CINECA IRIS Institutional Research Information System

PELOSINI, CATERINA
 Distribuzione geografica
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Continente #
NA - Nord America 1.182
EU - Europa 481
AS - Asia 152
AF - Africa 61
OC - Oceania 2
SA - Sud America 1
Totale 1.879
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Nazione #
US - Stati Uniti d'America 1.152
IT - Italia 128
SE - Svezia 92
CN - Cina 75
AT - Austria 63
DE - Germania 62
BG - Bulgaria 43
GB - Regno Unito 32
SG - Singapore 30
CA - Canada 29
CI - Costa d'Avorio 28
SN - Senegal 23
VN - Vietnam 16
TR - Turchia 15
UA - Ucraina 14
BE - Belgio 13
FI - Finlandia 10
FR - Francia 10
NG - Nigeria 10
CH - Svizzera 6
HK - Hong Kong 6
IN - India 4
KR - Corea 3
RU - Federazione Russa 3
AU - Australia 2
BO - Bolivia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
HU - Ungheria 1
IR - Iran 1
JP - Giappone 1
MX - Messico 1
NL - Olanda 1
NP - Nepal 1
SI - Slovenia 1
Totale 1.879
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Città #
Ann Arbor 152
Chandler 151
Fairfield 121
Ashburn 90
Woodbridge 90
Houston 69
Seattle 57
Vienna 56
Wilmington 44
Sofia 43
New York 37
Beijing 33
Cambridge 33
Florence 33
Abidjan 28
Ottawa 28
Dakar 23
Princeton 23
Lawrence 21
Medford 20
Pisa 19
Frankfurt am Main 17
Milan 17
Ogden 17
Izmir 15
Jacksonville 15
Brussels 13
Falls Church 11
Kent 11
San Diego 11
Serra 11
Bremen 10
Lagos 10
London 10
Nanjing 10
Marseille 8
Washington 8
Des Moines 7
Bern 6
Detroit 6
Hong Kong 6
Boulder 4
Düsseldorf 4
Jinan 4
Los Angeles 4
Phoenix 4
Porcari 4
Chicago 3
Dong Ket 3
Hebei 3
Jüchen 3
Nanchang 3
Norwalk 3
Redmond 3
Trieste 3
Bologna 2
Changsha 2
Dearborn 2
Jiaxing 2
Kunming 2
Lancaster 2
Pescara 2
Rheinfelden 2
Wandsworth 2
Ada 1
Adelaide 1
Andover 1
Ansbach 1
Anzio 1
Azzano San Paolo 1
Boardman 1
Boston 1
Brandon 1
Brdo 1
Capannori 1
Chehalis 1
Durham 1
Groningen 1
Hangzhou 1
Hefei 1
Huzhou 1
Islington 1
Jawalakhel 1
Kilburn 1
Kleve 1
Lanzhou 1
Leawood 1
Ljubljana 1
Lyngby 1
Massa 1
Melbourne 1
Mexico 1
Montpellier 1
Monza 1
Mountain View 1
Pieve 1
Pune 1
Redwood City 1
Rome 1
Roseto Degli Abruzzi 1
Totale 1.492
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Nome #
Identification of a novel mutation in the polymerase delta 1 (POLD1) gene in a lipodystrophic patient affected by mandibular hypoplasia, deafness, progeroid features (MDPL) syndrome 155
In vitro assay of thyroid disruptors affecting TSH-stimulated adenylate cyclase activity 145
Contribution of 32 GWAS-identified common variants to severe obesity in European adults referred for bariatric surgery 127
Lipodystrophy and obesity are associated with decreased number of T cells with regulatory function and pro-inflammatory macrophage phenotype 115
Serum concentrations of adiponectin and leptin in patients with thyroid dysfunctions 114
null 107
Serum haptoglobin: a novel marker of adiposity in humans 100
Melanocortin-4 receptor mutations in obesity 88
LDL-cholesterol lowering effect of a new dietary supplement: an open label, controlled, randomized, cross-over clinical trial in patients with mild-to-moderate hypercholesterolemia 88
null 88
Serum IGF-binding protein 2 (IGFBP-2) concentrations change early after gastric bypass bariatric surgery revealing a possible marker of leptin sensitivity in obese subjects 77
The complex interactions amongst serotonin, insulin, leptin and glycolipid metabolic parameters in human obesity 72
Atypical progeroid syndrome and partial lipodystrophy due to LMNA gene p.R349W mutation 57
Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel AGPAT2 Homozygous Variants Showing the Highly Heterogeneous Presentation of the Disease 57
Immunological features of patients affected by Barraquer-Simons syndrome 56
null 55
Acute exogenous TSH administration stimulates leptin secretion in vivo 53
null 51
Histological pattern and gene expression profiling of thyroid tissue in subjects with obesity 43
Autoimmunity in lipodystrophy syndromes 39
Partial lipodystrophy and lmna p.R545h variant 38
Weight Loss and Variation of Levothyroxine Requirements in Hypothyroid Obese Patients After Bariatric Surgery 37
Spot-light on microbiota in obesity and cancer 36
Circulating Levels of MiRNAs From 320 Family in Subjects With Lipodystrophy: Disclosing Novel Signatures of the Disease 31
Genetic screening for melanocortin-4 receptor (MC4-R) mutations in a cohort of italian obese patients: Description and functional characterization of a novel mutation 27
Oxidative and DNA damage in obese patients undergoing bariatric surgery: A one-year follow-up study 27
Frequency of the GPR7 Tyr135Phe allelic variant in lean and obese subjects. 19
Post-acute cardiac complications following SARS-CoV-2 infection in partial lipodystrophy due to LMNA gene p.R349W mutation 18
Effect of burosumab treatment on phosphate metabolism and bone health in patients with X-linked hypophosphatemic rickets (XLH). Preliminary data within an Italian sample 6
Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets 4
A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature 3
Totale 1.933
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Categoria #
all - tutte 6.143
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 6.143
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201978 0 0 0 0 0 0 0 0 0 0 40 38
2019/2020293 40 29 12 17 28 29 33 24 27 18 30 6
2020/2021147 9 8 4 5 13 18 14 16 15 10 10 25
2021/2022238 5 2 5 17 31 42 7 10 19 22 16 62
2022/2023536 40 87 45 44 56 59 5 27 114 2 46 11
2023/2024273 26 16 41 12 31 67 9 9 5 12 45 0
Totale 1.933