IRIS
RANZANI, GUGLIELMINA
 Distribuzione geografica
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Continente #
NA - Nord America 5.910
AS - Asia 3.585
EU - Europa 3.225
SA - Sud America 387
AF - Africa 130
Continente sconosciuto - Info sul continente non disponibili 112
OC - Oceania 4
Totale 13.353
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Nazione #
US - Stati Uniti d'America 5.681
CN - Cina 1.888
SG - Singapore 718
IE - Irlanda 653
UA - Ucraina 466
DE - Germania 358
HK - Hong Kong 352
FI - Finlandia 341
IT - Italia 327
RU - Federazione Russa 317
BR - Brasile 287
VN - Vietnam 248
FR - Francia 227
SE - Svezia 197
GB - Regno Unito 186
CA - Canada 115
IN - India 80
ZA - Sudafrica 74
BD - Bangladesh 59
IQ - Iraq 39
AR - Argentina 34
BE - Belgio 33
JP - Giappone 32
MX - Messico 30
PL - Polonia 27
TR - Turchia 23
ES - Italia 20
NL - Olanda 19
PK - Pakistan 19
CO - Colombia 18
EC - Ecuador 16
PH - Filippine 16
ID - Indonesia 13
CR - Costa Rica 12
PR - Porto Rico 12
AT - Austria 11
MA - Marocco 11
SA - Arabia Saudita 11
UZ - Uzbekistan 11
VE - Venezuela 11
IL - Israele 10
SV - El Salvador 10
KE - Kenya 9
NI - Nicaragua 9
AE - Emirati Arabi Uniti 8
CL - Cile 7
CW - ???statistics.table.value.countryCode.CW??? 7
EU - Europa 7
GT - Guatemala 7
JO - Giordania 7
LT - Lituania 7
AZ - Azerbaigian 6
EG - Egitto 6
HN - Honduras 6
TN - Tunisia 6
GP - Guadalupe 5
JM - Giamaica 5
KZ - Kazakistan 5
NP - Nepal 5
PE - Perù 5
TT - Trinidad e Tobago 5
DZ - Algeria 4
GR - Grecia 4
MU - Mauritius 4
PA - Panama 4
PT - Portogallo 4
UY - Uruguay 4
AU - Australia 3
CH - Svizzera 3
CI - Costa d'Avorio 3
CZ - Repubblica Ceca 3
DO - Repubblica Dominicana 3
ET - Etiopia 3
GE - Georgia 3
KG - Kirghizistan 3
OM - Oman 3
PY - Paraguay 3
RE - Reunion 3
SK - Slovacchia (Repubblica Slovacca) 3
AL - Albania 2
AW - Aruba 2
BY - Bielorussia 2
DK - Danimarca 2
EE - Estonia 2
HR - Croazia 2
IR - Iran 2
KH - Cambogia 2
LB - Libano 2
LV - Lettonia 2
MM - Myanmar 2
MY - Malesia 2
QA - Qatar 2
RS - Serbia 2
SC - Seychelles 2
TH - Thailandia 2
TJ - Tagikistan 2
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
Totale 13.232
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Città #
Chandler 662
Dublin 652
Jacksonville 508
San Jose 473
Ashburn 443
Nanjing 431
Singapore 378
Hong Kong 338
Beijing 329
Dallas 254
Council Bluffs 251
Boardman 226
Nanchang 160
Los Angeles 133
Ann Arbor 132
Princeton 130
Lawrence 126
Medford 125
Shenyang 121
Hebei 117
Lauterbourg 114
Wilmington 113
Jiaxing 105
Helsinki 98
Changsha 91
Ho Chi Minh City 90
New York 70
Tianjin 66
Shanghai 63
Johannesburg 61
Buffalo 58
Hangzhou 58
Moscow 57
Munich 57
Hanoi 56
Milan 54
Pavia 53
Santa Clara 53
Redondo Beach 46
Toronto 41
Woodbridge 41
Brooklyn 35
São Paulo 35
Verona 35
Brussels 32
Orem 32
Chicago 31
Houston 31
Tokyo 31
Atlanta 29
Montreal 24
Norwalk 24
Turku 21
Warsaw 21
Seattle 19
Chennai 18
Fairfield 17
Rome 17
Nuremberg 16
Rio de Janeiro 16
San Francisco 16
The Dalles 15
Da Nang 14
Denver 14
Frankfurt am Main 14
London 14
North Bergen 14
Phoenix 14
Falkenstein 12
Haiphong 12
Mexico City 12
Zhengzhou 12
Auburn Hills 11
Columbus 11
Des Moines 11
Kunming 11
Baghdad 10
Jinan 10
Latina 10
Tashkent 10
Washington 10
Amsterdam 9
Boston 9
Guangzhou 9
Jakarta 9
Newark 9
North Charleston 9
Queens 9
Stockholm 9
Brasília 8
Dearborn 8
Dhaka 8
Kolkata 8
Managua 8
Manchester 8
Nairobi 8
New Delhi 8
Cape Town 7
Hải Dương 7
Miami 7
Totale 8.332
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Nome #
Analysis and clinical implications of p53 gene mutations and human papillomavirus type 16 and 18 infection in primary adenocarcinoma of the uterine cervix 181
Caratterizzazione funzionale di mutazioni del gene MYH associate a poliposi adenomatosa familiare del colon. 178
Analysis and clinical implications of K-ras gene mutations and infection with human papillomavirus types 16 and 18 in primary adenocarcinoma of the uterine cervix 165
Caratterizzazione citogenetico-molecolare di estese delezioni di APC in pazienti con poliposi 164
Cancer incidence in eastern Adriatic isolates, Croatia: examples from the islands of Krk, Cres, Losinj, Rab and Pag 164
Gut Microbiota Analysis in Postoperative Lynch Syndrome Patients 158
Ricerca di mutazioni del gene MYH in pazienti con poliposi attenuata ed in soggetti di controllo, italiani e greci. 157
Molecular-cytogenetic characterization of APC (Adenomatous Polyposis Coli) gene deletions by means of “DNA combing” 157
CARATTERIZZAZIONE CITOGENETICO-MOLECOLARE DI DELEZIONI DEL GENE APC (ADENOMATOUS POLYPOSIS COLI) MEDIANTE “DNA COMBING” 156
Analysis and clinical implications of p53 gene mutations and human papillomavirus type 16 and 18 infection in primary adenocarcinoma of the uterine cervix. 147
Understanding the role of the Q338H MUTYH variant in oxidative damage repair. 146
Characterization of mutations in the base excision repair MYH (MUTYH) gene associated with familial adenomatous polyposis. 144
APC haploinsufficiency, but not CTNNB1 or CDH1 gene mutations, accounts for a fraction of familial adenomatous polyposis patients without APC truncating mutations 143
“COMBING” DI SINGOLE MOLECOLE DI DNA PER IDENTIFICARE RIARRANGIAMENTI DEL LOCUS APC UMANO 142
Effects of topoisomerase II inhibitors on gastric cancer cells characterized by different genetic lesions 140
MUTYH mutations associated with familial adenomatous polyposis: functional characterization by a mammalian cell-based assay 140
A novel APC promoter 1B deletion shows a founder effect in Italian patients with classical familial adenomatous polyposis phenotype 140
Caratterizzazione di delezioni del gene APC in pazienti con poliposi adenomatosa familiare del colon 139
K-ras gene mutations: an unfavorable prognostic marker in stage I lung adenocarcinoma 136
Frameshift mutations of human gastrin receptor gene (hGARE) in gastrointestinal cancers with microsatellite instability 129
Morphine metabolism, transport and brain disposition 129
Microsatellite instability in intestinal- and diffuse-type gastric carcinoma 127
Shifts of Faecal Microbiota During Sporadic Colorectal Carcinogenesis 127
Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis 126
Genetic variability at COMT but not at OPRM1 and UGT2B7 loci modulates morphine analgesic response in acute postoperative pain. 125
p53 codon 72 polymorphism does not affect the risk of cervical cancer in patients from northern Italy 124
A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. 124
Primary retroperitoneal mucinous cystoadenocarcinomas: an immunohistochemical and molecular study 124
Functional analysis and case-control study of -160C/A polymorphism in the E-cadherin gene promoter: association with cancer risk 123
Genetics of colorectal polyps 122
Colorectal Adenomatous Polyposis: Heterogeneity of Susceptibility Gene Mutations and Phenotypes in a Cohort of Italian Patients 122
K-ras and p53 gene mutations in pancreatic cancer: ductal and nonductal tumors progress through different genetic lesions 122
Intestinal and diffuse gastric cancers arise in a different background of Helicobacter pylori gastritis through different gene involvement 121
A novel endonuclease of human cells specific for single-stranded DNA 121
A study of several genetic biochemical markers in Sherpas with description of some variant phenotypes 120
Molecular combing for the detection of rearrangements involving the human APC locus 120
APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes 119
Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis 118
Elevata espressione costitutiva di un trascritto del gene APC dovuto a splicing alternativo tra gli esoni 10 e 15 in pazienti con poliposi. 116
Molecular mechanisms involved in the pathogenesis of gastric carcinoma: interactions between genetic alterations, cellular phenotype and cancer histotype 116
How and why to screen for CYP2D6 interindividual variability in patients under pharmacological treatments 115
Analisi mediante MLPA del gene APC in pazienti italiani e greci con diagnosi di poliposi attenuata. 115
Intraductal papillary-mucinous tumours represent a distinct group of pancreatic neoplasms: an investigation of tumour cell differentiation and K-ras, p53 and c-erbB-2 abnormalities in 26 patients. 114
Oxycodone pain management in cytochrome p450-impaired patients. 114
F-Cell distribution in normals and in Heterocellular HPFH (Swiss Type) 114
Ki-ras and p53 gene mutations in pancreatic ductal carcinoma: a relationship with tumor phenotype and survival 113
A 5'-truncated c-myc gene variant not associated with a risk of cancer 112
High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis 112
A study of ten red cell enzymatic markers in the Naples' population. Report of a new GPT variant phenotype. 111
Detection of a CDH1 rare transcript variant in fresh-frozen gastric cancer tissues by chip-based digital PCR 111
Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH 110
p53 gene mutations and protein nuclear accumulation are early events in intestinal type gastric cancer but late events in diffuse type 110
Genetic pattern, histological structure, and cellular phenotype in early and advanced gastric cancers: evidence for structure-related genetic subsets and for loss of glandular structure during progression of some tumors 110
Genetic events in sporadic colorectal adenomas; K-ras and p53 heterozygous mutations are not sufficient for malignant progression 110
Involvement of MYH in colorectal polyposis: where are we? 109
E-cadherin downregulation and microRNAs in sporadic intestinal-type gastric cancer 109
Hereditary diffuse gastric cancer in two families: A case report 108
Digital PCR identifies changes in CDH1 (E-cadherin) transcription pattern in intestinal-type gastric cancer 107
Absence of microsatellite instability in breast carcinomas with both p53 and c-erbB-2 alterations 105
Red cell and serum polymorphisms in the Oltrepò Pavese population (northern Italy) 105
Complementary molecular approaches reveal heterogeneous CDH1 germline defects in Italian patients with hereditary diffuse gastric cancer (HDGC) syndrome. 104
The polymorphism of red cell uridine monophosphate kinase in two samples of the Italian population 103
Base transitions are the most frequent genetic changes at P53 in gastric cancer 103
Loss of heterozygosity and K-ras gene mutations in gastric cancer 102
A study of several red cell enzyme markers in two samples of the Italian population. Report of new CA1 and PGD variant phenotypes 102
An analysis of red cell enzymatic markers in the province of Bologna (Italy) 102
Multigene Panel Testing Increases the Number of Loci Associated with Gastric Cancer Predisposition 102
Rb and TP53 pathway alterations in sporadic and NF1-related malignant peripheral nerve sheath tumors 101
Oxidative DNA damage drives carcinogenesis in MUTYH-associated-polyposis by specific mutations of mitochondrial and MAPK genes. 101
Study on aneuploidy and p53 mutations in astrocytomas 100
Heterogeneous protooncogene amplification correlates with tumor progression and presence of metastases in gastric cancer patients 100
Genetica molecolare dei tumori e nuovi approcci terapeutici. 99
Cytokine gene polymorphisms in gastric cancer patients from two Italian areas at high and low cancer prevalence 99
MUTYH-associated polyposis (MAP), the syndrome implicating Base Excision Repair in inherited predisposition to colorectal tumors 99
Rapid assessment of replication error phenotype in gastric cancer 98
Loss of heterozygosity for chromosome 11 in adenocarcinoma of the stomach. 98
Microsatellite instability in colorectal-cancer patients with suspected genetic predisposition 97
Red cell glyoxalase I polymorphism in Italians. Report of a variant phenotype 95
Constitutional high expression of an APC mRNA isoform in a subset of attenuated familial adenomatous polyposis patients 95
Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer 94
Clinical pharmacokinetics of morphine and its metabolites during morphine dose titration for chronic cancer pain. 94
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing 94
Influence of COMT Val158Met Polymorphism on Alzheimer's Disease and Mild Cognitive Impairment in Italian Patients. 92
DNA amplification in human gastric carcinomas 91
The significance of p53 mutations in human cancers 91
Subtyping of phosphoglucomutase locus 1 (PGM1) polymorphism in some populations of Rwanda: description of variant phenotypes, "haplotype" frequencies, and linkage disequilibrium data 89
Subtyping of human red cell phosphoglucomutase locus 1 (PGM1) polymorphism: a third PGM1(1) allele common among Twa Pygmies from North Rwanda 89
Oxidative damage repair and protein-protein interactions of the Q338H MUTYH polymorphic variant 89
Population genetic studies in Sikkim 88
Individualizing pain therapy with opioids: The rational approach based on pharmacogenetics and pharmacokinetics 88
TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studies 88
Surname as 'cancer risk' in extreme isolates: example from the island of Lastovo, Croatia 87
Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect 87
Somatic frameshift mutations in the Bloom syndrome BLM gene are frequent in sporadic gastric carcinomas with microsatellite mutator phenotype 87
Microsatellite instability and mutations of p53 and TGF-beta RII genes in gastric cancer 86
Effect of apoptogenic stimuli on colon carcinoma cell lines with a different c-myc expression level 86
Gene amplification and proliferative kinetics in relation to prognosis of patients with gastric carcinoma 86
Identification and classification of Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome): adapting old concepts to recent advancements.Report from the Italian Association for the Study of Hereditary Colorectal Tumors Consensus Group 85
Understanding the role of a polymorphic MUTYH variant in oxidative damage repair 84
Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes 82
Totale 11.443
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Categoria #
all - tutte 56.122
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 56.122
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022548 0 0 0 0 12 24 15 49 39 18 81 310
2022/20231.870 201 131 21 148 209 193 2 111 768 15 42 29
2023/2024579 89 117 17 56 52 116 4 49 8 11 21 39
2024/20251.699 41 159 43 52 19 80 71 169 431 56 161 417
2025/20263.672 296 282 370 348 529 219 687 149 302 315 91 84
2026/20271.273 138 205 292 459 179 0 0 0 0 0 0 0
Totale 13.353