CNR Institutional Research Information System

ESPOSITO, TERESA
 Distribuzione geografica
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Continente #
AS - Asia 2.316
NA - Nord America 1.754
EU - Europa 647
SA - Sud America 478
Continente sconosciuto - Info sul continente non disponibili 59
AF - Africa 52
OC - Oceania 3
Totale 5.309
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Nazione #
US - Stati Uniti d'America 1.646
SG - Singapore 1.003
CN - Cina 438
BR - Brasile 371
HK - Hong Kong 307
IT - Italia 275
VN - Vietnam 206
FR - Francia 137
BD - Bangladesh 87
JP - Giappone 66
NL - Olanda 61
KR - Corea 57
CA - Canada 37
GB - Regno Unito 37
IN - India 35
MX - Messico 30
AR - Argentina 29
DE - Germania 29
EC - Ecuador 28
CO - Colombia 21
ID - Indonesia 19
ZA - Sudafrica 17
ES - Italia 14
FI - Finlandia 14
RU - Federazione Russa 14
SA - Arabia Saudita 13
EG - Egitto 10
IQ - Iraq 10
UA - Ucraina 10
PY - Paraguay 9
MY - Malesia 8
PL - Polonia 8
TR - Turchia 8
IL - Israele 7
JM - Giamaica 7
PH - Filippine 7
TH - Thailandia 7
VE - Venezuela 7
AZ - Azerbaigian 6
CL - Cile 6
MA - Marocco 6
UZ - Uzbekistan 6
IE - Irlanda 5
KE - Kenya 5
PK - Pakistan 5
AT - Austria 4
CR - Costa Rica 4
CZ - Repubblica Ceca 4
HN - Honduras 4
SE - Svezia 4
SV - El Salvador 4
BB - Barbados 3
CH - Svizzera 3
DO - Repubblica Dominicana 3
GR - Grecia 3
GT - Guatemala 3
JO - Giordania 3
LT - Lituania 3
LV - Lettonia 3
PA - Panama 3
PE - Perù 3
UY - Uruguay 3
AE - Emirati Arabi Uniti 2
AO - Angola 2
EE - Estonia 2
HU - Ungheria 2
KH - Cambogia 2
KZ - Kazakistan 2
LB - Libano 2
LU - Lussemburgo 2
NI - Nicaragua 2
NP - Nepal 2
PR - Porto Rico 2
PT - Portogallo 2
RO - Romania 2
SC - Seychelles 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
AL - Albania 1
AM - Armenia 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BF - Burkina Faso 1
BS - Bahamas 1
BY - Bielorussia 1
BZ - Belize 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
HT - Haiti 1
IS - Islanda 1
MD - Moldavia 1
ME - Montenegro 1
Totale 5.241
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Città #
Singapore 566
Santa Clara 346
Hong Kong 304
San Jose 213
Ashburn 169
Hefei 123
Beijing 120
Lauterbourg 107
Ho Chi Minh City 73
Seoul 57
Tokyo 56
Los Angeles 52
Assemini 51
Hanoi 42
New York 38
Milan 32
Dallas 27
Rome 24
Council Bluffs 20
Naples 20
Buffalo 19
São Paulo 19
Brooklyn 14
Chicago 13
Haiphong 13
Biên Hòa 12
Brasília 12
Da Nang 12
Rio de Janeiro 12
Atlanta 11
Philadelphia 11
Florence 10
Cairo 9
Johannesburg 9
Marigliano 9
Toronto 9
Dhaka 8
Figino 8
Guayaquil 8
Houston 8
Minamishinagawa 8
Nuremberg 8
The Bronx 8
Curitiba 7
Lappeenranta 7
Miami 7
Montreal 7
Orem 7
Phoenix 7
Riyadh 7
Warsaw 7
Avellino 6
Boston 6
Can Tho 6
Charlotte 6
Columbia 6
Denver 6
Fortaleza 6
Helsinki 6
Mexico City 6
Portsmouth 6
Asunción 5
Baku 5
Bangkok 5
Bogotá 5
City of London 5
Dublin 5
Everett 5
Frankfurt am Main 5
Genoa 5
Hyderabad 5
Kyiv 5
Newark 5
Orlando 5
Plainfield 5
Quito 5
Quận Bình Thạnh 5
Sacramento 5
Tampa 5
Tashkent 5
Bologna 4
Catanduva 4
Chennai 4
Delhi 4
Düsseldorf 4
Falkenstein 4
Kingston 4
Milwaukee 4
Nairobi 4
Novo Hamburgo 4
Oklahoma City 4
Porto Alegre 4
Querétaro 4
Ribeirão Preto 4
San Salvador 4
Santo André 4
St Louis 4
Thái Bình 4
Washington 4
Ambato 3
Totale 2.980
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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. 121
Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix. 94
Multiomics approach discloses lipids and metabolites profiles associated to Parkinson's disease stages and applied therapies 83
Identification of sixteen novel candidate genes for late onset Parkinson's disease 82
Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage 81
piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene 77
The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone 75
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 70
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate. 68
The distinct clinical features of giant cell tumor of bone in pagetic and non-pagetic patients are associated with genetic, biochemical and histological differences 66
The Sex Chromosomes: Sequence, Evolution and Human Diseases. In: The Human Genome: Features, Variations and Genetic Disorders 65
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients 62
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease 61
The melatonin receptor 1a (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis 61
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology 60
Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 59
Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population 58
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. 57
Dysregulation of the Expression of Asparagine-Linked Glycosylation 13 Short Isoform 2 Affects Nephrin Function by Altering Its N-Linked Glycosylation. 57
ZNF687 mutations are frequently found in pagetic patients from South Italy: implication in the pathogenesis of Paget's disease of bone. 56
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 54
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 54
Novel autophagic vacuolar myopathies: Phenotype and genotype features 53
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. 52
Epidemiological, clinical, and genetic characteristics of Paget's disease of bone in a rural area of Calabria, Southern Italy 51
Exome-wide association study of levodopa-induced dyskinesia in Parkinson's disease 51
A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease 51
Vitamin D Receptor Gene Polymorphisms Predict Acquired Resistance to Clodronate Treatment in Patients with Paget Disease of Bone 50
Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 50
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere 50
Analysis of Genetic and Non-genetic Predictors of Levodopa Induced Dyskinesia in Parkinson's Disease 50
Rare variants in autophagy and non-autophagy genes in late-onset pompe disease: Suggestions of their disease-modifying role in two Italian families 49
Early posterior vitreous detachment is associated with LAMA5 dominant mutation 49
Role of Uncoupling Protein 2 Gene Polymorphisms on the Risk of Ischemic Stroke in a Sardinian Population. 48
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 48
Expressed STSs and transcription of human Xq28. 47
Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution. 46
Ogliastra Project: Population, Methodology and Results. 46
Geographic distribution of Ala62Thr variant associated to Uric Acid Nephrolithiasis in Sub-Saharan and Mediterranean area 45
Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy 44
SEQUENCE-TAGGED SITES (STSS) FROM YAC INSERT-ENDS AND X-SPECIFIC FLOW-SORTED CHROMOSOMES 44
YAC contig organization and CpG island analysis in Xq28 43
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations 42
Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigree. 42
Autosomal dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation. 42
Identification of a susceptibility gene for uric acid kidney stones. 42
From sequence analysis to diseases identification in the distal human xq28 41
Successful long-term therapy with flecainide in a family with paramyotonia congenita 41
Clinical characteristics and evolution of giant cell tumor occurring in paget's disease of bone. 41
A novel GBE1 mutation and features of polyglucosan bodies autophagy in Adult Polyglucosan Body Disease 41
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. 40
Genes, Diet and Uric Acid Nephrolithiasis 40
A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene 40
Procedimenti di analisi genetica della malattia di Parkinson 39
Genomic rearrangement in NEMO impairs NF-KAPPAB activation and is a cause of incontinentia pigmenti 39
Intrafamilial "DOA-plus" phenotype variability related to different OMI/HTRA2 expression. 39
Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN. 39
A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene. 39
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 39
Assembly of a YAC contig spanning 1.6 Mb of Xq28 DNA around the DXS304 locus 38
A functional allelic variant of the FGF23 gene is associated with renal phospate leak in calcium nephrolithiasis. 38
SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone 37
Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomes 37
A functional allelic variant of the FGF23 gene is associated with renal phosphate leak in calcium nephrolithiasis. 36
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 36
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases 35
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts 35
Concerted evolution in mammals of Talanin and uricase genes 35
ZNF687 Mutations in Severe Paget Disease of Bone Associated with Giant Cell Tumor. 34
ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses 33
FSHR gene polymorphisms influence bone mineral density and bone turnover in postmenopausal women 33
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 32
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti. 32
First study on the peptidergic innervation of the brain superior sagittal sinus in humans. 31
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility 31
Genetic variants of Y chromosome are associated with a protective lipid profile in black men 31
Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to XQ28 Close to the L1CAM Gene 31
Paget's disease of bone: epidemiology, pathogenesis and pharmacotherapy 31
Mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma) cause atypical forms of Incontinentia pigmenti 30
Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis 30
Molecular analysis of the mature T cell proliferation-1 (MTCP-1) gene in Xq28-linked incontinentia pigmenti 30
Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population. 30
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 30
PHYSICAL MAPPING BY YAC CONTIGS AND ANALYSIS FOR CPG ISLANDS IN XQ28 30
ASSEMBLY AND RARE-CUTTER RESTRICTION ENZYME ANALYSIS OF YACS COVERING 8.1 MB ACROSS XQ28 30
Genomic organization and transcriptional analysis of the long arm of the X chromosome. 30
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of Delta 7-sterol reductase in Italy and report of three novel mutations 29
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility 29
X-Cromosome STSs: a tool for mapping the human X chromosome. 29
From sequence analysis to diseases identification in the distal human xq28 29
Systematic generation of X-chromosome specific sequence-tagged sites (STSs). 29
Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome 28
Organization of a 1.2 Mb YAC contig spanning the entire iduronate sulfatase gene 28
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations. 27
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes 27
Association between the T239M missense variation in the FGF23 gene and renal phosphate leak 27
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes. 26
Incontinentia Pigmenti Type 2 (IP2): isolation and characterisation of the gene through trascriptional and sequence analysis 26
Multiple pathogenic and benign rearrangements arise from an ancient 35-kb genomic duplication involving the NEMO and LAGE2 genes 26
From Sequence Analysis to diseases identification in the distal human Xq28. 26
Totale 4.446
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Categoria #
all - tutte 19.573
article - articoli 16.253
book - libri 151
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 35.977
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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
2026/2027852 234 180 438 0 0 0 0 0 0 0 0 0
Totale 5.309