IRIS UniCatt

Minucci, Angelo
 Distribuzione geografica
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Continente #
EU - Europa 3.572
NA - Nord America 3.417
AS - Asia 1.614
SA - Sud America 281
AF - Africa 51
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 5
Totale 8.950
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Nazione #
US - Stati Uniti d'America 3.369
DE - Germania 994
SE - Svezia 725
IT - Italia 633
CN - Cina 589
SG - Singapore 563
BR - Brasile 259
UA - Ucraina 248
FR - Francia 228
IE - Irlanda 179
IN - India 141
FI - Finlandia 127
GB - Regno Unito 123
ID - Indonesia 120
RU - Federazione Russa 87
NL - Olanda 64
TR - Turchia 48
KR - Corea 41
BE - Belgio 32
CI - Costa d'Avorio 32
CA - Canada 29
PL - Polonia 28
AT - Austria 26
IR - Iran 22
HK - Hong Kong 19
CZ - Repubblica Ceca 15
JP - Giappone 14
VN - Vietnam 13
AR - Argentina 9
RO - Romania 9
CH - Svizzera 8
IQ - Iraq 8
ES - Italia 7
EU - Europa 7
MX - Messico 6
EE - Estonia 5
LT - Lituania 5
MA - Marocco 5
PE - Perù 5
AZ - Azerbaigian 4
DK - Danimarca 4
EC - Ecuador 4
LV - Lettonia 4
PT - Portogallo 4
TN - Tunisia 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AE - Emirati Arabi Uniti 3
AU - Australia 3
EG - Egitto 3
HU - Ungheria 3
IL - Israele 3
KG - Kirghizistan 3
MD - Moldavia 3
PA - Panama 3
PH - Filippine 3
RS - Serbia 3
BD - Bangladesh 2
BG - Bulgaria 2
CO - Colombia 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
HN - Honduras 2
JM - Giamaica 2
LK - Sri Lanka 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PK - Pakistan 2
PS - Palestinian Territory 2
SA - Arabia Saudita 2
UZ - Uzbekistan 2
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CY - Cipro 1
ET - Etiopia 1
GE - Georgia 1
HR - Croazia 1
KE - Kenya 1
KH - Cambogia 1
KZ - Kazakistan 1
LU - Lussemburgo 1
ML - Mali 1
MY - Malesia 1
PY - Paraguay 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
SV - El Salvador 1
TH - Thailandia 1
TJ - Tagikistan 1
TM - Turkmenistan 1
ZA - Sudafrica 1
Totale 8.950
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Città #
Chandler 734
Singapore 349
Ashburn 329
Dublin 178
San Mateo 161
Jacksonville 148
Rome 144
New York 126
Jakarta 117
Milan 114
Nanjing 94
Ann Arbor 89
Wilmington 86
The Dalles 73
Hyderabad 72
Boston 70
Helsinki 69
Cattolica 63
Moscow 56
Woodbridge 56
Los Angeles 51
Dearborn 48
Beijing 46
Hefei 46
Princeton 46
Bremen 45
Nürnberg 45
Izmir 43
Seattle 40
Lawrence 38
Munich 38
Seoul 38
Lancaster 34
Marseille 34
Nanchang 34
Abidjan 32
Frankfurt am Main 32
Chicago 31
Redwood City 31
Houston 30
Boardman 29
Fairfield 25
Düsseldorf 24
São Paulo 24
Lauterbourg 22
Mountain View 22
Shanghai 22
Hangzhou 21
Shenyang 20
Leawood 19
Nuremberg 19
Brussels 17
Hebei 17
Kunming 17
University Park 17
Hong Kong 16
Jiaxing 16
Zhengzhou 16
Augusta 15
London 15
Vienna 15
Tianjin 14
Guangzhou 13
Kraków 13
Naples 13
Toronto 13
North Bergen 12
Portsmouth 11
Pune 11
Waanrode 11
Belo Horizonte 10
Changsha 10
Falkenstein 10
Ottawa 10
Andover 9
Busto Arsizio 9
Hanoi 9
Norwalk 9
Enterprise 8
Lanzhou 8
Washington 8
Amsterdam 7
Detroit 7
Paris 7
Santa Clara 7
Warsaw 7
Bari 6
Brno 6
Buffalo 6
Cambridge 6
Henderson 6
Kish 6
Mumbai 6
Philadelphia 6
Turku 6
Bologna 5
Chengdu 5
Des Moines 5
Edinburgh 5
Florianópolis 5
Totale 4.643
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Nome #
Homocysteine lowering by folate-rich diet or pharmacological supplementations in subjects with moderate hyperhomocysteinemia 190
Alterations of energy metabolism and metabolism and glutathione levels af HL-60 cells induced by methacrylates present in composite resins 164
Effetto di monomeri metacrilici delle resine composite per uso odontoiatrico sul metabolismo redox del glutatione 164
Small Amplicons High Resolution Melting Analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population 160
Basic and Preclinical Research for Personalized Medicine 159
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation 146
DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism 146
Incidental Finding of a Homozygous p.M348K Asymptomatic Italian Patient Confirms the Many Faces of Cystic Fibrosis 145
Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia 142
A preliminary Quality Control (QC) for next generation sequencing (NGS) library evaluation turns out to be a very useful tool for a rapid detection of BRCA1/2 deleterious mutations 141
Multidisciplinary team for elucidation of any new mutation and how this approach can be useful to individualize any genetic result: the case of BRCA2 c.631G > A/c.7008-2A > T genotype 125
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement 124
A new founder BRCA1 haplotype identified in the Puglia region is associated with a specific age-related cancer onset in three unrelated families 122
Advanced tools for BRCA1/2 mutational screening: Comparison between two methods for large genomic rearrangements (LGRs) detection 120
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants 118
Role of distinct phospholipases A2 and their modulators in meconium aspiration syndrome in human neonates. 115
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: Comparison of two methods and implications in molecular diagnostics 112
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms? 108
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration. 105
Comparing different methods for homocysteine determination 105
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome 101
Inhibition of salivary enzymes by cigarette smoke and the protective role of glutathione 100
A rare case of juvenile hypertension: coexistence of type 2 multiple endocrine neoplasia -related bilateral pheochromocytoma and reninoma in a young patient with ACE gene polymorphism 100
Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants 99
Clinical and biological role of secretory phospholipase A2 in acute respiratory distress syndrome infants 98
High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism 97
Secretory phospholipase A₂ pathway during pediatric acute respiratory distress syndrome: a preliminary study. 97
Is Homocysteine a pro-oxidant ? 97
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the "old" and update of the new mutations 97
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia 96
Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population 91
A Prolonged Neonatal Jaundice Associated With a Rare G6PD Mutation 90
Molecular profile of brca-negative long survivor high grade serous ovarian cancer patients using a somatic multigene panel 90
Identification of RFLP G6PD mutations by using microcapillary electrophoretic chips (Experion(TM)). 88
Competitive PCR-High Resolution Melting Analysis (C-PCR-HRMA) for large genomic rearrangements (LGRs) detection: A new approach to assess quantitative status of BRCA1 gene in a reference laboratory 88
A rapid screening of a recurrent CYP24A1 pathogenic variant opens the way to molecular testing for Idiopathic Infantile Hypercalcemia (IIH) 87
A novel CYP24A1 genotype associated to a clinical picture of hypercalcemia, nephrolithiasis and low bone mass 87
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 86
Rapid UGT1A1 (TA)(n) genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosis 86
Ex Vivo Effect of Varespladib on Secretory Phospholipase A2 Alveolar Activity in Infants with ARDS 86
Red blood cell PK deficiency: An update of PK-LR gene mutation database 86
A whole germline BRCA2 gene deletion: How to learn from CNV in silico analysis 85
Feasibility of tumor testing for BRCA status in high-grade serous ovarian cancer using fresh-frozen tissue based approach 84
Surfactant and Varespladib Co-Administration in Stimulated Rat Alveolar Macrophages Culture 83
Lung cancer multi-omics digital human avatars for integrating precision medicine into clinical practice: the LANTERN study 81
BRCA testing delay during the COVID-19 pandemic: How to act? 81
Rapid and simple identification of the commonest glucose-6-phosphate dehydrogenase (G6PD) Italian mutations: From DNA extraction to genotyping 80
In silico investigation of the molecular effects caused by R123H variant in secretory phospholipase A2-IIA associated with ARDS 80
UGT1A1 Polymorphism and Mortality Outcome after Allogeneic Stem Cell Transplantation with Busulfan Based Regimen 80
G6PD Murcia, G6PD Ube and G6PD Orissa: report of three G6PD mutations unusual for Italian population. 79
Effect of whole body hypothermia on inflammation and surfactant function in asphyxiated neonates 79
A new founder BRCA1 haplotype identified in the Puglia region is associated with a specific age-related cancer onset in three unrelated families 79
A novel CYP24A1 genotype associated to a clinical picture of hypercalcemia, nephrolithiasis and low bone mass (vol 45, pg 291, 2016) 76
Spliceogenic analysis of BRCA1 c.439T>C (rs794727800) variant by High Resolution Melting Analysis 76
Multiplex Ligation-Dependent Probe Amplification Analysis Is Useful for Diagnosing Congenital Adrenal Hyperplasia but Requires a Deep Knowledge of CYP21A2 Genetics 75
Epithelial ovarian cancer and brain metastases: might the BRCA status, PARP inhibitor administration, and surgical treatment impact the survival? 74
Ovarian cancer onset across different BRCA mutation types: a view to a more tailored approach for BRCA mutated patients 73
Feasibility of extracellular competitive inhibition of phospholipase A2 in neonatal and pediatric lung injury 72
Prognostic factors value of germline and somatic brca in patients undergoing surgery for recurrent ovarian cancer with liver metastases 72
High Resolution Melting Analysis is Very Useful to Identify Breast Cancer Type 1 Susceptibility Protein (BRCA1) c.4964\_4982del19 (rs80359876) Founder Calabrian Pathogenic Variant on Peripheral Blood and Buccal Swab DNA 72
Effect of prenatal steroidal inhibition of sPLA2 in a rat model of preterm lung 71
Additional molecular and clinical evidence open the way to definitive IARC classification of the BRCA1 c.5332G > A (p.Asp1778Asn) variant 71
PCR experion automated electrophoresis system to detect Lysteria monocytogenes in food. 70
Identification of twenty-nine novel germline unclassified variants of BRCA1 and BRCA2 genes in 1400 Italian individuals 70
Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar Syndrome type II in an Italian patient 68
Role of SH levels and markers of immune response in the stroke 68
Characterization of a new BRCA1 rearrangement in an Italian woman with hereditary breast and ovarian cancer syndrome 68
Novel BRCA1 Large Genomic Rearrangements in Italian Breast/Ovarian Cancer Patients 68
Droplet digital PCR for large genomic rearrangements detection: A promising strategy in tissue BRCA1 testing 68
Integrating a Comprehensive Cancer Genome Profiling into Clinical Practice: A Blueprint in an Italian Referral Center 66
First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy 65
Oncocytic variant of medullary thyroid carcinoma: a rare case of sporadic multifocal and bilateral RET wild-type neoplasm with revision of the literature 65
BRCA Mutation Status in Triple-Negative Breast Cancer Patients Treated with Neoadjuvant Chemotherapy: A Pivotal Role for Treatment Decision-Making 63
The Relationship between ACE, ACTN3 and MCT1 Genetic Polymorphisms and Athletic Performance in Elite Rugby Union Players: A Preliminary Study 63
Deep-Learning to Predict BRCA Mutation and Survival from Digital H&E Slides of Epithelial Ovarian Cancer 61
New onset of Susac syndrome after mRNA COVID-19 vaccine: a case report 61
Medullary thyroid carcinoma with exon 2 p. L56M RET variant: Clinical particular features in two patients 60
A novel low-density lipoprotein receptor variant in a Ukrainian patient: a case report and overview of the disease-causing low-density lipoprotein receptor variants associated to familial hypercholesterolemia 60
Identification and Characterization of a New BRCA2 Rearrangement in an Italian Family with Hereditary Breast and Ovarian Cancer Syndrome 59
Molecular basis of favism triggered by ingestion of frozen pumpkin cross-contaminated with fava beans 56
Tumor BRCA testing in ovarian cancer and EQA scheme: our experience of a critical evaluation 56
BRCA testing on buccal swab to improve access to healthcare and cancer prevention: A performance evaluation 53
Corded and hyalinized endometrioid endometrial carcinoma with high-grade features: a clinicopathological and TCGA-based molecular analysis 53
High resolution melting profiles (HRMPs) obtained by magnetic induction cycler (MIC) have been used to monitor the BRCA2 status highlighted by next generation tumor sequencing (NGTS): a combined approach in a diagnostic environment 53
Identification of a novel gene signature predicting response to first-line chemotherapy in BRCA wild-type high-grade serous ovarian cancer patients 53
Impact of Comprehensive Genome Profiling on the Management of Advanced Non–Small Cell Lung Cancer: Preliminary Results From the Lung Cancer Cohort of the FPG500 Program 52
Survival outcomes in patients with BRCA mutated, variant of unknown significance, and wild type ovarian cancer treated with PARP inhibitors 51
BRCA Mutation Status to Personalize Management of Recurrent Ovarian Cancer: A Multicenter Study 51
Granulocyte oxidative activity and plasma oxygen reactive species in travertine-induced industrial bronchitis 51
Risk reducing surgery with peritoneal staging in BRCA1-2 mutation carriers. A prospective study 50
Multigenic panels in breast cancer: Clinical utility and management of patients with pathogenic variants other than BRCA1/2 50
Endometrial giant cell carcinoma: new insights from a morphological, immunohistochemical, and molecular analysis of three cases 50
Dual inhibition of CDK12 and CDK13 uncovers actionable vulnerabilities in patient-derived ovarian cancer organoids 49
The Pathogenic RET Val804Met Variant in Acromegaly: A New Clinical Phenotype? 49
NLR and BRCA mutational status in patients with high grade serous advanced ovarian cancer 48
A common pattern of somatic mutations in t-MDS/AML of patients treated with PARP inhibitors for metastatic ovarian cancer 47
Role of Homologous Recombination Repair (HRR) Genes in Uterine Leiomyosarcomas: A Retrospective Analysis 46
Genetics and Sport Injuries: New Perspectives for Athletic Excellence in an Italian Court of Rugby Union Players 45
A common pattern of somatic mutations in t-MDS/AML of patients treated with PARP inhibitors for metastatic ovarian cancer 44
The BRCA1 c.788G > T (NM_007294.4) variant in a high grade serous ovarian cancer (HGSOC) patient: foods for thought 43
Totale 8.434
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Categoria #
all - tutte 43.110
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 43.110
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020149 0 0 0 0 0 0 0 0 0 0 91 58
2020/2021649 34 60 16 57 68 24 99 19 84 31 125 32
2021/2022878 55 101 10 62 52 29 26 155 43 51 108 186
2022/20232.112 254 337 168 272 123 265 97 185 218 40 100 53
2023/20241.172 42 277 34 63 67 201 81 70 16 53 119 149
2024/20252.242 64 73 224 126 221 122 134 119 363 348 448 0
Totale 9.105