O'Connell JR - Search Results

1

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.

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 2nd, Shelton J, O'Connell JR, Shuldiner AR, Mitchell BD. Shen H, et al. Arch Intern Med. 2010 Nov 8;170(20):1850-5. doi: 10.1001/archinternmed.2010.384. Arch Intern Med. 2010. PMID: 21059979 Free PMC article.

2

Exploring the genetics of longevity in the Old Order Amish.

Sorkin J, Post W, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Sorkin J, et al. Mech Ageing Dev. 2005 Feb;126(2):347-50. doi: 10.1016/j.mad.2004.08.027. Mech Ageing Dev. 2005. PMID: 15621217

3

Vesicle-associated membrane protein 4, a positional candidate gene on 1q24-q25, is not associated with type 2 diabetes in the Old Order Amish.

Sabra MM, Damcott C, Fu M, Ott S, O'Connell JR, Mitchell BD, Shuldiner AR. Sabra MM, et al. Mol Genet Metab. 2005 Jun;85(2):133-9. doi: 10.1016/j.ymgme.2004.09.012. Mol Genet Metab. 2005. PMID: 15896658

4

Genetic variation in adiponectin receptor 1 and adiponectin receptor 2 is associated with type 2 diabetes in the Old Order Amish.

Damcott CM, Ott SH, Pollin TI, Reinhart LJ, Wang J, O'connell JR, Mitchell BD, Shuldiner AR. Damcott CM, et al. Diabetes. 2005 Jul;54(7):2245-50. doi: 10.2337/diabetes.54.7.2245. Diabetes. 2005. PMID: 15983228

5

Variants in the ghrelin gene are associated with metabolic syndrome in the Old Order Amish.

Steinle NI, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Steinle NI, et al. J Clin Endocrinol Metab. 2005 Dec;90(12):6672-7. doi: 10.1210/jc.2005-0549. Epub 2005 Oct 4. J Clin Endocrinol Metab. 2005. PMID: 16204371

6

A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection.

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. Pollin TI, et al. Science. 2008 Dec 12;322(5908):1702-5. doi: 10.1126/science.1161524. Science. 2008. PMID: 19074352 Free PMC article.

7

Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy.

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, Herzog W, Gurbel PA. Shuldiner AR, et al. JAMA. 2009 Aug 26;302(8):849-57. doi: 10.1001/jama.2009.1232. JAMA. 2009. PMID: 19706858 Free PMC article.

8

Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels.

Cheng YC, Kao WH, Mitchell BD, O'Connell JR, Shen H, McArdle PF, Gibson Q, Ryan KA, Shuldiner AR, Pollin TI. Cheng YC, et al. Circ Cardiovasc Genet. 2009 Aug;2(4):329-37. doi: 10.1161/CIRCGENETICS.108.834986. Epub 2009 May 14. Circ Cardiovasc Genet. 2009. PMID: 20031604 Free PMC article.

9

Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes.

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, Faraday N, Herzog W, Gong Y, Pepine CJ, Johnson JA, Gurbel PA, Shuldiner AR. Lewis JP, et al. Circ Cardiovasc Genet. 2013 Apr;6(2):184-92. doi: 10.1161/CIRCGENETICS.111.964627. Epub 2013 Feb 7. Circ Cardiovasc Genet. 2013. PMID: 23392654 Free PMC article. Clinical Trial.

10

Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels.

Lu W, Cheng YC, Chen K, Wang H, Gerhard GS, Still CD, Chu X, Yang R, Parihar A, O'Connell JR, Pollin TI, Angles-Cano E, Quon MJ, Mitchell BD, Shuldiner AR, Fu M. Lu W, et al. Hum Mol Genet. 2015 Apr 15;24(8):2390-400. doi: 10.1093/hmg/ddu731. Epub 2015 Jan 9. Hum Mol Genet. 2015. PMID: 25575512 Free PMC article.

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