The DOI matches its Crossref record; 294 of the 294 references it cites were found in a registry or an index.
Genetics of Human Longevity Within an Eco-Evolutionary Nature-Nurture Framework
Open accessAbstract
Human longevity is a complex trait, and to disentangle its basis has a great theoretical and practical consequences for biomedicine. The genetics of human longevity is still poorly understood despite several investigations that used different strategies and protocols. Here, we argue that such rather disappointing harvest is largely because of the extraordinary complexity of the longevity phenotype in humans. The capability to reach the extreme decades of human lifespan seems to be the result of an intriguing mixture of gene-environment interactions. Accordingly, the genetics of human longevity is here described as a highly context-dependent phenomenon, within a new integrated, ecological, and evolutionary perspective, and is presented as a dynamic process, both historically and individually. The available literature has been scrutinized within this perspective, paying particular attention to factors (sex, individual biography, family, population ancestry, social structure, economic status, and education, among others) that have been relatively neglected. The strength and limitations of the most powerful and used tools, such as genome-wide association study and whole-genome sequencing, have been discussed, focusing on prominently emerged genes and regions, such as apolipoprotein E, Forkhead box O3, interleukin 6, insulin-like growth factor-1, chromosome 9p21, 5q33.3, and somatic mutations among others. The major results of this approach suggest that (1) the genetics of longevity is highly population specific; (2) small-effect alleles, pleiotropy, and the complex allele timing likely play a major role; (3) genetic risk factors are age specific and need to be integrated in the light of the geroscience perspective; (4) a close relationship between genetics of longevity and genetics of age-related diseases (especially cardiovascular diseases) do exist. Finally, the urgent need of a global approach to the largely unexplored interactions between the 3 genetics of human body, that is, nuclear, mitochondrial, and microbiomes, is stressed. We surmise that the comprehensive approach here presented will help in increasing the above-mentioned harvest.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Our findings could well be integrated within current ideas on the biology of aging which suggest that aging rates, and consequently lifespans, evolve as a function of trade-offs with other characters including social, cognitive, and reproductive capacities (Yang, et al. 2016; Giuliani, et al. 2018; Snyder-Mackler, et al. 2020).”
From DLX5/6 GABAergic Expression Affects Social Vocalization: Implications for Human Evolution (2021) · cites this paper as Giuliani, et al. 2018
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Sudlow, C., Gallacher, J., Allen, N., Beral, V., Burton, P., Danesh, J., Downey, P., Elliott, P., Green, J., Landray, M., et al. (2015) · PLOS Medicine · doi:10.1371/journal.pmed.1001779 · Cited by 12,728
Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., & Pericak-Vance, M. A. (1993) · Science · doi:10.1126/science.8346443 · Cited by 9,429
Social Relationships and Mortality Risk: A Meta-analytic Review
Holt-Lunstad, J., Smith, T. B., & Layton, J. B. (2010) · PLoS Medicine · doi:10.1371/journal.pmed.1000316 · Cited by 7,272
DNA methylation age of human tissues and cell types
Horvath, S. (2013) · Genome Biology · doi:10.1186/gb-2013-14-10-r115 · Cited by 7,075
Davey Smith, G., & Ebrahim, S. (2003) · International Journal of Epidemiology · doi:10.1093/ije/dyg070 · Cited by 5,882
Age-related clonal hematopoiesis associated with adverse outcomes
Jaiswal, S., Fontanillas, P., Flannick, J., Manning, A., Grauman, P. V., Mar, B. G., Lindsley, R. C., Mermel, C. H., Burtt, N., Chavez, A., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1408617 · Cited by 4,841
Lloyd-Jones, D. M., Hong, Y., Labarthe, D., Mozaffarian, D., Appel, L. J., Van Horn, L., Greenlund, K., Daniels, S., Nichol, G., Tomaselli, G. F., et al. (2010) · Circulation · doi:10.1161/circulationaha.109.192703 · Cited by 4,750
Pleiotropy, natural selection, and the evolution of senescence.
Williams, G. C. (1957) · Evolution · doi:10.1111/j.1558-5646.1957.tb02911.x · Cited by 4,279
Interactions Between the Microbiota and the Immune System
Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173
Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases
Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891
ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering
Gaj, T., Gersbach, C. A., & Barbas, C. F. (2013) · Trends in Biotechnology · doi:10.1016/j.tibtech.2013.04.004 · Cited by 3,820
The impact of the gut microbiota on human health: an integrative view
Clemente, J. C., Ursell, L. K., Parfrey, L. W., & Knight, R. (2012) · Cell · doi:10.1016/j.cell.2012.01.035 · Cited by 3,710
Bacterial Community Variation in Human Body Habitats Across Space and Time
Costello, E. K., Lauber, C. L., Hamady, M., Fierer, N., Gordon, J. I., & Knight, R. (2009) · Science · doi:10.1126/science.1177486 · Cited by 3,231
Extending Healthy Life Span—From Yeast to Humans
Fontana, L., Partridge, L., & Longo, V. D. (2010) · Science · doi:10.1126/science.1172539 · Cited by 3,023
An Expanded View of Complex Traits: From Polygenic to Omnigenic
Boyle, E. A., Li, Y. I., & Pritchard, J. K. (2017) · Cell · doi:10.1016/j.cell.2017.05.038 · Cited by 2,851
Geroscience: Linking Aging to Chronic Disease
Kennedy, B. K., Berger, S. L., Brunet, A., Campisi, J., Cuervo, A. M., Epel, E. S., Franceschi, C., Lithgow, G. J., Morimoto, R. I., Pessin, J. E., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.039 · Cited by 2,764
Composition, variability, and temporal stability of the intestinal microbiota of the elderly
Claesson, M. J., Cusack, S., O'Sullivan, O., Greene-Diniz, R., de Weerd, H., Flannery, E., Marchesi, J. R., Falush, D., Dinan, T., Fitzgerald, G., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000097107 · Cited by 1,754
Gut microbiota in cardiovascular health and disease
Tang, W. H. W., Kitai, T., & Hazen, S. L. (2017) · Circulation Research · doi:10.1161/circresaha.117.309715 · Cited by 1,670
The mystery of missing heritability: Genetic interactions create phantom heritability
Zuk, O., Hechter, E., Sunyaev, S. R., & Lander, E. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119675109 · Cited by 1,542
Through Ageing, and Beyond: Gut Microbiota and Inflammatory Status in Seniors and Centenarians
Biagi, E., Nylund, L., Candela, M., Ostan, R., Bucci, L., Pini, E., Nikkïla, J., Monti, D., Satokari, R., Franceschi, C., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010667 · Cited by 1,483
Self-citationThe Application of Ecological Theory Toward an Understanding of the Human Microbiome
Costello, E. K., Stagaman, K., Dethlefsen, L., Bohannan, B. J. M., & Relman, D. A. (2012) · Science · doi:10.1126/science.1224203 · Cited by 1,437
Parental olfactory experience influences behavior and neural structure in subsequent generations
Dias, B. G., & Ressler, K. J. (2014) · Nature Neuroscience · doi:10.1038/nn.3594 · Cited by 1,338
The Endocrine Regulation of Aging by Insulin-like Signals
Tatar, M., Bartke, A., & Antebi, A. (2003) · Science · doi:10.1126/science.1081447 · Cited by 1,327
Chronic high-fat diet in fathers programs β-cell dysfunction in female rat offspring
Ng, S.-F., Lin, R. C. Y., Laybutt, D. R., Barres, R., Owens, J. A., & Morris, M. J. (2010) · Nature · doi:10.1038/nature09491 · Cited by 1,327
Houle, D., Govindaraju, D. R., & Omholt, S. W. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2897 · Cited by 1,319
(2012) · The Lancet · doi:10.1016/s0140-6736(12)60110-x · Cited by 1,146
van der Harst, P., & Verweij, N. (2018) · Circulation Research · doi:10.1161/circresaha.117.312086 · Cited by 1,141
Genetic associations with human longevity at the APOE and ACE loci
Schächter, F., Faure-Delanef, L., Guénot, F., Rouger, H., Froguel, P., Lesueur-Ginot, L., & Cohen, D. (1994) · Nature Genetics · doi:10.1038/ng0194-29 · Cited by 1,095
Gut Microbiota and Extreme Longevity
Biagi, E., Franceschi, C., Rampelli, S., Severgnini, M., Ostan, R., Turroni, S., Consolandi, C., Quercia, S., Scurti, M., Monti, D., et al. (2016) · Current Biology · doi:10.1016/j.cub.2016.04.016 · Cited by 1,025
Li, Y., Willer, C., Sanna, S., & Abecasis, G. (2009) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.9.081307.164242 · Cited by 990
Caesar, R., Tremaroli, V., Kovatcheva-Datchary, P., Cani, P. D., & Bäckhed, F. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.07.026 · Cited by 960
The evolution of the host microbiome as an ecosystem on a leash
Foster, K. R., Schlüter, J., Coyte, K. Z., & Rakoff-Nahoum, S. (2017) · Nature · doi:10.1038/nature23292 · Cited by 958
The nature of nurture: Effects of parental genotypes
Kong, A., Thorleifsson, G., Frigge, M. L., Vilhjalmsson, B. J., Young, A. I., Thorgeirsson, T. E., Benonisdottir, S., Oddsson, A., Halldorsson, B. V., Masson, G., et al. (2018) · Science · doi:10.1126/science.aan6877 · Cited by 949
Commensal bacteria at the interface of host metabolism and the immune system
Brestoff, J. R., & Artis, D. (2013) · Nature Immunology · doi:10.1038/ni.2640 · Cited by 945
The Continuum of Aging and Age-Related Diseases: Common Mechanisms but Different Rates
Franceschi, C., Garagnani, P., Morsiani, C., Conte, M., Santoro, A., Grignolio, A., Monti, D., Capri, M., & Salvioli, S. (2018) · Frontiers in Medicine · doi:10.3389/fmed.2018.00061 · Cited by 945
Self-citationHow culture shaped the human genome: bringing genetics and the human sciences together
Laland, K. N., Odling‐Smee, J., & Myles, S. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2734 · Cited by 891
(2012) · The Lancet · doi:10.1016/s0140-6736(11)61931-4 · Cited by 823
Association of apolipoprotein E genotypes with lipid levels and coronary risk
Bennet, A. M., Di Angelantonio, E., Ye, Z., Wensley, F., Dahlin, A., Ahlbom, A., Keavney, B., Collins, R., Wiman, B., de Faire, U., et al. (2007) · JAMA · doi:10.1001/jama.298.11.1300 · Cited by 794
Transgenerational epigenetic programming via sperm microRNA recapitulates effects of paternal stress
Rodgers, A. B., Morgan, C. P., Leu, N. A., & Bale, T. L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508347112 · Cited by 751
Functionally significant insulin-like growth factor I receptor mutations in centenarians
Suh, Y., Atzmon, G., Cho, M.-O., Hwang, D., Liu, B., Leahy, D. J., Barzilai, N., & Cohen, P. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705467105 · Cited by 703
Furman, D., Hejblum, B. P., Simon, N., Jojic, V., Dekker, C. L., Thiébaut, R., Tibshirani, R. J., & Davis, M. M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1321060111 · Cited by 700
Pollin, T. I., Damcott, C. M., Shen, H., Ott, S. H., Shelton, J., Horenstein, R. B., Post, W., McLenithan, J. C., Bielak, L. F., Peyser, P. A., et al. (2008) · Science · doi:10.1126/science.1161524 · Cited by 688
Evolution of the cancer genome
Yates, L. R., & Campbell, P. J. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3317 · Cited by 682
Danesh, J., Kaptoge, S., Mann, A. G., Sarwar, N., Wood, A., Angleman, S. B., Wensley, F., Higgins, J. P. T., Lennon, L., Eiriksdottir, G., et al. (2008) · PLoS Medicine · doi:10.1371/journal.pmed.0050078 · Cited by 676
Transgenerational epigenetic inheritance of longevity in Caenorhabditis elegans
Greer, E. L., Maures, T. J., Ucar, D., Hauswirth, A. G., Mancini, E., Lim, J. P., Benayoun, B. A., Shi, Y., & Brunet, A. (2011) · Nature · doi:10.1038/nature10572 · Cited by 660
Absence of effects of Sir2 overexpression on lifespan in C. elegans and Drosophila
Burnett, C., Valentini, S., Cabreiro, F., Goss, M., Somogyvári, M., Piper, M. D., Hoddinott, M., Sutphin, G. L., Leko, V., McElwee, J. J., et al. (2011) · Nature · doi:10.1038/nature10296 · Cited by 624
SIRT1 Mediates Central Circadian Control in the SCN by a Mechanism that Decays with Aging
Chang, H.-C., & Guarente, L. (2013) · Cell · doi:10.1016/j.cell.2013.05.027 · Cited by 615
Getting the Hologenome Concept Right: an Eco-Evolutionary Framework for Hosts and Their Microbiomes
Theis, K. R., Dheilly, N. M., Klassen, J. L., Brucker, R. M., Baines, J. F., Bosch, T. C. G., Cryan, J. F., Gilbert, S. F., Goodnight, C. J., Lloyd, E. A., et al. (2016) · mSystems · doi:10.1128/msystems.00028-16 · Cited by 613
Interventions to slow aging in humans: are we ready?
Longo, V. D., Antebi, A., Bartke, A., Barzilai, N., Brown‐Borg, H. M., Caruso, C., Curiel, T. J., Cabo, R., Franceschi, C., Gems, D., et al. (2015) · Aging Cell · doi:10.1111/acel.12338 · Cited by 592
Mechanisms of aging: public or private?
Partridge, L., & Gems, D. (2002) · Nature Reviews Genetics · doi:10.1038/nrg753 · Cited by 517
Morbidity Profiles of Centenarians: Survivors, Delayers, and Escapers
Evert, J., Lawler, E. V., Bogan, H., & Perls, T. T. (2003) · The Journals of Gerontology Series A · doi:10.1093/gerona/58.3.m232 · Cited by 517
The quest for genetic determinants of human longevity: challenges and insights
Christensen, K., Johnson, T. E., & Vaupel, J. W. (2006) · Nature Reviews Genetics · doi:10.1038/nrg1871 · Cited by 494
Accelerated epigenetic aging in Down syndrome
Horvath, S., Garagnani, P., Bacalini, M. G., Pirazzini, C., Salvioli, S., Gentilini, D., Blasio, A. M. D., Giuliani, C., Tung, S., Vinters, H. V., et al. (2015) · Aging Cell · doi:10.1111/acel.12325 · Cited by 487
The effects of sex hormones on immune function: a meta-analysis
Foo, Y. Z., Nakagawa, S., Rhodes, G., & Simmons, L. W. (2016) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12243 · Cited by 484
Interleukin‐6: A Cytokine for Gerontolgists
Ershler, W. B. (1993) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1993.tb02054.x · Cited by 475
Methylation of ELOVL 2 gene as a new epigenetic marker of age
Garagnani, P., Bacalini, M. G., Pirazzini, C., Gori, D., Giuliani, C., Mari, D., Di Blasio, A. M., Gentilini, D., Vitale, G., Collino, S., et al. (2012) · Aging Cell · doi:10.1111/acel.12005 · Cited by 473
Genetic signatures of exceptional longevity in humans
Sebastiani, P., Solovieff, N., DeWan, A. T., Walsh, K. M., Puca, A., Hartley, S. W., Melista, E., Andersen, S., Dworkis, D. A., Wilk, J. B., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029848 · Cited by 464
Niche Construction Theory: A Practical Guide for Ecologists
Odling‐Smee, J., Erwin, D. H., Palkovacs, E. P., Feldman, M. W., & Laland, K. N. (2013) · The Quarterly Review of Biology · doi:10.1086/669266 · Cited by 460
Van Meter, M., Kashyap, M., Rezazadeh, S., Geneva, A. J., Morello, T. D., Seluanov, A., & Gorbunova, V. (2014) · Nature Communications · doi:10.1038/ncomms6011 · Cited by 456
Fullerton, S. M., Clark, A. G., Weiss, K. M., Nickerson, D. A., Taylor, S. L., Stengård, J., Salomaa, V. V., Vartiainen, E. A., Perola, M., Boerwinkle, E., et al. (2000) · The American Journal of Human Genetics · doi:10.1086/303070 · Cited by 429
Finch, C. E. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909606106 · Cited by 417
Changes in DNA repair during aging
Gorbunova, V., Seluanov, A., Mao, Z., & Hine, C. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm756 · Cited by 405
Wain, L. V., Shrine, N. R. G., Miller, S., Jackson, V. E., Ntalla, I., Artigas, M. S., Billington, C. K., Kheirallah, A. K., Allen, R. J., Cook, J. P., et al. (2015) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(15)00283-0 · Cited by 393
Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans
BENEDICTIS, G. D., Rose, G., Carrieri, G., Luca, M. D., Falcone, E., Passarino, G., Bonafè, M., Monti, D., Baggio, G., Bertolini, S., et al. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.12.1532 · Cited by 390
Centenarians as a model for healthy aging
Franceschi, C., & Bonafè, M. (2003) · Biochemical Society Transactions · doi:10.1042/bst0310457 · Cited by 384
Bellizzi, D., Rose, G., Cavalcante, P., Covello, G., Dato, S., De Rango, F., Greco, V., Maggiolini, M., Feraco, E., Mari, V., et al. (2005) · Genomics · doi:10.1016/j.ygeno.2004.11.003 · Cited by 367
Schoenmaker, M., de Craen, A. J. M., de Meijer, P. H. E. M., Beekman, M., Blauw, G. J., Slagboom, P. E., & Westendorp, R. G. J. (2005) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201508 · Cited by 363
Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity
Pawlikowska, L., Hu, D., Huntsman, S., Sung, A., Chu, C., Chen, J., Joyner, A. H., Schork, N. J., Hsueh, W., Reiner, A. P., et al. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00493.x · Cited by 358
FOXO3: A Major Gene for Human Longevity - A Mini-Review
Morris, B. J., Willcox, D. C., Donlon, T. A., & Willcox, B. J. (2015) · Gerontology · doi:10.1159/000375235 · Cited by 353
APOE distribution in world populations with new data from India and the UK
Singh, P. P., Singh, M., & Mastana, S. S. (2006) · Annals of Human Biology · doi:10.1080/03014460600594513 · Cited by 351
Living by the clock: The circadian pacemaker in older people
Hofman, M. A., & Swaab, D. F. (2005) · Ageing Research Reviews · doi:10.1016/j.arr.2005.07.001 · Cited by 350
Human niche construction in interdisciplinary focus
Kendal, J. R., Tehrani, J. J., & Odling‐Smee, J. (2011) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2010.0306 · Cited by 350
Mechanisms of cancer resistance in long-lived mammals
Seluanov, A., Gladyshev, V. N., Vijg, J., & Gorbunova, V. A. (2018) · Nature reviews. Cancer · doi:10.1038/s41568-018-0004-9 · Cited by 349
A genome-wide scan for linkage to human exceptional longevity identifies a locus on chromosome 4
Puca, A. A., Daly, M. J., Brewster, S. J., Matise, T. C., Barrett, J. C., Shea-Drinkwater, M., Kang, S., Joyce, E., Nicoli, J., Benson, E. K., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.181337598 · Cited by 347
Xie, H., Guo, R., Zhong, H., Feng, Q., Lan, Z., Qin, B., Ward, K. J., Jackson, M. A., Xia, Y., Chen, X., et al. (2016) · Cell Systems · doi:10.1016/j.cels.2016.10.004 · Cited by 341
The network and the remodeling theories of aging: historical background and new perspectives
Franceschi, C., Valensin, S., Bonafè, M., Paolisso, G., Yashin, A. I., Monti, D., & De Benedictis, G. (2000) · Experimental Gerontology · doi:10.1016/s0531-5565(00)00172-8 · Cited by 335
Andersen, S. L., Sebastiani, P., Dworkis, D. A., Feldman, L., & Perls, T. T. (2012) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glr223 · Cited by 331
Mitochondrial genotype associated with longevity
Tanaka, M., Gong, J., Zhang, J., Yoneda, M., & Yagi, K. (1998) · The Lancet · doi:10.1016/s0140-6736(05)78211-8 · Cited by 316
Decreased epigenetic age of PBMCs from Italian semi-supercentenarians and their offspring
Horvath, S., Pirazzini, C., Bacalini, M. G., Gentilini, D., Di Blasio, A. M., Delledonne, M., Mari, D., Arosio, B., Monti, D., Passarino, G., et al. (2015) · Aging · doi:10.18632/aging.100861 · Cited by 316
Self-citationBonafè, M., Barbieri, M., Marchegiani, F., Olivieri, F., Ragno, E., Giampieri, C., Mugianesi, E., Centurelli, M., Franceschi, C., & Paolisso, G. (2003) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2002-021810 · Cited by 312
The Relationship Between the Human Genome and Microbiome Comes into View
Goodrich, J. K., Davenport, E. R., Clark, A. G., & Ley, R. E. (2017) · Annual Review of Genetics · doi:10.1146/annurev-genet-110711-155532 · Cited by 311
GWAS of Longevity in CHARGE Consortium Confirms APOE and FOXO3 Candidacy
Broer, L., Buchman, A. S., Deelen, J., Evans, D. S., Faul, J. D., Lunetta, K. L., Sebastiani, P., Smith, J. A., Smith, A. V., Tanaka, T., et al. (2014) · The Journals of Gerontology Series A · doi:10.1093/gerona/glu166 · Cited by 292
Franceschi, C., Salvioli, S., Garagnani, P., de Eguileor, M., Monti, D., & Capri, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00982 · Cited by 290
Self-citationExperimental Evidence Supports a Sex-Specific Selective Sieve in Mitochondrial Genome Evolution
Innocenti, P., Morrow, E. H., & Dowling, D. K. (2011) · Science · doi:10.1126/science.1201157 · Cited by 288
Poulain, M., Pes, G. M., Grasland, C., Carru, C., Ferrucci, L., Baggio, G., Franceschi, C., & Deiana, L. (2004) · Experimental Gerontology · doi:10.1016/j.exger.2004.06.016 · Cited by 286
Self-citationDeelen, J., Beekman, M., Uh, H., Helmer, Q., Kuningas, M., Christiansen, L., Kremer, D., van der Breggen, R., Suchiman, H. E. D., Lakenberg, N., et al. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00705.x · Cited by 285
Rose, G., Dato, S., Altomare, K., Bellizzi, D., Garasto, S., Greco, V, Passarino, G., Feraco, E., Mari, V, Barbi, C., et al. (2003) · Experimental Gerontology · doi:10.1016/s0531-5565(03)00209-2 · Cited by 282
Self-citationDNA end joining becomes less efficient and more error-prone during cellular senescence
Seluanov, A., Mittelman, D., Pereira-Smith, O. M., Wilson, J. H., & Gorbunova, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400726101 · Cited by 278
Collino, S., Montoliu, I., Martin, F.-P. J., Scherer, M., Mari, D., Salvioli, S., Bucci, L., Ostan, R., Monti, D., Biagi, E., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056564 · Cited by 270
Self-citationOstan, R., Monti, D., Gueresi, P., Bussolotto, M., Franceschi, C., & Baggio, G. (2016) · Clinical Science · doi:10.1042/cs20160004 · Cited by 270
Human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequency
Hancock, A. M., Witonsky, D., Ehler, E., Alkorta‐Aranburu, G., Beall, C. M., Gebremedhin, A., Sukernik, R. I., Utermann, G., Pritchard, J. K., Coop, G., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914625107 · Cited by 263
Deelen, J., Beekman, M., Uh, H., Broer, L., Ayers, K. L., Tan, Q., Kamatani, Y., Bennet, A. M., Tamm, R., Trompet, S., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu139 · Cited by 259
Cultural variation in Africa: role of mechanisms of transmission and adaptation.
Guglielmino, C. R., Viganotti, C., Hewlett, B. L., & Cavalli-Sforza, L. L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.16.7585 · Cited by 251
Evolution, human-microbe interactions, and life history plasticity
Rook, G., Bäckhed, F., Levin, B. R., McFall-Ngai, M. J., & McLean, A. R. (2017) · The Lancet · doi:10.1016/s0140-6736(17)30566-4 · Cited by 246
Mitochondrial DNA polymorphisms associated with longevity in a Finnish population
Niemi, A., Hervonen, A., Hurme, M., Karhunen, P. J., Jylhä, M. K., & Majamaa, K. (2003) · Human Genetics · doi:10.1007/s00439-002-0843-y · Cited by 245
Quantitative analysis of population-scale family trees with millions of relatives
Kaplanis, J., Gordon, A., Shor, T., Weissbrod, O., Geiger, D., Wahl, M., Gershovits, M., Markus, B., Sheikh, M., Gymrek, M., et al. (2018) · Science · doi:10.1126/science.aam9309 · Cited by 245
Latitudinal clines: an evolutionary view on biological rhythms,
Hut, R. A., Paolucci, S., Dor, R., Kyriacou, C. P., & Daan, S. (2013) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.0433 · Cited by 241
Bürkle, A., Moreno‐Villanueva, M., Bernhard, J., Blasco, M. A., Zondag, G. C. M., Hoeijmakers, J. H. J., Toussaint, O., Grubeck‐Loebenstein, B., Mocchegiani, E., Collino, S., et al. (2015) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2015.03.006 · Cited by 239
New insights into IGF-1 signaling in the heart
Troncoso, R., Ibarra, C., Vicencio, J. M., Jaimovich, E., & Lavandero, S. (2014) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2013.12.002 · Cited by 232
Mitonuclear interactions: evolutionary consequences over multiple biological scales
Wolff, J. N., Ladoukakis, E. D., Enríquez, J. A., & Dowling, D. K. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0443 · Cited by 232
Eisenberg, D. T. A., Kuzawa, C. W., & Hayes, M. G. (2010) · American Journal of Physical Anthropology · doi:10.1002/ajpa.21298 · Cited by 231
Lipoprotein Genotype and Conserved Pathway for Exceptional Longevity in Humans
Atzmon, G., Rincon, M., Schechter, C. B., Shuldiner, A. R., Lipton, R. B., Bergman, A., & Barzilai, N. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040113 · Cited by 222
Meat‐Adaptive Genes and the Evolution of Slower Aging in Humans
Finch, C. E., & Stanford, C. B. (2004) · The Quarterly Review of Biology · doi:10.1086/381662 · Cited by 216
Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes
Grarup, N., Moltke, I., Andersen, M. K., Dalby, M., Vitting-Seerup, K., Kern, T., Mahendran, Y., Jørsboe, E., Larsen, C. V. L., Dahl-Petersen, I. K., et al. (2018) · Nature Genetics · doi:10.1038/s41588-017-0022-7 · Cited by 216
Li, K., Ching, D., Luk, F. S., & Raffaı̈, R. L. (2015) · Circulation Research · doi:10.1161/circresaha.117.305844 · Cited by 211
Mitochondria, Maternal Inheritance, and Male Aging
Camus, M. F., Clancy, D. J., & Dowling, D. K. (2012) · Current Biology · doi:10.1016/j.cub.2012.07.018 · Cited by 209
Whole-genome sequencing of a healthy aging cohort
Erikson, G. A., Bodian, D. L., Rueda, M., Molparia, B., Scott, E. R., Scott-Van Zeeland, A. A., Topol, S. E., Wineinger, N. E., Niederhuber, J. E., Topol, E. J., et al. (2016) · Cell · doi:10.1016/j.cell.2016.03.022 · Cited by 202
Huebbe, P., & Rimbach, G. H. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.06.002 · Cited by 202
Nebel, A., Kleindorp, R., Caliebe, A., Nothnagel, M., Blanché, H., Junge, O., Wittig, M., Ellinghaus, D., Flachsbart, F., Wichmann, H. ‐., et al. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.06.008 · Cited by 201
Evolutionary public health: introducing the concept
Wells, J. C. K., Nesse, R. M., Sear, R., Johnstone, R. A., & Stearns, S. C. (2017) · The Lancet · doi:10.1016/s0140-6736(17)30572-x · Cited by 196
Novel loci and pathways significantly associated with longevity
Zeng, Y., Nie, C., Min, J., Liu, X., Li, M., Chen, H., Xu, H., Wang, M., Ni, T., Li, Y., et al. (2016) · Scientific Reports · doi:10.1038/srep21243 · Cited by 195
The lifespan of Korean eunuchs
Min, K., Lee, C., & Park, H.-N. (2012) · Current Biology · doi:10.1016/j.cub.2012.06.036 · Cited by 193
Lunetta, K. L., D’Agostino, R. B., Karasik, D., Benjamin, E. J., Guo, C., Govindaraju, R., Kiel, D. P., Kelly‐Hayes, M., Massaro, J. M., Pencina, M. J., et al. (2007) · BMC Medical Genetics · doi:10.1186/1471-2350-8-s1-s13 · Cited by 193
Genome-wide linkage analysis for human longevity: Genetics of Healthy Aging Study
Beekman, M., Blanché, H., Perola, M., Hervonen, A., Bezrukov, V., Sikora, E., Flachsbart, F., Christiansen, L., De Craen, A. J. M., Kirkwood, T. B. L., et al. (2013) · Aging Cell · doi:10.1111/acel.12039 · Cited by 190
Frank, S. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909343106 · Cited by 185
Suri, S., Heise, V., Trachtenberg, A. J., & Mackay, C. E. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.10.010 · Cited by 183
Mitochondrial DNA polymorphism: its role in longevity of the Irish population
Ross, O. A. (2001) · Experimental Gerontology · doi:10.1016/s0531-5565(01)00094-8 · Cited by 181
Genome-Wide Scan Informed by Age-Related Disease Identifies Loci for Exceptional Human Longevity
Fortney, K., Dobriban, E., Garagnani, P., Pirazzini, C., Monti, D., Mari, D., Atzmon, G., Barzilai, N., Franceschi, C., Owen, A. B., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005728 · Cited by 180
Somatic mosaicism in healthy human tissues
De, S. (2011) · Trends in Genetics · doi:10.1016/j.tig.2011.03.002 · Cited by 179
Baggio, G., Donazzan, S., Monti, D., Mari, D., Martini, S., Gabelli, C., Vestra, M. D., Previato, L., Guido, M., Pigozzo, S., et al. (1998) · The FASEB Journal · doi:10.1096/fasebj.12.6.433 · Cited by 178
Mao, Z., Tian, X., Van Meter, M., Ke, Z., Gorbunova, V., & Seluanov, A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1200583109 · Cited by 176
Majithia, A. R., Flannick, J. A., Shahinian, P., Guo, M. H., Bray, M., Fontanillas, P., Gabriel, S., NHGRI JHS/FHS Allelic Spectrum Project, Rosen, E. D., Altshuler, D., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1410428111 · Cited by 172
Joshi, P. K., Pirastu, N., Kentistou, K. A., Fischer, K., Hofer, E., Schraut, K. E., Clark, D. W., Nutile, T., Barnes, C. L. K., Timmers, P. R. H. J., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00934-5 · Cited by 161
Genotypic Context and Epistasis in Individuals and Populations
Sackton, T. B., & Hartl, D. L. (2016) · Cell · doi:10.1016/j.cell.2016.06.047 · Cited by 160
Corella, D., Carrasco, P., Sorlí, J. V., Estruch, R., Rico‐Sanz, J., Martínez‐González, M. Á., Salas‐Salvadó, J., Covas, M. I., Coltell, Ó., Arós, F., et al. (2013) · Diabetes Care · doi:10.2337/dc13-0955 · Cited by 157
The TOMM machinery is a molecular switch in PINK1 and PARK2/PARKIN-dependent mitochondrial clearance
Bertolin, G., Ferrando-Miguel, R., Jacoupy, M., Traver, S., Grenier, K., Greene, A. W., Dauphin, A., Waharte, F., Bayot, A., Salamero, J., et al. (2013) · Autophagy · doi:10.4161/auto.25884 · Cited by 156
Accelerated epigenetic aging in Werner syndrome
Maierhofer, A., Flunkert, J., Oshima, J., Martin, G. M., Haaf, T., & Horvath, S. (2017) · Aging · doi:10.18632/aging.101217 · Cited by 154
Beekman, M., Nederstigt, C., Suchiman, H. E. D., Kremer, D., van der Breggen, R., Lakenberg, N., Alemayehu, W. G., de Craen, A. J. M., Westendorp, R. G. J., Boomsma, D. I., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003540107 · Cited by 153
Somatic mutations, genome mosaicism, cancer and aging
Vijg, J. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2014.04.002 · Cited by 143
Emerging beneficial roles of sirtuins in heart failure
Tanno, M., Kuno, A., Horio, Y., & Miura, T. (2012) · Basic Research in Cardiology · doi:10.1007/s00395-012-0273-5 · Cited by 142
Global DNA Methylation Levels are Modulated by Mitochondrial DNA Variants
Bellizzi, D., D’Aquila, P., Giordano, M., Montesanto, A., & Passarino, G. (2012) · Epigenomics · doi:10.2217/epi.11.109 · Cited by 141
Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants
Pilling, L. C., Atkins, J. L., Bowman, K., Jones, S. E., Tyrrell, J., Beaumont, R. N., Ruth, K. S., Tuke, M. A., Yaghootkar, H., Wood, A. R., et al. (2016) · Aging · doi:10.18632/aging.100930 · Cited by 141
Yashin, A. I., BENEDICTIS, G. D., Vaupel, J. W., Tan, Q., Andreev, K. F., Iachine, I. A., Bonafè, M., DeLuca, M., Valensin, S., Carotenuto, L., et al. (1999) · The American Journal of Human Genetics · doi:10.1086/302572 · Cited by 139
Newman, A. B., Walter, S., Lunetta, K. L., Garcia, M. E., Slagboom, P. E., Christensen, K., Arnold, A. M., Aspelund, T., Aulchenko, Y. S., Benjamin, E. J., et al. (2010) · The Journals of Gerontology Series A · doi:10.1093/gerona/glq028 · Cited by 139
Engberg, H., Oksuzyan, A., Jeune, B., Vaupel, J. W., & Christensen, K. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00474.x · Cited by 137
Gender and longevity: Why do men die earlier than women? Comparative and experimental evidence
Regan, J. C., & Partridge, L. (2013) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2013.05.016 · Cited by 134
Genetic variants linked to education predict longevity
Marioni, R. E., Ritchie, S. J., Joshi, P. K., Hagenaars, S. P., Okbay, A., Fischer, K., Adams, M. J., Hill, W. D., Davies, G., Nagy, R., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1605334113 · Cited by 129
Genetics, lifestyle and longevity: Lessons from centenarians
Govindaraju, D., Atzmon, G., & Barzilai, N. (2015) · Applied & Translational Genomics · doi:10.1016/j.atg.2015.01.001 · Cited by 128
Knock-In Reporter Mice Demonstrate that DNA Repair by Non-homologous End Joining Declines with Age
Vaidya, A. M., Mao, Z., Tian, X., Spencer, B., Seluanov, A., & Gorbunova, V. A. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004511 · Cited by 125
IGF1 as predictor of all cause mortality and cardiovascular disease in an elderly population
Andreassen, M., Raymond, I. E., Kistorp, C., Hildebrandt, P. R., Faber, J. O., & Kristensen, L. Ø. (2008) · European Journal of Endocrinology · doi:10.1530/eje-08-0452 · Cited by 124
Cell-specific production, secretion, and function of apolipoprotein E
Kockx, M., Traini, M., & Kritharides, L. (2018) · Journal of Molecular Medicine · doi:10.1007/s00109-018-1632-y · Cited by 124
Serum N-glycan profile shift during human ageing
Vanhooren, V., Dewaele, S., Libert, C., Engelborghs, S., Deyn, P. P. D., Toussaint, O., Debacq‐Chainiaux, F., Poulain, M., Glupczynski, Y., Franceschi, C., et al. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.08.009 · Cited by 121
Genetic influence on social outcomes during and after the Soviet era in Estonia
Rimfeld, K., Krapohl, E. M. L., Trzaskowski, M., Coleman, J. R. I., Selzam, S., Dale, P. S., Esko, T., Metspalu, A., & Plomin, R. J. (2018) · Nature Human Behaviour · doi:10.1038/s41562-018-0332-5 · Cited by 118
Buffering Mechanisms in Aging: A Systems Approach Toward Uncovering the Genetic Component of Aging
Bergman, A., Atzmon, G., Ye, K. Q., MacCarthy, T., & Barzilai, N. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030170 · Cited by 117
Cancer prevalence and mortality in centenarians: a systematic review
Pavlidis, N., Stanta, G., & Audisio, R. A. (2012) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2011.09.007 · Cited by 115
Innate immunity and tolerance toward mitochondria
Rongvaux, A. (2017) · Mitochondrion · doi:10.1016/j.mito.2017.10.007 · Cited by 115
N-Glycomic Changes in Serum Proteins During Human Aging
Vanhooren, V., Desmyter, L., Liu, X., Cardelli, M., Franceschi, C., Federico, A., Libert, C., Laroy, W., Dewaele, S., Contreras, R., et al. (2007) · Rejuvenation Research · doi:10.1089/rej.2007.0556 · Cited by 113
Effect of interleukin-6 polymorphisms on human longevity: A systematic review and meta-analysis
Bona, D. D., Vasto, S., Capurso, C. A., Christiansen, L., Deiana, L., Franceschi, C., Hurme, M., Mocchegiani, E., Rea, I. M., Lio, D., et al. (2008) · Ageing Research Reviews · doi:10.1016/j.arr.2008.09.001 · Cited by 113
Identification and characterization of two functional variants in the human longevity gene FOXO3
Flachsbart, F., Dose, J., Gentschew, L., Geismann, C., Caliebe, A., Knecht, C., Nygaard, M., Badarinarayan, N., ElSharawy, A., May, S., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-02183-y · Cited by 110
Chromatin regulation at the frontier of synthetic biology
Keung, A. J., Joung, J. K., Khalil, A. S., & Collins, J. J. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3900 · Cited by 109
How a Mutation that Slows Aging Can Also Disproportionately Extend End-of-Life Decrepitude
Podshivalova, K., Kerr, R. A., & Kenyon, C. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.062 · Cited by 109
Grandparents' psychological well-being after loss of contact with their grandchildren.
Drew, L. M., & Silverstein, M. D. (2007) · Journal of Family Psychology · doi:10.1037/0893-3200.21.3.372 · Cited by 107
Trumble, B. C., Stieglitz, J., Blackwell, A. D., Allayee, H., Beheim, B., Finch, C. E., Gurven, M., & Kaplan, H. (2017) · The FASEB Journal · doi:10.1096/fj.201601084r · Cited by 106
Mitochondrial genotype associated with longevity and its inhibitory effect on mutagenesis
Tanaka, M., Gong, J., Zhang, J., Yamada, Y., Borgeld, H. W., & Yagi, K. (2000) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(00)00149-4 · Cited by 105
Testa, R., Vanhooren, V., Bonfigli, A. R., Boemi, M., Olivieri, F., Ceriello, A., Genovese, S., Spazzafumo, L., Borelli, V., Bacalini, M. G., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119983 · Cited by 104
SIRT1 Gene Polymorphisms Affect the Protein Expression in Cardiovascular Diseases
Kılıç, Ü., Gök, Ö., Bacaksız, A., İzmirli, M., Elibol, B., & Uysal, Ö. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090428 · Cited by 101
Association of the mitochondrial DNA haplogroup J with longevity is population specific
Dato, S., Passarino, G., Rose, G., Altomare, K., Bellizzi, D., Mari, V., Feraco, E., Franceschi, C., & Benedictis, G. D. (2004) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201278 · Cited by 100
Raule, N., Sevini, F., Li, S., Barbieri, A., Tallaro, F., Lomartire, L., Vianello, D., Montesanto, A., Moilanen, J. S., Bezrukov, V. V., et al. (2013) · Aging Cell · doi:10.1111/acel.12186 · Cited by 97
Tachmazidou, I., Dedoussis, G. V., Southam, L., Farmaki, A., Ritchie, G. R. S., Xifara, D. K., Matchan, A., Hatzikotoulas, K., Rayner, N. W., Chen, Y., et al. (2013) · Nature Communications · doi:10.1038/ncomms3872 · Cited by 96
Nebel, A., Croucher, P. J. P., Stiegeler, R., Nikolaus, S., Krawczak, M., & Schreiber, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408670102 · Cited by 96
Soerensen, M., Dato, S., Tan, Q., Thinggaard, M., Kleindorp, R., Beekman, M., Suchiman, H. E. D., Lindahl‐Jacobsen, R., McGue, M. K., Stevnsner, T., et al. (2012) · AGE · doi:10.1007/s11357-011-9373-7 · Cited by 95
Identifying genetic variants that affect viability in large cohorts
Mostafavi, H., Berisa, T., Day, F. R., Perry, J. R. B., Przeworski, M., & Pickrell, J. K. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2002458 · Cited by 94
Historical demography and longevity genetics: Back to the future
van den Berg, N., Beekman, M., Smith, K. R., Janssens, A. A. P. O., & Slagboom, P. E. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.06.005 · Cited by 93
Mandibuloacral dysplasia: A premature ageing disease with aspects of physiological ageing
Cenni, V., D’Apice, M. R., Garagnani, P., Columbaro, M., Novelli, G., Franceschi, C., & Lattanzi, G. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.12.001 · Cited by 92
Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan
Joshi, P. K., Fischer, K., Schraut, K. E., Campbell, H. J., Esko, T., & Wilson, J. F. (2016) · Nature Communications · doi:10.1038/ncomms11174 · Cited by 91
Sex Differences in Genetic Associations With Longevity
Zeng, Y., Nie, C., Min, J., Chen, H., Liu, X., Ye, R., Chen, Z., Bai, C., Xie, E., Yin, Z., et al. (2018) · JAMA Network Open · doi:10.1001/jamanetworkopen.2018.1670 · Cited by 91
In search of low-frequency and rare variants affecting complex traits
Panoutsopoulou, K., Tachmazidou, I., & Zeggini, E. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt376 · Cited by 90
Whole-Genome Sequencing of the World’s Oldest People
Gierman, H. J., Fortney, K., Roach, J. C., Coles, N. S., Li, H., Glusman, G., Markov, G. J., Smith, J., Hood, L., Coles, L. S., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112430 · Cited by 88
Uniparental Markers in Italy Reveal a Sex-Biased Genetic Structure and Different Historical Strata
Boattini, A., Martínez‐Cruz, B., Sarno, S., Harmant, C., Useli, A., Sanz, P., Yao, D. Y., Manry, J., Ciani, G., Luiselli, D., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065441 · Cited by 87
SIRT1 Gene, Age-Related Diseases, and Mortality: The Leiden 85-Plus Study
Kuningas, M., Putters, M., Westendorp, R. G. J., Slagboom, P. E., & van Heemst, D. (2007) · The Journals of Gerontology Series A · doi:10.1093/gerona/62.9.960 · Cited by 87
Why do centenarians escape or postpone cancer? The role of IGF-1, inflammation and p53
Salvioli, S., Capri, M., Bucci, L., Lanni, C., Racchi, M., Uberti, D. L., Memo, M., Mari, D., Govoni, S. M., & Franceschi, C. (2009) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-008-0639-6 · Cited by 87
Inferring chronological age from DNA methylation patterns of human teeth
Giuliani, C., Cilli, E., Bacalini, M. G., Pirazzini, C., Sazzini, M., Gruppioni, G., Franceschi, C., Garagnani, P., & Luiselli, D. (2015) · American Journal of Physical Anthropology · doi:10.1002/ajpa.22921 · Cited by 86
Family clustering in Sardinian longevity: A genealogical approach
Caselli, G., Pozzi, L., Vaupel, J. W., Deiana, L., Pes, G. M., Carru, C., Franceschi, C., & Baggio, G. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.05.009 · Cited by 85
ApoE gene and exceptional longevity: Insights from three independent cohorts
Garatachea, N., Emanuele, E., Calero, M., Fuku, N., Arai, Y., Abe, Y., Murakami, H., Miyachi, M., Yvert, T., Verde, Z., et al. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.02.004 · Cited by 84
Aging, exceptional longevity and comparisons of the Hannum and Horvath epigenetic clocks
Armstrong, N. J., Mather, K. A., Thalamuthu, A., Wright, M. J., Trollor, J. N., Ames, D. J., Brodaty, H., Schofield, P. R., Sachdev, P. S., & Kwok, J. B. (2017) · Epigenomics · doi:10.2217/epi-2016-0179 · Cited by 84
Nutrition and Inflammation: Are Centenarians Similar to Individuals on Calorie-Restricted Diets?
Franceschi, C., Ostan, R., & Santoro, A. (2018) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-082117-051637 · Cited by 84
Sirtuin 1 gene polymorphisms are associated with body fat and blood pressure in Japanese
Shimoyama, Y., Suzuki, K. A. O., Hamajima, N., & Niwa, T. (2011) · Translational research · doi:10.1016/j.trsl.2011.02.004 · Cited by 83
The unusual genetics of human longevity
De Benedictis, G., & Franceschi, C. (2006) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2006.10.pe20 · Cited by 83
Teumer, A., Qi, Q., Nethander, M., Aschard, H., Bandinelli, S., Beekman, M., Berndt, S. I., Bidlingmaier, M., Broer, L., CHARGE Longevity Working Group, et al. (2016) · Aging Cell · doi:10.1111/acel.12490 · Cited by 83
Joint influence of small-effect genetic variants on human longevity
Yashin, A. I., Wu, D., Arbeev, K. G., & Ukraintseva, S. V. (2010) · Aging · doi:10.18632/aging.100191 · Cited by 81
Rea, I. M., Ross, O. A., Armstrong, M., McNerlan, S., Alexander, D. H., Curran, M. D., & Middleton, D. (2003) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(03)00036-8 · Cited by 80
Sirtuin 1 (SIRT1) sequence variation is not associated with exceptional human longevity
Flachsbart, F., CROUCHER, P., Nikolaus, S., Hampe, J., CORDES, C., SCHREIBER, S., & Nebel, A. (2005) · Experimental Gerontology · doi:10.1016/j.exger.2005.09.008 · Cited by 80
Effect of APOE ε4 allele on survival and fertility in an adverse environment
van Exel, E. R., Koopman, J. J. E., van Bodegom, D., Meij, H. J., de Knijff, P., Ziem, J. B., Finch, C. E., & Westendorp, R. G. J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179497 · Cited by 79
Bayesian association scan reveals loci associated with human lifespan and linked biomarkers
McDaid, A. F., Joshi, P. K., Porcu, E., Komljenović, A., Li, H., Sorrentino, V., Litovchenko, M., Bevers, R. P. J., Rüeger, S., Reymond, A., et al. (2017) · Nature Communications · doi:10.1038/ncomms15842 · Cited by 79
Genetic evidence for common pathways in human age‐related diseases
Johnson, S. C., Dong, X., Vijg, J., & Suh, Y. (2015) · Aging Cell · doi:10.1111/acel.12362 · Cited by 78
Paolisso, G. (2001) · Experimental Gerontology · doi:10.1016/s0531-5565(01)00148-6 · Cited by 77
Grandmothering and natural selection
Kachel, A. F., Premo, L. S., & Hublin, J. (2010) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2010.1247 · Cited by 77
Cytoplasmic male sterility in Drosophila melanogaster associated with a mitochondrial CYTB variant
Clancy, D. J., Hime, G. R., & Shirras, A. D. (2011) · Heredity · doi:10.1038/hdy.2011.12 · Cited by 76
Male/female ratio in centenarians: a possible role played by population genetic structure
Passarino, G., Calignano, C., Vallone, A., Franceschi, C., Jeune, B., Robine, J., Yashin, A. I., Cavalli-Sforza, L. L., & BENEDICTIS, G. D. (2002) · Experimental Gerontology · doi:10.1016/s0531-5565(02)00140-7 · Cited by 76
Immunosenescence in Humans: Deterioration or Remodelling?
Franceschi, C., Monti, D., Barbieri, D., Grassilli, E., Troiano, L., Salvioli, S., Negro, P., Capri, M., Guido, M., Azzi, R., et al. (1995) · International Reviews of Immunology · doi:10.3109/08830189509056702 · Cited by 74
Sebastiani, P., Nussbaum, L. S., Andersen, S. L., Black, M. J., & Perls, T. T. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv020 · Cited by 74
Grossi, V., Forte, G., Sanese, P., Peserico, A., Tezil, T., Signorile, M. L., Fasano, C., Lovaglio, R., Bagnulo, R., Loconte, D. C., et al. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky331 · Cited by 74
Towards a Liquid Self: How Time, Geography, and Life Experiences Reshape the Biological Identity
Grignolio, A., Mishto, M., Faria, A. M. C., Garagnani, P., Franceschi, C., & Tieri, P. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00153 · Cited by 73
Malovini, A. L., Illario, M., Iaccarino, G., Villa, F., Ferrario, A., Roncarati, R., Anselmi, C. V., Novelli, V., Cipolletta, E., Leggiero, E., et al. (2011) · Rejuvenation Research · doi:10.1089/rej.2010.1114 · Cited by 72
Duration of Life and Causes of Death in Domestic Cats: Influence of Sex, Gonadectomy, and Inbreeding
Hamilton, J. B., Hamilton, R. S., & Mestler, G. E. (1969) · Journal of Gerontology · doi:10.1093/geronj/24.4.427 · Cited by 72
Association of the Sirtuin and Mitochondrial Uncoupling Protein Genes with Carotid Plaque
Dong, C., Della‐Morte, D., Wang, L., Cabral, D., Beecham, A. H., McClendon, M. S., Luca, C. C., Blanton, S. H., Sacco, R. L., & Rundek, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027157 · Cited by 69
Puzzling role of genetic risk factors in human longevity: “risk alleles” as pro-longevity variants
Ukraintseva, S. V., Yashin, A. I., Arbeev, K. G., Kulminski, A. M., Akushevich, I. V., Wu, D., Joshi, G., Land, K. C., & Stallard, E. (2015) · Biogerontology · doi:10.1007/s10522-015-9600-1 · Cited by 68
Rising premature mortality in the UK’s persistently deprived areas: Only a Scottish phenomenon?
Norman, P. D., Boyle, P., Exeter, D. J., Feng, Z., & Popham, F. (2011) · Social Science & Medicine · doi:10.1016/j.socscimed.2011.09.034 · Cited by 68
Garagnani, P., Giuliani, C., Pirazzini, C., Olivieri, F., Bacalini, M. G., Ostan, R., Mari, D., Passarino, G., Monti, D., Bonfigli, A. R., et al. (2013) · Aging · doi:10.18632/aging.100562 · Cited by 67
Andersen, S. L., Terry, D. F., Wilcox, M., Babineau, T. J., Malek, K. S., & Perls, T. T. (2004) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.08.019 · Cited by 65
Research works printed but not linked: 2
- 10.1016/j.mad.2017.01.008 · DOI
- Luca, B, Claudia, S, Nicola, M, Cristina, P, Cristina, G, Giovanni, M, Paolo, G, Oliviero, O, Giovanni, M, Claudio, F, Domenico, G. Clonal hematopoiesis of indeterminate potential (CHIP) in patients with coronary artery disease and in centenarians. Further clues linking chip with cardiovascular risk. 2017;130(suppl 1)1144.
Cited by
Sorted by citations
Melzer, D. R., Pilling, L. C., & Ferrucci, L. (2019) · Nature Reviews Genetics · doi:10.1038/s41576-019-0183-6 · Cited by 387
The Genetics of Aging: A Vertebrate Perspective
Singh, P. P., Demmitt, B. A., Nath, R. D., & Brunet, A. (2019) · Cell · doi:10.1016/j.cell.2019.02.038 · Cited by 259
“, Sardinia and Okinawa islands) could facilitate the identification of rare variants because of increased frequency in these populations (Giuliani et al., 2018) and decreased heterogeneity (Pala et al.”
BackgroundInfluentialThe Genetic Variability of APOE in Different Human Populations and Its Implications for Longevity
Abondio, P., Sazzini, M., Garagnani, P., Boattini, A., Monti, D., Franceschi, C., Luiselli, D., & Giuliani, C. (2019) · Genes · doi:10.3390/genes10030222 · Cited by 240
Rampelli, S., Soverini, M., D’Amico, F., Barone, M., Tavella, T., Monti, D., Capri, M., Astolfi, A., Brigidi, P., Biagi, E., et al. (2020) · mSystems · doi:10.1128/msystems.00124-20 · Cited by 166
“Longevity has been described as the result of a complex combination of variables, deriving from genetics, lifestyle, and environment (1, 2).”
BackgroundMechanisms of Lifespan Regulation by Calorie Restriction and Intermittent Fasting in Model Organisms
Hwangbo, D., Lee, H., Abozaid, L. S., & Min, K. (2020) · Nutrients · doi:10.3390/nu12041194 · Cited by 173
Metadata
- Authors
- Giuliani, C., Garagnani, P., & Franceschi, C.
- Affiliations
- University of Oxford (GB)
- Karolinska Institutet (SE)
- Istituto delle Scienze Neurologiche di Bologna (IT)
- Corresponding author
- Franceschi, Claudio
- Venue
- Circulation Research
- Published
- 2018-09-14
- Volume
- 123
- Issue
- 7
- Pages
- 745-772
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- OpenAlex
- W2890672865
- Cited by
- 92
- References
- 293
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 8 · 2023: 13 · 2022: 10 · 2021: 12 · 2020: 21 · 2019: 15 · 2018: 2
- FWCI
- 0.84
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- other-oa
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion, other-oa)
- Funders
- European Commission (602757, 634821)
- Ministry of Education and Science of the Russian Federation (074-02-2018-330)
- Lobachevsky State University of Nizhny Novgorod
- Horizon 2020 Framework Programme (634821)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Physical Performance
- Keywords
- human longevity, gene-environment interaction, apolipoprotein E, FOXO3, interleukin-6, insulin-like growth factor I, chromosome 9p21, somatic mutations, pleiotropy, geroscience, age-related diseases, cardiovascular disease, mitochondrial genetics, microbiome, sex differences, socioeconomic status
- MeSH terms
- Healthy Aging, Age Factors, Animals, Cardiovascular Diseases, Humans, Longevity, Risk Factors, Risk Assessment, Evolution, Molecular, Gene-Environment Interaction
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review