IRIS
LANTIERI, FRANCESCA
 Distribuzione geografica
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Continente #
EU - Europa 7.783
AS - Asia 814
NA - Nord America 807
Continente sconosciuto - Info sul continente non disponibili 130
SA - Sud America 86
AF - Africa 12
Totale 9.632
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Nazione #
IT - Italia 7.662
US - Stati Uniti d'America 756
SG - Singapore 324
CN - Cina 241
VN - Vietnam 120
FR - Francia 58
BR - Brasile 41
BD - Bangladesh 38
HK - Hong Kong 35
CA - Canada 23
AR - Argentina 15
JP - Giappone 13
GB - Regno Unito 10
FI - Finlandia 9
MX - Messico 9
NL - Olanda 9
DE - Germania 8
CO - Colombia 6
ID - Indonesia 6
IN - India 6
PH - Filippine 6
IE - Irlanda 5
TT - Trinidad e Tobago 5
CL - Cile 4
EC - Ecuador 4
MA - Marocco 4
RU - Federazione Russa 4
UY - Uruguay 4
VE - Venezuela 4
CH - Svizzera 3
CY - Cipro 3
GT - Guatemala 3
PE - Perù 3
PK - Pakistan 3
PT - Portogallo 3
PY - Paraguay 3
ZA - Sudafrica 3
BH - Bahrain 2
CR - Costa Rica 2
ES - Italia 2
IQ - Iraq 2
JM - Giamaica 2
KG - Kirghizistan 2
KR - Corea 2
NP - Nepal 2
PL - Polonia 2
SI - Slovenia 2
TR - Turchia 2
UA - Ucraina 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BB - Barbados 1
BG - Bulgaria 1
BO - Bolivia 1
BS - Bahamas 1
CI - Costa d'Avorio 1
EG - Egitto 1
GF - Guiana Francese 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
KE - Kenya 1
MT - Malta 1
NG - Nigeria 1
NI - Nicaragua 1
OM - Oman 1
PA - Panama 1
SA - Arabia Saudita 1
SC - Seychelles 1
SV - El Salvador 1
TC - Turks e Caicos 1
TW - Taiwan 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 9.503
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Città #
Genova 4.537
Genoa 1.831
Rapallo 494
Vado Ligure 470
Bordighera 245
San Jose 202
Singapore 152
Lauterbourg 56
Ashburn 53
Beijing 52
Ho Chi Minh City 40
New York 38
Hong Kong 34
Hanoi 23
Council Bluffs 22
Santa Clara 20
Los Angeles 13
Tokyo 13
Milan 10
Helsinki 9
Naples 8
Orem 8
Tianjin 8
Detroit 7
Montreal 7
Olive Branch 7
Cerritos 6
Dallas 6
Memphis 6
Mexico City 6
Rome 6
Charlotte 5
City of London 5
Frankfurt am Main 5
Phoenix 5
Amsterdam 4
Brescia 4
Chicago 4
Cleveland 4
Da Nang 4
Dublin 4
Haiphong 4
Philadelphia 4
Queens 4
The Bronx 4
Toronto 4
Turin 4
Acalanes Ridge 3
Atlanta 3
Biên Hòa 3
Boardman 3
Boston 3
Brooklyn 3
Bắc Giang 3
Carlsbad 3
Corvallis 3
Fayetteville 3
Grayslake 3
Guatemala City 3
Hudson 3
Johannesburg 3
Las Vegas 3
London 3
Miami 3
Montevideo 3
Nicosia 3
Tân Tiến 3
Zurich 3
Alpharetta 2
Asunción 2
Bari 2
Blytheville 2
Bogotá 2
Brasília 2
Buffalo 2
Can Tho 2
Cape Coral 2
Chennai 2
Columbus 2
Florence 2
Garland 2
Guangzhou 2
Guayaquil 2
Ha Long 2
Hamad Town 2
Hamilton 2
Houston 2
Jacksonville 2
Leme 2
Lima 2
Ljubljana 2
Long Xuyen 2
Manlius 2
Marrakesh 2
Mattoon 2
Mobile 2
Mumbai 2
Newark 2
Norristown 2
Omaha 2
Totale 8.584
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Nome #
Parental origin and somatic mosaicism of PHOX2B mutations in Congenital Central Hypoventilation Syndrome 387
Beneficial effects of long-term treatment with bosentan on the development of pulmonary arterial hypertension in patients with systemic sclerosis 231
A prospective observational study of associated anomalies in Hirschsprung's disease. 223
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 198
TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis 196
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 194
CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation 190
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum 189
The impact of stapled transanal rectal resection on anorectal function in patients with obstructed defecation syndrome 188
Gly101Trp germline mutation in the CDKN2A gene in familial and non familial Ligurian melanoma patients 183
Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A 182
Prevalence of erectile dysfunction in a cohort of Italian hypertensive subjects 182
The involvement of the RET variant G691S in medullary thyroid carcinoma: Conflicting results of meta-analyses need to be reconciled 181
A COMMON HAPLOTYPE AT THE 5' END OF THE RET PROTO-ONCOGENE, OVERREPRESENTED IN HIRSCHSPRUNG PATIENTS, IS ASSOCIATED WITH REDUCED GENE EXPRESSION 176
Behavior of serum human major histocompatibility complex class I antigen levels in human immunodeficiency virus-infected patients during antiretroviral therapy: correlation with clinical outcome 176
A multi-omics approach reveals impaired lipid metabolism and oxidative stress in a zebrafish model of Alexander disease 171
Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorder 170
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability 170
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities 169
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes 160
Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant Validation. 160
A metagenomics study on Hirschsprung's disease associated enterocolitis: Biodiversity and gut microbial homeostasis depend on resection length and patient's clinical history 159
Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study 157
High prevalence of the G101W germline mutation in the CDKN2A (P16INK4A) gene in 62 Italian malignant melanoma families 157
HLA-G expression in gastric carcinoma: clinicopathological correlations and prognostic impact 156
Varianti polimorfiche del gene MC1R (Melanocortin receptor 1) nella popolazione ligure ed associazione con il rischio di melanoma 155
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. 155
Molecular genetics of Hirschsprung disease. 154
Relevance of CD38 expression on CD8 T cells to evaluate antiretroviral therapy response in HIV-1-infected youths 154
Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease. 153
High prevalence of the Gly101Trp germline mutation in the CDKN2A gene in 62 small Italian families 149
Effectiveness of psychological support in patients undergoing primary total hip or knee arthroplasty: a controlled cohort study 147
Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from Hirschsprung patients. 147
Absence of melanocortin 1 receptor variants in Ligurian G101W families 143
Incorporating prior biological information in linkage studies increases power and limits multiple testing 137
Novel MC1R variants in Ligurian melanoma patients and controls 135
Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease 134
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles 133
A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung disease 132
Hirschsprung disease, associated syndromes and genetics: a review 131
Attention-deficit hyperactivity disorder 130
Soluble HLA-G serum levels in patients with the Acquired Immunodeficiency Syndrome affected by different AIDS-defining conditions before and after anti-retroviral treatment 129
Integration of Linkage Analysis and Next-Generation Sequencing Data 129
Absence of melanocortin 1 receptor variants in Ligurian Gly101trp families 127
DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients 126
The osmr gene is involved in hirschsprung associated enterocolitis susceptibility through an altered downstream signaling 126
Technological improvements in the treatment of haemorrhoids and obstructed defaecation syndrome 123
Flu and pneumococcal vaccine coverage in scleroderma patients still need to be prompted: A systematic review 123
Inclusion of a priori information in genome-wide association analysis 119
Pathways systematically associated to Hirschsprung's disease. 116
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease 114
Molecular mechanisms of RET-induced Hirschsprung pathogenesis 114
A Survey on Undergraduate Medical Students’ Perception of COVID-19 Vaccination 107
Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data 106
Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome 102
null 101
Prevalence of CDKN2A gene mutations in patients with early-onset sporadic melanoma 95
Deprescribing Strategies: A Prospective Study on Proton Pump Inhibitors 93
Effect of Aging on Deferasirox Therapy in Transfusion-dependent Patients. A Prospective-Retrospective, Cohort-study 91
Triple inhaled therapy in asthma: Beliefs, behaviours and doubts 87
Prevalenza della mutazione germinale G101W nel gene CDKN2A in pazienti liguri con melanoma sporadico 83
A pilot study on school of medicine students’ perception of ethical issues related to human specimens in anatomical museums 82
Melanoma Familiare: Il contributo di geni di suscettibilità ad alta e bassa penetranza 79
Correction: Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from hirschsprung patients (PLoS ONE) 61
Human Leukocyte Antigen Class II associations in late-onset Myasthenia Gravis 60
Editorial: Elucidation of the causes of human disease by multi-omics integration 51
The involvement of the RET variant G691S in medullary thyroid carcinoma enlightened by a meta-analysis study 46
OSM/OSMR and Interleukin 6 Family Cytokines in Physiological and Pathological Condition 28
Patients’ preferences, feelings, and benefits on Music-Based Intervention: A Pilot Study in COVID-19 Hospitalization 20
Totale 9.632
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Categoria #
all - tutte 29.337
article - articoli 25.007
book - libri 0
conference - conferenze 3.227
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.103
Totale 58.674
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20262.182 275 75 119 191 265 192 350 98 136 220 115 146
2026/2027345 345 0 0 0 0 0 0 0 0 0 0 0
Totale 9.632