2007年GWA論文

Nature, Science, Nature Genetics, PLoS Genetics
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Nature 447 661-678 (2007)
by The Wellcome Trust Case Control Consortium
PubMedリンク
A Common Variant on Chromosome 9p21 Affects the Rsk of Myocardial Infarction.
Science 316, 1491-1493 (2007)
by Anna Helgadottir, et al.
Science リンク
A Common Allele on Chromosome 9 Associated with Coronary Heart Disease.
Science 316, 1488-1491 (2007)
by Ruth McPherson, et al.
Science リンク
A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity.
Sceience 316, 889-894 (2007)
by Timothy M. Frayling, et al.
Science リンク
Genome-wide association study identifies novel breast cancer susceptibility loci.
Nature 447 1087-1093 (2007)
by DF Easton, et al.
PubMed リンク
Genome-Wide Association Analysis identifies Loci for Type 2 Diabetes and Triglyceride Levels.
Science 316, 1331-1336 (2007)
by BioMedical Research, et al.
Science リンク
A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants.
Science 316, 1341-1345 (2007)
by LJ Scott, et al.
Science リンク
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk.
Nat Genet 39 1315-1317 (2007)
by P Broderick, et al.
PubMed リンク
Effects of environment, genetics and data analysis pitfalls in an esophageal cancer genome-wide association study.
PLoS ONE. 2007 Sep 26;2(9):e958.
by Statnikov A, Li C, Aliferis CF.
PubMed リンク
A genome-wide association study of global gene expression.
Nat Genet. 2007 Oct;39(10):1202-7. Epub 2007 Sep 16.
by AL Dixon, et al.
PubMed リンク
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.
Nat Genet. 2007 Aug;39(8):1000-6. Epub 2007 Jul 18.
by J Winkelmann, et al.
PubMed リンク
Abstract A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
Nature. 2007 Aug 2;448(7153):591-4. Epub 2007 Jul 15.
by H Hakonarson, et al.
PubMed リンク
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.
Nat Genet. 2007 Aug;39(8):995-9. Epub 2007 Jul 15.
by S Buch, et al.
PubMed リンク
Abstract A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
Nat Genet. 2007 Aug;39(8):984-8. Epub 2007 Jul 8.
by I Tomlinson, et al.
PubMed リンク
Abstract Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.
Nature. 2007 Jul 26;448(7152):470-3. Epub 2007 Jul 4.
by MF Moffatt, et al.
PubMed リンク
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
Nat Genet. 2007 Jul;39(7):827-9. Epub 2007 Jun 10.
by DA van Heel, et al
PubMed リンク
Abstract Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
Nat Genet. 2007 Jul;39(7):857-64. Epub 2007 Jun 6.
by JA Todd, et al.
PubMed リンク
Abstract A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.
Nat Genet. 2007 Jul;39(7):870-4. Epub 2007 May 27.
by DJ Hunter, et al
PubMed リンク
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
Nat Genet. 2007 May;39(5):596-604. Epub 2007 Apr 15.Click here to read
by JD Rioux, et al.
PubMed リンク

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
Nat Genet. 2007 May;39(5):631-7. Epub 2007 Apr 1.
by J Gudmundsson, et al.
PubMed リンク
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.
Nat Genet. 2007 May;39(5):645-9. Epub 2007 Apr 1.
by M Yeager, et al.
PubMed リンク
A genome-wide association study identifies novel risk loci for type 2 diabetes.
Nature. 2007 Feb 22;445(7130):881-5. Epub 2007 Feb 11.
by R Sladek, et al.
PubMed リンク
Abstract A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
Nat Genet. 2007 Feb;39(2):207-11. Epub 2006 Dec 31.
by J Hampe, et al.
PubMed リンク