IRIS
LESCAI, FRANCESCO
 Distribuzione geografica
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Continente #
NA - Nord America 986
EU - Europa 418
AS - Asia 147
Continente sconosciuto - Info sul continente non disponibili 4
SA - Sud America 1
Totale 1.556
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Nazione #
US - Stati Uniti d'America 981
IE - Irlanda 288
CN - Cina 85
SG - Singapore 58
FI - Finlandia 54
DE - Germania 30
BE - Belgio 14
IT - Italia 13
GB - Regno Unito 7
CA - Canada 4
EU - Europa 4
SE - Svezia 4
FR - Francia 2
IR - Iran 2
NL - Olanda 2
AR - Argentina 1
CZ - Repubblica Ceca 1
EE - Estonia 1
IN - India 1
JP - Giappone 1
LT - Lituania 1
MX - Messico 1
RU - Federazione Russa 1
Totale 1.556
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Città #
Chandler 332
Dublin 285
Ashburn 101
Helsinki 54
Boardman 52
Princeton 49
Lawrence 48
Medford 47
Shanghai 41
Singapore 40
Wilmington 29
Washington 18
Chicago 16
Brussels 13
Los Angeles 13
Norwalk 9
Falls Church 8
New York 6
Beijing 5
Seattle 5
Bridgeton 4
San Francisco 4
Ann Arbor 3
Dallas 3
Falkenstein 3
Laurel 3
Liverpool 3
Sunderland 3
Toronto 3
Cinisello Balsamo 2
Des Moines 2
Florence 2
Hefei 2
Langfang 2
Phoenix 2
Pontremoli 2
Rockville 2
Santa Clara 2
Shijiazhuang 2
Benxi 1
Borås 1
Brno 1
Cambridge 1
Chongqing 1
Chuzhou 1
Clifton 1
Guangzhou 1
Handan 1
Houston 1
Karaj 1
Kish 1
Klaipėda 1
London 1
Markham 1
Menlo Park 1
Mexico City 1
Milan 1
Munich 1
Pavia 1
Pune 1
Redmond 1
Roseto degli Abruzzi 1
San Diego 1
Suzhou 1
Tallinn 1
Terlizzi 1
Tokyo 1
Wuhan 1
Yingkou 1
Zhengzhou 1
Zhongshan 1
Zhoukou 1
Totale 1.253
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Nome #
Association between the interleukin-1β polymorphisms and Alzheimer's disease: A systematic review and meta-analysis 52
An APOE haplotype associated with decreased 4 expression increases the risk of late onset alzheimer's disease 51
Helping young independent scientists: the EMBO Young Investigator Programme. Interview with Gerlind Wallon, Deputy Executive Director, EMBO Young Investigator Programme 49
Complexity of anti-immunosenescence strategies in humans 48
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients 46
Genes, ageing and longevity in humans: Problems, advantages and perspectives 46
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus 44
Do men and women follow different trajectories to reach extreme longevity? 44
Human longevity and 11p15.5: A study in 1321 centenarians 42
Identification and validation of loss of function variants in clinical contexts 42
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios 41
Characterisation and Validation of Insertions and Deletions in 173 Patient Exomes 41
Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq 41
Omics in a Digital World: The Role of Bioinformatics in Providing New Insights Into Human Aging 41
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference 40
High-quality exome sequencing of whole-genome amplified neonatal dried blood spot DNA 40
Young Scientist: Italian biotechnologists organize 39
Human models of aging and longevity 37
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies 37
Assembly and analysis of 100 full MHC haplotypes from the Danish population 36
Systems biology and longevity: An emerging approach to identify innovative anti-aging targets and strategies 36
Genotype of inflammatory cytokines in limbal stem cell graft in Italian patients 36
A genetic-demographic approach reveals male-specific association between survival and tumor necrosis factor (A/G)-308 polymorphism 35
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants 34
Role of mitochondrial DNA in longevity, aging and age-related diseases in humans: A reappraisal 32
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes 32
ParkDB: A Parkinson's disease gene expression database 31
Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder 31
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia 30
Rare coding variants in ten genes confer substantial risk for schizophrenia 30
Robertsonian Fusion and Centromere Repositioning Contributed to the Formation of Satellite-free Centromeres During the Evolution of Zebras 29
Special issue of new biotechnology in memory of professor Brian F.C. Clark (1936–2014) 29
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome 28
hgtseq: A Standard Pipeline to Study Horizontal Gene Transfer 25
The use of whole-exome sequencing to disentangle complex phenotypes 25
The Young European Biotech Network (YEBN) 24
Identification of single nucleotide polymorphisms in the p21 (CDKN1A) gene and correlations with longevity in the Italian population 22
Neuroinflammation and the genetics of Alzheimer's disease: The search for a pro-inflammatory phenotype 21
Network approaches to Genome-Wide association studies 21
PON1 is a longevity gene: Results of a meta-analysis 21
Pathological relevance of the natural immune system 20
Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population 19
STAG3 truncating variant as the cause of primary ovarian insufficiency 19
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder 18
Mutation of SALL2 causes recessive ocular coloboma in humans and mice 16
The impact of phenocopy on the genetic analysis of complex traits 16
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum 15
Marie Curie fellowships unraveled. An interview with Theodosius Lennon, Director Directorate T, DG Research, European Commission 15
Interview with Professor Fotis C. Kafatos, President of the European Research Council 14
In memory of Professor Brian Frederic Carl Clark: Contributions from friends 12
Scalable and efficient DNA sequencing analysis on different compute infrastructures aiding variant discovery 10
The promise of explainable deep learning for omics data analysis: Adding new discovery tools to AI 6
Totale 1.609
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Categoria #
all - tutte 10.761
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 10.761
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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
2022/2023779 88 58 14 80 56 75 0 60 316 4 21 7
2023/2024355 18 79 27 38 22 78 52 6 3 18 10 4
2024/2025199 25 59 19 18 22 56 0 0 0 0 0 0
Totale 1.609