlinden, AG, Vernooij, MW, Wang, JJ, Wong, TY, Wardlaw, JM, Windham, BG, Wittfeld, K, Wolf, C, Wright, CB, Yang, Q, Zhao, W, Zijdenbos, A, Jukema, JW, Sacco, RL, Kardia, SLR, Amouyel, P, Mosley, TH, Longstreth, WT, DeCarli, CC, Van Duijn, CM, Schmidt, R, Launer, LJ, Grabe, HJ
Publikováno v:
Verhaaren, BFJ; Debette, S; Bis, JC; Smith, JA; Ikram, MK; Adams, HH; et al.(2015). Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI. Circulation: Cardiovascular Genetics, 8(2), 398-409. doi: 10.1161/CIRCGENETICS.114.000858. UCLA: Retrieved from: http://www.escholarship.org/uc/item/7fq176q6
© 2015 American Heart Association, Inc. Background-The burden of cerebral white matter hyperintensities (WMH) is associated with an increased risk of stroke, dementia, and death. WMH are highly heritable, but their genetic underpinnings are incomple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::3605a7101c3d65aad35c5b43af70dea1
http://www.escholarship.org/uc/item/7fq176q6
http://www.escholarship.org/uc/item/7fq176q6
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