IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

TABANO, SILVIA MARIA
 Distribuzione geografica
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Continente #
EU - Europa 8.404
NA - Nord America 7.290
AS - Asia 2.754
SA - Sud America 224
OC - Oceania 36
AF - Africa 27
Continente sconosciuto - Info sul continente non disponibili 4
Totale 18.739
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Nazione #
US - Stati Uniti d'America 7.110
GB - Regno Unito 3.187
IT - Italia 2.267
CN - Cina 1.280
DE - Germania 866
SE - Svezia 724
SG - Singapore 569
RU - Federazione Russa 303
IN - India 245
FR - Francia 194
BR - Brasile 173
IE - Irlanda 165
CA - Canada 164
TR - Turchia 154
UA - Ucraina 122
FI - Finlandia 117
ID - Indonesia 110
KR - Corea 108
NL - Olanda 102
HK - Hong Kong 94
DK - Danimarca 85
EU - Europa 46
BE - Belgio 40
PL - Polonia 37
JP - Giappone 31
ES - Italia 30
AU - Australia 29
CH - Svizzera 29
AT - Austria 26
VN - Vietnam 26
GR - Grecia 22
PH - Filippine 22
TW - Taiwan 20
UZ - Uzbekistan 19
CO - Colombia 17
RO - Romania 16
IR - Iran 15
MX - Messico 13
PT - Portogallo 13
AR - Argentina 12
NO - Norvegia 12
CZ - Repubblica Ceca 11
AE - Emirati Arabi Uniti 7
NZ - Nuova Zelanda 7
PE - Perù 7
CL - Cile 6
MY - Malesia 6
KZ - Kazakistan 5
SK - Slovacchia (Repubblica Slovacca) 5
ZA - Sudafrica 5
EG - Egitto 4
HR - Croazia 4
HU - Ungheria 4
IQ - Iraq 4
KG - Kirghizistan 4
SA - Arabia Saudita 4
SC - Seychelles 4
VE - Venezuela 4
BG - Bulgaria 3
EC - Ecuador 3
IL - Israele 3
KE - Kenya 3
KW - Kuwait 3
LT - Lituania 3
LV - Lettonia 3
MM - Myanmar 3
PS - Palestinian Territory 3
RS - Serbia 3
TH - Thailandia 3
TN - Tunisia 3
AL - Albania 2
AM - Armenia 2
BD - Bangladesh 2
BO - Bolivia 2
DZ - Algeria 2
IS - Islanda 2
JO - Giordania 2
MO - Macao, regione amministrativa speciale della Cina 2
NI - Nicaragua 2
OM - Oman 2
PK - Pakistan 2
SI - Slovenia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BY - Bielorussia 1
EE - Estonia 1
GH - Ghana 1
KH - Cambogia 1
LK - Sri Lanka 1
LU - Lussemburgo 1
MA - Marocco 1
MD - Moldavia 1
MN - Mongolia 1
NG - Nigeria 1
PA - Panama 1
SN - Senegal 1
ZM - Zambia 1
Totale 18.782
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Città #
Southend 3.065
Milan 766
Chandler 575
Ashburn 560
Fairfield 376
Singapore 364
Frankfurt am Main 341
Seattle 304
Wilmington 275
Woodbridge 223
Beijing 212
Ann Arbor 207
Houston 203
Princeton 191
Dearborn 182
Dublin 161
Cambridge 159
Council Bluffs 151
Rome 145
Nanjing 103
Toronto 89
Jakarta 86
Shanghai 85
Santa Clara 81
Redwood City 74
Mountain View 73
Hong Kong 70
Hanover 66
Redmond 66
Des Moines 65
Boardman 63
Bengaluru 59
Florence 57
Guangzhou 57
Phoenix 57
New York 52
Helsinki 51
Jacksonville 51
Jinan 50
Verona 50
Turin 47
Ottawa 46
Naples 45
Berlin 37
Los Angeles 37
Sakarya 36
Shenyang 36
Hangzhou 35
Serra 34
Tianjin 34
Hebei 33
San Diego 30
Brussels 29
Mumbai 29
Roxbury 29
Andover 28
Falls Church 27
Nanchang 27
Bologna 25
Fuzhou 25
Zhengzhou 25
Changsha 21
Istanbul 21
London 21
Athens 20
Nuremberg 19
Somerville 19
Seoul 18
Bogotá 17
Eitensheim 17
Padova 17
Warsaw 17
Ningbo 16
Silver Spring 16
Xian 15
Kunming 14
Pavia 14
Chicago 13
Hefei 13
Medford 13
Bari 12
Jiaxing 12
Munich 12
São Paulo 12
Kiez 11
Lecco 11
Quanzhou 11
Wuhan 11
Bühl 10
Lainate 10
Taipei 10
Taizhou 10
Vicenza 10
Vienna 10
Bergamo 9
Chengdu 9
Cinisello Balsamo 9
Fremont 9
Lanzhou 9
Modena 9
Totale 11.086
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Nome #
Epigenetica della violenza sulle donne : lo studio pilota 2.833
Mitochondrial DNA content and methylation in fetal cord blood of pregnancies with placental insufficiency 626
Impact of Mutation Density and Heterogeneity on Papillary Thyroid Cancer Clinical Features and Remission Probability 547
Differential signature of the centrosomal MARK4 isoforms in glioma 523
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 310
The Genetic Landscape of Human Glioblastoma and Matched Primary Cancer Stem Cells Reveals Intratumour Similarity and Intertumour Heterogeneity 287
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry 267
X chromosome inactivation pattern in BRCA gene mutation carriers 265
Studio della nutrizione in gravidanza nell'ambito del progetto "HUMAN-BB": impatto dell'alimentazione sulla salute mterno/neonatale in un campione di 800 gravide fisiologiche 261
Role of epigenetics in human aging and longevity : genome-wide DNA methylation profile in centenarians and centenarians' offspring 258
Duplicazioni parziali di SHOX associate alla Sindrome di Mayer-Rokitansky-Kuster-Hauser 250
Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System Atrophy 248
Misbehaviour of XIST RNA in breast cancer cells 245
Intrauterine growth restriction is associated with alterations in placental lipoprotein receptors and maternal lipoprotein composition 239
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies 237
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 236
MARK4 : a tricky balance of L and S isoforms rules glial differentiation and glioma progression 226
Prognostic value of preoperative von Willebrand factor plasma levels in patients with Glioblastoma 225
Epigenetic effects of chromatin remodeling agents on organotypic cultures 223
Placental IGF2 expression in normal and intrauterine growth restricted (IUGR) pregnancies 217
Delineating the Cytogenomic and Epigenomic Landscapes of Glioma Stem Cell Lines 214
Transferrin Receptor 1 protein expression and localization in human IntraUterine Growth Restriction placentas 211
X monosomy in female systemic lupus erythematosus 209
Assessment of X chromosome Inactivation pattern in BRCA mutation carriers : evidence for an effect of chemotherapy 208
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes 204
Misbehaviour of XIST RNA in breast cancer cells 204
SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome 200
SNAT2 expression and regulation in human growth restricted placentas 199
Mass spectrometry-based assay for the molecular diagnosis of glioma : Concomitant detection of chromosome 1p/19q codeletion, and IDH1, IDH2, and TERT mutation status 198
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute 195
Triple-Negative Essential Thrombocythemia: Clinical-Pathological and Molecular Features. A Single-Center Cohort Study 195
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 194
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas 190
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction 189
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 184
Insulin-like growth factor II (IGF2) and H19 expression in IUGR 181
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 178
Angiotensin-converting enzyme and adducin-1 polymorphisms in women with preeclampsia and gestational hypertension 176
Transferrin receptor gene and protein expression and localization in human IUGR and normal term placentas 176
Placental LPL gene expression is increased in severe intrauterine growth-restricted pregnancies 173
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 172
DNA methylation and histone modifications modulate the B1,3 galactosyltransferase B3Gal-T5 native promoter in cancer cells 171
Synchronous pleural and peritoneal malignant mesothelioma : a case report and review of literature 171
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases 171
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosis 170
ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic men 169
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms 169
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome 169
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 167
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 167
ESX1 gene transcript as a spermatogenesis marker in infertile men 165
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion 161
TfR1 Protein Expression and Localization in Human IUGR Placentas 159
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men 159
Extensive placental methylation profiling in normal pregnancies 159
TP53, P14ARF, P16INK4a and H-ras gene molecular analysis in intestinal-type adenocarcinoma of the nasal cavity and paranasal sinuses 158
Genetic polymorphisms and sepsis in premature neonates 157
DNA methylation in the diagnosis of monogenic diseases 155
New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene 153
EpiWE project, the molecular signature of violence in women’s victim genome 152
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 151
Sodium coupled Neutral Aminoacid Transporter 2 (SNAT2) Intron1 methylation levels and Single Nucleotide Polymorphism in IUGR placentas 148
Fragile X syndrome : A review of clinical and molecular diagnoses 142
Analysis of BRCA1 and RAD51C promoter methylation in italian families at high-risk of breast and ovarian cancer 138
Mesenchymal stem cells : potential for therapy and treatment of chronic non-healing skin wounds 136
Angiotensin-converting enzyme and alpha-adducin polymorphisms in preeclamptic mothers and fetuses 131
Beckwith–Wiedemann and IMAGe syndromes : two very different diseases caused by mutations on the same gene 129
Gene Expression Profile Analysis of Human Mesenchymal Stem Cells from Herniated and Degenerated Intervertebral Discs Reveals Different Expression of Osteopontin 127
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls 127
Differential insulin receptor splicing in trophoblast vs endothelial cells 123
Constitutive X chromosome inactivation profile and BRCA genes germ-fine mutations 121
Lipoprotein lipase (LPL) mRNA expression in placentas from normal and IUGR (intrauterine growth restricted) pregnancies by real-time PCR 120
SNAT2 Intron1 Methylation Levels and Single Nucleotide Polymorphism in IUGR Placentas 119
Gestational diabetes modifies scavenger receptor class B type I receptor (SR-BI) expression in human placental tissue 119
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 118
TP53 status may predict pathological complete remission (pCR) to cisplatin plus fluorouracil plus leucovorin (PFL) in ethmoidal intestinal type adenocarcinoma (ITAC) treated with preoperative chemotherapy 116
MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma : the PTC-MA assay 110
Possible position effect on TRPS1 in a patient carrying t(2;8)(p16.1;q23.3) translocation with phenotype referring to trichorhinopahalangeal syndrome 109
Detection of Loss of Imprinting by Pyrosequencing 108
Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: cytogenetic, molecular and clinico-pathological studies 107
Only severe intrauterine growth restriction (IUGR) alters expression levels of low density lipoprotein receptor-related protein (LRP) and scavenger receptor class B type I (SR-BI) 106
SNAT2 and TfR1 Expression in human IUGR placentas 106
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study 105
STAR syndrome plus: The first description of a female patient with the lethal form 101
MV1035 Overcomes Temozolomide Resistance in Patient-Derived Glioblastoma Stem Cell Lines 100
Severe intrauterine growth restriction (IUGR) is associated with impaired lipoprotein receptor expression levels in human placenta 99
TP53, p14(ARF), p16(INK4a) and H-RAS gene molecular analysis in intestinal-type adenocarcinoma of the nasal cavity and paranasal sinuses 98
DNMT1-complex disorder caused by a novel mutation associated with an overlapping phenotype of autosomal-dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) and hereditary sensory neuropathy with dementia and hearing loss (HSN1E) 98
p15INK4b, p14ARF, and p16INK4a inactivation in sporadic and neurofibromatosis type 1-related malignant peripheral nerve sheath tumors 90
Mental health and the effects on methylation of stress-related genes in front-line versus other health care professionals during the second wave of COVID-19 pandemic: an Italian pilot study 88
Mitochondrial DNA methylation in fetal cord blood of IUGR and preeclamptic pregnancies 76
The classification of myeloproliferative neoplasms : Rationale, historical background and future perspectives with focus on unclassifiable cases 65
Primary cutaneous, epidermotropic mycosis fungoides-like presentation: critical appraisal and description of two novel cases, broadening the spectrum of ALK+ T-cell lymphoma 59
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis 45
Granular cell tumor of the neurohypophysis presenting as a third ventricle mass 42
A Rare Case of Urinary Bladder Hamartoma Clinically Mimicking an Urothelial Carcinoma: A Case Report and Review of the Literature 41
Liquid biopsy in non-small cell lung cancer: a meta-analysis of state-of-the-art and future perspectives 37
The unexpected guest: Cytotoxic, pseudolymphoma-like reaction at the site of primary cutaneous follicle centre B-cell lymphoma in a patient receiving secukinumab for psoriasis 19
Totale 19.549
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Categoria #
all - tutte 51.745
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 51.745
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020797 0 0 0 0 0 0 0 0 267 332 95 103
2020/20211.873 147 146 100 113 184 141 120 165 183 181 278 115
2021/20222.006 168 141 174 169 121 135 125 96 226 129 162 360
2022/20232.045 300 283 211 178 206 320 85 115 167 28 94 58
2023/20244.208 85 112 112 150 505 146 147 384 1.733 225 319 290
2024/20252.240 193 322 119 387 272 213 199 310 225 0 0 0
Totale 19.549