Francesco Lescai
Francesco Lescai
Head of Bioinformatics, Medicines and Healthcare products Regulatory Agency
Verified email at nibsc.org
Title
Cited by
Cited by
Year
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
3322000
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
3322000
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), 552-555, 2016
2572016
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), 1131-1136, 2012
1532012
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
1402008
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
1292010
“Mild” uncoupling of mitochondria
AA Starkov
Bioscience Reports 17 (3), 273-279, 1997
1231997
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 (1), 1-9, 2015
1152015
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
1152001
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
1102015
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), 902-909, 2012
1042012
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
952008
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
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), 1515-1519, 2009
752009
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
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
742006
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), 87-91, 2017
712017
PON1 is a longevity gene: results of a meta-analysis
F Lescai, F Marchegiani, C Franceschi
Ageing research reviews 8 (4), 277-284, 2009
692009
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
622014
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
582015
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