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Items where Author is "Schmidt, C. O."

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Number of items: 2.

2023

Shrine, N. and Izquierdo, A. G. and Chen, J. and Packer, R. and Hall, R. J. and Guyatt, A. L. and Batini, C. and Thompson, R. J. and Pavuluri, C. and Malik, V. and Hobbs, B. D. and Moll, M. and Kim, W. and Tal-Singer, R. and Bakke, P. and Fawcett, K. A. and John, C. and Coley, K. and Piga, N. N. and Pozarickij, A. and Lin, K. and Millwood, I. Y. and Chen, Z. and Li, L. and Wijnant, S. R. A. and Lahousse, L. and Brusselle, G. and Uitterlinden, A. G. and Manichaikul, A. and Oelsner, E. C. and Rich, S. S. and Barr, R. G. and Kerr, S. M. and Vitart, V. and Brown, M. R. and Wielscher, M. and Imboden, M. and Jeong, A. and Bartz, T. M. and Gharib, S. A. and Flexeder, C. and Karrasch, S. and Gieger, C. and Peters, A. and Stubbe, B. and Hu, X. and Ortega, V. E. and Meyers, D. A. and Bleecker, E. R. and Gabriel, S. B. and Gupta, N. and Smith, A. V. and Luan, J. and Zhao, J. H. and Hansen, A. F. and Langhammer, A. and Willer, C. and Bhatta, L. and Porteous, D. and Smith, B. H. and Campbell, A. and Sofer, T. and Lee, J. and Daviglus, M. L. and Yu, B. and Lim, E. and Xu, H. and O'Connor, G. T. and Thareja, G. and Albagha, O. M. E. and Qatar Genome Program Research Consortium, and Suhre, K. and Granell, R. and Faquih, T. O. and Hiemstra, P. S. and Slats, A. M. and Mullin, B. H. and Hui, J. and James, A. and Beilby, J. and Patasova, K. and Hysi, P. and Koskela, J. T. and Wyss, A. B. and Jin, J. and Sikdar, S. and Lee, M. and May-Wilson, S. and Pirastu, N. and Kentistou, K. A. and Joshi, P. K. and Timmers, Prhj and Williams, A. T. and Free, R. C. and Wang, X. and Morrison, J. L. and Gilliland, F. D. and Chen, Z. and Wang, C. A. and Foong, R. E. and Harris, S. E. and Taylor, A. and Redmond, P. and Cook, J. P. and Mahajan, A. and Lind, L. and Palviainen, T. and Lehtimäki, T. and Raitakari, O. T. and Kaprio, J. and Rantanen, T. and Pietiläinen, K. H. and Cox, S. R. and Pennell, C. E. and Hall, G. L. and Gauderman, W. J. and Brightling, C. and Wilson, J. F. and Vasankari, T. and Laitinen, T. and Salomaa, V. and Mook-Kanamori, D. O. and Timpson, N. J. and Zeggini, E. and Dupuis, J. and Hayward, C. and Brumpton, B. and Langenberg, C. and Weiss, S. and Homuth, G. and Schmidt, C. O. and Probst-Hensch, N. and Jarvelin, M. R. and Morrison, A. C. and Polasek, O. and Rudan, I. and Lee, J. H. and Sayers, I. and Rawlins, E. L. and Dudbridge, F. and Silverman, E. K. and Strachan, D. P. and Walters, R. G. and Morris, A. P. and London, S. J. and Cho, M. H. and Wain, L. V. and Hall, I. P. and Tobin, M. D.. (2023) Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Nat Genet, 55 (3). pp. 410-422.

2016

Ibrahim-Verbaas, C. A. and Bressler, J. and Debette, S. and Schuur, M. and Smith, A. V. and Bis, J. C. and Davies, G. and Trompet, S. and Smith, J. A. and Wolf, C. and Chibnik, L. B. and Liu, Y. and Vitart, V. and Kirin, M. and Petrovic, K. and Polasek, O. and Zgaga, L. and Fawns-Ritchie, C. and Hoffmann, P. and Karjalainen, J. and Lahti, J. and Llewellyn, D. J. and Schmidt, C. O. and Mather, K. A. and Chouraki, V. and Sun, Q. and Resnick, S. M. and Rose, L. M. and Oldmeadow, C. and Stewart, M. and Smith, B. H. and Gudnason, V. and Yang, Q. and Mirza, S. S. and Jukema, J. W. and deJager, P. L. and Harris, T. B. and Liewald, D. C. and Amin, N. and Coker, L. H. and Stegle, O. and Lopez, O. L. and Schmidt, R. and Teumer, A. and Ford, I. and Karbalai, N. and Becker, J. T. and Jonsdottir, M. K. and Au, R. and Fehrmann, R. S. and Herms, S. and Nalls, M. and Zhao, W. and Turner, S. T. and Yaffe, K. and Lohman, K. and van Swieten, J. C. and Kardia, S. L. and Knopman, D. S. and Meeks, W. M. and Heiss, G. and Holliday, E. G. and Schofield, P. W. and Tanaka, T. and Stott, D. J. and Wang, J. and Ridker, P. and Gow, A. J. and Pattie, A. and Starr, J. M. and Hocking, L. J. and Armstrong, N. J. and McLachlan, S. and Shulman, J. M. and Pilling, L. C. and Eiriksdottir, G. and Scott, R. J. and Kochan, N. A. and Palotie, A. and Hsieh, Y. C. and Eriksson, J. G. and Penman, A. and Gottesman, R. F. and Oostra, B. A. and Yu, L. and DeStefano, A. L. and Beiser, A. and Garcia, M. and Rotter, J. I. and Nothen, M. M. and Hofman, A. and Slagboom, P. E. and Westendorp, R. G. and Buckley, B. M. and Wolf, P. A. and Uitterlinden, A. G. and Psaty, B. M. and Grabe, H. J. and Bandinelli, S. and Chasman, D. I. and Grodstein, F. and Raikkonen, K. and Lambert, J. C. and Porteous, D. J. and Generation, Scotland and Price, J. F. and Sachdev, P. S. and Ferrucci, L. and Attia, J. R. and Rudan, I. and Hayward, C. and Wright, A. F. and Wilson, J. F. and Cichon, S. and Franke, L. and Schmidt, H. and Ding, J. and de Craen, A. J. and Fornage, M. and Bennett, D. A. and Deary, I. J. and Ikram, M. A. and Launer, L. J. and Fitzpatrick, A. L. and Seshadri, S. and van Duijn, C. M. and Mosley, T. H.. (2016) GWAS for executive function and processing speed suggests involvement of the CADM2 gene. Molecular Psychiatry, 21 (2). pp. 189-197.

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