IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

SIRCHIA, SILVIA MARIA
 Distribuzione geografica
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Continente #
EU - Europa 8.176
NA - Nord America 4.909
AS - Asia 2.666
SA - Sud America 253
AF - Africa 39
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 7
Totale 16.071
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Nazione #
US - Stati Uniti d'America 4.753
GB - Regno Unito 4.064
CN - Cina 1.266
IT - Italia 1.086
SE - Svezia 830
DE - Germania 649
SG - Singapore 534
RU - Federazione Russa 360
NL - Olanda 239
IN - India 198
FR - Francia 190
UA - Ucraina 190
BR - Brasile 178
IE - Irlanda 163
TR - Turchia 156
KR - Corea 140
FI - Finlandia 139
CA - Canada 130
HK - Hong Kong 96
EU - Europa 80
DK - Danimarca 72
ID - Indonesia 71
VN - Vietnam 59
NO - Norvegia 39
BE - Belgio 38
JP - Giappone 37
CO - Colombia 30
AU - Australia 21
MX - Messico 21
ES - Italia 17
ZA - Sudafrica 16
GR - Grecia 15
TW - Taiwan 15
PL - Polonia 14
AT - Austria 13
IR - Iran 12
RO - Romania 12
AR - Argentina 11
CH - Svizzera 11
CZ - Repubblica Ceca 11
PE - Perù 9
AE - Emirati Arabi Uniti 8
JO - Giordania 8
EC - Ecuador 7
EG - Egitto 7
PH - Filippine 7
AZ - Azerbaigian 6
MY - Malesia 6
PK - Pakistan 6
SA - Arabia Saudita 6
BD - Bangladesh 5
BO - Bolivia 5
CL - Cile 5
UZ - Uzbekistan 5
HU - Ungheria 4
KE - Kenya 4
MA - Marocco 4
PT - Portogallo 4
UY - Uruguay 4
IQ - Iraq 3
KZ - Kazakistan 3
SC - Seychelles 3
SK - Slovacchia (Repubblica Slovacca) 3
VE - Venezuela 3
BA - Bosnia-Erzegovina 2
IL - Israele 2
KG - Kirghizistan 2
LA - Repubblica Popolare Democratica del Laos 2
NI - Nicaragua 2
OM - Oman 2
PA - Panama 2
PS - Palestinian Territory 2
RS - Serbia 2
SI - Slovenia 2
SY - Repubblica araba siriana 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
BG - Bulgaria 1
BY - Bielorussia 1
GH - Ghana 1
IS - Islanda 1
JM - Giamaica 1
KH - Cambogia 1
KW - Kuwait 1
LB - Libano 1
LK - Sri Lanka 1
LT - Lituania 1
LU - Lussemburgo 1
MD - Moldavia 1
MN - Mongolia 1
NG - Nigeria 1
NP - Nepal 1
PY - Paraguay 1
SN - Senegal 1
TN - Tunisia 1
TZ - Tanzania 1
Totale 16.145
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Città #
Southend 3.901
Chandler 642
Milan 505
Singapore 360
Ann Arbor 310
Ashburn 307
Seattle 299
Fairfield 259
Wilmington 248
Princeton 217
Beijing 211
Dearborn 185
Woodbridge 168
Dublin 161
Houston 157
Frankfurt am Main 147
Council Bluffs 143
Redmond 119
Mountain View 118
Nanjing 115
Santa Clara 107
Cambridge 99
Jacksonville 88
Hong Kong 81
Toronto 78
Des Moines 68
Jinan 68
Sakarya 67
Shanghai 65
Bengaluru 63
Shenyang 61
Boardman 58
Jakarta 58
Redwood City 56
Serra 53
Helsinki 52
Phoenix 50
New York 45
Berlin 41
Hebei 37
Nanchang 37
Brussels 36
Tianjin 36
Guangzhou 35
Eitensheim 34
Verona 34
Los Angeles 33
Changsha 31
Hanover 30
Turin 30
Zhengzhou 29
Andover 28
Bogotá 27
Falls Church 26
Ottawa 26
Fuzhou 24
London 24
Ningbo 24
Somerville 24
Istanbul 23
San Diego 23
Grafing 20
Hangzhou 20
Buffalo 19
Rome 18
Medford 17
Dong Ket 16
Jiaxing 16
Roxbury 16
Seoul 15
Athens 14
Cagliari 14
Cangzhou 14
Haikou 14
Kiez 14
Saint Petersburg 14
Silver Spring 14
Munich 13
Nuremberg 13
Chicago 12
Mumbai 12
Nashua 12
Washington 12
Auburn Hills 11
Bitonto 11
Bologna 11
Quanzhou 11
São Paulo 11
Fremont 10
Kunming 10
Pisa 10
Bühl 9
Kent 9
Norwalk 9
Sunnyvale 9
Vienna 9
Brno 8
Hamburg 8
Hefei 8
Taipei 8
Totale 10.972
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Nome #
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 318
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 315
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry 273
X chromosome inactivation pattern in BRCA gene mutation carriers 269
Role of epigenetics in human aging and longevity : genome-wide DNA methylation profile in centenarians and centenarians' offspring 258
The methylation of the TSC2 promoter underlies the abnormal growth of TSC2 angiomyolipoma-derived smooth muscle cells 249
Misbehaviour of XIST RNA in breast cancer cells 249
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis 246
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 243
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 235
Epigenetic effects of chromatin remodeling agents on organotypic cultures 227
Characterization of LAM/TSC cells isolated from patient chylous 225
Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype 221
Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes 219
Placental IGF2 expression in normal and intrauterine growth restricted (IUGR) pregnancies 219
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 207
Misbehaviour of XIST RNA in breast cancer cells 206
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with changes in transcriptional profiles 202
Pathogenesis and pharmacological evaluation of human TSC2 smooth muscle cells. Possible treatment options for TSC and lymphangioleiomyomatosis 200
Endogenous reactivation of the RARbeta2 tumor suppressor gene epigenetically silenced in breast cancer 200
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies 200
Characterization of human TSC2 cells derived from a TSC/LAM patient chylous effusion 199
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 199
Ruolo di BRCA1 nella regolazione dell’espressione del gene XIST 197
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute 195
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction 193
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta2 promoter in breast cancer cells 193
TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival 193
Ruolo di ESX1L nella spermatogenesi umana 190
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 190
Insulin-like growth factor II (IGF2) and H19 expression in IUGR 183
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma 183
Regulatory element deletion cause a down-regulation of ZDHHC15 gene in a proband with Smith Magenis syndrome phenotype 182
GDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML 182
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 182
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 181
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells 179
Sindrome di Rubinstein Taybi: CREBBP e oltre 179
Promoter methylation of TSC2 gene is important for pathogenesis of TSC and LAM lesions 178
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases 177
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosis 175
An epigenetic event may underlies the TSC features in TSC2 ASM cells 174
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 174
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 173
X chromosome inactivation defects and breast tumorigenesis 171
DNA methylation and histone modifications modulate the B1,3 galactosyltransferase B3Gal-T5 native promoter in cancer cells 171
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome 171
ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic men 170
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms 169
Blood fetal microchimerism in primary biliary cirrhosis 166
ESX1 gene transcript as a spermatogenesis marker in infertile men 166
Highly sensitive chemiluminescent method for the detection of cell contamination 166
Extensive placental methylation profiling in normal pregnancies 166
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion 164
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men 162
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 159
Epigenetic Basis of Vitamin A Resistance in Breast Cancer. Implications for Prevention and Treatment 158
DNA methylation in the diagnosis of monogenic diseases 157
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected 154
Tuberin deficiency for an epigenetic modification in LAM cells from chylous of a TSC2 patient 154
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype 153
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism 152
Le basi biologiche della vita 150
Highly sensitive chemiluminescent method for the detection of maternal cell contamination in human cord blood stored for allotransplantation : the experience of the Milano cord blood bank 146
Thompson & Thompson : Genetica in medicina 146
Aneuploid correction and confined placental mosaicism 145
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters 145
Epigenetic alterations in cancer and personalized cancer treatment 145
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries 144
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery 144
Direct and indirect pharmacological regulation of mTOR affects fate of LAM/TSC cells. Epithelial to mesenchymal transition features of LAM/TSC cells 144
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas 137
Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics 137
Confined placental mosaicism 136
Loss of heterozigosity of chromosomal region 4q32-35 in basal cell carcinomas 136
Characterization of four microsatellites in an Italian population and their application to paternity testing 136
Increased loss of the Y chromosome in peripheral blood cells in male patients with autoimmune thyroiditis 132
Germline oncopharmacogenetics, a promising field in cancer therapy 131
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 126
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent method 123
Constitutive X chromosome inactivation profile and BRCA genes germ-fine mutations 122
Chromatin remodeling of the RAR gene in the pathogenesis and retinoid resistance to breast cancer 122
Intrauterine growth retardation (IUGR) : uniparental disomy or placental morpho-functional anomalies? 120
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study 117
Introduzione al genoma umano 115
Introduzione 113
OTX1 expression in breast cancer is regulated by p53 102
The mammary gland and the homeobox gene Otx1 97
Methylation status of RARbeta2 promoter in esophageal cancer 93
Targeting epigenetic changes associated with retinoid resistance : a novel strategy to treat breast cancer 91
Silencing of the retinoic acid receptor beta (RAR beta) gene by hypermethylation in human breast cancer 87
Molecular screening of families affected by familial adenomatous polyposis (FAP) 85
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome : a clinical, EEG, and molecular genetic study 82
Severe epilepsy in a patient with Prader-Willi-syndrome due to inversion-duplication of chromosome 15q11-q13 - a clinical neurophysiological, and molecular-genetic study 82
Significance of clustered tumor suppressor genes in cancer 82
p53 family members regulate the Otx1 gene expression in differentiation of breast cancer stem cells and in mammary gland development 76
The mammary gland and the homeobox gene Otx1 64
Erratum: The mammary gland and the homeobox gene otx1. (Breast Journal (2010) 16:1 (S53-S56)) 64
OTX1 expression in breast cancer is regulated by p53 64
Totale 16.650
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Categoria #
all - tutte 45.298
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 45.298
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020624 0 0 0 0 0 0 0 0 0 365 89 170
2020/20211.722 103 99 121 113 157 116 90 122 191 132 367 111
2021/20221.920 206 134 122 151 126 145 134 84 189 123 171 335
2022/20232.004 292 295 202 199 221 320 46 120 179 23 82 25
2023/20241.215 41 86 70 98 318 107 62 74 28 66 93 172
2024/20251.954 108 241 65 289 218 147 112 264 167 343 0 0
Totale 16.885