IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

TUCCI, ARIANNA
 Distribuzione geografica
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Continente #
NA - Nord America 386
EU - Europa 324
AS - Asia 207
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 2
OC - Oceania 1
Totale 922
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Nazione #
US - Stati Uniti d'America 370
GB - Regno Unito 138
CN - Cina 108
SG - Singapore 64
SE - Svezia 56
IT - Italia 32
CA - Canada 16
DE - Germania 16
BE - Belgio 15
IN - India 15
RU - Federazione Russa 13
FI - Finlandia 11
IE - Irlanda 11
DK - Danimarca 9
ID - Indonesia 7
FR - Francia 6
UA - Ucraina 6
HK - Hong Kong 5
NL - Olanda 3
RO - Romania 3
BG - Bulgaria 2
BR - Brasile 2
KR - Corea 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AU - Australia 1
ES - Italia 1
EU - Europa 1
IQ - Iraq 1
IR - Iran 1
LT - Lituania 1
MY - Malesia 1
PH - Filippine 1
RS - Serbia 1
TW - Taiwan 1
UZ - Uzbekistan 1
Totale 922
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Città #
Southend 129
Chandler 65
Ann Arbor 52
Singapore 47
Fairfield 42
Ashburn 24
Milan 21
Seattle 17
Princeton 16
Wilmington 16
Woodbridge 16
Cambridge 14
Toronto 14
Brussels 13
Guangzhou 12
Nanjing 12
Santa Clara 12
Dublin 11
Dearborn 10
Beijing 8
Jinan 8
Hangzhou 7
Helsinki 7
Bengaluru 6
Des Moines 6
Phoenix 5
Boardman 4
Hong Kong 4
Houston 4
Mumbai 4
Shenyang 4
Haikou 3
Jakarta 3
Los Angeles 3
Nanchang 3
Ningbo 3
Norwalk 3
Redwood City 3
Tianjin 3
Changsha 2
Edinburgh 2
Eschweiler 2
Fuzhou 2
Hanover 2
London 2
Ottawa 2
Rome 2
Sofia 2
São Paulo 2
Taiyuan 2
Taizhou 2
Waanrode 2
Zhengzhou 2
Alexandria 1
Amsterdam 1
Belgrade 1
Berlin 1
Bühl 1
Central District 1
Changchun 1
Chatsworth 1
Fremont 1
Görwihl 1
Jiaxing 1
Jinhua 1
Kaunas 1
Kent 1
Korbach 1
Kuala Lumpur 1
Lessolo 1
Luohe 1
Manila 1
North Bergen 1
Quanzhou 1
Redmond 1
San Diego 1
San Francisco 1
Seano 1
Shanghai 1
Shenzhen 1
Taipei 1
Wenzhou 1
Yubileyny 1
Ürümqi 1
Totale 693
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Nome #
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth 157
MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions 151
7p22.1 microduplication syndrome : refinement of the critical region 143
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome 137
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation 112
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review 110
The absence that makes the difference: choroidal abnormalities in Legius syndrome 98
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? : A case report and review of 62 cases 76
Totale 984
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Categoria #
all - tutte 2.810
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 2.810
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020109 0 0 0 0 0 16 14 10 36 22 3 8
2020/2021131 7 7 17 3 11 4 23 18 7 9 17 8
2021/2022125 15 8 8 5 2 6 3 3 24 11 8 32
2022/2023165 23 22 21 20 15 31 2 12 14 2 2 1
2023/202480 1 11 11 5 21 4 1 4 3 1 1 17
2024/2025102 7 40 13 27 13 2 0 0 0 0 0 0
Totale 984