H. M. Boezen (Groningen, The Netherlands), D. Jarvis (London, United Kingdom)
Late Breaking Abstract: Candidate-wide association study of lung function among European- and African-Americans in 8 population-based cohorts. The candidate-gene association resource (CARe)
K. Burkart, J. Wilk, P. Enright, F. Ahmed, N. Hansel, D. Haynes, S. Heckbert, L. Loehr, S. London, H. Lyon, G. O‘Connor, E. Oelsner, M. Petrini, S. Redline, W. White, S. Rich, R. Barr (New York, Boston, Tucson, Baltimore, Jackson, Seattle, Chapel Hill, Research Triangle Park, Cleveland, Tougaloo, Charlottesville, United States Of America)
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COPACETIC, a genome-wide association study on chronic obstructive pulmonary disease (COPD)
J. Smolonska, C. Wijmenga, B. van Ginneken, B. de Hoop, A. E. Dijkstra, M. Platteel, D. S. Postma, M. Oudkerk, W. Mali, J. W. Lammers, H. J. M. Groen, P. Zanen, H. M. Boezen (Groningen, Utrecht, Netherlands)
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Scavenger receptor AI/II truncation, lung function and COPD in 48,700 individuals
M. Thomsen, B. Nordestgaard, A. Tybjærg-Hansen, M. Dahl (Denmark)
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A single nucleotide polymorphism in NOD2 gene was associated with pathogenesis and severity of COPD
D. Kinose, E. Ogawa, T. Hirota, I. Ito, S. Muro, Y. Hoshino, T. Hirai, H. Sakai, M. Tamari, M. Mishima (Yokohama, Japan)
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Severe alpha-1-antitrypsin deficiency (A1ATD) caused by Q0Ourém mutation: A clinical characterization
L. Vaz-Rodrigues, F. Costa, S. Seixas, J. Rocha, C. Mendonça (Coimbra, Portugal)
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Association analysis between polymorphisms in the cytochrome P450 2J2, 2S1 and UDP-glucuronosyltransferase 2B7 genes with occupational chronic bronchitis
L. Akhmadishina, G. Korytina, O. Tselousova, T. Victorova (Ufa, Russian Federation)
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Association of GST gene polymorphism with the lung function of COPD patient in northern India population
R. K. Shukla, S. Kant, S. Bhattacharya, R. Upadhyay, B. Mittal (Lucknow, India)
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Association of TNF-α polymorphisms with COPD in a Spanish population
E. Córdoba-Lanús, R. Baz-Dávila, J. P. de-Torres, C. Rodríguez, N. Varo, N. Maca-Meyer, C. Medina, A. Aguirre-Jaime, C. Casanova (Santa Cruz de Tenerife, Navarra, Spain)
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Association of ET-1 gene polymorphisms with emphysematous and non-emphysematous phenotypes in a COPD caucasian population
F. Sampsonas, A. Kaparianos, D. Lykouras, G. Efremidis, A. Antonacopoulou, P. Drakatos, K. Karkoulias, H. Kalofonos, C. Gogos, K. Spiropoulos (Greece)
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Micro-RNA expression in induced sputum of smokers and patients with chronic obstructive pulmonary disease
G. Van Pottelberge, P. Mestdagh, K. Bracke, O. Thas, Y. Van Durme, G. Joos, J. Vandesompele, G. Brusselle (Belgium)
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Integrated analysis of COPD gene expression data reveals specific pathway signatures
D. Cheng, S. Sridhar, J. Patel, S. Visvanathan, J. Fine, B. Hans (Nutley, United States Of America)
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Genetics of the neonatal lung function – A genome wide analyses together with expressed genes and candidate genes
E. Kreiner-Møller, P. Sleiman, F. Baty, K. Bønnelykke, H. Hakonarsson, H. Bisgaard (Copenhagen, Denmark; Philadelphia, United States Of America)
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The interaction between maternal smoke exposure in utero and maternal and child GSTP1 polymorphisms on lung function in primary school children
J. Murdzoska, S. Devadason, S. K. Khoo, L. Landau, S. Young, J. Goldblatt, G. Zhang, P. Le Souef, C. Hayden (Perth, Australia)
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SERPINA1 MS and MZ heterozygotes and lung function decline in the SAPALDIA cohort study
G. A. Thun, I. Ferrarotti, M. Imboden, T. Rochat, M. Zorzetto, S. Ottaviani, E. W. Russi, M. Luisetti, N. M. Probst-Hensch (Basel, Switzerland; Pavia, Italy)
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Polymorphism T3801C of CYP1A1 influence the RDS development in neonates
L. Khamidullina, K. Danilko, T. Victorova, R. Fayzullina (Ufa, Russian Federation)
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PDCD4 polymorphisms in severe childhood asthma
A. Binia, W. Cookson, M. Moffatt (United Kingdom)
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The role of CD14 polymorphisms in the pathogenesis of RSV infection in infants
M. Goutaki, S. Pappa, K. Haidopoulou, M. Eboriadou, P. Tsakiridis, A. Papa, M. Hatzistilianou (Greece)
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Allele variants of C3435T multidrug resistance gene (MDR1), R130Q interleukin 13 (IL13) gene, 590C/T IL4 – Markers of steroid dependent bronchial asthma (BA) risk
M. Simakova, Z. Mironova, V. Trofimov, V. Belash, E. Iantchina, M. Dubina (St. Petersburg, Russian Federation)
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Interpopulation differences of allele and genotype frequencies of 12 SNP markers in 8 asthma susceptibility genes in Russians and Buryats
O. Voronko, M. Gabaeva, E. Dmitrieva-Zdorova, S. Lemza, N. Bodoev (Moscow, Ulan-Ude, Russian Federation)
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Identification of multiple asthma susceptibility loci within the lmr1 locus on mouse chromosome 17
B. Piavaux, M. Nawijn, R. Gras, L. den Boef, S. Foote, R. Korstanje, A. van Oosterhout (Groningen, Netherlands; Hobart, Australia; Bar Harbor, United States Of America)
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