Cupples LA - Search Results

1

Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease.

Erlich PM, Lunetta KL, Cupples LA, Abraham CR, Green RC, Baldwin CT, Farrer LA. Erlich PM, et al. Among authors: cupples la. Neurobiol Aging. 2012 May;33(5):1015.e7-23. doi: 10.1016/j.neurobiolaging.2010.08.003. Epub 2010 Oct 27. Neurobiol Aging. 2012. PMID: 20980077 Free PMC article.

2

Absence of linkage or association for osteoarthritis with the vitamin D receptor/type II collagen locus: the Framingham Osteoarthritis Study.

Baldwin CT, Cupples LA, Joost O, Demissie S, Chaisson C, Mcalindon T, Myers RH, Felson D. Baldwin CT, et al. Among authors: cupples la. J Rheumatol. 2002 Jan;29(1):161-5. J Rheumatol. 2002. PMID: 11824954

3

Genetic loci influencing lung function: a genome-wide scan in the Framingham Study.

Joost O, Wilk JB, Cupples LA, Harmon M, Shearman AM, Baldwin CT, O'Connor GT, Myers RH, Gottlieb DJ. Joost O, et al. Among authors: cupples la. Am J Respir Crit Care Med. 2002 Mar 15;165(6):795-9. doi: 10.1164/ajrccm.165.6.2102057. Am J Respir Crit Care Med. 2002. PMID: 11897646

4

Expectation maximization algorithm based haplotype relative risk (EM-HRR): test of linkage disequilibrium using incomplete case-parents trios.

Guo CY, DeStefano AL, Lunetta KL, Dupuis J, Cupples LA. Guo CY, et al. Among authors: cupples la. Hum Hered. 2005;59(3):125-35. doi: 10.1159/000085571. Epub 2005 May 2. Hum Hered. 2005. PMID: 15867473

5

Polymorphisms in the PON gene cluster are associated with Alzheimer disease.

Erlich PM, Lunetta KL, Cupples LA, Huyck M, Green RC, Baldwin CT, Farrer LA; MIRAGE Study Group. Erlich PM, et al. Among authors: cupples la. Hum Mol Genet. 2006 Jan 1;15(1):77-85. doi: 10.1093/hmg/ddi428. Epub 2005 Nov 30. Hum Mol Genet. 2006. PMID: 16319130

6

Estrogen receptor alpha gene variation is associated with risk of myocardial infarction in more than seven thousand men from five cohorts.

Shearman AM, Cooper JA, Kotwinski PJ, Miller GJ, Humphries SE, Ardlie KG, Jordan B, Irenze K, Lunetta KL, Schuit SC, Uitterlinden AG, Pols HA, Demissie S, Cupples LA, Mendelsohn ME, Levy D, Housman DE. Shearman AM, et al. Among authors: cupples la. Circ Res. 2006 Mar 17;98(5):590-2. doi: 10.1161/01.RES.0000210578.62102.a6. Epub 2006 Feb 16. Circ Res. 2006. PMID: 16484614

7

Informative-transmission disequilibrium test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring.

Guo CY, Lunetta KL, DeStefano AL, Ordovas JM, Cupples LA. Guo CY, et al. Among authors: cupples la. Genet Epidemiol. 2007 Feb;31(2):115-33. doi: 10.1002/gepi.20195. Genet Epidemiol. 2007. PMID: 17123304

8

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease.

Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F, Katayama T, Baldwin CT, Cheng R, Hasegawa H, Chen F, Shibata N, Lunetta KL, Pardossi-Piquard R, Bohm C, Wakutani Y, Cupples LA, Cuenco KT, Green RC, Pinessi L, Rainero I, Sorbi S, Bruni A, Duara R, Friedland RP, Inzelberg R, Hampe W, Bujo H, Song YQ, Andersen OM, Willnow TE, Graff-Radford N, Petersen RC, Dickson D, Der SD, Fraser PE, Schmitt-Ulms G, Younkin S, Mayeux R, Farrer LA, St George-Hyslop P. Rogaeva E, et al. Among authors: cupples la. Nat Genet. 2007 Feb;39(2):168-77. doi: 10.1038/ng1943. Epub 2007 Jan 14. Nat Genet. 2007. PMID: 17220890 Free PMC article.

9

Heritability of magnetic resonance imaging (MRI) traits in Alzheimer disease cases and their siblings in the MIRAGE study.

Lunetta KL, Erlich PM, Cuenco KT, Cupples LA, Green RC, Farrer LA, Decarli C; MIRAGE Study Group. Lunetta KL, et al. Among authors: cupples la. Alzheimer Dis Assoc Disord. 2007 Apr-Jun;21(2):85-91. doi: 10.1097/WAD.0b013e3180653bf7. Alzheimer Dis Assoc Disord. 2007. PMID: 17545732 Clinical Trial.

10

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.

Cupples LA, Arruda HT, Benjamin EJ, D'Agostino RB Sr, Demissie S, DeStefano AL, Dupuis J, Falls KM, Fox CS, Gottlieb DJ, Govindaraju DR, Guo CY, Heard-Costa NL, Hwang SJ, Kathiresan S, Kiel DP, Laramie JM, Larson MG, Levy D, Liu CY, Lunetta KL, Mailman MD, Manning AK, Meigs JB, Murabito JM, Newton-Cheh C, O'Connor GT, O'Donnell CJ, Pandey M, Seshadri S, Vasan RS, Wang ZY, Wilk JB, Wolf PA, Yang Q, Atwood LD. Cupples LA, et al. BMC Med Genet. 2007;8 Suppl 1(Suppl 1):S1. doi: 10.1186/1471-2350-8-S1-S1. BMC Med Genet. 2007. PMID: 17903291 Free PMC article.

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