IRIS
LANTIERI, FRANCESCA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 7.744
AS - Asia 761
NA - Nord America 403
SA - Sud America 77
AF - Africa 12
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.998
Salva come PNG Salva come JPEG
Nazione #
IT - Italia 7.631
US - Stati Uniti d'America 374
SG - Singapore 318
CN - Cina 227
VN - Vietnam 118
FR - Francia 58
BR - Brasile 37
HK - Hong Kong 34
CA - Canada 15
AR - Argentina 14
JP - Giappone 13
GB - Regno Unito 10
BD - Bangladesh 9
FI - Finlandia 9
MX - Messico 9
DE - Germania 8
NL - Olanda 7
IN - India 6
PH - Filippine 6
ID - Indonesia 5
IE - Irlanda 5
CL - Cile 4
EC - Ecuador 4
MA - Marocco 4
RU - Federazione Russa 4
UY - Uruguay 4
CH - Svizzera 3
CO - Colombia 3
CY - Cipro 3
PE - Perù 3
PK - Pakistan 3
PY - Paraguay 3
VE - Venezuela 3
ZA - Sudafrica 3
BH - Bahrain 2
IQ - Iraq 2
KG - Kirghizistan 2
KR - Corea 2
NP - Nepal 2
PT - Portogallo 2
TR - Turchia 2
TT - Trinidad e Tobago 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BO - Bolivia 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
EG - Egitto 1
ES - Italia 1
GF - Guiana Francese 1
HR - Croazia 1
JM - Giamaica 1
KE - Kenya 1
MT - Malta 1
NG - Nigeria 1
OM - Oman 1
PA - Panama 1
PL - Polonia 1
SA - Arabia Saudita 1
SC - Seychelles 1
SI - Slovenia 1
TW - Taiwan 1
UA - Ucraina 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 8.998
Salva come PNG Salva come JPEG
Città #
Genova 4.537
Genoa 1.831
Rapallo 494
Vado Ligure 470
Bordighera 245
Singapore 146
San Jose 138
Lauterbourg 56
Beijing 42
Ho Chi Minh City 38
Hong Kong 34
New York 32
Ashburn 29
Hanoi 23
Council Bluffs 22
Santa Clara 13
Tokyo 13
Helsinki 9
Tianjin 8
Orem 7
Los Angeles 6
Mexico City 6
Montreal 6
City of London 5
Frankfurt am Main 5
Milan 5
Naples 5
Amsterdam 4
Brescia 4
Charlotte 4
Da Nang 4
Dublin 4
Haiphong 4
Acalanes Ridge 3
Biên Hòa 3
Bắc Giang 3
Chicago 3
Cleveland 3
Johannesburg 3
London 3
Montevideo 3
Nicosia 3
Phoenix 3
Rome 3
Turin 3
Tân Tiến 3
Zurich 3
Asunción 2
Bari 2
Boston 2
Brasília 2
Can Tho 2
Cape Coral 2
Chennai 2
Dallas 2
Guangzhou 2
Guayaquil 2
Ha Long 2
Hamad Town 2
Houston 2
Las Vegas 2
Leme 2
Lima 2
Long Xuyen 2
Marrakesh 2
Mumbai 2
Poplar 2
Ramos Mejía 2
Tashkent 2
The Bronx 2
Toronto 2
Valparaíso de Goiás 2
Windsor 2
Abidjan 1
Acarigua 1
Amadora 1
Ankara 1
Araçariguama 1
Artur Nogueira 1
Atlanta 1
Baghdad 1
Banī Suwayf 1
Barranquilla 1
Bishkek 1
Blair 1
Bologna 1
Bonito 1
Botucatu 1
Bragado 1
Brainerd 1
Brantford 1
Brooklyn 1
Brusque 1
Buenos Aires 1
Buffalo 1
Buon Ma Thuot 1
Burke 1
Bình Dương 1
Bến Tre 1
Camaquã 1
Totale 8.370
Salva come PNG Salva come JPEG
Nome #
Parental origin and somatic mosaicism of PHOX2B mutations in Congenital Central Hypoventilation Syndrome 385
Beneficial effects of long-term treatment with bosentan on the development of pulmonary arterial hypertension in patients with systemic sclerosis 225
A prospective observational study of associated anomalies in Hirschsprung's disease. 213
TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis 193
Measurement of sorafenib plasma concentration by high-performance liquid chromatography in patients with advanced hepatocellular carcinoma: is it useful the application in clinical practice? A pilot study 188
The impact of stapled transanal rectal resection on anorectal function in patients with obstructed defecation syndrome 181
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum 181
Behavior of soluble HLA-A, -B, -C and HLA-G molecules in patients with chronic hepatitis C virus infection undergoing pegylated interferon-α and ribavirin treatment: potential role as markers of response to antiviral therapy 181
CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation 180
Prevalence of erectile dysfunction in a cohort of Italian hypertensive subjects 180
Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A 173
Gly101Trp germline mutation in the CDKN2A gene in familial and non familial Ligurian melanoma patients 172
The involvement of the RET variant G691S in medullary thyroid carcinoma: Conflicting results of meta-analyses need to be reconciled 171
Behavior of serum human major histocompatibility complex class I antigen levels in human immunodeficiency virus-infected patients during antiretroviral therapy: correlation with clinical outcome 171
A COMMON HAPLOTYPE AT THE 5' END OF THE RET PROTO-ONCOGENE, OVERREPRESENTED IN HIRSCHSPRUNG PATIENTS, IS ASSOCIATED WITH REDUCED GENE EXPRESSION 165
Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorder 165
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability 165
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities 163
A multi-omics approach reveals impaired lipid metabolism and oxidative stress in a zebrafish model of Alexander disease 160
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes 157
Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant Validation. 154
Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study 151
A metagenomics study on Hirschsprung's disease associated enterocolitis: Biodiversity and gut microbial homeostasis depend on resection length and patient's clinical history 151
Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease. 150
Behavior of non-classical soluble HLA class G antigens in human immunodeficiency virus 1-infected patients before and after HAART: comparison with classical soluble HLA-A, -B, -C antigens and potential role in immune-reconstitution. 150
Relevance of CD38 expression on CD8 T cells to evaluate antiretroviral therapy response in HIV-1-infected youths 150
Varianti polimorfiche del gene MC1R (Melanocortin receptor 1) nella popolazione ligure ed associazione con il rischio di melanoma 148
HLA-G expression in gastric carcinoma: clinicopathological correlations and prognostic impact 147
High prevalence of the G101W germline mutation in the CDKN2A (P16INK4A) gene in 62 Italian malignant melanoma families 145
Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from Hirschsprung patients. 144
High prevalence of the Gly101Trp germline mutation in the CDKN2A gene in 62 small Italian families 143
Molecular genetics of Hirschsprung disease. 143
Absence of melanocortin 1 receptor variants in Ligurian G101W families 142
Incorporating prior biological information in linkage studies increases power and limits multiple testing 134
Effectiveness of psychological support in patients undergoing primary total hip or knee arthroplasty: a controlled cohort study 134
Novel MC1R variants in Ligurian melanoma patients and controls 131
Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease 128
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles 127
Hirschsprung disease, associated syndromes and genetics: a review 127
Soluble HLA-G serum levels in patients with the Acquired Immunodeficiency Syndrome affected by different AIDS-defining conditions before and after anti-retroviral treatment 127
DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients 123
Absence of melanocortin 1 receptor variants in Ligurian Gly101trp families 123
A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung disease 122
Attention-deficit hyperactivity disorder 122
Integration of Linkage Analysis and Next-Generation Sequencing Data 122
The osmr gene is involved in hirschsprung associated enterocolitis susceptibility through an altered downstream signaling 121
Flu and pneumococcal vaccine coverage in scleroderma patients still need to be prompted: A systematic review 117
Pathways systematically associated to Hirschsprung's disease. 114
Inclusion of a priori information in genome-wide association analysis 114
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease 109
Technological improvements in the treatment of haemorrhoids and obstructed defaecation syndrome 109
Molecular mechanisms of RET-induced Hirschsprung pathogenesis 109
Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data 104
null 101
Prevalence of CDKN2A gene mutations in patients with early-onset sporadic melanoma 92
A Survey on Undergraduate Medical Students’ Perception of COVID-19 Vaccination 89
Deprescribing Strategies: A Prospective Study on Proton Pump Inhibitors 82
Prevalenza della mutazione germinale G101W nel gene CDKN2A in pazienti liguri con melanoma sporadico 81
Effect of Aging on Deferasirox Therapy in Transfusion-dependent Patients. A Prospective-Retrospective, Cohort-study 79
Melanoma Familiare: Il contributo di geni di suscettibilità ad alta e bassa penetranza 76
A pilot study on school of medicine students’ perception of ethical issues related to human specimens in anatomical museums 75
Triple inhaled therapy in asthma: Beliefs, behaviours and doubts 75
Correction: Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from hirschsprung patients (PLoS ONE) 58
Human Leukocyte Antigen Class II associations in late-onset Myasthenia Gravis 47
Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome 44
The involvement of the RET variant G691S in medullary thyroid carcinoma enlightened by a meta-analysis study 42
Editorial: Elucidation of the causes of human disease by multi-omics integration 39
OSM/OSMR and Interleukin 6 Family Cytokines in Physiological and Pathological Condition 25
Patients’ preferences, feelings, and benefits on Music-Based Intervention: A Pilot Study in COVID-19 Hospitalization 16
Totale 9.125
Salva come PNG Salva come JPEG
Categoria #
all - tutte 27.431
article - articoli 23.366
book - libri 0
conference - conferenze 3.034
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.031
Totale 54.862
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202176 0 0 0 0 0 0 0 0 0 0 37 39
2021/2022729 19 44 81 82 23 40 58 154 36 67 43 82
2022/2023604 58 59 4 49 110 88 2 40 98 10 79 7
2023/2024584 20 36 6 44 30 62 34 247 12 22 21 50
2024/20251.275 61 83 33 75 155 128 113 221 59 63 125 159
2025/20262.020 275 75 119 191 265 192 350 98 136 220 99 0
Totale 9.125