SIRCHIA, SILVIA MARIA
 Distribuzione geografica
Continente #
NA - Nord America 2.271
EU - Europa 1.482
AS - Asia 624
AF - Africa 57
SA - Sud America 53
OC - Oceania 25
Continente sconosciuto - Info sul continente non disponibili 3
Totale 4.515
Nazione #
US - Stati Uniti d'America 2.226
DE - Germania 612
IT - Italia 355
CN - Cina 330
GB - Regno Unito 126
FR - Francia 111
IN - India 57
NL - Olanda 56
ID - Indonesia 50
RU - Federazione Russa 48
JP - Giappone 40
KR - Corea 39
CA - Canada 36
CZ - Repubblica Ceca 28
IR - Iran 24
ZA - Sudafrica 23
AU - Australia 21
ES - Italia 19
EU - Europa 19
PE - Perù 17
RO - Romania 17
BR - Brasile 16
IE - Irlanda 16
UA - Ucraina 15
VN - Vietnam 15
EG - Egitto 14
AE - Emirati Arabi Uniti 13
PL - Polonia 13
FI - Finlandia 12
TR - Turchia 11
CL - Cile 9
MY - Malesia 9
PK - Pakistan 9
TW - Taiwan 8
GR - Grecia 7
MX - Messico 7
SE - Svezia 7
HK - Hong Kong 6
AR - Argentina 5
HU - Ungheria 5
ZM - Zambia 5
BE - Belgio 4
CH - Svizzera 4
EE - Estonia 4
NZ - Nuova Zelanda 4
AT - Austria 3
BY - Bielorussia 3
DK - Danimarca 3
DZ - Algeria 3
GH - Ghana 3
HR - Croazia 3
MV - Maldive 3
SG - Singapore 3
UG - Uganda 3
CO - Colombia 2
KE - Kenya 2
MK - Macedonia 2
MT - Malta 2
NG - Nigeria 2
PH - Filippine 2
SK - Slovacchia (Repubblica Slovacca) 2
UY - Uruguay 2
A1 - Anonimo 1
BD - Bangladesh 1
CR - Costa Rica 1
ET - Etiopia 1
HN - Honduras 1
IL - Israele 1
KH - Cambogia 1
LI - Liechtenstein 1
LV - Lettonia 1
MA - Marocco 1
NO - Norvegia 1
PT - Portogallo 1
RS - Serbia 1
SA - Arabia Saudita 1
SR - Suriname 1
TH - Thailandia 1
VE - Venezuela 1
Totale 4.532
Città #
Fairfield 242
Ashburn 166
Seattle 147
Woodbridge 143
Milan 141
Buffalo 123
Houston 108
Beijing 101
Santa Cruz 87
Cambridge 85
Wilmington 75
Mountain View 60
Ann Arbor 58
Shanghai 38
Columbus 35
Wuhan 35
Jakarta 32
Redmond 27
Chicago 26
Southend 25
University Park 24
Kiez 23
Nürnberg 23
Rome 21
Las Vegas 19
Boardman 18
Muizenberg 17
Phoenix 17
London 15
Los Angeles 15
San Diego 15
Monmouth Junction 14
Dublin 13
Guangzhou 13
Ottawa 13
Piscataway 13
Campi Bisenzio 12
Dallas 11
Amsterdam 10
Changsha 9
Helsinki 9
Tacna 9
Cairo 8
Sydney 8
Tokyo 8
Clearwater 7
Coimbatore 7
Des Moines 7
Hanoi 7
Henderson 7
Jersey City 7
Nanjing 7
Paris 7
Bengaluru 6
Council Bluffs 6
Fasano 6
New York 6
Scranton 6
Shenyang 6
Sunnyvale 6
Athens 5
Caserta 5
Chennai 5
Dearborn 5
Hangzhou 5
Herndon 5
Lake Forest 5
Leawood 5
Lima 5
Milpitas 5
Moscow 5
Mumbai 5
Nashville 5
Philadelphia 5
Rochester 5
San Francisco 5
San Jose 5
Taipei 5
Vigo 5
Xian 5
Auckland 4
Aurora 4
Bologna 4
Boston 4
Delhi 4
Florence 4
Hamilton 4
Nuremberg 4
Provo 4
Seoul 4
Stockholm 4
Torino 4
Turin 4
Valencia 4
Accra 3
Albuquerque 3
Ankara 3
Ballymoney 3
Cinisello Balsamo 3
Colatina 3
Totale 2.383
Nome #
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta2 promoter in breast cancer cells, file dfa8b990-eebe-748b-e053-3a05fe0a3a96 489
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, file dfa8b990-5187-748b-e053-3a05fe0a3a96 303
TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival, file dfa8b991-1b3a-748b-e053-3a05fe0a3a96 283
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms, file dfa8b98f-c6ab-748b-e053-3a05fe0a3a96 264
Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype, file dfa8b98f-b895-748b-e053-3a05fe0a3a96 250
The methylation of the TSC2 promoter underlies the abnormal growth of TSC2 angiomyolipoma-derived smooth muscle cells, file dfa8b98f-5895-748b-e053-3a05fe0a3a96 238
Endogenous reactivation of the RARbeta2 tumor suppressor gene epigenetically silenced in breast cancer, file dfa8b990-5e1a-748b-e053-3a05fe0a3a96 211
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes, file dfa8b995-f1e5-748b-e053-3a05fe0a3a96 207
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins, file dfa8b99d-8fb0-748b-e053-3a05fe0a3a96 191
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer, file dfa8b99d-ddd9-748b-e053-3a05fe0a3a96 176
Epigenetic Basis of Vitamin A Resistance in Breast Cancer. Implications for Prevention and Treatment, file dfa8b990-59ad-748b-e053-3a05fe0a3a96 175
Misbehaviour of XIST RNA in breast cancer cells, file dfa8b98f-6fb8-748b-e053-3a05fe0a3a96 173
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders, file dfa8b99c-7e70-748b-e053-3a05fe0a3a96 169
Epigenetic effects of chromatin remodeling agents on organotypic cultures, file dfa8b996-3420-748b-e053-3a05fe0a3a96 157
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry, file dfa8b99a-88d4-748b-e053-3a05fe0a3a96 152
GDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML, file dfa8b99b-058e-748b-e053-3a05fe0a3a96 139
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study, file 8b318451-dc63-410e-a441-d0778dc86835 122
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases, file dfa8b99a-4931-748b-e053-3a05fe0a3a96 118
Extensive placental methylation profiling in normal pregnancies, file dfa8b9a6-05fd-748b-e053-3a05fe0a3a96 116
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion, file dfa8b996-dcb6-748b-e053-3a05fe0a3a96 102
DNA methylation in the diagnosis of monogenic diseases, file dfa8b9a2-149a-748b-e053-3a05fe0a3a96 99
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome, file dfa8b9a3-8db8-748b-e053-3a05fe0a3a96 97
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients, file dfa8b9a2-2082-748b-e053-3a05fe0a3a96 88
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes, file dfa8b9a9-4cb1-748b-e053-3a05fe0a3a96 80
The mammary gland and the homeobox gene Otx1, file dfa8b9a8-5d25-748b-e053-3a05fe0a3a96 75
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines, file dfa8b9a8-a051-748b-e053-3a05fe0a3a96 64
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance, file dfa8b9a7-69c9-748b-e053-3a05fe0a3a96 63
OTX1 expression in breast cancer is regulated by p53, file dfa8b9a9-1ff0-748b-e053-3a05fe0a3a96 41
Epigenetic effects of chromatin remodeling agents on organotypic cultures, file dfa8b996-b533-748b-e053-3a05fe0a3a96 34
Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model, file 07faa77c-b282-4a02-b831-5f3adb23a50c 31
The mammary gland and the homeobox gene Otx1, file dfa8b990-4e93-748b-e053-3a05fe0a3a96 19
Characterization of four microsatellites in an Italian population and their application to paternity testing, file dfa8b990-524d-748b-e053-3a05fe0a3a96 15
Role of epigenetics in human aging and longevity : genome-wide DNA methylation profile in centenarians and centenarians' offspring, file dfa8b990-503d-748b-e053-3a05fe0a3a96 11
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute, file dfa8b995-2c84-748b-e053-3a05fe0a3a96 9
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi, file dfa8b992-ec91-748b-e053-3a05fe0a3a96 8
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men, file dfa8b994-ac83-748b-e053-3a05fe0a3a96 8
Germline oncopharmacogenetics, a promising field in cancer therapy, file dfa8b996-ba01-748b-e053-3a05fe0a3a96 7
Highly sensitive chemiluminescent method for the detection of cell contamination, file dfa8b990-5473-748b-e053-3a05fe0a3a96 5
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome : a clinical, EEG, and molecular genetic study, file dfa8b990-573b-748b-e053-3a05fe0a3a96 5
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism, file dfa8b990-5a57-748b-e053-3a05fe0a3a96 5
X chromosome inactivation pattern in BRCA gene mutation carriers, file dfa8b996-a141-748b-e053-3a05fe0a3a96 5
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosis, file dfa8b997-01c5-748b-e053-3a05fe0a3a96 5
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with changes in transcriptional profiles, file dfa8b990-6756-748b-e053-3a05fe0a3a96 4
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas, file dfa8b990-4f29-748b-e053-3a05fe0a3a96 3
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma, file dfa8b990-5201-748b-e053-3a05fe0a3a96 3
Losses of heterozygosity in endometrial adenocarcinomas : positive correlations with histopathological parameters, file dfa8b990-56c5-748b-e053-3a05fe0a3a96 3
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome, file dfa8b990-c22c-748b-e053-3a05fe0a3a96 2
ESX1 gene transcript as a spermatogenesis marker in infertile men, file dfa8b996-34d9-748b-e053-3a05fe0a3a96 2
Erratum: The mammary gland and the homeobox gene otx1. (Breast Journal (2010) 16:1 (S53-S56)), file dfa8b9a8-a3a2-748b-e053-3a05fe0a3a96 2
A perspective on diet, epigenetics and complex diseases: where is the field headed next?, file fb79ffe4-9af9-4c90-9378-cc11d179dd17 2
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction, file dfa8b996-5448-748b-e053-3a05fe0a3a96 1
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome, file dfa8b99b-7fae-748b-e053-3a05fe0a3a96 1
null, file dfa8b99e-bae1-748b-e053-3a05fe0a3a96 1
Thompson & Thompson : Genetica in medicina, file dfa8b99e-ed0d-748b-e053-3a05fe0a3a96 1
The mammary gland and the homeobox gene Otx1, file dfa8b9a8-e34e-748b-e053-3a05fe0a3a96 1
OTX1 expression in breast cancer is regulated by p53, file dfa8b9a8-fb47-748b-e053-3a05fe0a3a96 1
Totale 4.836
Categoria #
all - tutte 10.134
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 10.134


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201969 0 0 0 0 0 0 0 0 0 0 0 69
2019/2020672 55 36 48 85 70 58 51 63 70 40 46 50
2020/2021588 30 56 20 67 52 58 47 53 39 60 68 38
2021/2022673 36 42 45 45 61 36 59 48 47 23 163 68
2022/2023528 19 31 164 85 27 51 16 19 14 21 68 13
2023/2024522 28 16 36 30 57 37 50 69 52 29 71 47
Totale 4.836