| Year |
Citation |
Score |
| 2017 |
Richard MA, Huan T, Ligthart S, Gondalia R, Jhun MA, Brody JA, Irvin MR, Marioni R, Shen J, Tsai PC, Montasser ME, Jia Y, Syme C, Salfati EL, Boerwinkle E, ... ... Damcott CM, et al. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation. American Journal of Human Genetics. 101: 888-902. PMID 29198723 DOI: 10.1016/J.Ajhg.2017.09.028 |
0.341 |
|
| 2016 |
Yerges-Armstrong LM, Chai S, O'Connell JR, Curran JE, Blangero J, Mitchell BD, Shuldiner AR, Damcott CM. Gene Expression Differences Between Offspring of Long-Lived Individuals and Controls in Candidate Longevity Regions: Evidence for PAPSS2 as a Longevity Gene. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 26896383 DOI: 10.1093/Gerona/Glv212 |
0.396 |
|
| 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 |
0.385 |
|
| 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 |
0.393 |
|
| 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 |
0.495 |
|
| 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 |
0.423 |
|
| 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 |
0.51 |
|
| 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 |
0.313 |
|
| 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 |
0.322 |
|
| 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 |
0.399 |
|
| 2007 |
Njajou OT, Cawthon RM, Damcott CM, Wu SH, Ott S, Garant MJ, Blackburn EH, Mitchell BD, Shuldiner AR, Hsueh WC. Telomere length is paternally inherited and is associated with parental lifespan. Proceedings of the National Academy of Sciences of the United States of America. 104: 12135-9. PMID 17623782 DOI: 10.1073/Pnas.0702703104 |
0.332 |
|
| 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 |
0.404 |
|
| 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 |
0.449 |
|
| 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 |
0.497 |
|
| 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 |
0.491 |
|
| 2007 |
Dotson C, Elson A, Shaw H, Shi X, Damcott C, Naj A, Snitker S, Steinle N, Munger S. Taste receptor polymorphisms in the Old Order Amish: Associations with obesity and related traits Appetite. 49: 288. DOI: 10.1016/J.Appet.2007.03.060 |
0.499 |
|
| 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 |
0.547 |
|
| 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 |
0.479 |
|
| 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 |
0.715 |
|
| 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 |
0.495 |
|
| 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 |
0.375 |
|
| 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 |
0.446 |
|
| 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 |
0.51 |
|
| 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 |
0.509 |
|
| 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 |
0.708 |
|
| 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 |
0.719 |
|
| 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 |
0.348 |
|
| 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 |
0.732 |
|
| 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 DOI: 10.1093/Ajcn/75.4.714 |
0.55 |
|
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