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Items where Author is "Li, X."

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Number of items: 6.

2019

Shrine, N. and Guyatt, A. L. and Erzurumluoglu, A. M. and Jackson, V. E. and Hobbs, B. D. and Melbourne, C. A. and Batini, C. and Fawcett, K. A. and Song, K. and Sakornsakolpat, P. and Li, X. and Boxall, R. and Reeve, N. F. and Obeidat, M. and Zhao, J. H. and Wielscher, M. and Understanding Society Scientific Group, and Weiss, S. and Kentistou, K. A. and Cook, J. P. and Sun, B. B. and Zhou, J. and Hui, J. and Karrasch, S. and Imboden, M. and Harris, S. E. and Marten, J. and Enroth, S. and Kerr, S. M. and Surakka, I. and Vitart, V. and Lehtimaki, T. and Allen, R. J. and Bakke, P. S. and Beaty, T. H. and Bleecker, E. R. and Bosse, Y. and Brandsma, C. A. and Chen, Z. and Crapo, J. D. and Danesh, J. and DeMeo, D. L. and Dudbridge, F. and Ewert, R. and Gieger, C. and Gulsvik, A. and Hansell, A. L. and Hao, K. and Hoffman, J. D. and Hokanson, J. E. and Homuth, G. and Joshi, P. K. and Joubert, P. and Langenberg, C. and Li, X. and Li, L. and Lin, K. and Lind, L. and Locantore, N. and Luan, J. and Mahajan, A. and Maranville, J. C. and Murray, A. and Nickle, D. C. and Packer, R. and Parker, M. M. and Paynton, M. L. and Porteous, D. J. and Prokopenko, D. and Qiao, D. and Rawal, R. and Runz, H. and Sayers, I. and Sin, D. D. and Smith, B. H. and Artigas, M. S. and Sparrow, D. and Tal-Singer, R. and Timmers, P. and Van den Berge, M. and Whittaker, J. C. and Woodruff, P. G. and Yerges-Armstrong, L. M. and Troyanskaya, O. G. and Raitakari, O. T. and Kahonen, M. and Polasek, O. and Gyllensten, U. and Rudan, I. and Deary, I. J. and Probst-Hensch, N. M. and Schulz, H. and James, A. L. and Wilson, J. F. and Stubbe, B. and Zeggini, E. and Jarvelin, M. R. and Wareham, N. and Silverman, E. K. and Hayward, C. and Morris, A. P. and Butterworth, A. S. and Scott, R. A. and Walters, R. G. and Meyers, D. A. and Cho, M. H. and Strachan, D. P. and Hall, I. P. and Tobin, M. D. and Wain, L. V.. (2019) Author correction : New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nature genetics, 51. pp. 1067-1068.

2018

Waage, J. and Standl, M. and Curtin, J. A. and Jessen, L. E. and Thorsen, J. and Tian, C. and Schoettler, N. and andMe Research Team, and Aagc collaborators, and Flores, C. and Abdellaoui, A. and Ahluwalia, T. S. and Alves, A. C. and Amaral, A. F. S. and Anto, J. M. and Arnold, A. and Barreto-Luis, A. and Baurecht, H. and van Beijsterveldt, C. E. M. and Bleecker, E. R. and Bonas-Guarch, S. and Boomsma, D. I. and Brix, S. and Bunyavanich, S. and Burchard, E. G. and Chen, Z. and Curjuric, I. and Custovic, A. and den Dekker, H. T. and Dharmage, S. C. and Dmitrieva, J. and Duijts, L. and Ege, M. J. and Gauderman, W. J. and Georges, M. and Gieger, C. and Gilliland, F. and Granell, R. and Gui, H. and Hansen, T. and Heinrich, J. and Henderson, J. and Hernandez-Pacheco, N. and Holt, P. and Imboden, M. and Jaddoe, V. W. V. and Jarvelin, M. R. and Jarvis, D. L. and Jensen, K. K. and Jonsdottir, I. and Kabesch, M. and Kaprio, J. and Kumar, A. and Lee, Y. A. and Levin, A. M. and Li, X. and Lorenzo-Diaz, F. and Melen, E. and Mercader, J. M. and Meyers, D. A. and Myers, R. and Nicolae, D. L. and Nohr, E. A. and Palviainen, T. and Paternoster, L. and Pennell, C. E. and Pershagen, G. and Pino-Yanes, M. and Probst-Hensch, N. M. and Ruschendorf, F. and Simpson, A. and Stefansson, K. and Sunyer, J. and Sveinbjornsson, G. and Thiering, E. and Thompson, P. J. and Torrent, M. and Torrents, D. and Tung, J. Y. and Wang, C. A. and Weidinger, S. and Weiss, S. and Willemsen, G. and Williams, L. K. and Ober, C. and Hinds, D. A. and Ferreira, M. A. and Bisgaard, H. and Strachan, D. P. and Bonnelykke, K.. (2018) Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nature genetics, 50 (8). pp. 1072-1080.

2016

Li, M. and Luo, X. J. and Landen, M. and Bergen, S. E. and Hultman, C. M. and Li, X. and Zhang, W. and Yao, Y. G. and Zhang, C. and Liu, J. and Mattheisen, M. and Cichon, S. and Muhleisen, T. W. and Degenhardt, F. A. and Nothen, M. M. and Schulze, T. G. and Grigoroiu-Serbanescu, M. and Li, H. and Fuller, C. K. and Chen, C. and Dong, Q. and Chen, C. and Jamain, S. and Leboyer, M. and Bellivier, F. and Etain, B. and Kahn, J. P. and Henry, C. and Preisig, M. and Kutalik, Z. and Castelao, E. and Wright, A. and Mitchell, P. B. and Fullerton, J. M. and Schofield, P. R. and Montgomery, G. W. and Medland, S. E. and Gordon, S. D. and Martin, N. G. and Moo, D. S. Consortium and Swedish Bipolar Study, Group and Rietschel, M. and Liu, C. and Kleinman, J. E. and Hyde, T. M. and Weinberger, D. R. and Su, B.. (2016) Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. The British Journal of Psychiatry, 208 (2). pp. 128-137.

2013

Köttgen, A. and Albrecht, E. and Teumer, A. and Vitart, V. and Krumsiek, J. and Hundertmark, C. and Pistis, G. and Ruggiero, D. and O'Seaghdha, C. M. and Haller, T. and Yang, Q. and Tanaka, T. and Johnson, A. D. and Kutalik, Z. and Smith, A. V. and Shi, J. and Struchalin, M. and Middelberg, R. P. and Brown, M. J. and Gaffo, A. L. and Pirastu, N. and Li, G. and Hayward, C. and Zemunik, T. and Huffman, J. and Yengo, L. and Zhao, J. H. and Demirkan, A. and Feitosa, M. F. and Liu, X. and Malerba, G. and Lopez, L. M. and van der Harst, P. and Li, X. and Kleber, M. E. and Hicks, A. A. and Nolte, I. M. and Johansson, A. and Murgia, F. and Wild, S. H. and Bakker, S. J. and Peden, J. F. and Dehghan, A. and Steri, M. and Tenesa, A. and Lagou, V. and Salo, P. and Mangino, M. and Rose, L. M. and Lehtimaki, T. and Woodward, O. M. and Okada, Y. and Tin, A. and Muller, C. and Oldmeadow, C. and Putku, M. and Czamara, D. and Kraft, P. and Frogheri, L. and Thun, G. A. and Grotevendt, A. and Gislason, G. K. and Harris, T. B. and Launer, L. J. and McArdle, P. and Shuldiner, A. R. and Boerwinkle, E. and Coresh, J. and Schmidt, H. and Schallert, M. and Martin, N. G. and Montgomery, G. W. and Kubo, M. and Nakamura, Y. and Tanaka, T. and Munroe, P. B. and Samani, N. J. and Jacobs, DR Jr and Liu, K. and D'Adamo, P. and Ulivi, S. and Rotter, J. I. and Psaty, B. M. and Vollenweider, P. and Waeber, G. and Campbell, S. and Devuyst, O. and Navarro, P. and Kolcic, I. and Hastie, N. and Balkau, B. and Froguel, P. and Esko, T. and Salumets, A. and Khaw, K.. (2013) Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature genetics, Vol. 45, H. 2. pp. 145-154.

2011

Viscidi, R. P. and Khanna, N. and Tan, C. S. and Li, X. and Jacobson, L. and Clifford, D. B. and Nath, A. and Margolick, J. B. and Shah, K. V. and Hirsch, H. H. and Koralnik, I. J.. (2011) JC virus antibody and viremia as predictors of progressive multifocal leukoencephalopathy in human immunodeficiency virus-1-infected individuals. Clinical infectious diseases, Vol. 53, H. 7. pp. 711-715.

2010

Elowe, S. and Dulla, K. and Uldschmid, A. and Li, X. and Dou, Z. and Nigg, E. A.. (2010) Uncoupling of the spindle-checkpoint and chromosome-congression functions of BubR1. Journal of cell science, Vol. 123, H. 1. pp. 84-94.

This list was generated on Wed Nov 20 19:21:02 2019 CET.