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Population Architecture using Genomics and Epidemiology (PAGE) Consortium

Population Architecture using Genomics and Epidemiology (PAGE) Consortium

Published Manuscripts

PAGE-Wide
  • Matise TM, Ambite JL, Buyske S, Carlson CC, Cole SA, Crawford DC, Haiman CA, Heiss G, Kooperberg C, Marchand LL, Manolio TA, North KE, Peters U, Ritchie MD, Hindorff LA, Haines JL,; for the PAGE Study. The Next PAGE in Understanding Complex Traits: Design for the Analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study. American Journal of Epidemiology, 174(7):849-859. 2011. [PubMed]
  • Pendergrass SA, Brown-Gentry K, Dudek SM, Torstenson ES, Ambite JL, Avery CL, Buyske S, Cai C, Fesinmeyer MD, Haiman C, Heiss G, Hindorff LA, Hsu CN, Jackson RD, Kooperberg C, Le Marchand L, Lin Y, Matise TC, Moreland L, Monroe K, Reiner AP, Wallace R, Wilkens LR, Crawford DC, Ritchie MD. The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery. Genetic Epidemiology, 35(5):410-22. 2011. [PubMed]
  • Dumitrescu L, Carty CL, Taylor K, Schumacher FR, Hindorff LA, Ambite JL, Anderson G, Best LG, Brown-Gentry K, Buzkova P, Carlson CS, Cochran B, Cole SA, Devereux RB, Duggan D, Easton CB, Fornage M, Franceschini N, Haessler J, Howard BV, Johnson KC, Laston S, Kolonel LN, Lee ET, MacCluer JW, Manolio TA, Pendergrass SA, Quibrera M, Shohet RV, Wilkens LR, Haiman CA, Le Marchand L, Buyske S, Kooperberg C, North KE, Crawford DC. Genetic Determinants of Lipid Traits in Diverse Populations from the Population Architecture using Genomics and Epidemiology (PAGE) Study. PLoS Genetics, 7(6):e1002138. 2011. [PubMed]
  • Chun-Nan Hsu, Cheng-Ju Kuo, Congxing Cai, Sarah A. Pendergrass, Marylyn D. Ritchie and Jose Luis Ambite. "Learning Phenotype Mapping for Integrating Large Genetic Data." BIONLP '11: Proceedings of the Workshop on Current Trends in Biomedical Natural Language Processing, 2011. Association of Computational Linguistics, Portland, Ore.
  • Cheng I, Caberto CP, Lum-Jones A, Seifried A, Wilkens LR, Schumacher FR, Monroe KR, Lim U, Tiirikainen M, Kolonel LN, Henderson BE, Stram DO, Haiman CA, Le Marchand L. Type 2 diabetes risk variants and colorectal cancer risk: the Multiethnic Cohort and PAGE studies. Gut, 60(12):1703-11.2011. [PubMed]
  • Avery CL, He Q, North KE, Ambite JL, Boerwinkle E, Fornage M, Hindorff LA, Kooperberg C, Meigs Consistent Directions of Effect for Established Type 2 Diabetes Risk Variants Across Populations: The Population Architecture using Genomics and Epidemiology (PAGE) Consortium maccJB, Pankow JS, Pendergrass SA, Psaty BM, Ritchie MD, Rotter JI, Taylor KD, Wilkens LR, Heiss G, Lin GY. A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains. PLoS Genet, 7(10):e1002322. 2011. [PubMed
  • Franceschini N, Carty C, Buzkova P, Reiner A, Garrett T, Lin Y, Vockler JS, Hindorff LA, Cole SA, Boerwinkle E, Lin DY, Bookman E, Best LG, Bella JN, Eaton C, Greenland P, Jenny N, North KE, Taverna D, Young AM, Deelman E, Kooperberg C, Psaty B, Heiss G. Association of genetic variants and incident coronary heart disease in multi-ethnic cohorts. The PAGE Study. Circ Cardiovasc Genet, 4(6):661-72. 2011. [PubMed]
  • Setiawan VW, Haessler J, Schumacher F, Cote ML, Deelman E, Fesinmeyer MD, Henderson BE, Jackson RD, Vockler JS, Wilkens LR, Yasmeen S, Haiman CA, Peters U, LeMarchand L, Kooperberg C. HNF1B and endometrial cancer risk: results from the PAGE study. PLoS One, 7(1):e30390. 2012. [PubMed]
  • Haiman CA, Fesinmeyer MD, Spencer KL, Buzkova P, Voruganti VA, Wan P, Haessler J, Franceschini N, Monroe KR, Howard BV, Jackson RD, FLorez JC, Kolonel LN, Buyske S, Goodloe RJ, Liu S, Manson JE, Meigs JB, Waters K, Mukamal KJ, Pendergrass SA, Shrader P, Wilkens LR, Hindorff LA, Ambite JL, North KE, Peters U, Crawford DC, LeMarchand L, Pankow JS. Consistent Directions of Effect for Established Type 2 Diabetes Risk Variants Across Populations: The Population Architecture using Genomics and Epidemiology (PAGE) Consortium. Diabetes, 61(6):1642-7. 2012. [PubMed]
  • Buyske S, Wu Y, Carty CL, Cheng I, Assimes TL, Dumitrescu L, Hindorff LA, Mitchell S, Ambite JL, Boerwinkle E, Buzkova P, Carlson CS, Cochran B, Duggan D, Eaton CB, Fesinmeyer MD, Franceschini N, Haessler J, Jenny N, Kang HM, Kooperberg C, Lin Y, LeMarchand L, Matise TC, Robinson JG, Rodriguez C, Schumacher FR. Voight BF, Young A, Manolio TA, Mohlke KL, Haiman CA, Peters U, Crawford DC, North KE. Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study. PLoS One, 7(4):e35651. 2012. [PubMed]
  • Carty Cl, Buzkova P, Fornage M, Franceschini N, Cole S, Heiss G, Hindorff LA, Howard BV, Mann S, Martin LW, Zhang Y, Matise TC, Prentice R, Reiner AP, Kooperberg C. Associations between incident ischemic stroke events and stroke and cardiovascular disease-related genome-wide association studies single nucleotide polymorphisms in the Population Architecture Using Genomics and Epidemiology study. Circ Cardiovasc Genet, 5(2):210-6. 2012. [PubMed]

Single Site

CALICo
  • Franceschini N, Reiner AP, Heiss G. Recent findings in the genetics of blood pressure and hypertension traits. American Journal of Hypertension, 24(4):392-400. 2011. [PubMed]
  • Franceschini N, Shara NM, Wang H, Voruganti VS, Laston S, Haack K, Lee ET, Best LG, Maccluer JW, Cochran BJ, Dyer TD, Howard BV, Cole SA, North KE, Umans JG. The association of genetic variants of type 2 diabetes with kidney function. Kidney Int, 10.1038/ki.2012.107. 2012. [PubMed]
EAGLE
  • Pendergrass, SA, Dudek, SM, Crawford, DC, Ritchie, MD. Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis. BioData Min, 3:10. 2010. [PubMed]
  • Pendergrass S, Dudek SM, Roden DM, Crawford DC, Ritchie MD. Visual integration of results from a large DNA biobank (biovu) using synthesis-view. Pac Symp Biocomput, 265-75. 2011. [PubMed]
  • Spencer K, Glenn K, Brown-Gentry K, Haines JL, Crawford DC. Population differences in genetic risk for age-related macular degeneration and implications for genetic testing. Arch Opthalmol, 130(1):116-7. 2012. [PubMed]
MEC
  • Waters KM, Wilkens LR, Monroe KR, Stram DO, Kolonel LN, Henderson BE, Le Marchand L, Haiman CA. No association of type 2 diabetes risk variants and prostate cancer risk: the multiethnic cohort and PAGE. Cancer Epidemiol Biomarkers Prev, 20(9):1979-81. 2011. [PubMed]
  • Chen F, Wilkens LR, Monroe KR, Stram DO, Kolonel LN, Henderson BE, Marchand LL, Haiman CA. No Association of Risk Variants for Diabetes and Obesity with Breast Cancer: The Multiethnic Cohort and PAGE Studies. Cancer Epidemiology, Biomarkers & Prevention, 20(5):1039-42. 2011. [PubMed]
  • Cheng I, Caberto CP, Lum-Jones A, Seifried A, Wilkens LR, Schumacher FR, Monroe KR, Lim U, Tiirkainen M, Kolonel LN, Henderson BE, Stram DO, Haiman CA, LeMarchand L. Type-2 Diabetes Risk Variants and Colorectal Cancer Risk: The Multiethnic Cohort and PAGE Studies. Gut, 20;60(12):1703-11. 2011. [PubMed]
  • Waters KM, Stram DO, Hassanein MT, Le Marchand L, Wilkens LR, Maskarinec G, Monroe KR, Kolonel LN, Altshuler D, Henderson BE, Haiman CA. Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups. PLoS Genetics, 26;6(8). 2010. [PubMed]
  • Lim U, Wilkens LR, Monroe KR, Caberto C, Tiirikainen M, Cheng I, Park SL, Stram DO, Henderson BE, Kolonel LN, Haiman CA, LeMarchand L. Susceptibility variants for obesity and colorectal cancer risk: The multiethnic cohort and PAGE studies. Int J Cancer, Apr 17, 2012. [PubMed]
Coordinating Center
  • Mehta G, Deelman E, Knowles JA, Chen T, Wang Y, Vöckler J, Buyske S, Matise TC. Enabling Data and Compute Intensive Workflows in Bioinformatics. High Performance Bioinformatics and Biomedicine (HiBB). 2011.

Last updated: June 19, 2012