IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

COLAPIETRO, PATRIZIA
 Distribuzione geografica
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Continente #
EU - Europa 4.815
NA - Nord America 2.483
AS - Asia 1.301
SA - Sud America 35
OC - Oceania 19
AF - Africa 7
Continente sconosciuto - Info sul continente non disponibili 4
Totale 8.664
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Nazione #
US - Stati Uniti d'America 2.374
GB - Regno Unito 2.051
IT - Italia 894
CN - Cina 591
DE - Germania 571
SE - Svezia 490
SG - Singapore 189
IN - India 162
RU - Federazione Russa 158
FR - Francia 113
CA - Canada 102
UA - Ucraina 95
IE - Irlanda 92
FI - Finlandia 90
TR - Turchia 81
HK - Hong Kong 70
KR - Corea 70
DK - Danimarca 54
NL - Olanda 54
ID - Indonesia 43
JP - Giappone 40
EU - Europa 32
GR - Grecia 32
BE - Belgio 27
ES - Italia 20
CO - Colombia 19
AU - Australia 18
PL - Polonia 14
NO - Norvegia 12
VN - Vietnam 12
CH - Svizzera 11
CZ - Repubblica Ceca 10
RO - Romania 10
BR - Brasile 7
MX - Messico 7
PH - Filippine 7
IL - Israele 6
IR - Iran 6
TW - Taiwan 5
UZ - Uzbekistan 5
PE - Perù 4
PT - Portogallo 4
SA - Arabia Saudita 4
SC - Seychelles 4
AT - Austria 3
AR - Argentina 2
HU - Ungheria 2
MM - Myanmar 2
QA - Qatar 2
RS - Serbia 2
SI - Slovenia 2
VE - Venezuela 2
XK - ???statistics.table.value.countryCode.XK??? 2
AE - Emirati Arabi Uniti 1
CL - Cile 1
EE - Estonia 1
GH - Ghana 1
HR - Croazia 1
KE - Kenya 1
KW - Kuwait 1
LB - Libano 1
LT - Lituania 1
MK - Macedonia 1
MY - Malesia 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
TH - Thailandia 1
Totale 8.694
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Città #
Southend 1.960
Chandler 339
Milan 318
Frankfurt am Main 276
Seattle 138
Fairfield 126
Ashburn 124
Beijing 122
Wilmington 121
Princeton 120
Singapore 120
Dearborn 110
Ann Arbor 101
Dublin 92
Houston 90
Woodbridge 88
Nanjing 64
Mountain View 60
Hong Kong 56
Toronto 56
Jacksonville 54
Cambridge 51
Helsinki 46
Redmond 43
Bengaluru 41
Redwood City 39
Des Moines 37
Shanghai 36
Rome 33
Berlin 31
Boardman 30
Athens 29
New York 28
Phoenix 28
Jakarta 27
Sakarya 27
Guangzhou 25
Chicago 24
Andover 23
Ottawa 23
Hanover 21
Jinan 21
Shenyang 21
Verona 21
Falls Church 20
Nanchang 20
Brussels 19
Bühl 18
Somerville 18
Turin 18
Bogotá 17
Santa Clara 17
Serra 17
Istanbul 15
Zhengzhou 15
Eitensheim 14
Hebei 14
San Diego 14
Tianjin 12
Changsha 11
Jiaxing 11
Bologna 10
Hamburg 10
Mumbai 10
Ningbo 10
Pavia 10
Silver Spring 10
Tokyo 10
Brno 9
Fremont 9
Hangzhou 9
Lainate 9
Medford 9
Roxbury 9
Auburn Hills 8
Kunming 8
Lanzhou 8
Lodi 8
Los Angeles 8
Palermo 8
Sunnyvale 8
Taizhou 8
Waanrode 8
Barcelona 7
Hefei 7
Kiez 7
London 7
Monza 7
Norwalk 7
Nürnberg 7
Paris 7
Vancouver 7
Warsaw 7
Aprilia 6
Carini 6
Cincinnati 6
Florence 6
Naples 6
Nashua 6
Philadelphia 6
Totale 5.818
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Nome #
KIT activating mutations : incidence in adult and pediatric AML, and identification of an internal tandem duplication 436
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 288
Smith-Magenis sindrome and growth hormone deficiency 275
Mismatch repair protein loss as a prognostic and predictive biomarker in breast cancers regardless of microsatellite instability 266
X chromosome inactivation pattern in BRCA gene mutation carriers 250
Rubinstein-Taybi syndrome : spectrum of CREBBP mutations in Italian patients. 247
Duplicazioni parziali di SHOX associate alla Sindrome di Mayer-Rokitansky-Kuster-Hauser 242
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 224
NUOVE MUTAZIONI PUNTIFORMI E DELEZIONI ESONICHE DEL GENE EP300 IN PAZIENTI CON SINDROME DI RUBINSTEIN-TAYBI 222
The expression pattern of small nucleolar and small cajal body-specific RNAS characterizes distinct molecular subtypes of multiple myeloma 220
DELEZIONI IN 16p13.2 COINVOLGENTI TOTALMENTE O PARZIALMENTE IL GENE CREBBP IN PAZIENTI CON SINDROME DI RUBINSTEIN-TAYBI 213
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene 212
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions 210
From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients : New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks 198
Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34(+)38(-) compartment 197
SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome 194
Transferrin Receptor 1 protein expression and localization in human IntraUterine Growth Restriction placentas 190
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas 183
SNAT2 expression and regulation in human growth restricted placentas 179
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction 173
TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival 171
Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome : an update of the CREBBP deletion repertoire 169
APPROCCI TECNOLOGICI MULTIPLI PER L'IDENTIFICAZIONE DI MUTAZIONI E MECCANISMI PATOGENETICI IN PAZIENTI CON SINDROME DI RUBINSTEIN-TAYBI 168
Transferrin receptor gene and protein expression and localization in human IUGR and normal term placentas 165
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi Syndrome patients 161
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 159
Genotype-phenotype correlation in patients with NF1 microdeletion syndrome : identification of candidate genes for mental retardation 156
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms 155
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome 154
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men 148
Distinct expression pattern of microtubule-associated protein/microtubule affinity-regulating kinase 4 in differentiated neurons 143
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 143
NEW POINTMUTATIONS AND EXON DELETIONS OF THE EP300 GENE IN PATIENTS WITH RUBINSTEIN-TAYBI SYNDROME 141
Extensive placental methylation profiling in normal pregnancies 141
NF1 exon 7 skipping by disruption of exonic splice enhancers (ESEs) in neurofibromatosis 1 137
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 135
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 133
Sodium coupled Neutral Aminoacid Transporter 2 (SNAT2) Intron1 methylation levels and Single Nucleotide Polymorphism in IUGR placentas 132
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements 130
Molecular screening of PDGFRA and PDGFRB genes in KIT and FLT3 negative core binding factor leukemias 126
Prevalence and prognostic impact of KIT mutations in acute myeloid leukaemia with inv(16). A retrospective study 120
Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorfism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation 118
Prognostic impact of c-KIT mutations in core binding factor leukemias. an Italian retrospective study 118
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements 117
IMPACT OF KIT MUTATIONS IN ACUTE MYELOID LEUKAEMIA WITH INV(16) 115
Serum tryptase levels in AML at diagnosis : a multicenter retrospective study 108
Mismatch repair protein loss is a prognostic and predictive biomarker in breast cancers regardless of microsatellite instability 106
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls 105
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 101
KIT mutations in core binding factor leukemias: outcome prediction and therapeutic implications 95
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 93
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study 71
Circulating microRNAs Suggest Networks Associated with Biological Functions in Aggressive Refractory Type 2 Celiac Disease 56
Mental health and the effects on methylation of stress-related genes in front-line versus other health care professionals during the second wave of COVID-19 pandemic: an Italian pilot study 56
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology 52
Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorphism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation 37
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis 26
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines 13
Totale 9.093
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Categoria #
all - tutte 24.763
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 24.763
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020891 0 0 0 121 89 113 157 77 113 134 46 41
2020/20211.032 74 61 59 47 97 71 58 64 130 88 208 75
2021/20221.258 105 75 100 97 100 85 100 60 152 87 105 192
2022/20231.276 180 174 102 130 126 194 58 77 106 30 64 35
2023/20241.015 40 48 68 70 239 77 65 89 33 66 97 123
2024/2025363 117 159 72 15 0 0 0 0 0 0 0 0
Totale 9.093