Items where Author is "Rawal, R."

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.

2014

Medici, M. and Porcu, E. and Pistis, G. and Teumer, A. and Brown, S. J. and Jensen, R. A. and Rawal, R. and Roef, G. L. and Plantinga, T. S. and Vermeulen, S. H. and Lahti, J. and Simmonds, M. J. and Husemoen, L. L. and Freathy, R. M. and Shields, B. M. and Pietzner, D. and Nagy, R. and Broer, L. and Chaker, L. and Korevaar, T. I. and Plia, M. G. and Sala, C. and Völker, U. and Richards, J. B. and Sweep, F. C. and Gieger, C. and Corre, T. and Kajantie, E. and Thuesen, B. and Taes, Y. E. and Visser, W. E. and Hattersley, A. T. and Kratzsch, J. and Hamilton, A. and Li, W. and Homuth, G. and Lobina, M. and Mariotti, S. and Soranzo, N. and Cocca, M. and Nauck, M. and Spielhagen, C. and Ross, A. and Arnold, A. and van de Bunt, M. and Liyanarachchi, S. and Heier, M. and Grabe, H. J. and Masciullo, C. and Galesloot, T. E. and Lim, E. M. and Reischl, E. and Leedman, P. J. and Lai, S. and Delitala, A. and Bremner, A. P. and Philips, D. I. and Beilby, J. P. and Mulas, A. and Vocale, M. and Abecasis, G. and Forsen, T. and James, A. and Widen, E. and Hui, J. and Prokisch, H. and Rietzschel, E. E. and Palotie, A. and Feddema, P. and Fletcher, S. J. and Schramm, K. and Rotter, J. I. and Kluttig, A. and Radke, D. and Traglia, M. and Surdulescu, G. L. and He, H. and Franklyn, J. A. and Tiller, D. and Vaidya, B. and de Meyer, T. and Jørgensen, T. and Eriksson, J. G. and O'Leary, P. C. and Wichmann, E. and Hermus, A. R. and Psaty, B. M. and Ittermann, T. and Hofman, A. and Bosi, E. and Schlessinger, D. and Wallaschofski, H. and Pirastu, N. and Aulchenko, Y. S. and de la Chapelle, A. and Netea-Maier, R. T. and Gough, S. C. and Meyer zu Schwabedissen, H. E. U. and Frayling, T. M. and Kaufman, J. M. and Linneberg, A. and Räikkönen, K. and Smit, J. W. and Kiemeney, L. A. and Rivadeneira, F. and Uitterlinden, A. G. and Walsh, J. P. and Meisinger, C. and den Heijer, M. and Visser, T. J. and Spector, T. D. and Wilson, S. G. and Völzke, H. and Cappola, A. and Toniolo, D. and Sanna, S. and Naitza, S. and Peeters, R. P.. (2014) Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease. PLoS genetics, Vol. 10, H. 2. pp. 1-13.