Coleen M. Damcott, Ph.D. - Publications

University of Pittsburgh, Pittsburgh, PA, United States 
biochemistry, genetics

29 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Albert JS, Yerges-Armstrong LM, Horenstein RB, Pollin TI, Sreenivasan UT, Chai S, Blaner WS, Snitker S, O'Connell JR, Gong DW, Breyer RJ, Ryan AS, McLenithan JC, Shuldiner AR, Sztalryd C, ... Damcott CM, et al. Null mutation in hormone-sensitive lipase gene and risk of type 2 diabetes. The New England Journal of Medicine. 370: 2307-15. PMID 24848981 DOI: 10.1056/NEJMoa1315496  0.32
2013 Lewis JP, Ryan K, O'Connell JR, Horenstein RB, Damcott CM, Gibson Q, Pollin TI, Mitchell BD, Beitelshees AL, Pakzy R, Tanner K, Parsa A, Tantry US, Bliden KP, Post WS, et al. Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes. Circulation. Cardiovascular Genetics. 6: 184-92. PMID 23392654 DOI: 10.1161/CIRCGENETICS.111.964627  0.32
2011 Shen H, Damcott C, Shuldiner SR, Chai S, Yang R, Hu H, Gibson Q, Ryan KA, Mitchell BD, Gong DW. Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels. Journal of Human Genetics. 56: 801-5. PMID 21900944 DOI: 10.1038/jhg.2011.105  0.32
2011 Streeten EA, Zarbalian K, Damcott CM. To the editor New England Journal of Medicine. 365: 1741-1742. DOI: 10.1056/NEJMc1110226  0.32
2010 Shen H, Damcott CM, Rampersaud E, Pollin TI, Horenstein RB, McArdle PF, Peyser PA, Bielak LF, Post WS, Chang YP, Ryan KA, Miller M, Rumberger JA, Sheedy PF, Shelton J, et al. Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. Archives of Internal Medicine. 170: 1850-5. PMID 21059979 DOI: 10.1001/archinternmed.2010.384  0.32
2010 Jenkins NT, McKenzie JA, Damcott CM, Witkowski S, Hagberg JM. Endurance exercise training effects on body fatness, VO2max, HDL-C subfractions, and glucose tolerance are influenced by a PLIN haplotype in older Caucasians. Journal of Applied Physiology (Bethesda, Md. : 1985). 108: 498-506. PMID 19850727 DOI: 10.1152/japplphysiol.01018.2009  0.32
2009 Shuldiner AR, O'Connell JR, Bliden KP, Gandhi A, Ryan K, Horenstein RB, Damcott CM, Pakyz R, Tantry US, Gibson Q, Pollin TI, Post W, Parsa A, Mitchell BD, Faraday N, et al. Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy. Jama. 302: 849-57. PMID 19706858 DOI: 10.1001/jama.2009.1232  0.32
2009 Shen H, Pollin TI, Damcott CM, McLenithan JC, Mitchell BD, Shuldiner AR. Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study. Human Genetics. 126: 567-74. PMID 19526250 DOI: 10.1007/s00439-009-0700-3  0.32
2008 Pollin TI, Damcott CM, Shen H, Ott SH, Shelton J, Horenstein RB, Post W, McLenithan JC, Bielak LF, Peyser PA, Mitchell BD, Miller M, O'Connell JR, Shuldiner AR. A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. Science (New York, N.Y.). 322: 1702-5. PMID 19074352 DOI: 10.1126/science.1161524  0.32
2008 McArdle PF, Rutherford S, Mitchell BD, Damcott CM, Wang Y, Ramachandran V, Ott S, Chang YP, Levy D, Steinle N. Nicotinic acetylcholine receptor subunit variants are associated with blood pressure; findings in the Old Order Amish and replication in the Framingham Heart Study. Bmc Medical Genetics. 9: 67. PMID 18625075 DOI: 10.1186/1471-2350-9-67  0.32
2008 Mitchell BD, McArdle PF, Shen H, Rampersaud E, Pollin TI, Bielak LF, Jaquish C, Douglas JA, Roy-Gagnon MH, Sack P, Naglieri R, Hines S, Horenstein RB, Chang YP, Post W, ... ... Damcott CM, et al. The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study. American Heart Journal. 155: 823-8. PMID 18440328 DOI: 10.1016/j.ahj.2008.01.019  0.32
2007 Rampersaud E, Damcott CM, Fu M, Shen H, McArdle P, Shi X, Shelton J, Yin J, Chang YP, Ott SH, Zhang L, Zhao Y, Mitchell BD, O'Connell J, Shuldiner AR. Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations. Diabetes. 56: 3053-62. PMID 17846126 DOI: 10.2337/db07-0457  0.32
2007 Post W, Shen H, Damcott C, Arking DE, Kao WHL, Sack PA, Ryan KA, Chakravarti A, Mitchell BD, Shuldiner AR. Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the Old Order Amish Human Heredity. 64: 214-219. PMID 17565224 DOI: 10.1159/000103630  0.32
2007 Roberts CG, Shen H, Mitchell BD, Damcott CM, Shuldiner AR, Rodriguez A. Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women. Human Heredity. 64: 107-13. PMID 17476110 DOI: 10.1159/000101962  0.32
2007 Fu M, Sabra MM, Damcott C, Pollin TI, Ma L, Ott S, Shelton JC, Shi X, Reinhart L, O'Connell J, Mitchell BD, Baier LJ, Shuldiner AR. Evidence that Rho guanine nucleotide exchange factor 11 (ARHGEF11) on 1q21 is a type 2 diabetes susceptibility gene in the Old Order Amish Diabetes. 56: 1363-1368. PMID 17369523 DOI: 10.2337/db06-1421  0.32
2007 Chu WS, Das SK, Wang H, Chan JC, Deloukas P, Froguel P, Baier LJ, Jia W, McCarthy MI, Ng MCY, Damcott C, Shuldiner AR, Zeggini E, Elbein SC. Activating transcription factor 6 (ATF6) sequence polymorphisms in type 2 diabetes and pre-diabetic traits Diabetes. 56: 856-862. PMID 17327457 DOI: 10.2337/db06-1305  0.32
2006 Damcott CM, Pollin TI, Reinhart LJ, Ott SH, Shen H, Silver KD, Mitchell BD, Shuldiner AR. Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance. Diabetes. 55: 2654-9. PMID 16936218 DOI: 10.2337/db06-0338  0.32
2006 Zeggini E, Damcott CM, Hanson RL, Karim MA, Rayner NW, Groves CJ, Baier LJ, Hale TC, Hattersley AT, Hitman GA, Hunt SE, Knowler WC, Mitchell BD, Ng MC, O'Connell JR, et al. Variation within the gene encoding the upstream stimulatory factor 1 does not influence susceptibility to type 2 diabetes in samples from populations with replicated evidence of linkage to chromosome 1q. Diabetes. 55: 2541-8. PMID 16936202 DOI: 10.2337/db06-0088  0.32
2005 Moffett SP, Feingold E, Barmada MM, Damcott CM, Marshall JA, Hamman RF, Ferrell RE. The C161-->T polymorphism in peroxisome proliferator-activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator-activated receptor gamma. Metabolism: Clinical and Experimental. 54: 1552-6. PMID 16253648 DOI: 10.1016/j.metabol.2005.05.025  0.32
2005 Damcott CM, Ott SH, Pollin TI, Reinhart LJ, Wang J, O'connell JR, Mitchell BD, Shuldiner AR. Genetic variation in adiponectin receptor 1 and adiponectin receptor 2 is associated with type 2 diabetes in the Old Order Amish. Diabetes. 54: 2245-50. PMID 15983228 DOI: 10.2337/diabetes.54.7.2245  0.32
2005 Sabra MM, Damcott C, Fu M, Ott S, O'Connell JR, Mitchell BD, Shuldiner AR. Vesicle-associated membrane protein 4, a positional candidate gene on 1q24-q25, is not associated with type 2 diabetes in the Old Order Amish Molecular Genetics and Metabolism. 85: 133-139. PMID 15896658 DOI: 10.1016/j.ymgme.2004.09.012  0.32
2005 Pollin TI, Tanner K, O'connell JR, Ott SH, Damcott CM, Shuldiner AR, McLenithan JC, Mitchell BD. Linkage of plasma adiponectin levels to 3q27 explained by association with variation in the APM1 gene. Diabetes. 54: 268-74. PMID 15616038 DOI: 10.2337/diabetes.54.1.268  0.32
2004 Damcott CM, Hoppman N, Ott SH, Reinhart LJ, Wang J, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Polymorphisms in both promoters of hepatocyte nuclear factor 4-alpha are associated with type 2 diabetes in the Amish. Diabetes. 53: 3337-41. PMID 15561969 DOI: 10.2337/diabetes.53.12.3337  0.32
2004 Fu M, Damcott CM, Sabra M, Pollin TI, Ott SH, Wang J, Garant MJ, O'Connell JR, Mitchell BD, Shuldiner AR. Polymorphism in the calsequestrin 1 (CASQ1) gene on chromosome 1q21 is associated with type 2 diabetes in the old order Amish. Diabetes. 53: 3292-9. PMID 15561962 DOI: 10.2337/diabetes.53.12.3292  0.32
2004 Damcott CM, Feingold E, Moffett SP, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females. Metabolism: Clinical and Experimental. 53: 458-64. PMID 15045692 DOI: 10.1016/j.metabol.2003.11.019  0.32
2004 Damcott CM, Moffett SP, Feingold E, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males. Metabolism: Clinical and Experimental. 53: 303-9. PMID 15015141 DOI: 10.1016/j.metabol.2003.10.010  0.32
2003 Damcott CM, Sack P, Shuldiner AR. The genetics of obesity. Endocrinology and Metabolism Clinics of North America. 32: 761-86. PMID 14711061 DOI: 10.1016/S0889-8529(03)00076-8  0.32
2003 Damcott CM, Feingold E, Moffett SP, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels. Human Genetics. 112: 610-6. PMID 12634920 DOI: 10.1007/s00439-003-0937-1  0.32
2002 Kimm SY, Glynn NW, Aston CE, Damcott CM, Poehlman ET, Daniels SR, Ferrell RE. Racial differences in the relation between uncoupling protein genes and resting energy expenditure. The American Journal of Clinical Nutrition. 75: 714-9. PMID 11916758  0.32
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