CNR Institutional Research Information System

FORABOSCO, PAOLA
 Distribuzione geografica
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Continente #
AS - Asia 1.435
NA - Nord America 716
EU - Europa 298
SA - Sud America 215
AF - Africa 25
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.693
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Nazione #
US - Stati Uniti d'America 685
SG - Singapore 632
CN - Cina 328
BR - Brasile 176
HK - Hong Kong 160
VN - Vietnam 148
IT - Italia 101
FR - Francia 82
KR - Corea 42
BD - Bangladesh 27
NL - Olanda 24
GB - Regno Unito 22
IN - India 21
JP - Giappone 20
DE - Germania 18
AR - Argentina 12
CA - Canada 12
FI - Finlandia 8
IL - Israele 8
MX - Messico 8
TN - Tunisia 8
EC - Ecuador 7
SA - Arabia Saudita 7
ZA - Sudafrica 7
CO - Colombia 6
PK - Pakistan 6
RU - Federazione Russa 6
UZ - Uzbekistan 6
EG - Egitto 5
ES - Italia 5
ID - Indonesia 5
PL - Polonia 5
UA - Ucraina 5
IQ - Iraq 4
PY - Paraguay 4
TR - Turchia 4
JM - Giamaica 3
PE - Perù 3
PH - Filippine 3
SE - Svezia 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
AU - Australia 2
BO - Bolivia 2
CL - Cile 2
CR - Costa Rica 2
DK - Danimarca 2
LA - Repubblica Popolare Democratica del Laos 2
LT - Lituania 2
LV - Lettonia 2
OM - Oman 2
PT - Portogallo 2
VE - Venezuela 2
VI - Stati Uniti Isole Vergini 2
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BE - Belgio 1
BS - Bahamas 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
GF - Guiana Francese 1
GR - Grecia 1
GT - Guatemala 1
HN - Honduras 1
IE - Irlanda 1
IS - Islanda 1
JO - Giordania 1
KE - Kenya 1
KZ - Kazakistan 1
LB - Libano 1
LC - Santa Lucia 1
MR - Mauritania 1
MT - Malta 1
MV - Maldive 1
MY - Malesia 1
NA - Namibia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
RO - Romania 1
TJ - Tagikistan 1
TW - Taiwan 1
TZ - Tanzania 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 2.693
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Città #
Singapore 371
Santa Clara 268
Hong Kong 158
Hefei 106
San Jose 83
Lauterbourg 69
Beijing 61
Ho Chi Minh City 59
Seoul 42
Hanoi 40
Ashburn 36
Assemini 30
Los Angeles 28
Tokyo 14
Dallas 13
New York 13
Orem 13
São Paulo 13
Buffalo 11
Gubbio 10
Guangzhou 9
Rio de Janeiro 8
Council Bluffs 6
Frankfurt am Main 6
Milan 6
Belo Horizonte 5
Campinas 5
Chennai 5
Haiphong 5
Helsinki 5
Johannesburg 5
Minamishinagawa 5
Warsaw 5
Bengaluru 4
Chicago 4
Da Nang 4
Falkenstein 4
Goiânia 4
Ha Long 4
Hải Dương 4
London 4
Montreal 4
Phủ Lý 4
Tashkent 4
Brasília 3
Capua 3
Curitiba 3
Guayaquil 3
Islamabad 3
Istanbul 3
Lappeenranta 3
Lucknow 3
Manaus 3
Miami 3
Nabeul 3
Naples 3
Phoenix 3
Quito 3
Rome 3
Seattle 3
Baghdad 2
Bari 2
Biên Hòa 2
Brooklyn 2
Buenos Aires 2
Cagliari 2
Cairo 2
Chengdu 2
Christiansted 2
Contagem 2
Copenhagen 2
Denver 2
Dhaka 2
Fortaleza 2
Go Vap 2
Greenwich 2
Hangzhou 2
Ipatinga 2
Jeddah 2
João Pessoa 2
Kansas City 2
Kingston 2
Kyiv 2
La Paz 2
Lima 2
Lisbon 2
Maceió 2
Manchester 2
Modena 2
Montes Claros 2
Muscat 2
Newark 2
Ponta Grossa 2
Poplar 2
Pouso Alegre 2
Quezon City 2
Quảng Ngãi 2
Quận Bình Thạnh 2
Raleigh 2
Riga 2
Totale 1.685
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Nome #
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset 73
Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis method. 72
Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy. 70
Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia 69
A Sardinian founder mutation in glycoprotein Ib platelet subunit beta(GP1BB) that impacts thrombocytopenia 69
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank 67
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders 61
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate. 60
Association studies of candidate genes for Alzheimer's disease in a North Sardinian population. 56
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information 56
Segregation analysis of ovarian cancer using diathesis to include other cancers 53
Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis. 52
A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia 50
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease 50
Association of the IL-10 Gene Family Locus on Chromosome 1 with Juvenile Idiopathic Arthritis (JIA) 49
Identification of a new candidate locus for uric acid nephrolithiasis. 48
A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia 43
lincRNA-mRNA transcriptional regulatory co-expression network from RNA-seq data in 624 Sardinian individuals 43
Identification of new nephrolithiasis loci in a genetic isolate. 41
Identification of a new candidate locus for uric acid nephrolithiasis 39
First evidence of candidate loci for uric acid nephrolithiasis using an ideal genetic-isolate. 39
Extent and distribuition of linkage disequilibrium on Xq13.3 in nested Sardinian subpopulations 39
Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor gene. 39
Genome-wide screen for essential hypertension in a deep rooted pedigree from an isolated Sardinian subpopulation. 38
Predicting the Risk of Rheumatoid Arthritis and Its Age of Onset through Modelling Genetic Risk Variants with Smoking 38
Association of a GABA(B) gene haplotype and temporal lobe epilepsy. 37
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks 37
Not all isolates are equal: Linkage disequilibrium analysis on Xq13.3 reveals different patterns in Sardinian sub-populations 37
High resolution genetic maps and complete genealogy of an isolated Sardinian sub-population as prerequisite for the study of complex traits. 36
Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis 36
Prediction model for rheumatoid arthritis: modelling 46 genetic risk variants with smoking 35
Insights into TREM2 biology by network analysis of human brain gene expression data 35
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. 35
Inheritance of hyperbilirubinemia: evidence for a major autosomal recessive gene. 34
Gene co-expression networks shed light into diseases of brain iron accumulation 33
Analisi di geni candidati nella malattia di Alzheimer in Sardegna. 33
Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity 32
White matter involvement may explain phenotypic pleiotropy amongst genes involved in episodic movement disorders 32
Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA method. 31
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy. 31
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits 31
Inheritance of astigmatism: Evidence for a major autosomal dominant locus 30
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genes 30
Frontotemporal dementia: Insights into the biological underpinnings of disease through gene co-expression network analysis 30
Genome-wide screen for essential hypertension genes in a deep rooted Sardinian pedigree. 29
Meta-analysis of genome-wide linkage studies across autoimmune diseases 29
ASSOCIATION OF A GABA(B) GENE HAPLOTYPE AND TEMPORAL LOBE EPILEPSY 29
Meta-analysis of 32 genome-wide linkage studies of schizophreniaGenome-wide linkage studies of SCZ 29
Linkage of ulcerative colitis to the pericentromeric region of chromosome 16 in Italian inflammatory bowel disease families is independent of the presence of common CARD15 mutations 29
Genome-wide screen for essential hypertension genes in a deep rooted Sardinian pedigree 28
Meta-analysis of genome-wide linkage studies across autoimmune diseases 27
Feasibility of complex pedigrees in an isolated population for QTL mapping of cholesterol levels. 26
Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder 25
Studio di linkage in tre famiglie calabresi con epilessia frontale notturna autosomica dominante 25
Meta-analysis of linkage studies for Alzheimer's disease--a web resource 25
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstruction [1] 24
Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus. 24
Linkage analysis on Alzheimer's disease candidate genes in a Sardinian population. 23
Inheritance of cleft palate in Italy. Evidence for a major autosomal recessive locus 23
Meta-analysis of genome-wide linkage studies in celiac disease 23
Empirical significance of association tests of related cases and controls in isolated populations with known genealogy 23
Localisation of the gene responsible for Fechtner syndrome in a region < 600 Kb on 22q11-q13 22
Genetic of bitter taste: identification of a Ch 7q35 locus in a Sardinian genetic isolate. 22
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy 22
Statistical tools for linkage analysis and genetic association studies. 21
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy 21
Genetic heterogeneity in inherited spastic paraplegia associated with epilepsy 21
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis 21
Optic disc drusen, angioid streaks, and mottled fundus in various combinations in a Sicilian family 20
Integration of gene maps: updating chromosome 1 19
Association of Crohn's disease and ulcerative colitis with haplotypes of the MLH1 gene in Italian inflammatory bowel disease patients [2] 19
An integrated map of chromosome 9 19
Autosomal dominant aplasia cutis congenita: Report of a large Italian family and no hint for candidate chromosomal regions 19
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2 18
Mutational and linkage analysis in three calabrian families with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 18
Linkage and mutational study in two families with Familial Hemiplegic Migraine . 16
Mutational and linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy 15
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus - A GISC study 15
Totale 2.718
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Categoria #
all - tutte 9.015
article - articoli 7.562
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 16.577
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202428 0 0 0 0 0 0 0 0 3 0 5 20
2024/20251.040 4 3 85 43 259 18 11 80 39 37 256 205
2025/20261.650 73 117 141 242 342 46 251 105 92 135 106 0
Totale 2.718