Weiss ST, Raby BA, Rogers A: Asthma genetics and genomics 2009. Current Opinion in Genetics & Development. 2009, 19 (3): 279-282. 10.1016/j.gde.2009.05.001.
Vercelli D: Discovering susceptibility genes for asthma and allergy. Nature Reviews Immunology. 2008, 8 (3): 169-182. 10.1038/nri2257.
Gu ML, Dong XQ, Zhao J: New Insight Into the Genes Susceptible to Asthma. Journal of Asthma. 2010, 47 (2): 113-116. 10.3109/02770900903498442.
Moffatt MF, Kabesch M, Liang LM, Dixon AL, Strachan D, Heath S, Depner M, von Berg A, Bufe A, Rietschel E, et al: Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature. 2007, 448 (7152): 470-U475. 10.1038/nature06014.
Ober C, Tan Z, Sun Y, Possick JD, Pan L, Nicolae R, Radford S, Parry RR, Heinzmann A, Deichmann KA, et al: Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function. New England Journal of Medicine. 2008, 358 (16): 1682-1691. 10.1056/NEJMoa0708801.
Sleiman PMA, Flory J, Imielinski M, Bradfield JP, Annaiah K, Willis-Owen SAG, Wang K, Rafaels NM, Michel S, Bonnelykke K, et al: Variants of DENND1B Associated with Asthma in Children. New England Journal of Medicine. 2010, 362 (1): 36-44. 10.1056/NEJMoa0901867.
Hancock DB, Romieu I, Shi M, Sienra-Monge JJ, Wu H, Chiu GY, Li HL, del Rio-Navarro BE, Willis-Owens SAG, Weiss ST, et al: Genome-Wide Association Study Implicates Chromosome 9q21.31 as a Susceptibility Locus for Asthma in Mexican Children. PLoS Genetics. 2009, 5 (8):
Himes BE, Hunninghake GM, Baurley JW, Rafaels NM, Sleiman P, Strachan DP, Wilk JB, Willis-Owen SAG, Klanderman B, Lasky-Su J, et al: Genome-wide Association Analysis Identifies PDE4D as an Asthma-Susceptibility Gene. American Journal of Human Genetics. 2009, 84 (5): 581-593. 10.1016/j.ajhg.2009.04.006.
Wu H, Romieu I, Shi M, Hancock DB, Li HL, Sienra-Monge JJ, Chiu GY, Xu H, del Rio-Navarro BE, London SJ: Evaluation of candidate genes in a genome-wide association study of childhood asthma in Mexicans. Journal of Allergy and Clinical Immunology. 2010, 125 (2): 321-327. 10.1016/j.jaci.2009.09.007.
Li XN, Howard TD, Zheng SL, Haselkorn T, Peters SP, Meyers DA, Bleecker ER: Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. Journal of Allergy and Clinical Immunology. 2010, 125 (2): 328-335. 10.1016/j.jaci.2009.11.018.
Noguchi E, Sakamoto H, Hirota T, Ochiai K, Imoto Y, Sakashita M, Kurosaka F, Akasawa A, Yoshihara S, Kanno N, et al: Genome-Wide Association Study Identifies HLA-DP as a Susceptibility Gene for Pediatric Asthma in Asian Populations. PLos Genetics. 2011, 7 (7):
Moffatt MF, Gut IG, Demenais F, Strachan DP, Bouzigon E, Heath S, von Mutius E, Farrall M, Lathrop M, Cookson W, et al: A Large-Scale, Consortium-Based Genomewide Association Study of Asthma. New England Journal of Medicine. 2010, 363 (13): 1211-1221. 10.1056/NEJMoa0906312.
Torgerson DG, Ampleford EJ, Chiu GY, Gauderman WJ, Gignoux CR, Graves PE, Himes BE, Levin AM, Mathias RA, Hancock DB, et al: Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nature Genetics. 2011, 43 (9): 887-892. 10.1038/ng.888.
Zhao YH, Wang S: Optimal DNA Pooling-Based Two-Stage Designs in Case-Control Association Studies. Human Heredity. 2009, 67 (1): 46-56. 10.1159/000164398.
Ronald A, Butcher LM, Docherty S, Davis OSP, Schalkwyk LC, Craig IW, Plomin R: A Genome-Wide Association Study of Social and Non-Social Autistic-Like Traits in the General Population Using Pooled DNA, 500 K SNP Microarrays and Both Community and Diagnosed Autism Replication Samples. Behavior Genetics. 2010, 40 (1): 31-45. 10.1007/s10519-009-9308-6.
Shifman S, Johannesson M, Bronstein M, Chen SX, Collier DA, Craddock NJ, Kendler KS, Li T, O'Donovan M, O'Neill FA, et al: Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. PLoS Genetics. 2008, 4 (2):
Castro-Giner F, Bustamante M, Gonzalez JR, Kogevinas M, Jarvis D, Heinrich J, Anto JM, Wjst M, Estivill X, de Cid R: A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS). BMC Medical Genetics. 2009, 10:
Anantharaman R, Chew FT: Validation of pooled genotyping on the Affymetrix 500 k and SNP6.0 genotyping platforms using the polynomial-based probe-specific correction. BMC Genetics. 2009, 10:
Andiappan AK, Anantharaman R, Nilkanth PP, Wang DY, Chew FT: Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population. BMC Genetics. 2010, 11:
Moore D, Dowhan D: Unit 2.1A: Purification and Concentration of DNA from Aqueous Solutions. Current Protocols in Molecular Biology. 2002
Parate PN, Wang D, Chew FT: Linkage Disequilibrium Pattern in Asthma Candidate Genes from 5q31-q33 in the Singapore Chinese Population. Annals of Human Genetics. 2010, 74: 137-145. 10.1111/j.1469-1809.2009.00558.x.
Asher MI, Keil U, Anderson HR, Beasley R, Crane J, Martinez F, Mitchell EA, Pearce N, Sibbald B, Stewart AW, et al: International study of asthma and allergies in childhood (ISAAC): rationale and methods. European Respiratory Journal. 1995, 8: 483-491. 10.1183/09031936.95.08030483.
Chew FT, Lim SH, Goh DYT, Lee BW: Sensitization to local dust-mite fauna in Singapore. Allergy. 1999, 54 (11): 1150-1159. 10.1034/j.1398-9995.1999.00050.x.
Brohede J, Dunne R, McKay JD, Hannan GN: PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays. Nucleic Acids Research. 2005, 33 (17):
Team RDC: R: A Language and Environment for Statistical Computing. Vienna, Austria: R Foundation for Statistical Computing. 2011
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, Bender D, Maller J, Sklar P, de Bakker PIW, Daly MJ, et al: PLINK: A tool set for whole-genome association and population-based linkage analyses. American Journal of Human Genetics. 2007, 81 (3): 559-575. 10.1086/519795.
Lewis CM: Genetic association studies: Design, analysis and interpretation. Brief Bioinform. 2002, 3 (2): 146-153. 10.1093/bib/3.2.146.
F-SNP: A collection of functional SNPs, specifically prioritized for disease association studies. [http://compbio.cs.queensu.ca/F-SNP/]
Human Splicing Finder: an online bioinformatics tool to predict splicing signals. [http://www.umd.be/HSF/]
Zuo Y, Zou G, Zhao H: Two-Stage Designs in Case-Control Association Analysis. Genetics. 2006, 173: 1747-1760. 10.1534/genetics.105.042648.
Skol AD, Scott LJ, Abecasis GR, Boehnke M: Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nature Genetics. 2006, 38 (2): 209-213. 10.1038/ng1706.
Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, et al: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007, 447 (7145): 661-678. 10.1038/nature05911.
Hindorff LA, Junkins HA, Hall PN, Mehta JP, Manolio TA: A Catalog of Published Genome-Wide Association Studies. Accessed Sept. 2010, [http://www.genome.gov/gwastudies/]
Sleiman PMA, Hakonarson H: Recent advances in the genetics and genomics of asthma and related traits. Current Opinion in Pediatrics. 2010, 22 (3): 307-312. 10.1097/MOP.0b013e328339553d.
Holloway JW, Yang IA, Holgate ST: Genetics of allergic disease. Journal of Allergy and Clinical Immunology. 2010, 125 (2): S81-S94. 10.1016/j.jaci.2009.10.071.
Postma DS, Koppelman GH: Genetics of Asthma: Where Are We and Where Do We Go?. Proceedings of the American Thoracic Society. 2009, 6 (3): 283-287. 10.1513/pats.200806-047RM.
Ricci G, Astolfi A, Remondini D, Cipriani F, Formica S, Dondi A, Pession A: Pooled Genome-Wide Analysis to Identify Novel Risk Loci for Pediatric Allergic Asthma. PLoS One. 2011, 6 (2): e16912-10.1371/journal.pone.0016912.
Dizier MH, Besse-Schmittler C, Guilloud-Bataille M, Annesi-Maesano I, Boussaha M, Bousquet J, Charpin D, Degioanni A, Gormand F, Grimfeld A, et al: Genome screen for asthma and related phenotypes in the French EGEA study. American Journal of Respiratory and Critical Care Medicine. 2000, 162 (5): 1812-1818.
Koppelman GH, Stine OC, Xu JF, Howard TD, Zheng SQL, Kauffman HF, Bleecker ER, Meyers DA, Postma DS: Genome-wide search for atopy susceptibility genes in Dutch families with asthma. Journal of Allergy and Clinical Immunology. 2002, 109 (3): 498-506. 10.1067/mai.2002.122235.
Bouzigon E, Forabosco P, Koppelman GH, Cookson W, Dizier MH, Duffy DL, Evans DM, Ferreira MAR, Kere J, Laitinen T, et al: Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy. European Journal of Human Genetics. 2010, 18 (6): 700-706. 10.1038/ejhg.2009.224.
Denham S, Koppelman GH, Blakey J, Wjst M, Ferreira MA, Hall IP, Sayers I: Meta-analysis of genome-wide linkage studies of asthma and related traits. Respiratory Research. 2008, 9:
Galanter J, Choudhry S, Eng C, Nazario S, Rodriguez-Santana JR, Casal J, Torres-Palacios A, Salas J, Chapela R, Watson HG, et al: ORMDL3 gene is associated with asthma in three ethnically diverse populations. American Journal of Respiratory and Critical Care Medicine. 2008, 177 (11): 1194-1200. 10.1164/rccm.200711-1644OC.
Madore AM, Tremblay K, Hudson TJ, Laprise C: Replication of an association between 17q21 SNPs and asthma in a French-Canadian familial collection. Human Genetics. 2008, 123 (1): 93-95. 10.1007/s00439-007-0444-x.
Halapi E, Gudbjartsson DF, Jonsdottir GM, Bjornsdottir US, Thorleifsson G, Helgadottir H, Williams C, Koppelman GH, Heinzmann A, Boezen HM, et al: A sequence variant on 17q21 is associated with age at onset and severity of asthma. European Journal of Human Genetics. 2010, 18 (8): 902-908. 10.1038/ejhg.2010.38.
Bisgaard H, Bonnelykke K, Sleiman PMA, Brasholt M, Chawes B, Kreiner-Moller E, Stage M, Kim C, Tavendale R, Baty F, et al: Chromosome 17q21 Gene Variants Are Associated with Asthma and Exacerbations but Not Atopy in Early Childhood. American Journal of Respiratory and Critical Care Medicine. 2009, 179 (3): 179-185.
Sleiman PMA, Annaiah K, Imielinski M, Bradfield JP, Kim CE, Frackelton EC, Glessner JT, Eckert AW, Otieno FG, Santa E, et al: ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry. Journal of Allergy and Clinical Immunology. 2008, 122 (6): 1225-1227. 10.1016/j.jaci.2008.06.041.
Weinmayr G, Weiland SK, Bjorksten B, Brunekreef B, Buchele G, Cookson WOC, Garcia-Marcos L, Gotua M, Gratziou C, van Hage M, et al: Atopic sensitization and the international variation of asthma symptom prevalence in children. American Journal of Respiratory and Critical Care Medicine. 2007, 176 (6): 565-574. 10.1164/rccm.200607-994OC.
Simpson A, Tan VYF, Winn J, Svensen M, Bishop CM, Heckerman DE, Buchan I, Custovic A: Beyond Atopy Multiple Patterns of Sensitization in Relation to Asthma in a Birth Cohort Study. American Journal of Respiratory and Critical Care Medicine. 2010, 181 (11): 1200-1206. 10.1164/rccm.200907-1101OC.
Fujita M, Umemura M, Yoko-o T, Jigami Y: PER1 is required for GPI-phospholipase A(2) activity and involved in lipid remodeling of GPI-anchored proteins. Molecular Biology of the Cell. 2006, 17 (12): 5253-5264. 10.1091/mbc.E06-08-0715.
Okazaki I, Moss J: The Function of GPI-Anchored Proteins. PNH and the GPI-Linked Proteins. 2000, Moss NSYaJ: Academic Press
Loertscher R, Lavery P: The role of glycosyl phosphatidyl inositol (GPI)-anchored cell surface proteins in T-cell activation. Transplant Immunology. 2002, 9 (2-4): 93-96. 10.1016/S0966-3274(02)00013-8.
Munitz A, Bachelet I, Finkelman FD, Rothenberg ME, Levi-Schaffer F: CD48 is critically involved in allergic eosinophilic airway inflammation. American Journal of Respiratory and Critical Care Medicine. 2007, 175 (9): 911-918. 10.1164/rccm.200605-695OC.
Moran M, Miceli MC: Engagement of GPI-linked CD48 contributes to TCR signals and cytoskeletal reorganization: A role for lipid rafts in T cell activation. Immunity. 1998, 9 (6): 787-796. 10.1016/S1074-7613(00)80644-5.
Muhammad A, Schiller HB, Forster F, Eckerstorfer P, Geyeregger R, Leksa V, Zlabinger GJ, Sibilia M, Sonnleitner A, Paster W, et al: Sequential Cooperation of CD2 and CD48 in the Buildup of the Early TCR Signalosome. Journal of Immunology. 2009, 182 (12): 7672-7680. 10.4049/jimmunol.0800691.
Munitz A, Bachelet I, Levi-Schaffer F: CD48 as a Novel Target in Asthma Therapy. Recent Patents on Inflammation & Allergy Drug Discovery. 2007, 1: 9-12. 10.2174/187221307779815057.
Deckert M, Ticchioni M, Mari B, Mary D, Bernard A: The Glycosylphosphatidylinositol-Anchored CD59 Protein Stimulates Both T-Cell Receptor Zeta/Zap-70-Dependent and Zeta/Zap-70-Independent Signaling Pathways in T-Cell. European Journal of Immunology. 1995, 25 (7): 1815-1822. 10.1002/eji.1830250704.
Katagiri T, Qi ZR, Ohtake S, Nakao S: GPI-anchored protein-deficient T cells in patients with aplastic anemia and low-risk myelodysplastic syndrome: implications for the immunopathophysiology of bone marrow failure. European Journal of Haematology. 2011, 86 (3): 226-236. 10.1111/j.1600-0609.2010.01563.x.
Schubert J, Stroehmann A, Scholz C, Schmidt RE: Glycosylphosphatidylinositol (GPI)-Anchored Surface-Antigens in the Allogeneic Activation of T-Cells. Clinical and Experimental Immunology. 1995, 102 (1): 199-203.
Macgregor S: Most Pooling Variation in Array-Based DNA Pooling is Attributable to Array Error Rather Than Pool Construction Error. European Journal of Human Genetics. 2007, 15: 501-504. 10.1038/sj.ejhg.5201768.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2350/12/170/prepub