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Results 21-30 of 48 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2011Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung functionArtigas, M.; Wain, L.; Repapi, E.; Obeidat, M.; Sayers, I.; Burton, P.; Johnson, T.; Zhao, J.; Albrecht, E.; Dominiczak, A.; Kerr, S.; Smith, B.; Cadby, G.; Hui, J.; Palmer, L.; Hingorani, A.; Wannamethee, S.; Whincup, P.; Ebrahim, S.; Smith, G.; et al.
2011Genome-wide association and large-scale follow up identifies 16 new loci influencing lung functionArtigas, M.; Loth, D.; Wain, L.; Gharib, S.; Obeidat, M.; Tang, W.; Zhai, G.; Zhao, J.; Smith, A.; Huffman, J.; Albrecht, E.; Jackson, C.; Evans, D.; Cadby, G.; Fornage, M.; Manichaikul, A.; Lopez, L.; Johnson, T.; Aldrich, M.; Aspelund, T.; et al.
2011Genetic diversity and population structure of the endangered marsupial Sarcophilus harrisii (Tasmanian devil)Miller, W.; Hayes, V.; Ratan, A.; Petersen, D.; Wittekindt, N.; Miller, J.; Walenz, B.; Knight, J.; Qi, J.; Zhao, F.; Wang, Q.; Bedoya-Reina, O.; Katiyar, N.; Tomsho, L.; Kasson, L.; Hardie, R.; Woodbridge, P.; Tindall, E.; Bertelsen, M.; Dixon, D.; et al.
2011A genome-wide significant linkage for severe depression on chromosome 3: the depression network studyBreen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; et al.
2011Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)Roberts, A.; Nancarrow, D.; Clendenning, M.; Buchanan, D.; Jenkins, M.; Duggan, D.; Taverna, D.; McKeone, D.; Walters, R.; Walsh, M.; Young, B.; Jass, J.; Rosty, C.; Gattas, M.; Pelzer, E.; Hopper, J.; Goldblatt, J.; George, J.; Suthers, G.; Phillips, K.; et al.
2011Convergent animal and human evidence suggests a role of PPM1A gene in response to antidepressantsMalki, K.; Uher, R.; Paya-Cano, J.; Binder, E.; Rietschel, M.; Zobel, A.; Mors, O.; Hauser, J.; Henigsberg, N.; Jerman, B.; Souery, D.; Placentino, A.; Ng, M.; Cohen-Woods, S.; Sluyter, F.; Farmer, A.; Aitchison, K.; Craig, I.; Lewis, C.; McGuffin, P.; et al.
2011The exposure of the hybrid detector of the Pierre Auger ObservatoryAbreu, P.; Aglietta, M.; Ahn, E.; Allard, D.; Allekotte, I.; Allen, J.; Alvarez Castillo, J.; Alvarez-Muñiz, J.; Ambrosio, M.; Aminaei, A.; Anchordoqui, L.; Andringa, S.; Antičić, T.; Anzalone, A.; Aramo, C.; Arganda, E.; Arisaka, K.; Arqueros, F.; Asorey, H.; Assis, P.; et al.
2011Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucomaKhan, K.; Rudkin, A.; Parry, D.; Burdon, K.; McKibbin, M.; Logan, C.; Abdelhamed, Z.; Muecke, J.; Fernandez-Fuentes, N.; Laurie, K.; Shires, M.; Fogarty, R.; Carr, I.; Poulter, J.; Morgan, J.; Mohamed, M.; Jafri, H.; Raashid, Y.; Meng, N.; Piseth, H.; et al.
2011Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1Jensen, L.; Wei, C.; Moser, B.; Lipkowitz, B.; Schroeder, C.; Musante, L.; Tzschach, A.; Kalscheuer, V.; Meloni, I.; Raynaud, M.; Van Esch, H.; Chelly, J.; de Brouwer, A.; Hackett, A.; van der Haar, S.; Henn, W.; Gecz, J.; Riess, O.; Bonin, M.; Reinhardt, R.; et al.
2011Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1Burdon, K.; MacGregor, S.; Hewitt, A.; Sharma, S.; Chidlow, G.; Mills, R.; Danoy, P.; Casson, R.; Viswanathan, A.; Liu, J.; Landers, J.; Henders, A.; Wood, J.; Souzeau, E.; Crawford, A.; Leo, P.; Wang, J.; Rochtchina, E.; Nyholt, D.; Martin, N.; et al.

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