CNR Institutional Research Information System

ESPOSITO, TERESA
 Distribuzione geografica
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Continente #
AS - Asia 2.218
NA - Nord America 1.029
EU - Europa 522
SA - Sud America 438
AF - Africa 50
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.261
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Nazione #
SG - Singapore 1.000
US - Stati Uniti d'America 972
CN - Cina 436
BR - Brasile 356
HK - Hong Kong 304
VN - Vietnam 197
IT - Italia 169
FR - Francia 134
JP - Giappone 66
NL - Olanda 59
KR - Corea 57
IN - India 34
BD - Bangladesh 31
GB - Regno Unito 31
DE - Germania 29
AR - Argentina 27
MX - Messico 24
EC - Ecuador 21
CA - Canada 17
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
CH - Svizzera 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
CZ - Repubblica Ceca 2
HU - Ungheria 2
JM - Giamaica 2
JO - Giordania 2
KH - Cambogia 2
KZ - Kazakistan 2
LB - Libano 2
LU - Lussemburgo 2
PA - Panama 2
PT - Portogallo 2
RO - Romania 2
SN - Senegal 2
SV - El Salvador 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
CR - Costa Rica 1
DK - Danimarca 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GM - Gambi 1
GT - Guatemala 1
GU - Guam 1
GY - Guiana 1
IS - Islanda 1
ME - Montenegro 1
MK - Macedonia 1
MN - Mongolia 1
MU - Mauritius 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
OM - Oman 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
TW - Taiwan 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 4.261
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Città #
Singapore 564
Santa Clara 333
Hong Kong 301
San Jose 133
Hefei 123
Beijing 119
Ashburn 107
Lauterbourg 107
Ho Chi Minh City 71
Seoul 57
Tokyo 56
Assemini 51
Hanoi 41
Los Angeles 40
New York 26
Milan 20
Buffalo 19
São Paulo 19
Dallas 18
Naples 15
Haiphong 13
Biên Hòa 12
Da Nang 11
Rome 11
Rio de Janeiro 10
Cairo 9
Johannesburg 9
Marigliano 9
Council Bluffs 8
Minamishinagawa 8
Nuremberg 8
Brasília 7
Curitiba 7
Dhaka 7
Lappeenranta 7
Orem 7
Riyadh 7
Warsaw 7
Avellino 6
Fortaleza 6
Guayaquil 6
Helsinki 6
Montreal 6
Portsmouth 6
Asunción 5
Baku 5
Brooklyn 5
Can Tho 5
City of London 5
Dublin 5
Frankfurt am Main 5
Hyderabad 5
Kyiv 5
Quận Bình Thạnh 5
Tashkent 5
Toronto 5
Atlanta 4
Catanduva 4
Chennai 4
Chicago 4
Delhi 4
Denver 4
Düsseldorf 4
Falkenstein 4
Mexico City 4
Nairobi 4
Novo Hamburgo 4
Phoenix 4
Porto Alegre 4
Querétaro 4
Ribeirão Preto 4
Santo André 4
Thái Bình 4
Ambato 3
Amsterdam 3
Athens 3
Baghdad 3
Belo Horizonte 3
Bogotá 3
Campinas 3
Cape Town 3
Chengdu 3
Cotia 3
Florence 3
Franca 3
Guangzhou 3
Guarulhos 3
Ha Long 3
Istanbul 3
Jeddah 3
Oklahoma City 3
Phủ Lý 3
Pinhais 3
Quito 3
Riga 3
Rostov-on-Don 3
Salvador 3
Santiago 3
St Louis 3
Sumaré 3
Totale 2.622
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Nome #
Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage 77
Multiomics approach discloses lipids and metabolites profiles associated to Parkinson's disease stages and applied therapies 77
Identification of sixteen novel candidate genes for late onset Parkinson's disease 72
Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix. 66
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
The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone 62
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate. 60
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients 55
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology 53
Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population 51
The distinct clinical features of giant cell tumor of bone in pagetic and non-pagetic patients are associated with genetic, biochemical and histological differences 51
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 49
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease 49
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 49
Evidence for epistatic interaction between VDR and SLC13A2 genes in the pathogenesis of hypocitraturia in recurrent calcium oxalate stone formers. 49
Vitamin D Receptor Gene Polymorphisms Predict Acquired Resistance to Clodronate Treatment in Patients with Paget Disease of Bone 48
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. 47
ZNF687 mutations are frequently found in pagetic patients from South Italy: implication in the pathogenesis of Paget's disease of bone. 47
Exome-wide association study of levodopa-induced dyskinesia in Parkinson's disease 46
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 45
Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution. 44
Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 44
Dysregulation of the Expression of Asparagine-Linked Glycosylation 13 Short Isoform 2 Affects Nephrin Function by Altering Its N-Linked Glycosylation. 44
Rare variants in autophagy and non-autophagy genes in late-onset pompe disease: Suggestions of their disease-modifying role in two Italian families 43
Novel autophagic vacuolar myopathies: Phenotype and genotype features 43
Early posterior vitreous detachment is associated with LAMA5 dominant mutation 43
The melatonin receptor 1a (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis 42
A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease 41
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 40
Ogliastra Project: Population, Methodology and Results. 40
Geographic distribution of Ala62Thr variant associated to Uric Acid Nephrolithiasis in Sub-Saharan and Mediterranean area 40
YAC contig organization and CpG island analysis in Xq28 40
piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene 39
Role of Uncoupling Protein 2 Gene Polymorphisms on the Risk of Ischemic Stroke in a Sardinian Population. 39
Epidemiological, clinical, and genetic characteristics of Paget's disease of bone in a rural area of Calabria, Southern Italy 38
Analysis of Genetic and Non-genetic Predictors of Levodopa Induced Dyskinesia in Parkinson's Disease 38
Identification of a susceptibility gene for uric acid kidney stones. 38
Assembly of a YAC contig spanning 1.6 Mb of Xq28 DNA around the DXS304 locus 37
From sequence analysis to diseases identification in the distal human xq28 37
Expressed STSs and transcription of human Xq28. 36
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy 36
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 36
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 35
Procedimenti di analisi genetica della malattia di Parkinson 35
A functional allelic variant of the FGF23 gene is associated with renal phospate leak in calcium nephrolithiasis. 35
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 35
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 34
Autosomal dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation. 34
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 34
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 33
Intrafamilial "DOA-plus" phenotype variability related to different OMI/HTRA2 expression. 32
Genes, Diet and Uric Acid Nephrolithiasis 31
Concerted evolution in mammals of Talanin and uricase genes 31
Successful long-term therapy with flecainide in a family with paramyotonia congenita 31
Clinical characteristics and evolution of giant cell tumor occurring in paget's disease of bone. 31
A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease 31
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts 30
Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN. 30
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 30
A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene. 29
Genomic rearrangement in NEMO impairs NF-KAPPAB activation and is a cause of incontinentia pigmenti 28
Genetic variants of Y chromosome are associated with a protective lipid profile in black men 28
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 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
ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses 28
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 27
Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to XQ28 Close to the L1CAM Gene 27
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 27
Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis 27
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 27
Genomic organization and transcriptional analysis of the long arm of the X chromosome. 27
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti. 26
ZNF687 Mutations in Severe Paget Disease of Bone Associated with Giant Cell Tumor. 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
Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigree. 25
First study on the peptidergic innervation of the brain superior sagittal sinus in humans. 25
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti 25
PHYSICAL MAPPING BY YAC CONTIGS AND ANALYSIS FOR CPG ISLANDS IN XQ28 25
A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene 25
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of Delta 7-sterol reductase in Italy and report of three novel mutations 24
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
SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone 24
Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome 24
From sequence analysis to diseases identification in the distal human xq28 24
FSHR gene polymorphisms influence bone mineral density and bone turnover in postmenopausal women 24
ASSEMBLY AND RARE-CUTTER RESTRICTION ENZYME ANALYSIS OF YACS COVERING 8.1 MB ACROSS XQ28 24
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility 23
Incontinentia Pigmenti Type 2 (IP2): isolation and characterisation of the gene through trascriptional and sequence analysis 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
From Sequence Analysis to diseases identification in the distal human Xq28. 23
Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population. 23
Association between the T239M missense variation in the FGF23 gene and renal phosphate leak 23
A functional allelic variant of the FGF23 gene is associated with renal phosphate leak in calcium nephrolithiasis. 22
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations. 22
Totale 3.619
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Categoria #
all - tutte 14.927
article - articoli 12.304
book - libri 128
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 27.359
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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
2025/20262.615 101 229 237 390 499 83 393 141 211 187 144 0
Totale 4.313