Francesco Lescai
Francesco Lescai
Associate Professor in Genomics and Bioinformatics, Aarhus University
Verified email at hum-gen.au.dk
TitleCited byYear
Do men and women follow different trajectories to reach extreme longevity?
C Franceschi, L Motta, S Valensin, R Rapisarda, A Franzone, M Berardelli, ...
Aging Clinical and Experimental Research 12 (2), 77-84, 2000
3262000
Do men and women follow different trajectories to reach extreme longevity?
C Franceschi, L Motta, S Valensin, R Rapisarda, A Franzone, M Berardelli, ...
Aging Clinical and Experimental Research 12 (2), 77-84, 2000
3262000
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ...
Nature genetics 48 (5), 552, 2016
2152016
Common variants at the MHC locus and at chromosome 16q24. 1 predispose to Barrett's esophagus
Z Su, LJ Gay, A Strange, C Palles, G Band, DC Whiteman, F Lescai, ...
Nature genetics 44 (10), 1131, 2012
1502012
Human models of aging and longevity
E Cevenini, L Invidia, F Lescai, S Salvioli, P Tieri, G Castellani, ...
Expert opinion on biological therapy 8 (9), 1393-1405, 2008
1262008
Low grade inflammation as a common pathogenetic denominator in age-related diseases: novel drug targets for anti-ageing strategies and successful ageing achievement
G Candore, C Caruso, E Jirillo, T Magrone, S Vasto
Current pharmaceutical design 16 (6), 584-596, 2010
1232010
“Mild” uncoupling of mitochondria
AA Starkov
Bioscience reports 17 (3), 273-279, 1997
1171997
Neuroinflammation and the genetics of Alzheimer’s disease: the search for a pro-inflammatory phenotype
C Franceschi, S Valensin, F Lescai, F Olivieri, F Licastro, LME Grimaldi, ...
Aging Clinical and Experimental Research 13 (3), 163-170, 2001
1122001
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia
E Ellinghaus, M Stanulla, G Richter, D Ellinghaus, G Te Kronnie, G Cario, ...
Leukemia 26 (5), 902, 2012
1002012
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios
S Besenbacher, S Liu, JMG Izarzugaza, J Grove, K Belling, J Bork-Jensen, ...
Nature communications 6, 5969, 2015
982015
Association between the interleukin-1β polymorphisms and Alzheimer's disease: a systematic review and meta-analysis
D Di Bona, A Plaia, S Vasto, L Cavallone, F Lescai, C Franceschi, ...
Brain research reviews 59 (1), 155-163, 2008
932008
Genes, ageing and longevity in humans: problems, advantages and perspectives
S Salvioli, F Olivieri, F Marchegiani, M Cardelli, A Santoro, E Bellavista, ...
Free Radical Research 40 (12), 1303-1323, 2006
832006
Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq
AP Rajkumar, P Qvist, R Lazarus, F Lescai, J Ju, M Nyegaard, O Mors, ...
BMC genomics 16 (1), 548, 2015
792015
Complexity of anti‐immunosenescence strategies in humans
M Capri, D Monti, S Salvioli, F Lescai, M Pierini, S Altilia, F Sevini, ...
Artificial organs 30 (10), 730-742, 2006
752006
Systems biology and longevity: an emerging approach to identify innovative anti-aging targets and strategies
E Cevenini, E Bellavista, P Tieri, G Castellani, F Lescai, M Francesconi, ...
Current pharmaceutical design 16 (7), 802-813, 2010
742010
Human longevity and 11p15. 5: a study in 1321 centenarians
F Lescai, H Blanché, A Nebel, M Beekman, M Sahbatou, F Flachsbart, ...
European Journal of Human Genetics 17 (11), 1515, 2009
732009
PON1 is a longevity gene: results of a meta-analysis
F Lescai, F Marchegiani, C Franceschi
Ageing research reviews 8 (4), 277-284, 2009
642009
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
L Maretty, JM Jensen, B Petersen, JA Sibbesen, S Liu, P Villesen, L Skov, ...
Nature 548 (7665), 87, 2017
522017
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes
AM Waters, R Asfahani, P Carroll, L Bicknell, F Lescai, A Bright, ...
Journal of medical genetics 52 (3), 147-156, 2015
522015
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome
AC Thomas, H Williams, N Setó-Salvia, C Bacchelli, D Jenkins, ...
The American Journal of Human Genetics 95 (5), 611-621, 2014
492014
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