CNR Institutional Research Information System

FORABOSCO, PAOLA
 Distribuzione geografica
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Continente #
AS - Asia 1.445
NA - Nord America 820
EU - Europa 314
SA - Sud America 216
AF - Africa 25
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.824
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Nazione #
US - Stati Uniti d'America 781
SG - Singapore 627
CN - Cina 327
BR - Brasile 176
HK - Hong Kong 158
VN - Vietnam 146
IT - Italia 116
FR - Francia 82
BD - Bangladesh 50
KR - Corea 42
NL - Olanda 25
GB - Regno Unito 22
IN - India 21
DE - Germania 18
JP - Giappone 18
CA - Canada 16
AR - Argentina 12
FI - Finlandia 8
IL - Israele 8
MX - Messico 8
TN - Tunisia 8
CO - Colombia 7
EC - Ecuador 7
ZA - Sudafrica 7
PK - Pakistan 6
RU - Federazione Russa 6
SA - Arabia Saudita 6
UZ - Uzbekistan 6
EG - Egitto 5
ES - Italia 5
ID - Indonesia 5
PL - Polonia 5
UA - Ucraina 5
IQ - Iraq 4
JM - Giamaica 4
CL - Cile 3
PE - Perù 3
PH - Filippine 3
PY - Paraguay 3
SE - Svezia 3
TR - Turchia 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
AU - Australia 2
BO - Bolivia 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
BB - Barbados 1
BE - Belgio 1
BS - Bahamas 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
GF - Guiana Francese 1
GP - Guadalupe 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
TH - Thailandia 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
TW - Taiwan 1
TZ - Tanzania 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 2.824
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Città #
Singapore 367
Santa Clara 265
Hong Kong 156
Hefei 106
San Jose 82
Lauterbourg 68
Beijing 61
Ho Chi Minh City 58
Ashburn 55
Seoul 42
Hanoi 40
Assemini 30
Los Angeles 29
Dallas 15
New York 15
São Paulo 14
Orem 13
Tokyo 12
Buffalo 11
Gubbio 10
Guangzhou 9
Milan 9
Rio de Janeiro 8
Chicago 7
Council Bluffs 6
Frankfurt am Main 6
Belo Horizonte 5
Campinas 5
Chennai 5
Haiphong 5
Helsinki 5
Johannesburg 5
Minamishinagawa 5
Montreal 5
Warsaw 5
Bengaluru 4
Da Nang 4
Falkenstein 4
Goiânia 4
Ha Long 4
Hải Dương 4
London 4
Phủ Lý 4
Rome 4
San Antonio 4
Tashkent 4
Brasília 3
Guayaquil 3
Islamabad 3
Lappeenranta 3
Lucknow 3
Manaus 3
Miami 3
Nabeul 3
Naples 3
Padua 3
Phoenix 3
Quito 3
Seattle 3
Wilmington 3
Alexandria 2
Arlington 2
Baghdad 2
Bari 2
Biên Hòa 2
Boardman 2
Brooklyn 2
Buenos Aires 2
Cagliari 2
Cairo 2
Catania 2
Chengdu 2
Christiansted 2
Clementon 2
Contagem 2
Copenhagen 2
Corpus Christi 2
Curitiba 2
Denver 2
Dhaka 2
Edison 2
Fortaleza 2
Garfield 2
Go Vap 2
Greenwich 2
Hangzhou 2
Hemet 2
Houston 2
Ipatinga 2
Irvine 2
Istanbul 2
Jacksonville 2
Jeddah 2
João Pessoa 2
Kansas City 2
Kingston 2
Kyiv 2
La Paz 2
Lake Worth 2
Lima 2
Totale 1.705
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Nome #
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset 77
Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis method. 74
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders 74
A Sardinian founder mutation in glycoprotein Ib platelet subunit beta(GP1BB) that impacts thrombocytopenia 74
Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy. 72
Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia 70
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank 70
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate. 62
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information 60
A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia 58
Association studies of candidate genes for Alzheimer's disease in a North Sardinian population. 56
Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis. 54
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease 54
Segregation analysis of ovarian cancer using diathesis to include other cancers 53
Association of the IL-10 Gene Family Locus on Chromosome 1 with Juvenile Idiopathic Arthritis (JIA) 53
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 51
Identification of a new candidate locus for uric acid nephrolithiasis. 48
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks 48
lincRNA-mRNA transcriptional regulatory co-expression network from RNA-seq data in 624 Sardinian individuals 47
Extent and distribuition of linkage disequilibrium on Xq13.3 in nested Sardinian subpopulations 43
Identification of a new candidate locus for uric acid nephrolithiasis 41
First evidence of candidate loci for uric acid nephrolithiasis using an ideal genetic-isolate. 41
Identification of new nephrolithiasis loci in a genetic isolate. 41
Not all isolates are equal: Linkage disequilibrium analysis on Xq13.3 reveals different patterns in Sardinian sub-populations 40
Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor gene. 40
Association of a GABA(B) gene haplotype and temporal lobe epilepsy. 39
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy. 39
Insights into TREM2 biology by network analysis of human brain gene expression data 38
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
High resolution genetic maps and complete genealogy of an isolated Sardinian sub-population as prerequisite for the study of complex traits. 38
Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis 38
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. 37
Prediction model for rheumatoid arthritis: modelling 46 genetic risk variants with smoking 36
Analisi di geni candidati nella malattia di Alzheimer in Sardegna. 35
Inheritance of hyperbilirubinemia: evidence for a major autosomal recessive gene. 34
Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity 34
White matter involvement may explain phenotypic pleiotropy amongst genes involved in episodic movement disorders 34
Inheritance of astigmatism: Evidence for a major autosomal dominant locus 33
Gene co-expression networks shed light into diseases of brain iron accumulation 33
Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA method. 32
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits 31
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genes 31
Frontotemporal dementia: Insights into the biological underpinnings of disease through gene co-expression network analysis 31
Meta-analysis of 32 genome-wide linkage studies of schizophreniaGenome-wide linkage studies of SCZ 31
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
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
Feasibility of complex pedigrees in an isolated population for QTL mapping of cholesterol levels. 28
Meta-analysis of genome-wide linkage studies across autoimmune diseases 28
Studio di linkage in tre famiglie calabresi con epilessia frontale notturna autosomica dominante 27
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis 27
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstruction [1] 26
Linkage analysis on Alzheimer's disease candidate genes in a Sardinian population. 25
Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder 25
Meta-analysis of linkage studies for Alzheimer's disease--a web resource 25
Genetic of bitter taste: identification of a Ch 7q35 locus in a Sardinian genetic isolate. 24
Statistical tools for linkage analysis and genetic association studies. 24
Inheritance of cleft palate in Italy. Evidence for a major autosomal recessive locus 24
Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus. 24
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
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy 23
Localisation of the gene responsible for Fechtner syndrome in a region < 600 Kb on 22q11-q13 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
Genetic heterogeneity in inherited spastic paraplegia associated with epilepsy 22
Optic disc drusen, angioid streaks, and mottled fundus in various combinations in a Sicilian family 22
An integrated map of chromosome 9 21
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2 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
Mutational and linkage analysis in three calabrian families with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 19
Linkage and mutational study in two families with Familial Hemiplegic Migraine . 19
Autosomal dominant aplasia cutis congenita: Report of a large Italian family and no hint for candidate chromosomal regions 19
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus - A GISC study 18
Mutational and linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy 15
Totale 2.849
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Categoria #
all - tutte 9.922
article - articoli 8.399
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 18.321
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202425 0 0 0 0 0 0 0 0 0 0 5 20
2024/20251.030 4 3 85 42 256 18 11 80 39 37 254 201
2025/20261.711 73 116 140 239 339 46 249 102 90 134 111 72
2026/202783 83 0 0 0 0 0 0 0 0 0 0 0
Totale 2.849