@article {1263,
	title = {Health and function of participants in the Long Life Family Study: A comparison with other cohorts.},
	journal = {Aging (Albany NY)},
	volume = {3},
	year = {2011},
	month = {2011 Jan},
	pages = {63-76},
	abstract = {<p>Individuals from families recruited for the Long Life Family Study (LLFS) (n= 4559) were examined and compared to individuals from other cohorts to determine whether the recruitment targeting longevity resulted in a cohort of individuals with better health and function. Other cohorts with similar data included the Cardiovascular Health Study, the Framingham Heart Study, and the New England Centenarian Study. Diabetes, chronic pulmonary disease and peripheral artery disease tended to be less common in LLFS probands and offspring compared to similar aged persons in the other cohorts. Pulse pressure and triglycerides were lower, high density lipids were higher, and a perceptual speed task and gait speed were better in LLFS. Age-specific comparisons showed differences that would be consistent with a higher peak, later onset of decline or slower rate of change across age in LLFS participants. These findings suggest several priority phenotypes for inclusion in future genetic analysis to identify loci contributing to exceptional survival.</p>},
	keywords = {Aged, Aged, 80 and over, Aging, Blood Pressure, Cardiovascular Diseases, Cohort Studies, Female, Gait, Humans, Longevity, Male, Middle Aged, Psychomotor Performance, Research Design},
	issn = {1945-4589},
	doi = {10.18632/aging.100242},
	author = {Newman, Anne B and Glynn, Nancy W and Taylor, Christopher A and Sebastiani, Paola and Perls, Thomas T and Mayeux, Richard and Christensen, Kaare and Zmuda, Joseph M and Barral, Sandra and Lee, Joseph H and Simonsick, Eleanor M and Walston, Jeremy D and Yashin, Anatoli I and Hadley, Evan}
}
@article {6789,
	title = {Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson{\textquoteright}s disease.},
	journal = {Nat Genet},
	volume = {46},
	year = {2014},
	month = {2014 Sep},
	pages = {989-93},
	abstract = {<p>We conducted a meta-analysis of Parkinson{\textquoteright}s disease genome-wide association studies using a common set of 7,893,274 variants across 13,708 cases and 95,282 controls. Twenty-six loci were identified as having genome-wide significant association; these and 6 additional previously reported loci were then tested in an independent set of 5,353 cases and 5,551 controls. Of the 32 tested SNPs, 24 replicated, including 6 newly identified loci. Conditional analyses within loci showed that four loci, including GBA, GAK-DGKQ, SNCA and the HLA region, contain a secondary independent risk variant. In total, we identified and replicated 28 independent risk variants for Parkinson{\textquoteright}s disease across 24 loci. Although the effect of each individual locus was small, risk profile analysis showed substantial cumulative risk in a comparison of the highest and lowest quintiles of genetic risk (odds ratio (OR) = 3.31, 95\% confidence interval (CI) = 2.55-4.30; P = 2 {\texttimes} 10(-16)). We also show six risk loci associated with proximal gene expression or DNA methylation.</p>},
	keywords = {Case-Control Studies, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Parkinson Disease, Polymorphism, Single Nucleotide, Risk Factors},
	issn = {1546-1718},
	doi = {10.1038/ng.3043},
	author = {Nalls, Mike A and Pankratz, Nathan and Lill, Christina M and Do, Chuong B and Hernandez, Dena G and Saad, Mohamad and DeStefano, Anita L and Kara, Eleanna and Bras, Jose and Sharma, Manu and Schulte, Claudia and Keller, Margaux F and Arepalli, Sampath and Letson, Christopher and Edsall, Connor and Stefansson, Hreinn and Liu, Xinmin and Pliner, Hannah and Lee, Joseph H and Cheng, Rong and Ikram, M Arfan and Ioannidis, John P A and Hadjigeorgiou, Georgios M and Bis, Joshua C and Martinez, Maria and Perlmutter, Joel S and Goate, Alison and Marder, Karen and Fiske, Brian and Sutherland, Margaret and Xiromerisiou, Georgia and Myers, Richard H and Clark, Lorraine N and Stefansson, Kari and Hardy, John A and Heutink, Peter and Chen, Honglei and Wood, Nicholas W and Houlden, Henry and Payami, Haydeh and Brice, Alexis and Scott, William K and Gasser, Thomas and Bertram, Lars and Eriksson, Nicholas and Foroud, Tatiana and Singleton, Andrew B}
}
