Distribuzione geografica
Continente #
NA - Nord America 651
EU - Europa 369
Continente sconosciuto - Info sul continente non disponibili 4
AS - Asia 3
SA - Sud America 1
Totale 1028
Nazione #
US - Stati Uniti d'America 648
IE - Irlanda 316
BE - Belgio 18
DE - Germania 10
FI - Finlandia 10
IT - Italia 6
EU - Europa 4
SE - Svezia 4
CA - Canada 3
CN - Cina 2
NL - Olanda 2
AR - Argentina 1
EE - Estonia 1
FR - Francia 1
IR - Iran 1
RU - Federazione Russa 1
Totale 1028
Città #
Chandler 332
Dublin 313
Princeton 49
Lawrence 48
Medford 47
Wilmington 28
Brussels 17
Helsinki 10
Norwalk 9
Falls Church 8
San Francisco 4
Ann Arbor 3
Laurel 3
Cinisello Balsamo 2
Des Moines 2
Hefei 2
Rockville 2
Toronto 2
Borås 1
Cambridge 1
Houston 1
Kish 1
Markham 1
Menlo Park 1
Redmond 1
Roseto degli Abruzzi 1
San Diego 1
Tallinn 1
Terlizzi 1
Totale 892
Nome #
Association between the interleukin-1β polymorphisms and Alzheimer's disease: A systematic review and meta-analysis 39
Helping young independent scientists: the EMBO Young Investigator Programme. Interview with Gerlind Wallon, Deputy Executive Director, EMBO Young Investigator Programme 36
An APOE haplotype associated with decreased 4 expression increases the risk of late onset alzheimer's disease 34
Do men and women follow different trajectories to reach extreme longevity? 34
Young Scientist: Italian biotechnologists organize 33
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients 31
Omics in a Digital World: The Role of Bioinformatics in Providing New Insights Into Human Aging 31
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus 30
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios 29
Genes, ageing and longevity in humans: Problems, advantages and perspectives 29
Systems biology and longevity: An emerging approach to identify innovative anti-aging targets and strategies 29
High-quality exome sequencing of whole-genome amplified neonatal dried blood spot DNA 29
Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq 29
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies 27
Complexity of anti-immunosenescence strategies in humans 27
Characterisation and Validation of Insertions and Deletions in 173 Patient Exomes 27
Assembly and analysis of 100 full MHC haplotypes from the Danish population 26
Human longevity and 11p15.5: A study in 1321 centenarians 26
Rare coding variants in ten genes confer substantial risk for schizophrenia 26
A genetic-demographic approach reveals male-specific association between survival and tumor necrosis factor (A/G)-308 polymorphism 24
Identification and validation of loss of function variants in clinical contexts 23
ParkDB: A Parkinson's disease gene expression database 23
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants 23
Genotype of inflammatory cytokines in limbal stem cell graft in Italian patients 23
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference 21
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes 21
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia 20
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome 19
Special issue of new biotechnology in memory of professor Brian F.C. Clark (1936–2014) 19
Human models of aging and longevity 18
Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder 18
The use of whole-exome sequencing to disentangle complex phenotypes 17
Role of mitochondrial DNA in longevity, aging and age-related diseases in humans: A reappraisal 17
Neuroinflammation and the genetics of Alzheimer's disease: The search for a pro-inflammatory phenotype 17
The Young European Biotech Network (YEBN) 16
PON1 is a longevity gene: Results of a meta-analysis 16
Robertsonian Fusion and Centromere Repositioning Contributed to the Formation of Satellite-free Centromeres During the Evolution of Zebras 15
Identification of single nucleotide polymorphisms in the p21 (CDKN1A) gene and correlations with longevity in the Italian population 15
Pathological relevance of the natural immune system 14
STAG3 truncating variant as the cause of primary ovarian insufficiency 14
Network approaches to Genome-Wide association studies 14
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder 12
Marie Curie fellowships unraveled. An interview with Theodosius Lennon, Director Directorate T, DG Research, European Commission 12
Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population 12
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum 11
Mutation of SALL2 causes recessive ocular coloboma in humans and mice 11
In memory of Professor Brian Frederic Carl Clark: Contributions from friends 11
The impact of phenocopy on the genetic analysis of complex traits 11
hgtseq: A Standard Pipeline to Study Horizontal Gene Transfer 10
Interview with Professor Fotis C. Kafatos, President of the European Research Council 9
Totale 1078
Categoria #
all - tutte 3477
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 3477

Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202153 0000 00 00 49103
2021/2022223 4030 34 314 7145139
2022/2023802 88581480 5675 360 368000
Totale 1078