Research Topics
Genomes and Genes
Species | Marilyn C CornelisSummaryAffiliation: Harvard University Country: USA Publications
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Detail Information
Publications
The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditionsMarilyn C Cornelis
Department of Nutrition, Harvard School of Public Health, 665 Huntington Avenue, Boston, MA 02115
Genet Epidemiol 34:364-72. 2010..By maximizing knowledge obtained through collaborative GWAS incorporating environmental exposure information, GENEVA aims to enhance our understanding of disease etiology, potentially identifying opportunities for intervention...
Gene-environment interactions in genome-wide association studies: a comparative study of tests applied to empirical studies of type 2 diabetesMarilyn C Cornelis
Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, USA
Am J Epidemiol 175:191-202. 2012..Study findings suggest that methods exploiting G-E independence can be efficient and valid options for investigating G-E interactions in GWAS...
Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestryMarilyn C Cornelis
Harvard School of Public Health, Channing Laboratory, Boston, MA 02115, USA
Ann Intern Med 150:541-50. 2009..Genome-wide association studies have identified novel type 2 diabetes loci, each of which has a modest impact on risk...
Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levelsQi Sun
Department of Nutrition, Harvard School of Public Health, 655 Huntington Avenue, Boston, MA 02115, USA
Hum Mol Genet 19:1846-55. 2010..These data provide novel evidence revealing the role of polymorphisms in LEPR in modulating plasma levels of sOB-R and may further our understanding of the complex relationships among leptin, leptin receptor and diabetes-related traits...
Obesity genotype score and cardiovascular risk in women with type 2 diabetes mellitusMeian He
Department of Nutrition, Harvard School of Public Health, Boston, MA 02115, USA
Arterioscler Thromb Vasc Biol 30:327-32. 2010..To investigate the associations between obesity-predisposing genetic variants, cardiovascular biomarkers, and cardiovascular disease (CVD) risk in women with preexisting type 2 diabetes mellitus...
Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetesLu Qi
Department of Nutrition, Harvard School of Public Health, Boston, MA 02115, USA
Hum Mol Genet 19:1856-62. 2010..Our findings indicate that the genetic variants at ABO locus affect plasma sE-selectin levels and diabetes risk. The genetic associations with diabetes risk were independent of sE-selectin levels...
Genetic predisposition, Western dietary pattern, and the risk of type 2 diabetes in menLu Qi
Department of Nutrition, Harvard School of Public Health, Boston, MA, USA
Am J Clin Nutr 89:1453-8. 2009..A widely held hypothesis is that interactions between genetic predisposition and Western-type lifestyle contribute to the epidemic of type 2 diabetes (T2D). No study has tested this hypothesis...
Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levelsMeian He
Department of Nutrition, Harvard School of Public Health, Boston, MA 02115, USA
Arterioscler Thromb Vasc Biol 30:885-90. 2010..We sought to identify the common genetic variants associated with IL-18 levels...
Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumptionMarilyn C Cornelis
Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, United States of America
PLoS Genet 7:e1002033. 2011..4 × 10(-19)), near AHR, and 15q24 (P = 5.2 × 10(-14)), between CYP1A1 and CYP1A2. Both the AHR and CYP1A2 genes are biologically plausible candidates as CYP1A2 metabolizes caffeine and AHR regulates CYP1A2...
Integrating genetic association, genetics of gene expression, and single nucleotide polymorphism set analysis to identify susceptibility Loci for type 2 diabetes mellitusDanielle M Greenawalt
Department of Genetics, Merck Research Laboratories, Pasteur, Boston, MA 02115, USA
Am J Epidemiol 176:423-30. 2012....
Genetic variants at 2q24 are associated with susceptibility to type 2 diabetesLu Qi
Department of Nutrition, Harvard School of Public Health, and Brigham and Women s Hospital, Boston, MA, USA
Hum Mol Genet 19:2706-15. 2010..05). These data suggest that the 2q24 locus may influence the T2D risk by affecting glucose metabolism and insulin resistance...
Beyond odds ratios--communicating disease risk based on genetic profilesPeter Kraft
Harvard School of Public Health, Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts 02115, USA
Nat Rev Genet 10:264-9. 2009..We argue that other measures--such as sensitivity, specificity, and positive and negative predictive values--are more useful when proposing a genetic profile for risk prediction...
Inclusion of gene-gene and gene-environment interactions unlikely to dramatically improve risk prediction for complex diseasesHugues Aschard
Program in Molecular and Genetic Epidemiology, Harvard School of Public Health, Boston, MA 02115, USA
Am J Hum Genet 90:962-72. 2012..We show that the inclusion of G-G and G-E interaction effects in risk-prediction models is unlikely to dramatically improve the discrimination ability of these models...
Plasma levels of fetuin-A and hepatic enzymes and risk of type 2 diabetes in women in the U.SQi Sun
Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, USA
Diabetes 62:49-55. 2013..69 (1.39-2.05) (P for heterogeneity = 0.45). These findings suggest that plasma fetuin-A levels were independently associated with higher risk of developing type 2 diabetes...
TCF7L2, dietary carbohydrate, and risk of type 2 diabetes in US womenMarilyn C Cornelis
Department of Nutrition, Harvard School of Public Health, Boston, MA 02115, USA
Am J Clin Nutr 89:1256-62. 2009..Dietary factors that increase the insulin demand might enhance the risk of T2D associated with TCF7L2 variants...
Exploring the genetic architecture of circulating 25-hydroxyvitamin DLinda T Hiraki
Program in Molecular and Genetic Epidemiology, Harvard School of Public Health, Boston, Massachusetts 02215, USA
Genet Epidemiol 37:92-8. 2013..The absence of a significant polygenic effect in this relatively large sample suggests an oligogenetic architecture for 25(OH)D...
Gene-environment interactions in the development of type 2 diabetes: recent progress and continuing challengesMarilyn C Cornelis
Department of Nutrition, Harvard School of Public Health, Harvard University, Boston, Massachusetts 02115, USA
Annu Rev Nutr 32:245-59. 2012..Nonetheless, continued investment in gene-environment interaction studies through large collaborative efforts holds promise in furthering our understanding of the interplay between genetic and environmental factors...
Genetic predisposition to higher body mass index or type 2 diabetes and leukocyte telomere length in the Nurses' Health StudyMengmeng Du
Department of Epidemiology, University of Washington School of Public Health, Seattle, Washington, United States of America
PLoS ONE 8:e52240. 2013..We therefore examined whether genetic predisposition to higher BMI or T2D was associated with shortened leukocyte telomere length (LTL)...
Coffee intakeMarilyn C Cornelis
Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, USA
Prog Mol Biol Transl Sci 108:293-322. 2012..This chapter focuses on those factors that are genetically determined and briefly summarizes progress in applying this knowledge to epidemiological studies of coffee and disease...
Genetics of post-traumatic stress disorder: review and recommendations for genome-wide association studiesMarilyn C Cornelis
Department of Nutrition, Harvard School of Public Health, Boston, MA 02115, USA
Curr Psychiatry Rep 12:313-26. 2010..Genome-wide association studies offer the best opportunity to identify novel "true" risk variants for the disorder that in turn has the potential to inform our understanding of PTSD etiology...
