Publications
305 results found
Binia A, Khorasani N, Bhavsar PK, et al., 2010, Chromosome 17q21 SNP and severe asthma, Journal of Human Genetics, Vol: 56, Pages: 97-98, ISSN: 1435-232X
Speliotes EK, Willer CJ, Berndt SI, et al., 2010, Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index, Nature Genetics, Vol: 42, Pages: 937-948, ISSN: 1546-1718
Obesity is globally prevalent and highly heritable, but its underlying genetic factors remain largely elusive. To identify genetic loci for obesity susceptibility, we examined associations between body mass index and approximately 2.8 million SNPs in up to 123,865 individuals with targeted follow up of 42 SNPs in up to 125,931 additional individuals. We confirmed 14 known obesity susceptibility loci and identified 18 new loci associated with body mass index (P < 5 x 10(-)(8)), one of which includes a copy number variant near GPRC5B. Some loci (at MC4R, POMC, SH2B1 and BDNF) map near key hypothalamic regulators of energy balance, and one of these loci is near GIPR, an incretin receptor. Furthermore, genes in other newly associated loci may provide new insights into human body weight regulation.
DeWan AT, Triche EW, Xu X, et al., 2010, <i>PDE11A</i> associations with asthma: Results of a genome-wide association scan, JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, Vol: 126, Pages: 871-U321, ISSN: 0091-6749
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- Citations: 39
Moffatt MF, Gut IG, Demenais F, et al., 2010, A Large-Scale, Consortium-Based Genomewide Association Study of Asthma, NEW ENGLAND JOURNAL OF MEDICINE, Vol: 363, Pages: 1211-1221, ISSN: 0028-4793
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- Citations: 1474
Hsu Y-H, Zillikens MC, Wilson SG, et al., 2010, An Integration of Genome-Wide Association Study and Gene Expression Profiling to Prioritize the Discovery of Novel Susceptibility Loci for Osteoporosis-Related Traits, PLOS GENETICS, Vol: 6, ISSN: 1553-7404
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- Citations: 151
Bouzigon E, Forabosco P, Koppelman GH, et al., 2010, Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy., Eur J Hum Genet, Vol: 18, Pages: 700-706
Asthma is caused by a heterogeneous combination of environmental and genetic factors. In the context of GA2LEN (Global Allergy and Asthma European Network), we carried out meta-analyses of almost all genome-wide linkage screens conducted to date in 20 independent populations from different ethnic origins (>or=3024 families with >or=10 027 subjects) for asthma, atopic asthma, bronchial hyper-responsiveness and five atopy-related traits (total immunoglobulin E level, positive skin test response (SPT) to at least one allergen or to House Dust Mite, quantitative score of SPT (SPTQ) and eosinophils (EOS)). We used the genome scan meta-analysis method to assess evidence for linkage within bins of traditionally 30-cM width, and explored the manner in which these results were affected by bin definition. Meta-analyses were conducted in all studies and repeated in families of European ancestry. Genome-wide evidence for linkage was detected for asthma in two regions (2p21-p14 and 6p21) in European families ascertained through two asthmatic sibs. With regard to atopy phenotypes, four regions reached genome-wide significance: 3p25.3-q24 in all families for SPT and three other regions in European families (2q32-q34 for EOS, 5q23-q33 for SPTQ and 17q12-q24 for SPT). Tests of heterogeneity showed consistent evidence of linkage of SPTQ to 3p11-3q21, whereas between-study heterogeneity was detected for asthma in 2p22-p13 and 6p21, and for atopic asthma in 1q23-q25. This large-scale meta-analysis provides an important resource of information that can be used to prioritize further fine-mapping studies and also be integrated with genome-wide association studies to increase power and better interpret the outcomes of these studies.
Bouzigon E, Forabosco P, Koppelman GH, et al., 2010, Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy, EUROPEAN JOURNAL OF HUMAN GENETICS, Vol: 18, Pages: 700-706, ISSN: 1018-4813
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- Citations: 41
Beghe B, Hall IP, Parker SG, et al., 2010, Polymorphisms in IL13 pathway genes in asthma and chronic obstructive pulmonary disease, ALLERGY, Vol: 65, Pages: 474-481, ISSN: 0105-4538
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- Citations: 73
Harper JI, Godwin H, Green A, et al., 2010, A study of matrix metalloproteinase expression and activity in atopic dermatitis using a novel skin wash sampling assay for functional biomarker analysis, BRITISH JOURNAL OF DERMATOLOGY, Vol: 162, Pages: 397-403, ISSN: 0007-0963
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- Citations: 52
Mathias RA, Grant AV, Rafaels N, et al., 2010, A genome-wide association study on African-ancestry populations for asthma, JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, Vol: 125, Pages: 336-346, ISSN: 0091-6749
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- Citations: 140
Sleiman PMA, Flory J, Imielinski M, et al., 2010, Variants of <i>DENND1B</i> Associated with Asthma in Children, NEW ENGLAND JOURNAL OF MEDICINE, Vol: 362, Pages: 36-44, ISSN: 0028-4793
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- Citations: 253
Hilty M, Burke C, Pedro H, et al., 2010, Disordered Microbial Communities in Asthmatic Airways, PLOS ONE, Vol: 5, ISSN: 1932-6203
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- Citations: 1171
Hsu Y-H, Zillikens MC, Wilson SG, et al., 2009, An Integration of Genome-Wide Association Study and Gene Expression Profiling to Prioritize the Discovery of Novel Susceptibility Loci for Osteoporosis Related Traits, 18th Annual Meeting of the International-Genetic-Epidemiology-Society, Publisher: WILEY-LISS, Pages: 752-753, ISSN: 0741-0395
Genuneit J, Cantelmo JL, Weinmayr G, et al., 2009, A multi-centre study of candidate genes for wheeze and allergy: the International Study of Asthma and Allergies in Childhood Phase 2, CLINICAL AND EXPERIMENTAL ALLERGY, Vol: 39, Pages: 1875-1888, ISSN: 0954-7894
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- Citations: 41
Taylor JM, Street TL, Hao L, et al., 2009, Dynamic and Physical Clustering of Gene Expression during Epidermal Barrier Formation in Differentiating Keratinocytes, PLOS ONE, Vol: 4, ISSN: 1932-6203
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- Citations: 26
Zhang Y, Cookson W, Moffatt M, 2009, Pharmacogenetics and Pharmacogenomics of Airway Diseases, Pharmacology and Therapeutics of Airway Disease, Editors: Barnes, Chung, Publisher: Taylor & Francis Group
I. Introduction Asthma and chronic obstructive pulmonary disease (COPD) are complex syndromes of airway inflammation. Asthma is a disease of the small airways of the lung. Intermittent narrowing of the respiratory bronchioles produces airway limitation and the symptoms of wheezing, chest tightness, and breathlessness. By contrast, in COPD the limitation of airflow is poorly reversible and usually gets progressively worse over time. The disease is primarily, but not exclusively, seen in smokers and former smokers. Environmental and genetic factors contribute to the etiology of both diseases. Cigarette smoking is the main risk factor for COPD, although less than 20% of chronic heavy smokers will develop symptoms of airway obstruction (1). Bronchodilators and corticosteroids are currently the most common medications used in the treatment of asthma and COPD.
GaoJ, Li W, Willis-Owen SA, et al., 2009, Polymorphisms of PHF11 and DPP10 are associated with asthma and related traits in a Chinese population., Respiration, Vol: 79, Pages: 17-24, ISSN: 1423-0356
Background: Initial studies by positional cloning have identified the genes encoding the plant homeodomain zinc finger protein 11 (PHF11) and dipeptidyl-peptidase 10 (DPP10) as asthma susceptibility genes. The variants in the two genes have been associated with asthma in several populations of European or Latin American origin. Objective: The aim of this study was to assess the common PHF11 and DPP10 polymorphisms for associations to asthma and asthma-related traits in a Han Chinese population. Methods: We genotyped six polymorphic markers in PHF11 and five polymorphic markers in DPP10 in a Han Chinese case-control cohort consisting of 408 asthma patients and 288 unrelated disease-free controls recruited from the Northern region of China. We analyzed the association between these markers and asthma as well as a number of intermediate, asthma-related traits. Linkage disequilibrium and haplotype patterns were also evaluated. Results: Significant associations were identified between two makers in PHF11 (rs1046295 and rs16659) and asthma susceptibility (odds ratio, OR = 1.32, 95% con fidence interval, CI = 1.06–1.65, p = 0.0096, for rs1046295, and OR = 1.41, 95% CI = 1.12–1.75, p = 0.0026, for rs16659). A strong association was observed between an SNP in DPP10 (rs10208402) and loge-transformed total IgE (p = 0.0003) and the percentage of peripheral blood eosinophils (p = 0.0023). A weak association between rs1430090 in DPP10 and forced expiratory volume in 1 s was also observed (p = 0.048). Haplotype analysis revealed two protective haplotypes in PHF11 against asthma. Conclusion: The results provide supporting evidence for genetic variants in PHF11 and DPP10 genes underlying asthma susceptibility and asthma-related quantitative traits in a Han Chinese population.
Yates L, McMurray F, Zhang Y, et al., 2009, ENU mutagenesis as a tool for understanding lung development and disease Biochemical Society Transactions 37: 838–842.
Himes BE, Hunninghake GM, Baurley JW, et al., 2009, Genome-wide Association Analysis Identifies <i>PDE4D</i> as an Asthma-Susceptibility Gene, AMERICAN JOURNAL OF HUMAN GENETICS, Vol: 84, Pages: 581-593, ISSN: 0002-9297
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- Citations: 248
Cookson W, Liang L, Abecasis G, et al., 2009, Mapping complex disease traits with global gene expression, NATURE REVIEWS GENETICS, Vol: 10, Pages: 184-194, ISSN: 1471-0056
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- Citations: 590
Willis-Owen SA, Moffatt MF, Cookson WO, 2009, The genetics of asthma and atopic dermatitis., Allergy and Allergic Diseases., Oxford, Publisher: Blackwell Publishing
Willis-Owen SAG, Cookson WO, Moffatt MF, 2009, Genome-Wide Association Studies in the Genetics of Asthma, CURRENT ALLERGY AND ASTHMA REPORTS, Vol: 9, Pages: 3-9, ISSN: 1529-7322
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- Citations: 22
Gao J, Willis-Owen SA, Moffatt M, et al., 2009, Polymorphisms of <i>PHF11</i> and <i>DPP10</i> Are Associated with Asthma and Related Traits in a Chinese Population., AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, Vol: 179, ISSN: 1073-449X
Rodriguez E, Gieger C, Baurecht H, et al., 2009, Genome-wide scan on total serum IgE levels identifies <i>FC</i>E<i>R1a</i> as novel susceptibility locus, 28th Congress of the European-Academy-of-Allergy-and-Clinical-Immunology, Publisher: WILEY-BLACKWELL PUBLISHING, INC, Pages: 50-50, ISSN: 0105-4538
Genuneit J, Cantelmo JL, Weinmayr G, et al., 2009, A Multi-Centre Study of Candidate Genes for Asthma and Allergy. The <i>International Study of Asthma and Allergies in Childhood Phase 2</i>., AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, Vol: 179, ISSN: 1073-449X
Moffatt MF, 2008, Genes in asthma: new genes and new ways, CURRENT OPINION IN ALLERGY AND CLINICAL IMMUNOLOGY, Vol: 8, Pages: 411-417, ISSN: 1528-4050
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- Citations: 29
Weidinger S, Gieger C, Rodriguez E, et al., 2008, Genome-Wide Scan on Total Serum IgE Levels Identifies <i>FCER1A</i> as Novel Susceptibility Locus, PLOS GENETICS, Vol: 4, ISSN: 1553-7404
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- Citations: 215
Moffatt MF, Cookson WOCM, 2008, Asthma and chitinases, NEW ENGLAND JOURNAL OF MEDICINE, Vol: 358, Pages: 1725-1726, ISSN: 0028-4793
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- Citations: 3
Dixon AL, Liang L, Moffatt MF, et al., 2007, A genome-wide association study of global gene expression, NATURE GENETICS, Vol: 39, Pages: 1202-1207, ISSN: 1061-4036
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- Citations: 779
Moffatt MF, Kabesch M, Liang L, et al., 2007, Genetic variants regulating <i>ORMDL3</i> expression contribute to the risk of childhood asthma, NATURE, Vol: 448, Pages: 470-U5, ISSN: 0028-0836
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- Citations: 1194
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