@article {315308,
	title = {Four Genome-Wide Association Studies Identify New Extreme Longevity Variants},
	journal = {J Gerontol A Biol Sci Med Sci},
	volume = {72},
	year = {2017},
	note = {<p>10.1093/gerona/glx027</p>
},
	month = {2017/10/12},
	pages = {1453 - 1464},
	abstract = {<p>The search for the genetic determinants of extreme human longevity has been challenged by the phenotype{\textquoteright}s rarity and its nonspecific definition by investigators. To address these issues, we established a consortium of four studies of extreme longevity that contributed 2,070 individuals who survived to the oldest one percentile of survival for the 1900 U.S. birth year cohort. We conducted various analyses to discover longevity-associated variants (LAV) and characterized those LAVs that differentiate survival to extreme age at death (eSAVs) from those LAVs that become more frequent in centenarians because of mortality selection (eg, survival to younger years). The analyses identified new rare variants in chromosomes 4 and 7 associated with extreme survival and with reduced risk for cardiovascular disease and Alzheimer{\textquoteright}s disease. The results confirm the importance of studying truly rare survival to discover those combinations of common and rare variants associated with extreme longevity and longer health span.</p>
},
	isbn = {1079-5006},
	doi = {https://doi.org/10.1093/gerona/glx027},
	url = {https://academic.oup.com/biomedgerontology/article-lookup/doi/10.1093/gerona/glx027},
	author = {Sebastiani, Paola and Gurinovich, Anastasia and Bae, Harold and Andersen, Stacy and Malovini, Alberto and Atzmon, Gil and Villa, Francesco and Kraja, Aldi T and Ben-Avraham, Danny and Barzilai, Nir and Puca, Annibale and Perls, Thomas T}
}
