IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

SIRCHIA, SILVIA MARIA
 Distribuzione geografica
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Continente #
EU - Europa 9.114
NA - Nord America 7.136
AS - Asia 5.927
SA - Sud America 504
AF - Africa 145
OC - Oceania 26
Continente sconosciuto - Info sul continente non disponibili 7
Totale 22.859
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Nazione #
US - Stati Uniti d'America 6.881
GB - Regno Unito 4.105
CN - Cina 2.034
SG - Singapore 1.594
IT - Italia 1.395
SE - Svezia 847
DE - Germania 737
HK - Hong Kong 586
RU - Federazione Russa 574
VN - Vietnam 431
BR - Brasile 366
FR - Francia 329
IN - India 277
BD - Bangladesh 275
NL - Olanda 255
UA - Ucraina 193
CA - Canada 180
KR - Corea 174
TR - Turchia 174
FI - Finlandia 171
IE - Irlanda 166
JP - Giappone 92
ID - Indonesia 87
EU - Europa 80
DK - Danimarca 72
CI - Costa d'Avorio 66
MX - Messico 45
ES - Italia 41
BE - Belgio 40
NO - Norvegia 39
PL - Polonia 39
CO - Colombia 34
AR - Argentina 32
ZA - Sudafrica 28
AU - Australia 25
IQ - Iraq 23
SA - Arabia Saudita 17
GR - Grecia 16
EC - Ecuador 15
IR - Iran 15
RO - Romania 15
TW - Taiwan 15
AT - Austria 14
PH - Filippine 14
CL - Cile 13
PK - Pakistan 13
AE - Emirati Arabi Uniti 12
CZ - Repubblica Ceca 12
KE - Kenya 12
UZ - Uzbekistan 12
CH - Svizzera 11
EG - Egitto 11
MA - Marocco 11
PE - Perù 11
JO - Giordania 10
VE - Venezuela 10
AZ - Azerbaigian 8
MY - Malesia 8
PT - Portogallo 8
PY - Paraguay 8
BO - Bolivia 7
IL - Israele 7
KZ - Kazakistan 7
LB - Libano 5
TH - Thailandia 5
UY - Uruguay 5
AL - Albania 4
AM - Armenia 4
HU - Ungheria 4
JM - Giamaica 4
LK - Sri Lanka 4
LT - Lituania 4
LU - Lussemburgo 4
PA - Panama 4
PS - Palestinian Territory 4
RS - Serbia 4
CR - Costa Rica 3
DO - Repubblica Dominicana 3
KG - Kirghizistan 3
NG - Nigeria 3
NI - Nicaragua 3
NP - Nepal 3
OM - Oman 3
SC - Seychelles 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
TT - Trinidad e Tobago 3
BA - Bosnia-Erzegovina 2
BG - Bulgaria 2
GT - Guatemala 2
GY - Guiana 2
HN - Honduras 2
KH - Cambogia 2
LA - Repubblica Popolare Democratica del Laos 2
MD - Moldavia 2
PR - Porto Rico 2
QA - Qatar 2
SN - Senegal 2
SV - El Salvador 2
Totale 22.914
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Città #
Southend 3.901
Singapore 917
Ashburn 790
Chandler 642
Milan 560
Hong Kong 537
San Jose 424
Beijing 370
Ann Arbor 310
Seattle 306
Fairfield 259
Wilmington 248
Dallas 221
Princeton 217
Council Bluffs 202
Frankfurt am Main 188
Dearborn 186
Los Angeles 178
Woodbridge 170
Dublin 164
Houston 164
Santa Clara 147
Ho Chi Minh City 131
New York 130
Redmond 119
Mountain View 118
Nanjing 115
Hanoi 104
Buffalo 100
Cambridge 99
Lauterbourg 99
Bengaluru 92
Jacksonville 88
Toronto 87
Moscow 82
Shanghai 81
Guangzhou 73
Des Moines 70
Helsinki 70
Jakarta 70
Jinan 69
The Dalles 69
Sakarya 67
Abidjan 66
Shenyang 64
Phoenix 60
Boardman 59
Hefei 57
Redwood City 56
Rome 55
Serra 53
Tokyo 50
Tianjin 47
Munich 45
Changsha 43
Columbus 43
Berlin 42
Brussels 38
Seoul 38
Hebei 37
Nanchang 37
Cangzhou 36
São Paulo 35
Verona 35
Zhengzhou 35
Eitensheim 34
Istanbul 34
Turin 34
London 33
Hanover 30
Andover 28
Bogotá 27
Ottawa 27
Falls Church 26
Fuzhou 25
Ningbo 25
San Diego 25
Warsaw 25
Bologna 24
Cagliari 24
Chicago 24
Hangzhou 24
Somerville 24
Atlanta 23
Delhi 21
Mumbai 21
Grafing 20
Nuremberg 20
Shenzhen 19
Haiphong 17
Medford 17
Dong Ket 16
Jiaxing 16
Naples 16
Roxbury 16
Washington 16
Athens 15
Montreal 15
Palermo 15
Silver Spring 15
Totale 14.856
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Nome #
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 406
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 403
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 380
X chromosome inactivation pattern in BRCA gene mutation carriers 370
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry 362
Role of epigenetics in human aging and longevity : genome-wide DNA methylation profile in centenarians and centenarians' offspring 341
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 340
The methylation of the TSC2 promoter underlies the abnormal growth of TSC2 angiomyolipoma-derived smooth muscle cells 328
Thompson & Thompson : Genetica in medicina 325
Misbehaviour of XIST RNA in breast cancer cells 323
Epigenetic effects of chromatin remodeling agents on organotypic cultures 317
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis 312
Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype 297
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 294
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 291
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 291
Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes 287
Characterization of LAM/TSC cells isolated from patient chylous 287
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 286
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells 283
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction 281
Placental IGF2 expression in normal and intrauterine growth restricted (IUGR) pregnancies 279
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases 273
Endogenous reactivation of the RARbeta2 tumor suppressor gene epigenetically silenced in breast cancer 270
DNA methylation in the diagnosis of monogenic diseases 269
TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival 269
Extensive placental methylation profiling in normal pregnancies 269
Pathogenesis and pharmacological evaluation of human TSC2 smooth muscle cells. Possible treatment options for TSC and lymphangioleiomyomatosis 267
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute 266
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes 266
GDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML 266
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with changes in transcriptional profiles 265
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 265
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies 264
Regulatory element deletion cause a down-regulation of ZDHHC15 gene in a proband with Smith Magenis syndrome phenotype 264
ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic men 263
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 263
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 261
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome 260
Assessment of X chromosome Inactivation pattern in BRCA mutation carriers : evidence for an effect of chemotherapy 257
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 252
Misbehaviour of XIST RNA in breast cancer cells 249
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta2 promoter in breast cancer cells 245
Ruolo di BRCA1 nella regolazione dell’espressione del gene XIST 243
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study 243
Characterization of human TSC2 cells derived from a TSC/LAM patient chylous effusion 242
Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics 240
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosis 239
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men 237
Ruolo di ESX1L nella spermatogenesi umana 236
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion 235
Insulin-like growth factor II (IGF2) and H19 expression in IUGR 234
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma 234
Promoter methylation of TSC2 gene is important for pathogenesis of TSC and LAM lesions 231
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected 231
An epigenetic event may underlies the TSC features in TSC2 ASM cells 230
Sindrome di Rubinstein Taybi: CREBBP e oltre 226
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms 225
ESX1 gene transcript as a spermatogenesis marker in infertile men 220
Blood fetal microchimerism in primary biliary cirrhosis 219
DNA methylation and histone modifications modulate the B1,3 galactosyltransferase B3Gal-T5 native promoter in cancer cells 218
X chromosome inactivation defects and breast tumorigenesis 217
Le basi biologiche della vita 208
Highly sensitive chemiluminescent method for the detection of cell contamination 207
Epigenetic Basis of Vitamin A Resistance in Breast Cancer. Implications for Prevention and Treatment 207
Tuberin deficiency for an epigenetic modification in LAM cells from chylous of a TSC2 patient 196
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas 192
Direct and indirect pharmacological regulation of mTOR affects fate of LAM/TSC cells. Epithelial to mesenchymal transition features of LAM/TSC cells 191
Germline oncopharmacogenetics, a promising field in cancer therapy 191
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries 190
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters 189
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism 186
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype 185
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 181
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines 176
Loss of heterozigosity of chromosomal region 4q32-35 in basal cell carcinomas 175
Introduzione al genoma umano 174
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery 173
Epigenetic alterations in cancer and personalized cancer treatment 172
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent method 171
Aneuploid correction and confined placental mosaicism 170
Increased loss of the Y chromosome in peripheral blood cells in male patients with autoimmune thyroiditis 169
Characterization of four microsatellites in an Italian population and their application to paternity testing 169
Introduzione 168
Confined placental mosaicism 167
Chromatin remodeling of the RAR gene in the pathogenesis and retinoid resistance to breast cancer 167
A perspective on diet, epigenetics and complex diseases: where is the field headed next? 162
Constitutive X chromosome inactivation profile and BRCA genes germ-fine mutations 150
Intrauterine growth retardation (IUGR) : uniparental disomy or placental morpho-functional anomalies? 149
The mammary gland and the homeobox gene Otx1 147
OTX1 expression in breast cancer is regulated by p53 137
Methylation status of RARbeta2 promoter in esophageal cancer 137
Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model 133
Targeting epigenetic changes associated with retinoid resistance : a novel strategy to treat breast cancer 126
OTX1 expression in breast cancer is regulated by p53 123
Non-invasive biomarkers for sperm retrieval in non-obstructive patients: a comprehensive review 122
Erratum: The mammary gland and the homeobox gene otx1. (Breast Journal (2010) 16:1 (S53-S56)) 120
Molecular screening of families affected by familial adenomatous polyposis (FAP) 117
Silencing of the retinoic acid receptor beta (RAR beta) gene by hypermethylation in human breast cancer 108
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome : a clinical, EEG, and molecular genetic study 107
Totale 23.218
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Categoria #
all - tutte 59.422
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 59.422
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021478 0 0 0 0 0 0 0 0 0 0 367 111
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
2024/20252.828 108 241 65 289 218 147 112 264 167 348 252 617
2025/20266.059 586 380 617 471 531 384 983 254 660 460 733 0
Totale 23.818