Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

[1]  Jake K. Byrnes,et al.  Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls , 2010 .

[2]  P. Deloukas,et al.  Multiple common variants for celiac disease influencing immune gene expression , 2010, Nature Genetics.

[3]  M. Hurles,et al.  Large, rare chromosomal deletions associated with severe early-onset obesity , 2010, Nature.

[4]  William W. Busse,et al.  Asthma: Clinical expression and molecular mechanisms , 2010, Journal of Allergy and Clinical Immunology.

[5]  E. Bleecker,et al.  Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. , 2010, The Journal of allergy and clinical immunology.

[6]  Michael M. Ward,et al.  Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci , 2010, Nature Genetics.

[7]  L. Liang,et al.  A genome-wide association study on African-ancestry populations for asthma. , 2010, The Journal of allergy and clinical immunology.

[8]  Ingo Ruczinski,et al.  Variants of DENND1B associated with asthma in children. , 2010, The New England journal of medicine.

[9]  Nicole Soranzo,et al.  Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. , 2010, American journal of human genetics.

[10]  Manuel A. R. Ferreira,et al.  Common variants in the trichohyalin gene are associated with straight hair in Europeans. , 2009, American journal of human genetics.

[11]  M. Chance,et al.  Crystal structure of native RPE65, the retinoid isomerase of the visual cycle , 2009, Proceedings of the National Academy of Sciences.

[12]  P. Sullivan,et al.  Genome-Wide Association Study Implicates Chromosome 9q21.31 as a Susceptibility Locus for Asthma in Mexican Children , 2009, PLoS genetics.

[13]  F. Collins,et al.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits , 2009, Proceedings of the National Academy of Sciences.

[14]  Ingo Ruczinski,et al.  Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. , 2009, American journal of human genetics.

[15]  D. Postma,et al.  Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction , 2009, Nature Genetics.

[16]  J. Stockman.  Association between Microdeletion and Microduplication at 16p11.2 and Autism , 2009 .

[17]  M. Daly,et al.  Genetic Mapping in Human Disease , 2008, Science.

[18]  P. Visscher,et al.  Rare chromosomal deletions and duplications increase risk of schizophrenia , 2008, Nature.

[19]  Ross Lazarus,et al.  Chromosome 17: association of a large inversion polymorphism with corticosteroid response in asthma , 2008, Pharmacogenetics and genomics.

[20]  Judy H. Cho,et al.  Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease , 2008, Nature Genetics.

[21]  L. Liang,et al.  Genome-Wide Scan on Total Serum IgE Levels Identifies FCER1A as Novel Susceptibility Locus , 2008, PLoS genetics.

[22]  Ying Sun,et al.  Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function. , 2008, The New England journal of medicine.

[23]  R. Mei,et al.  Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region , 2008, Human Genetics.

[24]  Iuliana Ionita-Laza,et al.  On the analysis of copy‐number variations in genome‐wide association studies: a translation of the family‐based association test , 2008, Genetic epidemiology.

[25]  Joshua M. Korn,et al.  Association between microdeletion and microduplication at 16p11.2 and autism. , 2008, The New England journal of medicine.

[26]  K. Deichmann,et al.  Effect of Variation in CHI 3 L 1 on Serum YKL-40 Level , Risk of Asthma , and Lung Function , 2008 .

[27]  Zhaohui S. Qin,et al.  A second generation human haplotype map of over 3.1 million SNPs , 2007, Nature.

[28]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.

[29]  Jacques Fellay,et al.  A Whole-Genome Association Study of Major Determinants for Host Control of HIV-1 , 2007, Science.

[30]  Gonçalo R. Abecasis,et al.  Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma , 2007, Nature.

[31]  E. Birney,et al.  Challenges and standards in integrating surveys of structural variation , 2007, Nature Genetics.

[32]  Judy H Cho,et al.  Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis , 2007, Nature Genetics.

[33]  C. Yau,et al.  QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data , 2007, Nucleic acids research.

[34]  R. Ferris,et al.  Loss of new chemokine CXCL14 in tumor tissue is associated with low infiltration by dendritic cells (DC), while restoration of human CXCL14 expression in tumor cells causes attraction of DC both in vitro and in vivo. , 2006, The Journal of Immunology.

[35]  R. Ferris,et al.  Loss of New Chemokine CXCL14 in Tumor Tissue Is Associated with Low Infiltration by Dendritic Cells (DC), while Restoration of Human CXCL14 Expression in Tumor Cells Causes Attraction of DC Both In Vitro and In Vivo1 , 2005, The Journal of Immunology.

[36]  H. Stefánsson,et al.  A common inversion under selection in Europeans , 2005, Nature Genetics.

[37]  L. Almasy,et al.  Multipoint oligogenic linkage analysis of quantitative traits , 1997, Genetic epidemiology.