IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

MIOZZO, MONICA ROSA
 Distribuzione geografica
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Continente #
EU - Europa 17.210
NA - Nord America 14.481
AS - Asia 11.904
Continente sconosciuto - Info sul continente non disponibili 1.690
SA - Sud America 1.053
AF - Africa 268
OC - Oceania 66
Totale 46.672
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Nazione #
US - Stati Uniti d'America 13.823
GB - Regno Unito 5.533
IT - Italia 4.815
CN - Cina 3.756
SG - Singapore 3.156
DE - Germania 1.577
SE - Svezia 1.252
BD - Bangladesh 1.189
HK - Hong Kong 1.048
RU - Federazione Russa 990
VN - Vietnam 918
BR - Brasile 763
NL - Olanda 669
FR - Francia 624
IN - India 498
CA - Canada 466
FI - Finlandia 341
IE - Irlanda 322
TR - Turchia 304
UA - Ucraina 262
KR - Corea 237
ID - Indonesia 206
JP - Giappone 155
DK - Danimarca 143
ES - Italia 115
CI - Costa d'Avorio 105
MX - Messico 94
BE - Belgio 85
PL - Polonia 85
EU - Europa 79
AR - Argentina 75
CO - Colombia 75
CH - Svizzera 69
AT - Austria 61
AU - Australia 57
IQ - Iraq 56
PH - Filippine 55
TW - Taiwan 46
GR - Grecia 41
ZA - Sudafrica 38
NO - Norvegia 37
EC - Ecuador 34
UZ - Uzbekistan 32
CL - Cile 31
RO - Romania 30
CZ - Repubblica Ceca 27
IR - Iran 27
SA - Arabia Saudita 27
KE - Kenya 22
PT - Portogallo 22
PE - Perù 20
PK - Pakistan 20
EG - Egitto 19
JM - Giamaica 19
MY - Malesia 19
VE - Venezuela 19
AE - Emirati Arabi Uniti 17
KZ - Kazakistan 17
LU - Lussemburgo 17
MA - Marocco 16
TH - Thailandia 14
HU - Ungheria 13
JO - Giordania 13
NI - Nicaragua 13
AL - Albania 12
BO - Bolivia 12
CR - Costa Rica 12
PY - Paraguay 12
GT - Guatemala 11
HR - Croazia 11
LB - Libano 11
LT - Lituania 11
NG - Nigeria 11
PS - Palestinian Territory 11
TN - Tunisia 11
UY - Uruguay 11
DZ - Algeria 10
LV - Lettonia 9
NP - Nepal 9
NZ - Nuova Zelanda 9
SC - Seychelles 9
IL - Israele 8
PR - Porto Rico 8
TT - Trinidad e Tobago 8
AZ - Azerbaigian 7
OM - Oman 7
KG - Kirghizistan 6
KW - Kuwait 6
MO - Macao, regione amministrativa speciale della Cina 6
RS - Serbia 6
SI - Slovenia 6
SK - Slovacchia (Repubblica Slovacca) 6
HN - Honduras 5
BG - Bulgaria 4
ET - Etiopia 4
KH - Cambogia 4
SN - Senegal 4
SV - El Salvador 4
AM - Armenia 3
AO - Angola 3
Totale 44.995
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Città #
Southend 5.181
Singapore 1.828
Ashburn 1.685
Milan 1.371
Hong Kong 962
Chandler 932
San Jose 781
Council Bluffs 699
Frankfurt am Main 644
Beijing 605
Dallas 579
Seattle 528
Santa Clara 495
Fairfield 488
Ann Arbor 444
Wilmington 404
Los Angeles 379
Princeton 349
New York 330
Dublin 317
Woodbridge 308
Dearborn 298
Houston 271
Ho Chi Minh City 256
Boardman 233
Hanoi 218
Nanjing 207
Cambridge 206
Rome 206
Buffalo 190
Moscow 186
Hefei 182
Lauterbourg 181
Guangzhou 178
Toronto 171
Helsinki 169
Shanghai 169
Bengaluru 166
Jacksonville 151
Jakarta 146
The Dalles 138
Mountain View 118
Redwood City 114
Phoenix 113
Des Moines 112
Redmond 108
Abidjan 104
Columbus 100
Turin 88
Berlin 87
Munich 87
São Paulo 86
Naples 83
Jinan 78
Tokyo 78
Shenyang 75
Cangzhou 74
Hanover 74
Chicago 73
Serra 72
Tianjin 68
Seoul 67
Brussels 64
Istanbul 64
Sakarya 63
Hangzhou 59
Changsha 58
Verona 58
Hebei 55
San Diego 55
Atlanta 50
Bogotá 50
Nuremberg 50
Ottawa 50
London 48
Mumbai 48
Nanchang 48
Andover 47
Florence 47
Zhengzhou 47
Montreal 44
Bologna 42
Brooklyn 42
Palermo 42
Fuzhou 41
Warsaw 41
Shenzhen 40
Da Nang 39
Dong Ket 38
Washington 38
Haiphong 36
Orem 35
Paris 33
Somerville 32
Falls Church 31
Roxbury 31
Athens 30
Philadelphia 29
Rio de Janeiro 29
Silver Spring 29
Totale 26.773
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Nome #
A second update on mapping the human genetic architecture of COVID-19 1.573
Mapping the human genetic architecture of COVID-19 1.267
Mitochondrial DNA content and methylation in fetal cord blood of pregnancies with placental insufficiency 761
Impact of Mutation Density and Heterogeneity on Papillary Thyroid Cancer Clinical Features and Remission Probability 696
Genomewide Association Study of Severe Covid-19 with Respiratory Failure 648
The Adipose Mesenchymal Stem Cell Secretome Inhibits Inflammatory Responses of Microglia : Evidence for an Involvement of Sphingosine-1-Phosphate Signalling 472
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 437
Mismatch repair protein loss as a prognostic and predictive biomarker in breast cancers regardless of microsatellite instability 423
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 421
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 415
The Genetic Landscape of Human Glioblastoma and Matched Primary Cancer Stem Cells Reveals Intratumour Similarity and Intertumour Heterogeneity 415
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 397
X chromosome inactivation pattern in BRCA gene mutation carriers 394
Thompson & Thompson : Genetica in medicina 382
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry 381
Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System Atrophy 373
X chromosome monosomy : a common mechanism for autoimmune diseases 370
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 366
SARS-CoV-2 specific serological pattern in healthcare workers of an Italian COVID-19 forefront hospital 352
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies 343
Misbehaviour of XIST RNA in breast cancer cells 341
Prognostic value of preoperative von Willebrand factor plasma levels in patients with Glioblastoma 341
The expression pattern of small nucleolar and small cajal body-specific RNAS characterizes distinct molecular subtypes of multiple myeloma 336
Molecular Insights into the Classification of Luminal Breast Cancers : the Genomic Heterogeneity of Progesterone-Negative Tumors 336
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis 332
Epigenetic effects of chromatin remodeling agents on organotypic cultures 331
Mass spectrometry-based assay for the molecular diagnosis of glioma : Concomitant detection of chromosome 1p/19q codeletion, and IDH1, IDH2, and TERT mutation status 326
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 323
Angiogenesis in human brain tumors : screening of drug response through a patient-specific cell platform for personalized therapy 317
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 317
Human cholangiocarcinoma development is associated with dysregulation of opioidergic modulation of cholangiocyte growth 315
Duplicazioni parziali di SHOX associate alla Sindrome di Mayer-Rokitansky-Kuster-Hauser 314
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 313
Women victims of intimate partner violence: psychological aspects and future epigenetics perspectives 309
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 307
A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability : a case report 307
Transferrin Receptor 1 protein expression and localization in human IntraUterine Growth Restriction placentas 305
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 302
X monosomy in female systemic lupus erythematosus 300
Placental IGF2 expression in normal and intrauterine growth restricted (IUGR) pregnancies 297
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction 297
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases 296
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells 293
Extensive placental methylation profiling in normal pregnancies 291
SNAT2 expression and regulation in human growth restricted placentas 286
Fetal growth restriction : a workshop report 286
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes 284
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 284
DNA methylation in the diagnosis of monogenic diseases 284
Placental LPL gene expression is increased in severe intrauterine growth-restricted pregnancies 279
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 278
Fragile X syndrome : A review of clinical and molecular diagnoses 277
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients 277
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome 275
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas 274
19p deletion in recurring leiomyosarcoma lesions from the same patient 273
EpiWE project, the molecular signature of violence in women’s victim genome 273
Epigenetics of functional hypothalamic amenorrhea 272
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies 270
ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic men 267
Transferrin receptor gene and protein expression and localization in human IUGR and normal term placentas 267
Angiotensin-converting enzyme and adducin-1 polymorphisms in women with preeclampsia and gestational hypertension 266
Frequency of monosomy X in women with primary biliary cirrhosis 265
SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome 265
The Genetic Basis, Lung Involvement, and Therapeutic Options in Niemann–Pick Disease: A Comprehensive Review 264
Assessment of X chromosome Inactivation pattern in BRCA mutation carriers : evidence for an effect of chemotherapy 264
Three cases with de novo 6q imbalance and variable prenatal phenotype 262
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosis 262
Genome-wide analysis of DNA methylation, copy number variation, and gene expression in monozygotic twins discordant for primary biliary cirrhosis 262
Role of polymorphisms of toll-like receptor (TLR) 4, TLR9, toll-interleukin 1 receptor domain containing adaptor protein (TIRAP) and FCGR2A genes in malaria susceptibility and severity in Burundian children 262
Nutrizione nelle prime epoche della vita : Ruolo della genetica e dell’epigenetica 259
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study 259
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion 258
Males with primary biliary cirrhosis manifest enhanced rates of Y chromosome loss compared to healthy subjects 257
Decreased serum level of sphingosine-1-phosphate: a novel predictor of clinical severity in COVID-19 257
Investigating the Impact of Epstein-Barr Virus on Sphingolipid Composition in Extracellular Vesicles of Multiple Sclerosis Patients 256
Delineating the Cytogenomic and Epigenomic Landscapes of Glioma Stem Cell Lines 255
Misbehaviour of XIST RNA in breast cancer cells 255
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men 255
Genetic polymorphisms and sepsis in premature neonates 252
Aspirin Affects Tumor Angiogenesis and Sensitizes Human Glioblastoma Endothelial Cells to Temozolomide, Bevacizumab, and Sunitinib, Impairing Vascular Endothelial Growth Factor-Related Signaling 252
Ruolo di BRCA1 nella regolazione dell’espressione del gene XIST 249
Y chromosome loss in male patients with primary biliary cirrhosis 248
Dysmorphologic assessment in 115 Mayer-Rokitansky-Küster-Hauser patients 247
MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma : the PTC-MA assay 244
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms 243
Ruolo di ESX1L nella spermatogenesi umana 242
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36 240
Insulin-like growth factor II (IGF2) and H19 expression in IUGR 238
Biomarker testing implementation for molecularly targeted therapy in non-small cell lung cancer patients 237
First cytogenetic study of a recurrent familial chordoma of the clivus 237
Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression 237
Analysis of BRCA1 and RAD51C promoter methylation in italian families at high-risk of breast and ovarian cancer 235
Mismatch repair protein loss is a prognostic and predictive biomarker in breast cancers regardless of microsatellite instability 234
High-phosphate Causes Endothelial Extracellular Matrix Calcification by Inducing Endothelial Cell Mesenchymal Transition and Osteoblastic Differentiation 233
Mesenchymal stem cells : potential for therapy and treatment of chronic non-healing skin wounds 229
Males with primary biliary cirrhosis manifest enhanced rates of Y chromosome loss in peripheral white blood cells 228
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls 226
Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele : new highlights on phenotype-genotype correlations in Beckwith-Wiedemann syndrome 225
X chromosome inactivation defects and breast tumorigenesis 223
Totale 32.820
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Categoria #
all - tutte 120.234
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 120.234
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20223.138 0 249 264 299 220 204 234 176 396 245 282 569
2022/20233.551 489 440 307 353 382 572 163 217 307 64 174 83
2023/20242.738 108 172 171 232 631 200 213 191 78 170 250 322
2024/20256.330 252 540 245 647 418 335 332 642 433 699 613 1.174
2025/202614.489 1.211 881 1.354 1.063 1.222 989 1.931 704 1.427 933 1.591 1.183
2026/20271.810 951 859 0 0 0 0 0 0 0 0 0 0
Totale 46.672