IRIS
LESCAI, FRANCESCO
 Distribuzione geografica
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Continente #
NA - Nord America 865
EU - Europa 465
AS - Asia 4
Continente sconosciuto - Info sul continente non disponibili 4
SA - Sud America 1
Totale 1.339
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Nazione #
US - Stati Uniti d'America 862
IE - Irlanda 344
FI - Finlandia 45
BE - Belgio 32
DE - Germania 26
IT - Italia 9
EU - Europa 4
SE - Svezia 4
CA - Canada 3
CN - Cina 2
NL - Olanda 2
AR - Argentina 1
EE - Estonia 1
FR - Francia 1
IN - India 1
IR - Iran 1
RU - Federazione Russa 1
Totale 1.339
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Città #
Dublin 341
Chandler 332
Ashburn 94
Princeton 49
Lawrence 48
Medford 47
Helsinki 45
Brussels 31
Wilmington 28
Washington 18
Norwalk 9
Falls Church 8
New York 6
San Francisco 4
Ann Arbor 3
Laurel 3
Cinisello Balsamo 2
Des Moines 2
Falkenstein 2
Hefei 2
Pontremoli 2
Rockville 2
Toronto 2
Borås 1
Cambridge 1
Houston 1
Kish 1
Markham 1
Menlo Park 1
Pune 1
Redmond 1
Roseto degli Abruzzi 1
San Diego 1
Tallinn 1
Terlizzi 1
Totale 1.092
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Nome #
Association between the interleukin-1β polymorphisms and Alzheimer's disease: A systematic review and meta-analysis 48
Helping young independent scientists: the EMBO Young Investigator Programme. Interview with Gerlind Wallon, Deputy Executive Director, EMBO Young Investigator Programme 45
An APOE haplotype associated with decreased 4 expression increases the risk of late onset alzheimer's disease 44
Do men and women follow different trajectories to reach extreme longevity? 43
Young Scientist: Italian biotechnologists organize 41
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients 40
Omics in a Digital World: The Role of Bioinformatics in Providing New Insights Into Human Aging 40
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus 37
Genes, ageing and longevity in humans: Problems, advantages and perspectives 37
Complexity of anti-immunosenescence strategies in humans 37
High-quality exome sequencing of whole-genome amplified neonatal dried blood spot DNA 37
Characterisation and Validation of Insertions and Deletions in 173 Patient Exomes 36
Systems biology and longevity: An emerging approach to identify innovative anti-aging targets and strategies 35
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference 35
Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq 34
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios 33
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies 33
Human longevity and 11p15.5: A study in 1321 centenarians 33
Assembly and analysis of 100 full MHC haplotypes from the Danish population 32
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes 31
Genotype of inflammatory cytokines in limbal stem cell graft in Italian patients 31
Identification and validation of loss of function variants in clinical contexts 30
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants 30
Rare coding variants in ten genes confer substantial risk for schizophrenia 29
A genetic-demographic approach reveals male-specific association between survival and tumor necrosis factor (A/G)-308 polymorphism 27
ParkDB: A Parkinson's disease gene expression database 27
Special issue of new biotechnology in memory of professor Brian F.C. Clark (1936–2014) 26
Human models of aging and longevity 25
The use of whole-exome sequencing to disentangle complex phenotypes 24
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia 24
Role of mitochondrial DNA in longevity, aging and age-related diseases in humans: A reappraisal 24
Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder 24
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome 23
Robertsonian Fusion and Centromere Repositioning Contributed to the Formation of Satellite-free Centromeres During the Evolution of Zebras 21
Neuroinflammation and the genetics of Alzheimer's disease: The search for a pro-inflammatory phenotype 21
PON1 is a longevity gene: Results of a meta-analysis 21
The Young European Biotech Network (YEBN) 20
Identification of single nucleotide polymorphisms in the p21 (CDKN1A) gene and correlations with longevity in the Italian population 20
STAG3 truncating variant as the cause of primary ovarian insufficiency 19
hgtseq: A Standard Pipeline to Study Horizontal Gene Transfer 18
Pathological relevance of the natural immune system 18
Network approaches to Genome-Wide association studies 18
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder 17
Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population 16
Marie Curie fellowships unraveled. An interview with Theodosius Lennon, Director Directorate T, DG Research, European Commission 15
The impact of phenocopy on the genetic analysis of complex traits 15
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum 14
In memory of Professor Brian Frederic Carl Clark: Contributions from friends 14
Mutation of SALL2 causes recessive ocular coloboma in humans and mice 13
Interview with Professor Fotis C. Kafatos, President of the European Research Council 11
The promise of explainable deep learning for omics data analysis: Adding new discovery tools to AI 4
Totale 1.390
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Categoria #
all - tutte 6.275
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.275
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202153 0 0 0 0 0 0 0 0 49 1 0 3
2021/2022223 4 0 3 0 3 4 3 14 7 1 45 139
2022/2023841 88 58 14 80 56 75 3 60 370 7 21 9
2023/2024273 20 80 29 44 23 77 0 0 0 0 0 0
Totale 1.390