CNR Institutional Research Information System

FORABOSCO, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 303
AS - Asia 118
EU - Europa 41
SA - Sud America 2
Totale 464
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Nazione #
US - Stati Uniti d'America 303
SG - Singapore 112
IT - Italia 30
DE - Germania 4
FI - Finlandia 4
CN - Cina 3
KR - Corea 2
AE - Emirati Arabi Uniti 1
BO - Bolivia 1
EC - Ecuador 1
IE - Irlanda 1
LV - Lettonia 1
UA - Ucraina 1
Totale 464
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Città #
Santa Clara 268
Singapore 81
Assemini 18
Falkenstein 4
Helsinki 4
Capua 3
Guangzhou 2
Seoul 2
Ashburn 1
Boardman 1
Dublin 1
Guayaquil 1
La Paz 1
Milan 1
Riga 1
Rome 1
Sala Baganza 1
Totale 391
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Nome #
Not all isolates are equal: Linkage disequilibrium analysis on Xq13.3 reveals different patterns in Sardinian sub-populations 11
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset 11
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate. 11
Extent and distribuition of linkage disequilibrium on Xq13.3 in nested Sardinian subpopulations 10
Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy. 9
Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis. 9
Association of the IL-10 Gene Family Locus on Chromosome 1 with Juvenile Idiopathic Arthritis (JIA) 9
Association studies of candidate genes for Alzheimer's disease in a North Sardinian population. 8
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 8
Identification of a new candidate locus for uric acid nephrolithiasis. 8
A Sardinian founder mutation in glycoprotein Ib platelet subunit beta(GP1BB) that impacts thrombocytopenia 8
Genome-wide screen for essential hypertension genes in a deep rooted Sardinian pedigree 8
Genome-wide screen for essential hypertension in a deep rooted pedigree from an isolated Sardinian subpopulation. 8
High resolution genetic maps and complete genealogy of an isolated Sardinian sub-population as prerequisite for the study of complex traits. 8
Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis method. 7
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits 7
Prediction model for rheumatoid arthritis: modelling 46 genetic risk variants with smoking 7
First evidence of candidate loci for uric acid nephrolithiasis using an ideal genetic-isolate. 7
Identification of new nephrolithiasis loci in a genetic isolate. 7
ASSOCIATION OF A GABA(B) GENE HAPLOTYPE AND TEMPORAL LOBE EPILEPSY 7
lincRNA-mRNA transcriptional regulatory co-expression network from RNA-seq data in 624 Sardinian individuals 7
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank 7
Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia 6
Inheritance of hyperbilirubinemia: evidence for a major autosomal recessive gene. 6
Ogliastra Project: Epidemiological Survey 6
Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA method. 6
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy. 6
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders 6
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks 6
Genetic of bitter taste: identification of a Ch 7q35 locus in a Sardinian genetic isolate. 6
Insights into TREM2 biology by network analysis of human brain gene expression data 6
Feasibility of complex pedigrees in an isolated population for QTL mapping of cholesterol levels. 6
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information 6
Predicting the Risk of Rheumatoid Arthritis and Its Age of Onset through Modelling Genetic Risk Variants with Smoking 6
A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia 6
Meta-analysis of linkage studies for Alzheimer's disease--a web resource 6
Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor gene. 6
Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus. 6
Integration of gene maps: updating chromosome 1 5
Inheritance of astigmatism: Evidence for a major autosomal dominant locus 5
Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity 5
Localisation of the gene responsible for Fechtner syndrome in a region < 600 Kb on 22q11-q13 5
Association of Crohn's disease and ulcerative colitis with haplotypes of the MLH1 gene in Italian inflammatory bowel disease patients [2] 5
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genes 5
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2 5
Genome-wide screen for essential hypertension genes in a deep rooted Sardinian pedigree. 5
Frontotemporal dementia: Insights into the biological underpinnings of disease through gene co-expression network analysis 5
Identification of a new candidate locus for uric acid nephrolithiasis 5
Statistical tools for linkage analysis and genetic association studies. 5
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstruction [1] 5
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. 5
White matter involvement may explain phenotypic pleiotropy amongst genes involved in episodic movement disorders 5
Inheritance of cleft palate in Italy. Evidence for a major autosomal recessive locus 5
Meta-analysis of genome-wide linkage studies in celiac disease 5
Gene co-expression networks shed light into diseases of brain iron accumulation 5
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 5
Empirical significance of association tests of related cases and controls in isolated populations with known genealogy 5
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease 5
An integrated map of chromosome 9 5
Meta-analysis of genome-wide linkage studies across autoimmune diseases 5
Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder 5
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy 5
Analisi di geni candidati nella malattia di Alzheimer in Sardegna. 5
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus - A GISC study 5
Genetic heterogeneity in inherited spastic paraplegia associated with epilepsy 5
Meta-analysis of genome-wide linkage studies across autoimmune diseases 5
Studio di linkage in tre famiglie calabresi con epilessia frontale notturna autosomica dominante 5
Meta-analysis of 32 genome-wide linkage studies of schizophreniaGenome-wide linkage studies of SCZ 5
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 5
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis 5
Autosomal dominant aplasia cutis congenita: Report of a large Italian family and no hint for candidate chromosomal regions 5
Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis 5
Optic disc drusen, angioid streaks, and mottled fundus in various combinations in a Sicilian family 5
Segregation analysis of ovarian cancer using diathesis to include other cancers 4
Association of a GABA(B) gene haplotype and temporal lobe epilepsy. 4
Mutational and linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy 2
Mutational and linkage analysis in three calabrian families with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 2
Linkage and mutational study in two families with Familial Hemiplegic Migraine . 2
Totale 467
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Categoria #
all - tutte 2.472
article - articoli 2.011
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.483
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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
2024/2025439 5 5 85 43 262 18 11 10 0 0 0 0
Totale 467