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  1. Gong, J., Nishimura, K., Bien, S., Graff, M., Fornage, M., Gross, M., Peters., U. (2017) Trans-Ethnic Analysis of Metabochip Data Identifies Two New Loci Associated with BMI. International Journal of Obesity. In press.

  2. Bien S., Pankow J., Haessler J., Lu Y., Pankratz N., Peters U., Kooperberg C. (2017) Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. Diabetologia. PMID: 28905132

  3. Yoneyama, S., Yao, J., Guo, X., Fernandez-Rhodes, L., Lim, U., Buzková, P., ... & Ehret, G. (2017). Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations. International Journal of Obesity. PMID: 27867202
  4. Fernández-Rhodes, L., Gong, J., Haessler, J., Franceschini, N., Graff, M., Nishimura, K. K., ... & Goodloe, R. (2017). Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci. Human Genetics, 1-30. PMID: 28391526
  5. Carlson, C. S. (2016). Ethnicity: Diversity is future for genetic analysis. Nature, 540(7633), 341-341. PMID: 27974770
  6. Bien, S. A., Wojcik, G. L., Zubair, N., Gignoux, C. R., Martin, A. R., Kocarnik, J. M., ... & Cheng, I. (2016). Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array. PloS one, 11(12), e0167758. PMID 27973554
  7. Yoneyama, S., Yao, J., Guo, X., Fernandez-Rhodes, L., Lim, U., Boston, J., Cooper, R. (2016). Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations. International Journal of Obesity. PMID 27867202
  8. Avery, C. L., Wassel, C. L., Richard, M. A., Highland, H. M., Bien, S., Zubair, N., ... & Seyerle, A. A. (2016). Fine-mapping of QT regions in global populations refines previously identified QT loci and identifies signals unique to african and hispanic descent populations. Heart Rhythm. PMID 27988371
  9. Franceschini, N., Carty, C. L., Lu, Y., Tao, R., Sung, Y. J., Manichaikul, A., Bien, S., et al. (2016). Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans. PloS one, 11(10), e0164132. PMID 27736895
  10. Kocarnik, J.M., Park, S.L., Han, J., Dumitrescu, L., Cheng, I., Wilkens, L.R., Schumacher, F.R., Kolonel, L., Carlson, C.S., Crawford, D.C., et al. (2015). Pleiotropic and Sex-Specific Effects of Cancer GWAS SNPs on Melanoma Risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study. PLoS One 10, e0120491. PMC4366224
  11. Wood, A.R., Esko, T., Yang, J., Vedantam, S., Pers, T.H., Gustafsson, S., Chu, A.Y., Estrada, K., Luan, J., Kutalik, Z., et al. (2014). Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet 46, 1173-1186. PMC4250049
  12. Shungin, D., Winkler, T.W., Croteau-Chonka, D.C., Ferreira, T., Locke, A.E., Magi, R., Strawbridge, R.J., Pers, T.H., Fischer, K., Justice, A.E., et al. (2015). New genetic loci link adipose and insulin biology to body fat distribution. Nature 518, 187-196. PMC4338562
  13. Locke, A.E., Kahali, B., Berndt, S.I., Justice, A.E., Pers, T.H., Day, F.R., Powell, C., Vedantam, S., Buchkovich, M.L., Yang, J., et al. (2015). Genetic studies of body mass index yield new insights for obesity biology. Nature 518, 197-206. PMC4382211
  14. Franceschini, N., Hu, Y., Reiner, A.P., Buyske, S., Nalls, M., Yanek, L.R., Li, Y., Hindorff, L.A., Cole, S.A., Howard, B.V., et al. (2014). Prospective Associations of Coronary Heart Disease Loci in African Americans Using the MetaboChip: The PAGE Study. PLoS One 9, e113203. PMC4277270
  15. Park, S.L., Caberto, C.P., Lin, Y., Goodloe, R.J., Dumitrescu, L., Love, S.A., Matise, T.C., Hindorff, L.A., Fowke, J.H., Schumacher, F.R., et al. (2014). Association of Cancer Susceptibility Variants with Risk of Multiple Primary Cancers: the Population Architecture using Genomics and Epidemiology Study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. PMID: 25139936
  16. Restrepo, N.A., Spencer, K.M., Goodloe, R., Garrett, T.A., Heiss, G., Buzkova, P., Jorgensen, N., Jensen, R.A., Matise, T.C., Hindorff, L.A., et al. (2014). Genetic determinants of age-related macular degeneration in diverse populations from the PAGE Study. Investigative ophthalmology & visual science. PMID: 25205864
  17. Carty, C.L., Bhattacharjee, S., Haessler, J., Cheng, I., Hindorff, L.A., Aroda, V., Carlson, C.S., Hsu, C.N., Wilkens, L., Liu, S., et al. (2014). Comparative Analysis of Metabolic Syndrome Components in over 15,000 African Americans Identifies Pleiotropic Variants: Results from the PAGE Study. Circulation Cardiovascular genetics. PMID: 25023634
  18. Seyerle, A.A., Young, A.M., Jeff, J.M., Melton, P.E., Jorgensen, N.W., Lin, Y., Carty, C.L., Deelman, E., Heckbert, S.R., Hindorff, L.A., et al. (2014). Evidence of Heterogeneity by Race/Ethnicity in Genetic Determinants of QT Interval. Epidemiology. PMID: 25166880
  19. Setiawan, V.W., Schumacher, F., Prescott, J., Haessler, J., Malinowski, J., Wentzensen, N., Yang, H., Chanock, S., Brinton, L., Hartge, P., et al. (2014). Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia. Carcinogenesis . PMID: 24832084
  20. Park, S.L., Fesinmeyer, M.D., Timofeeva, M., Caberto, C.P., Kocarnik, J.M., Han, Y., Love, S.A., Young, A., Dumitrescu, L., Lin, Y., et al. (2014). Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia. Journal of the National Cancer Institute 106, dju061. PMID: 24681604
  21. Kocarnik, J.M., Pendergrass, S.A., Carty, C.L., Pankow, J.S., Schumacher, F.R., Cheng, I., Durda, P., Ambite, J.L., Deelman, E., Cook, N.R., et al. (2014). Multi-Ancestral Analysis of Inflammation-Related Genetic Variants and C-Reactive Protein in the Population Architecture using Genomics and Epidemiology (PAGE) Study. Circulation Cardiovascular genetics . PMID: 24622110
  22. Lim, U., Kocarnik, J.M., Bush, W.S., Matise, T.C., Caberto, C., Park, S.L., Carlson, C.S., Deelman, E., Duggan, D., Fesinmeyer, M., et al. (2014). Pleiotropy of Cancer Susceptibility Variants on the Risk of Non-Hodgkin Lymphoma: The PAGE Consortium. PLoS One 9, e89791. PMID: 24598796
  23. Kocarnik, J.M., Park, S.L., Han, J., Dumitrescu, L., Cheng, I., Wilkens, L.R., Schumacher, F.R., Kolonel, L., Carlson, C.S., Crawford, D.C., et al. (2014). Replication of Associations Between GWAS SNPs and Melanoma Risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study. The Journal of investigative dermatology . PMID: 24480881
  24. Zhang, L., Spencer, K.L., Voruganti, V.S., Jorgensen, N.W., Fornage, M., Best, L.G., Brown-Gentry, K.D., Cole, S.A., Crawford, D.C., Deelman, E., et al. (2013). Association of Functional Polymorphism rs2231142 (Q141K) in the ABCG2 Gene With Serum Uric Acid and Gout in 4 US Populations: The PAGE Study. Am J Epidemiol , April 2013. PMID: 23552988
  25. Zhang, L., Buzkova, P., Wassel, C.L., Roman, M.J., North, K.E., Crawford, D.C., Boston, J., Brown-Gentry, K.D., Cole, S.A., Deelman, E., et al. (2013). Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four U.S. populations: The Population Architecture using Genomics and Epidemiology (PAGE) study. Atherosclerosis 228, 390-399. PMID: 23587283
  26. Wu, Y., Waite, L.L., Jackson, A.U., Sheu, W.H.H., Buyske, S., Absher, D., Arnett, D.K., Boerwinkle, E., Bonnycastle, L.L., Carty, C.L., et al. (2013). Trans-Ethnic Fine-Mapping of Lipid Loci Identifies Population-Specific Signals and Allelic Heterogeneity That Increases the Trait Variance Explained. PLoS Genet 9, e1003379. PMID:23555291
  27. Taylor, K.C., Carty, C.L., Dumitrescu, L., Buzkova, P., Cole, S.A., Hindorff, L., Schumacher, F.R., Wilkens, L.R., Shohet, R.V., Quibrera, P.M., et al. (2013). Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study. BMC genetics 14, 33. PMID: 23634756
  28. Spencer, K.L., Malinowski, J., Carty, C.L., Franceschini, N., Fernández-Rhodes, L., Young, A., Cheng, I., Ritchie, M.D., Haiman, C.A., Wilkens, L., et al. (2013). Genetic Variation and Reproductive Timing: African American Women from the Population Architecture Using Genomics and Epidemiology (PAGE) Study. PLoS One 8, e55258. PMC3570525
  29. Peters, U., North, K.E., Sethupathy, P., Buyske, S., Haessler, J., Jiao, S., Fesinmeyer, M.D., Jackson, R.D., Kuller, L.H., Rajkovic, A., et al. (2013). A Systematic Mapping Approach of 16q12.2/FTO and BMI in More Than 20,000 African Americans Narrows in on the Underlying Functional Variation: Results from the Population Architecture using Genomics and Epidemiology (PAGE) Study. PLoS Genet 9, e1003171. PMC3547789
  30. Pendergrass, S.A., Brown-Gentry, K., Dudek, S., Frase, A., Torstenson, E.S., Goodloe, R., Ambite, J.L., Avery, C.L., Buyske, S., Buzkova, P., et al. (2013). Phenome-Wide Association Study (PheWAS) for Detection of Pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network. PLoS Genet 9, e1003087. PMC3561060
  31. Park, S.L., Cheng, I., Pendergrass, S.A., Kucharska-Newton, A.M., Lim, U., Ambite, J.L., Caberto, C.P., Monroe, K.R., Schumacher, F., Hindorff, L.A., et al. (2013). Association of the FTO Obesity Risk Variant rs8050136 With Percentage of Energy Intake From Fat in Multiple Racial/Ethnic Populations: The PAGE Study. Am J Epidemiol 178, 780-790. PMC3755639
  32. Graff, M., Gordon-Larsen, P., Lim, U., Fowke, J.H., Love, S.A., Fesinmeyer, M., Wilkens, L.R., Vertilus, S., Ritchie, M.D., Prentice, R.L., et al. (2013). The influence of obesity-related single nucleotide polymorphisms on BMI across the life course: the PAGE study. Diabetes 62, 1763-1767. PMC3636619
  33. Gong, J., Schumacher, F., Lim, U., Hindorff, L.A., Haessler, J., Buyske, S., Carlson, C.S., Rosse, S., Buzkova, P., Fornage, M., et al. (2013). Fine Mapping and Identification of BMI Loci in African Americans. American journal of human genetics 93, 661-671. PMC3791273
  34. Fesinmeyer, M.D., North, K.E., Lim, U., Bůžková, P., Crawford, D.C., Haessler, J., Gross, M.D., Fowke, J.H., Goodloe, R., Love, S.-A., et al. (2013). Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study. BMC Med Genet 14. PMC3564691
  35. Fesinmeyer, M.D., Meigs, J.B., North, K.E., Schumacher, F.R., P, B.K., Franceschini, N., Haessler, J., Goodloe, R., Spencer, K.L., Voruganti, V.S., et al. (2013). Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. BMC Med Genet 14, 98. PMC3849560
  36. Dumitrescu, L., Carty, C.L., Franceschini, N., Hindorff, L.A., Cole, S.A., Buzkova, P., Schumacher, F.R., Eaton, C.B., Goodloe, R.J., Duggan, D.J., et al. (2013). No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population. Human genetics 132, 1427-1431. PMC3895337
  37. Dumitrescu, L., Carty, C.L., Franceschini, N., Hindorff, L.A., Cole, S.A., Buzkova, P., Schumacher, F.R., Eaton, C.B., Goodloe, R.J., Duggan, D.J., et al. (2013). Post-Genome-Wide Association Study Challenges for Lipid Traits: Describing Age as a Modifier of Gene-Lipid Associations in the Population Architecture Using Genomics and Epidemiology (PAGE) Study. Ann Hum Genet , June 2013. PMC3796061
  38. Duan, Q., Liu, E.Y., Auer, P.L., Zhang, G., Lange, E.M., Jun, G., Bizon, C., Jiao, S., Buyske, S., Franceschini, N., et al. (2013). Imputation of Coding Variants in African Americans: Better Performance using Data from the Exome Sequencing Project. Bioinformatics , August 2013. PMC3799474
  39. Cheng, I., Kocarnik, J.M., Dumitrescu, L., Lindor, N.M., Chang-Claude, J., Avery, C.L., Caberto, C.P., Love, S.A., Slattery, M.L., Chan, A.T., et al. (2013). Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia. Gut , August 2013. PMID23935004
  40. Carty, C.L., Spencer, K.L., Setiawan, V.W., Fernandez-Rhodes, L., Malinowski, J., Buyske, S., Young, A., Jorgensen, N.W., Cheng, I., Carlson, C.S., et al. (2013). Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study. Hum Reprod 28, 1695-1706. PMC3657124
  41. Carlson, C.S., Matise, T.C., North, K.E., Haiman, C.A., Fesinmeyer, M.D., Buyske, S., Schumacher, F.R., Peters, U., Franceschini, N., Ritchie, M.D., et al. (2013). Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study. PLoS Biol 11, e1001661. PMC3775722
  42. Setiawan, V.W., Haessler, J., Schumacher, F., Cote, M.L., Deelman, E., Fesinmeyer, M.D., Henderson, B.E., Jackson, R.D., Vockler, J.S., Wilkens, L.R., et al. (2012). HNF1B and endometrial cancer risk: results from the PAGE study. PLoS One 7, e30390. PMC3267708
  43. Liu, E.Y., Buyske, S., Aragaki, A.K., Peters, U., Boerwinkle, E., Carlson, C., Carty, C., Crawford, D.C., Haessler, J., Hindorff, L.A., et al. (2012). Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative. Genet Epidemiol 36, 107-117. PMC3410659
  44. Haiman, C.A., Fesinmeyer, M.D., Spencer, K.L., Buzkova, P., Voruganti, V.S., Wan, P., Haessler, J., Franceschini, N., Monroe, K.R., Howard, B.V., et al. (2012). Consistent directions of effect for established type 2 diabetes risk variants across populations: the population architecture using Genomics and Epidemiology (PAGE) Consortium. Diabetes 61, 1642-1647. PMC3357304
  45. Fesinmeyer, M.D., North, K.E., Ritchie, M.D., Lim, U., Franceschini, N., Wilkens, L.R., Gross, M.D., Buzkova, P., Glenn, K., Quibrera, P.M., et al. (2012). Genetic Risk Factors for BMI and Obesity in an Ethnically Diverse Population: Results From the Population Architecture Using Genomics and Epidemiology (PAGE) Study. Obesity , July 2012. PMC3482415
  46. Carty, C.L., Buzkova, P., Fornage, M., Franceschini, N., Cole, S., Heiss, G., Hindorff, L.A., Howard, B.V., Mann, S., Martin, L.W., et al. (2012). 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. Circulation Cardiovascular genetics 5, 210-216. PMC3402178
  47. Buyske, S., Wu, Y., Carty, C.L., Cheng, I., Assimes, T.L., Dumitrescu, L., Hindorff, L.A., Mitchell, S., Ambite, J.L., Boerwinkle, E., et al. (2012). Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. PLoS One 7, e35651. PMC3335090
  48. Avery, C.L., Sethupathy, P., Buyske, S., He, Q., Lin, D.Y., Arking, D.E., Carty, C.L., Duggan, D., Fesinmeyer, M.D., Hindorff, L.A., et al. (2012). Fine-Mapping and Initial Characterization of QT Interval Loci in African Americans. PLOS Genet 8, e1002870. PMC3415454
  49. Pendergrass, S.A., Brown-Gentry, K., Dudek, S.M., Torstenson, E.S., Ambite, J.L., Avery, C.L., Buyske, S., Cai, C., Fesinmeyer, M.D., Haiman, C., et al. (2011). The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery. Genet Epidemiol 35, 410-422. PMC3116446
  50. Matise, T.C., Ambite, J.L., Buyske, S., Carlson, C.S., Cole, S.A., Crawford, D.C., Haiman, C.A., Heiss, G., Kooperberg, C., Marchand, L.L., et al. (2011). The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study. Am J Epidemiol 174, 849-859. PMC3176830
  51. Hsu, C., Kuo, C., Cai, C., Pendergrass, S., Ritchie, M.D., and Ambite, J.L. (2011). Learning Phenotype Mapping for Integrating Large Genetic Data. In  BioNLP. (Portland, OR), pp 19-27
  52. Franceschini, N., Carty, C., Buzkova, P., Reiner, A.P., Garrett, T., Lin, Y., Vockler, J.S., Hindorff, L.A., Cole, S.A., Boerwinkle, E., et al. (2011). Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study. Circulation Cardiovascular genetics 4, 661-672. PMC3293207
  53. Dumitrescu, L., Carty, C.L., Taylor, K., Schumacher, F.R., Hindorff, L.A., Ambite, J.L., Anderson, G., Best, L.G., Brown-Gentry, K., Buzkova, P., et al. (2011). Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study. PLoS Genet 7, e1002138. PMC3128106
  54. Avery, C.L., He, Q., North, K.E., Ambite, J.L., Boerwinkle, E., Fornage, M., Hindorff, L.A., Kooperberg, C., Meigs, J.B., Pankow, J.S., et al. (2011). A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains. PLOS Genet 7, e1002322. PMC3192835

 Single Site:

CALiCo:

  1. Lin, D.Y., Tao, R., Kalsbeek, W.D., Zeng, D., Gonzalez, F., 2nd, Fernandez-Rhodes, L., Graff, M., Koch, G.G., North, K.E., and Heiss, G. (2014). Genetic Association Analysis under Complex Survey Sampling: The Hispanic Community Health Study/Study of Latinos. American journal of human genetics 95, 675-688. PMID: 25480034
  2. Voruganti, V.S., Franceschini, N., Haack, K., Laston, S., Maccluer, J.W., Umans, J.G., Comuzzie, A.G., North, K.E., and Cole, S.A. (2013). Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American Indians. European journal of human genetics : EJHG , December 2013. PMID: 24301058. PAGE MS 33.
  3. Franceschini, N., Haack, K., Goring, H.H., Voruganti, V.S., Laston, S., Almasy, L., Lee, E.T., Best, L.G., Fabsitz, R.R., North, K.E., et al. (2013). Epidemiology and genetic determinants of progressive deterioration of glycaemia in American Indians: the Strong Heart Family Study. Diabetologia 56, 2194-2202. PMC3773080. PAGE MS 61.
  4. Franceschini, N., Shara, N.M., Wang, H., Voruganti, V.S., Laston, S., Haack, K., Lee, E.T., Best, L.G., Maccluer, J.W., Cochran, B.J., et al. (2012). The association of genetic variants of type 2 diabetes with kidney function. Kidney international 82, 220-225. PMID: 22513821. PAGE MS 34.
  5. Franceschini, N., Reiner, A.P., and Heiss, G. (2011). Recent findings in the genetics of blood pressure and hypertension traits. Am J Hypertens 24, 392-400. PMC3110743. PAGE MS 03.

EAGLE:

  1. Jeff, J., Brown-Gentry, K., Goodloe, R., Ritchie, M., Denny, J., Kho, A., Armstrong, L., McClellan, B., Jr., Mayo, P., Allen, M., et al. (2014). Replication of SCN5A Associations with Electrocardiographic Traits in African Americans from Clinical and Epidemiologic Studies. In Applications of Evolutionary Computation, A.I. Esparcia-Alcázar and A.M. Mora, eds. (Springer Berlin Heidelberg), pp 939-951.
  2. Hall, M.A., Verma, A., Brown-Gentry, K.D., Goodloe, R., Boston, J., Wilson, S., McClellan, B., Sutcliffe, C., Ritchie, M.D., Pendergrass, S.A., et al. (2014). Detection of Pleiotropy through a Phenome-Wide Association Study (PheWAS) of Epidemiologic Data as Part of the Environmental Architecture for Genes Linked to Environment (EAGLE) Study. PLoS Genet 10, e1004678. PMID: 25474351
  3. Crawford, D.C., Dumitrescu, L., Goodloe, R., Brown-Gentry, K., Boston, J., McClellan, B., Jr., Sutcliffe, C., Wiseman, R., Baker, P., Pericak-Vance, M.A., et al. (2014). Rare Variant APOC3 R19X Is Associated with Cardio-Protective Profiles in a Diverse Population-Based Survey as Part of the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) Study. Circulation Cardiovascular genetics. PMID: 25363704
  4. Villegas, R., Goodloe, R.J., McClellan, B.E., Jr., Boston, J., and Crawford, D.C. (2014). Gene-carbohydrate and gene-fiber interactions and type 2 diabetes in diverse populations from the National Health and Nutrition Examination Surveys (NHANES) as part of the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study. BMC genetics 15, 69. PMID: 24929251
  5. Malinowski, J., Farber-Eger, E., and Crawford, D.C. (2014). Development of a data-mining algorithm to identify ages at reproductive milestones in electronic medical records. Pac Symp Biocomput , 376-387. PMID: 24297563
  6. Mitchell, S.L., Hall, J.B., Goodloe, R.J., Boston, J., Farber-Eger, E., Pendergrass, S.A., Bush, W.S., and Crawford, D.C. (2014). Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies. BioData Min 7, 6. PMID: 24731735. PAGE MS 16.
  7. Wiley, L.K., Shah, A., Xu, H., and Bush, W.S. (2013). ICD-9 tobacco use codes are effective identifiers of smoking status. J Am Med Inform Assoc : JAMIA 20, 652-658. PMC3721171. PAGE MS 57.
  8. Voruganti, V.S., Franceschini, N., Haack, K., Laston, S., Maccluer, J.W., Umans, J.G., Comuzzie, A.G., North, K.E., and Cole, S.A. (2013). Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American Indians. European journal of human genetics : EJHG , December 2013. PMID: 24301058
  9. Goodloe, R., Brown-Gentry, K., Gillani, N.B., Jin, H., Mayo, P., Allen, M., McClellan, B., Jr., Boston, J., Sutcliffe, C., Schnetz-Boutaud, N., et al. (2013). Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III). BMC Med Genet 14, 120. PMC3870971
  10. Bush, W.S., Boston, J., Pendergrass, S.A., Dumitrescu, L., Goodloe, R., Brown-Gentry, K., Wilson, S., McClellan, B., Torstenson, E., Basford, M.A., et al. (2013). Enabling high-throughput genotype-phenotype associations in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project as part of the Population Architecture using Genomics and Epidemiology (PAGE) study. Pac Symp Biocomput, 373-384. PMC3579641. PAGE MS 55.
  11. Crawford, D.C., Goodloe, R., Brown-Gentry, K., Wilson, S., Roberson, J., Gillani, N.B., Ritchie, M.D., Dilks, H.H., and Bush, W.S. (2013). Characterization of the metabochip in diverse populations from the international hapmap project in the epidemiologic architecture for genes linked to environment (eagle) project. Pac Symp Biocomput, 188-199. PMC3584704. PAGE MS 56.
  12. Spencer, K.L., Glenn, K., Brown-Gentry, K., Haines, J.L., and Crawford, D.C. (2012). Population differences in genetic risk for age-related macular degeneration and implications for genetic testing. Arch Ophthalmol 130, 116-117. PMC3326353
  13. Ritchie, M.D., and Pendergrass, S. (2012). Phenotype-Wide Association Study for Exploration of Novel SNP and Phenotype Relationships within EAGLE/NHANES. In Translational Bioinformatics Conference (Jeju Island, Korea). PAGE MS18.
  14. Dumitrescu, L., Goodloe, R., Brown-Gentry, K., Mayo, P., Allen, M., Jin, H., Gillani, N.B., Schnetz-Boutaud, N., Dilks, H.H., and Crawford, D.C. (2012). Serum vitamins A and E as modifiers of lipid trait genetics in the National Health and Nutrition Examination Surveys as part of the Population Architecture using Genomics and Epidemiology (PAGE) study. Human genetics 131, 1699-1708. PMC3472117. PAGE MS26.
  15. Pendergrass, S., Dudek, S.M., Roden, D.M., Crawford, D.C., and Ritchie, M.D. (2011). Visual integration of results from a large DNA biobank (biovu) using synthesis-view. Pac Symp Biocomput, 265-275. PMC3065108
  16. Pendergrass, S.A., Dudek, S.M., Crawford, D.C., and Ritchie, M.D. (2010). Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis. BioData Min 3, 10. PMC3012023.

MEC:

  1. Lim, U., Wilkens, L.R., Monroe, K.R., Caberto, C., Tiirikainen, M., Cheng, I., Park, S.L., Stram, D.O., Henderson, B.E., Kolonel, L.N., et al. (2012). Susceptibility variants for obesity and colorectal cancer risk: the multiethnic cohort and PAGE studies. International journal of cancer Journal international du cancer 131, E1038-1043. PMC3402643. PAGE MS11E
  2. Chen, F., Wilkens, L.R., Monroe, K.R., Stram, D.O., Kolonel, L.N., Henderson, B.E., Le Marchand, L., and Haiman, C.A. (2011). No association of risk variants for diabetes and obesity with breast cancer: the Multiethnic Cohort and PAGE studies. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 20, 1039-1042. PMID: 21357383. PAGE MS11B.
  3. Cheng, I., Caberto, C.P., Lum-Jones, A., Seifried, A., Wilkens, L.R., Schumacher, F.R., Monroe, K.R., Lim, U., Tiirikainen, M., Kolonel, L.N., et al. (2011). Type 2 diabetes risk variants and colorectal cancer risk: the Multiethnic Cohort and PAGE studies. Gut 60, 1703-1711. PMID: 21602532. PAGE MS11A.
  4. Waters, K.M., Stram, D.O., Hassanein, M.T., Le Marchand, L., Wilkens, L.R., Maskarinec, G., Monroe, K.R., Kolonel, L.N., Altshuler, D., Henderson, B.E., et al. (2010). Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups. PLoS Genet 6, e1001078. PMC2928808. PAGE MS11C.

WHI:

  1. Pashova, H., Leblanc, M., and Kooperberg, C. (2012). Boosting for detection of gene-environment interactions. Stat Med 32, 255-266. PMC3561470. PAGE MS38.

CC:

  1. Mehta, G., Deelman, E., Knowles, J.A., Chen, T., Wang, Y., Vöckler, J., Buyske, S., and Matise, T.C. (2011). Enabling Data and Compute Intensive Workflows in Bioinformatics. In  High Performance Bioinformatics and Biomedicine. (Bordeaux, France), pp 22-32. PAGE MS 42.