CNR Institutional Research Information System

ESPOSITO, TERESA
 Distribuzione geografica
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Continente #
AS - Asia 2.270
NA - Nord America 1.260
EU - Europa 551
SA - Sud America 440
AF - Africa 50
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.575
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Nazione #
US - Stati Uniti d'America 1.186
SG - Singapore 1.001
CN - Cina 438
BR - Brasile 357
HK - Hong Kong 307
VN - Vietnam 199
IT - Italia 195
FR - Francia 134
BD - Bangladesh 75
JP - Giappone 66
NL - Olanda 60
KR - Corea 57
IN - India 34
GB - Regno Unito 31
DE - Germania 29
AR - Argentina 28
CA - Canada 27
MX - Messico 24
EC - Ecuador 21
ZA - Sudafrica 17
FI - Finlandia 14
RU - Federazione Russa 14
ES - Italia 12
ID - Indonesia 12
SA - Arabia Saudita 12
EG - Egitto 10
IQ - Iraq 10
CO - Colombia 9
PY - Paraguay 9
UA - Ucraina 9
PL - Polonia 8
TR - Turchia 7
AZ - Azerbaigian 6
CL - Cile 6
IL - Israele 6
MA - Marocco 6
UZ - Uzbekistan 6
IE - Irlanda 5
KE - Kenya 5
PH - Filippine 5
PK - Pakistan 5
AT - Austria 4
MY - Malesia 4
SE - Svezia 4
SV - El Salvador 4
CH - Svizzera 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
DO - Repubblica Dominicana 3
GR - Grecia 3
HN - Honduras 3
LT - Lituania 3
LV - Lettonia 3
PE - Perù 3
TH - Thailandia 3
UY - Uruguay 3
VE - Venezuela 3
AO - Angola 2
GT - Guatemala 2
HU - Ungheria 2
JM - Giamaica 2
JO - Giordania 2
KH - Cambogia 2
KZ - Kazakistan 2
LB - Libano 2
LU - Lussemburgo 2
NI - Nicaragua 2
PA - Panama 2
PT - Portogallo 2
RO - Romania 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AM - Armenia 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BF - Burkina Faso 1
BY - Bielorussia 1
CD - Congo 1
DK - Danimarca 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GM - Gambi 1
GU - Guam 1
GY - Guiana 1
IS - Islanda 1
MD - Moldavia 1
ME - Montenegro 1
MK - Macedonia 1
MN - Mongolia 1
MU - Mauritius 1
NZ - Nuova Zelanda 1
OM - Oman 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
TW - Taiwan 1
Totale 4.573
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Città #
Singapore 565
Santa Clara 337
Hong Kong 304
San Jose 142
Ashburn 136
Hefei 123
Beijing 120
Lauterbourg 107
Ho Chi Minh City 71
Seoul 57
Tokyo 56
Assemini 51
Los Angeles 43
Hanoi 41
New York 28
Dallas 23
Milan 23
Buffalo 19
São Paulo 19
Naples 15
Haiphong 13
Rome 13
Biên Hòa 12
Da Nang 11
Rio de Janeiro 10
Brooklyn 9
Cairo 9
Johannesburg 9
Marigliano 9
Council Bluffs 8
Minamishinagawa 8
Nuremberg 8
Atlanta 7
Brasília 7
Chicago 7
Curitiba 7
Dhaka 7
Lappeenranta 7
Montreal 7
Orem 7
Riyadh 7
Toronto 7
Warsaw 7
Avellino 6
Fortaleza 6
Guayaquil 6
Helsinki 6
Portsmouth 6
Asunción 5
Baku 5
Can Tho 5
City of London 5
Dublin 5
Florence 5
Frankfurt am Main 5
Hyderabad 5
Kyiv 5
Phoenix 5
Quận Bình Thạnh 5
Sacramento 5
Tashkent 5
Catanduva 4
Chennai 4
Delhi 4
Denver 4
Düsseldorf 4
Everett 4
Falkenstein 4
Mexico City 4
Nairobi 4
Novo Hamburgo 4
Porto Alegre 4
Querétaro 4
Ribeirão Preto 4
San Salvador 4
Santo André 4
St Louis 4
Thái Bình 4
Ambato 3
Amsterdam 3
Athens 3
Baghdad 3
Belo Horizonte 3
Bogotá 3
Boston 3
Brampton 3
Campinas 3
Cape Town 3
Charlotte 3
Chengdu 3
Cotia 3
Franca 3
Genoa 3
Guangzhou 3
Guarulhos 3
Ha Long 3
Houston 3
Istanbul 3
Jeddah 3
Lebanon 3
Totale 2.705
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Nome #
Evidence for epistatic interaction between VDR and SLC13A2 genes in the pathogenesis of hypocitraturia in recurrent calcium oxalate stone formers. 116
Multiomics approach discloses lipids and metabolites profiles associated to Parkinson's disease stages and applied therapies 80
Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage 79
Identification of sixteen novel candidate genes for late onset Parkinson's disease 74
The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone 70
Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix. 67
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 63
The Sex Chromosomes: Sequence, Evolution and Human Diseases. In: The Human Genome: Features, Variations and Genetic Disorders 62
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate. 62
The distinct clinical features of giant cell tumor of bone in pagetic and non-pagetic patients are associated with genetic, biochemical and histological differences 62
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology 57
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients 57
Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 55
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease 53
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 53
The melatonin receptor 1a (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis 52
Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population 51
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 49
The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this location 49
ZNF687 mutations are frequently found in pagetic patients from South Italy: implication in the pathogenesis of Paget's disease of bone. 49
Vitamin D Receptor Gene Polymorphisms Predict Acquired Resistance to Clodronate Treatment in Patients with Paget Disease of Bone 48
Epidemiological, clinical, and genetic characteristics of Paget's disease of bone in a rural area of Calabria, Southern Italy 48
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. 48
Dysregulation of the Expression of Asparagine-Linked Glycosylation 13 Short Isoform 2 Affects Nephrin Function by Altering Its N-Linked Glycosylation. 47
Novel autophagic vacuolar myopathies: Phenotype and genotype features 47
Exome-wide association study of levodopa-induced dyskinesia in Parkinson's disease 46
Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution. 45
Rare variants in autophagy and non-autophagy genes in late-onset pompe disease: Suggestions of their disease-modifying role in two Italian families 45
Ogliastra Project: Population, Methodology and Results. 44
A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease 44
Early posterior vitreous detachment is associated with LAMA5 dominant mutation 44
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 43
Role of Uncoupling Protein 2 Gene Polymorphisms on the Risk of Ischemic Stroke in a Sardinian Population. 42
Analysis of Genetic and Non-genetic Predictors of Levodopa Induced Dyskinesia in Parkinson's Disease 42
YAC contig organization and CpG island analysis in Xq28 42
Geographic distribution of Ala62Thr variant associated to Uric Acid Nephrolithiasis in Sub-Saharan and Mediterranean area 41
piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene 40
From sequence analysis to diseases identification in the distal human xq28 39
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy 39
Identification of a susceptibility gene for uric acid kidney stones. 39
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 39
Expressed STSs and transcription of human Xq28. 38
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 38
Autosomal dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation. 38
Assembly of a YAC contig spanning 1.6 Mb of Xq28 DNA around the DXS304 locus 37
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 37
Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigree. 37
Procedimenti di analisi genetica della malattia di Parkinson 37
Clinical characteristics and evolution of giant cell tumor occurring in paget's disease of bone. 37
A functional allelic variant of the FGF23 gene is associated with renal phospate leak in calcium nephrolithiasis. 36
Intrafamilial "DOA-plus" phenotype variability related to different OMI/HTRA2 expression. 35
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 35
A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease 35
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 35
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 34
Successful long-term therapy with flecainide in a family with paramyotonia congenita 34
Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN. 33
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 33
Genes, Diet and Uric Acid Nephrolithiasis 33
Concerted evolution in mammals of Talanin and uricase genes 33
Genomic rearrangement in NEMO impairs NF-KAPPAB activation and is a cause of incontinentia pigmenti 32
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 32
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts 31
A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene. 31
Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to XQ28 Close to the L1CAM Gene 30
A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene 30
Genetic variants of Y chromosome are associated with a protective lipid profile in black men 29
ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses 29
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 29
SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone 28
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 28
Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis 28
Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomes 28
Paget's disease of bone: epidemiology, pathogenesis and pharmacotherapy 28
Genomic organization and transcriptional analysis of the long arm of the X chromosome. 28
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 27
First study on the peptidergic innervation of the brain superior sagittal sinus in humans. 27
ZNF687 Mutations in Severe Paget Disease of Bone Associated with Giant Cell Tumor. 27
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility 26
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti. 26
X-Cromosome STSs: a tool for mapping the human X chromosome. 26
Organization of a 1.2 Mb YAC contig spanning the entire iduronate sulfatase gene 26
Systematic generation of X-chromosome specific sequence-tagged sites (STSs). 26
PHYSICAL MAPPING BY YAC CONTIGS AND ANALYSIS FOR CPG ISLANDS IN XQ28 26
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of Delta 7-sterol reductase in Italy and report of three novel mutations 25
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti 25
From sequence analysis to diseases identification in the distal human xq28 25
FSHR gene polymorphisms influence bone mineral density and bone turnover in postmenopausal women 25
ASSEMBLY AND RARE-CUTTER RESTRICTION ENZYME ANALYSIS OF YACS COVERING 8.1 MB ACROSS XQ28 25
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes. 24
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes 24
Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome 24
Molecular analysis of the mature T cell proliferation-1 (MTCP-1) gene in Xq28-linked incontinentia pigmenti 24
From Sequence Analysis to diseases identification in the distal human Xq28. 24
Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population. 24
Incontinentia Pigmenti Type 2 (IP2): isolation and characterisation of the gene through trascriptional and sequence analysis 23
Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease. 23
Paget disease of bone-associated UBA domain mutations of SQSTM1 exert distinct effects on protein structure and function 23
Multiple pathogenic and benign rearrangements arise from an ancient 35-kb genomic duplication involving the NEMO and LAGE2 genes 23
Association between the T239M missense variation in the FGF23 gene and renal phosphate leak 23
Totale 3.909
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Categoria #
all - tutte 16.895
article - articoli 13.948
book - libri 138
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 30.981
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202464 0 0 0 0 0 0 0 0 7 0 5 52
2024/20251.634 9 11 128 72 331 31 12 84 35 89 445 387
2025/20262.759 101 229 237 390 499 83 393 141 211 187 167 121
2026/2027170 170 0 0 0 0 0 0 0 0 0 0 0
Totale 4.627