SIRCHIA, SILVIA MARIA
 Distribuzione geografica
Continente #
EU - Europa 7.587
NA - Nord America 4.400
AS - Asia 1.986
SA - Sud America 71
AF - Africa 21
OC - Oceania 18
Continente sconosciuto - Info sul continente non disponibili 7
Totale 14.090
Nazione #
US - Stati Uniti d'America 4.255
GB - Regno Unito 4.057
CN - Cina 1.036
IT - Italia 1.008
SE - Svezia 824
DE - Germania 572
IN - India 197
UA - Ucraina 186
FR - Francia 178
SG - Singapore 176
RU - Federazione Russa 168
IE - Irlanda 158
TR - Turchia 153
KR - Corea 140
FI - Finlandia 128
CA - Canada 126
HK - Hong Kong 88
EU - Europa 80
NL - Olanda 79
DK - Danimarca 72
VN - Vietnam 52
ID - Indonesia 43
BE - Belgio 37
NO - Norvegia 37
JP - Giappone 36
CO - Colombia 29
AU - Australia 18
MX - Messico 18
GR - Grecia 15
BR - Brasile 14
ES - Italia 14
TW - Taiwan 14
IR - Iran 12
CH - Svizzera 11
PL - Polonia 11
RO - Romania 10
PE - Perù 8
ZA - Sudafrica 7
EG - Egitto 6
AR - Argentina 5
EC - Ecuador 5
MY - Malesia 5
PH - Filippine 5
PK - Pakistan 5
SA - Arabia Saudita 5
AE - Emirati Arabi Uniti 4
CZ - Repubblica Ceca 4
JO - Giordania 4
PT - Portogallo 4
UY - Uruguay 4
CL - Cile 3
SC - Seychelles 3
UZ - Uzbekistan 3
BA - Bosnia-Erzegovina 2
BD - Bangladesh 2
HU - Ungheria 2
IL - Israele 2
KE - Kenya 2
RS - Serbia 2
SI - Slovenia 2
SY - Repubblica araba siriana 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AT - Austria 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
GH - Ghana 1
KW - Kuwait 1
MD - Moldavia 1
NG - Nigeria 1
NP - Nepal 1
PA - Panama 1
PY - Paraguay 1
SK - Slovacchia (Repubblica Slovacca) 1
TZ - Tanzania 1
VE - Venezuela 1
Totale 14.164
Città #
Southend 3.901
Chandler 642
Milan 479
Ann Arbor 310
Seattle 299
Ashburn 261
Fairfield 259
Wilmington 248
Princeton 217
Beijing 207
Dearborn 185
Woodbridge 168
Houston 157
Dublin 156
Redmond 119
Mountain View 118
Nanjing 109
Frankfurt am Main 103
Cambridge 99
Jacksonville 88
Toronto 78
Hong Kong 75
Singapore 74
Des Moines 68
Jinan 67
Sakarya 67
Bengaluru 63
Shenyang 61
Boardman 58
Redwood City 56
Serra 53
Phoenix 50
Shanghai 48
Helsinki 46
New York 44
Berlin 41
Hebei 37
Nanchang 37
Tianjin 36
Brussels 35
Eitensheim 34
Changsha 31
Verona 31
Hanover 30
Jakarta 30
Turin 29
Zhengzhou 29
Andover 28
Guangzhou 28
Bogotá 26
Falls Church 26
Ottawa 26
Somerville 24
Ningbo 23
San Diego 23
Istanbul 22
Grafing 20
Hangzhou 20
London 19
Buffalo 18
Medford 17
Dong Ket 16
Jiaxing 16
Roxbury 16
Seoul 15
Athens 14
Cagliari 14
Haikou 14
Kiez 14
Saint Petersburg 14
Rome 13
Chicago 12
Los Angeles 12
Mumbai 12
Nashua 12
Silver Spring 12
Washington 12
Auburn Hills 11
Bitonto 11
Fremont 10
Kunming 10
Pisa 10
Bühl 9
Norwalk 9
Sunnyvale 9
Fuzhou 8
Hefei 8
Cinisello Balsamo 7
Hamburg 7
Lanzhou 7
Munich 7
Pune 7
Scranton 7
Sydney 7
Taipei 7
Taizhou 7
Bologna 6
Minoh 6
Torino 6
Vancouver 6
Totale 10.153
Nome #
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 288
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 285
Role of epigenetics in human aging and longevity : genome-wide DNA methylation profile in centenarians and centenarians' offspring 245
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry 243
X chromosome inactivation pattern in BRCA gene mutation carriers 240
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis 238
The methylation of the TSC2 promoter underlies the abnormal growth of TSC2 angiomyolipoma-derived smooth muscle cells 233
Misbehaviour of XIST RNA in breast cancer cells 227
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 218
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 217
Characterization of LAM/TSC cells isolated from patient chylous 209
Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype 206
Placental IGF2 expression in normal and intrauterine growth restricted (IUGR) pregnancies 204
Epigenetic effects of chromatin remodeling agents on organotypic cultures 203
Assessment of X chromosome Inactivation pattern in BRCA mutation carriers : evidence for an effect of chemotherapy 200
Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes 195
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes 194
Misbehaviour of XIST RNA in breast cancer cells 193
Pathogenesis and pharmacological evaluation of human TSC2 smooth muscle cells. Possible treatment options for TSC and lymphangioleiomyomatosis 182
Ruolo di BRCA1 nella regolazione dell’espressione del gene XIST 181
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 181
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies 178
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 174
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction 173
Insulin-like growth factor II (IGF2) and H19 expression in IUGR 172
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute 172
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with changes in transcriptional profiles 169
Regulatory element deletion cause a down-regulation of ZDHHC15 gene in a proband with Smith Magenis syndrome phenotype 168
Sindrome di Rubinstein Taybi: CREBBP e oltre 167
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells 166
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta2 promoter in breast cancer cells 165
Endogenous reactivation of the RARbeta2 tumor suppressor gene epigenetically silenced in breast cancer 164
TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival 163
Ruolo di ESX1L nella spermatogenesi umana 162
DNA methylation and histone modifications modulate the B1,3 galactosyltransferase B3Gal-T5 native promoter in cancer cells 161
Promoter methylation of TSC2 gene is important for pathogenesis of TSC and LAM lesions 160
GDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML 160
An epigenetic event may underlies the TSC features in TSC2 ASM cells 157
Highly sensitive chemiluminescent method for the detection of cell contamination 157
X chromosome inactivation defects and breast tumorigenesis 156
ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic men 156
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosis 155
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases 155
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms 153
ESX1 gene transcript as a spermatogenesis marker in infertile men 153
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 153
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma 151
Characterization of human TSC2 cells derived from a TSC/LAM patient chylous effusion 151
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 151
Blood fetal microchimerism in primary biliary cirrhosis 150
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome 150
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 148
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion 145
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men 145
Le basi biologiche della vita 144
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype 143
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 142
Tuberin deficiency for an epigenetic modification in LAM cells from chylous of a TSC2 patient 140
Aneuploid correction and confined placental mosaicism 139
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected 138
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism 135
Extensive placental methylation profiling in normal pregnancies 134
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 134
Epigenetic alterations in cancer and personalized cancer treatment 133
Direct and indirect pharmacological regulation of mTOR affects fate of LAM/TSC cells. Epithelial to mesenchymal transition features of LAM/TSC cells 132
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries 130
Confined placental mosaicism 128
Epigenetic Basis of Vitamin A Resistance in Breast Cancer. Implications for Prevention and Treatment 128
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery 127
Microtubule-associated protein/microtubule affinity-regulating kinase 4 (MARK4) plays a role in cell cycle progression and cytoskeletal dynamics 127
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 127
Characterization of four microsatellites in an Italian population and their application to paternity testing 124
DNA methylation in the diagnosis of monogenic diseases 124
Increased loss of the Y chromosome in peripheral blood cells in male patients with autoimmune thyroiditis 123
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters 122
Loss of heterozigosity of chromosomal region 4q32-35 in basal cell carcinomas 118
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas 118
Constitutive X chromosome inactivation profile and BRCA genes germ-fine mutations 115
Thompson & Thompson : Genetica in medicina 115
Germline oncopharmacogenetics, a promising field in cancer therapy 111
Intrauterine growth retardation (IUGR) : uniparental disomy or placental morpho-functional anomalies? 109
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent method 109
Chromatin remodeling of the RAR gene in the pathogenesis and retinoid resistance to breast cancer 106
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 96
Introduzione 93
OTX1 expression in breast cancer is regulated by p53 91
The mammary gland and the homeobox gene Otx1 89
Introduzione al genoma umano 87
Methylation status of RARbeta2 promoter in esophageal cancer 84
Molecular screening of families affected by familial adenomatous polyposis (FAP) 77
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome : a clinical, EEG, and molecular genetic study 77
Severe epilepsy in a patient with Prader-Willi-syndrome due to inversion-duplication of chromosome 15q11-q13 - a clinical neurophysiological, and molecular-genetic study 77
Silencing of the retinoic acid receptor beta (RAR beta) gene by hypermethylation in human breast cancer 77
Significance of clustered tumor suppressor genes in cancer 76
Targeting epigenetic changes associated with retinoid resistance : a novel strategy to treat breast cancer 74
p53 family members regulate the Otx1 gene expression in differentiation of breast cancer stem cells and in mammary gland development 68
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study 57
Development of epigenetic resistance to retinoic acid in breast cancer : implications for chemoprevention 55
Erratum: The mammary gland and the homeobox gene otx1. (Breast Journal (2010) 16:1 (S53-S56)) 49
OTX1 expression in breast cancer is regulated by p53 49
Totale 14.793
Categoria #
all - tutte 34.119
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 34.119


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019133 0 0 0 0 0 0 0 0 0 0 0 133
2019/20202.443 320 85 56 255 160 234 302 152 255 365 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
2023/20241.186 41 86 70 98 318 107 62 74 28 66 93 143
Totale 14.902