CINECA IRIS Institutional Research Information System

CARANDO, Adriana
 Distribuzione geografica
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Continente #
NA - Nord America 1.476
EU - Europa 1.118
AS - Asia 436
OC - Oceania 9
SA - Sud America 4
AF - Africa 3
Totale 3.046
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Nazione #
US - Stati Uniti d'America 1.456
IT - Italia 294
CN - Cina 216
SE - Svezia 182
DE - Germania 108
IE - Irlanda 107
AT - Austria 76
FI - Finlandia 67
UA - Ucraina 64
SG - Singapore 60
FR - Francia 55
KR - Corea 46
GB - Regno Unito 45
PL - Polonia 41
TW - Taiwan 31
NL - Olanda 27
JP - Giappone 24
VN - Vietnam 23
CA - Canada 19
IN - India 16
BE - Belgio 15
ES - Italia 12
AU - Australia 9
RU - Federazione Russa 8
GR - Grecia 7
TR - Turchia 6
CZ - Repubblica Ceca 4
HK - Hong Kong 4
CH - Svizzera 3
CY - Cipro 3
BR - Brasile 2
PH - Filippine 2
PK - Pakistan 2
ZA - Sudafrica 2
AR - Argentina 1
BG - Bulgaria 1
CL - Cile 1
DK - Danimarca 1
IR - Iran 1
NO - Norvegia 1
PR - Porto Rico 1
SA - Arabia Saudita 1
SN - Senegal 1
UZ - Uzbekistan 1
Totale 3.046
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Città #
Chandler 269
Beijing 139
Dublin 107
Houston 106
Torino 98
Vienna 75
Ann Arbor 67
Dearborn 65
Fairfield 57
Jacksonville 53
Singapore 50
Nyköping 46
Fremont 39
Ashburn 37
Warsaw 37
Medford 35
Villeurbanne 32
Wilmington 31
Princeton 30
Tainan City 30
Redwood City 27
Boardman 26
Seattle 25
Woodbridge 22
Turin 21
Milan 17
Helsinki 15
New York 15
Cambridge 14
Dong Ket 14
Boston 13
Guangzhou 13
Brussels 12
Santa Clara 11
Chicago 10
Toronto 10
Buffalo 9
Pune 9
Rome 9
Pavia 8
Pisa 8
Los Angeles 7
Verona 7
Bethesda 6
Dronten 6
Hefei 6
Kunming 6
Norwalk 5
Padova 5
Piemonte 5
Takamatsu 5
Tianjin 5
Blackpool 4
Bologna 4
Chengdu 4
Dorchester 4
Falls Church 4
Jinan 4
San Diego 4
Wuhan 4
Xian 4
Ankara 3
Basel 3
Carini 3
Columbus 3
Florence 3
Lachine 3
Larnaca 3
London 3
Mountain View 3
Nanjing 3
Nürnberg 3
Paderno 3
San Mateo 3
Shenzhen 3
Wietrzychowice 3
Adelaide 2
Albertville 2
Aylesbury 2
Barcelona 2
Beaverton 2
Bursa 2
Chiba 2
Clearwater 2
Düsseldorf 2
Ferrara 2
Hanwell 2
Harbin 2
Huelva 2
Kofu 2
Las Vegas 2
Lodi 2
Ludhiana 2
Lund 2
Monselice 2
Muizenberg 2
Nagoya 2
Peshawar 2
Petaluma 2
Plymouth Meeting 2
Totale 1.903
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Nome #
Spontaneous remission in a Diamond-Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation 250
Design of a multiplex ligation-dependent probe amplification assay for SLC20A2: identification of two novel deletions in primary familial brain calcification 231
A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease? 223
High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay 175
Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia 143
Diamond-Blackfan anemia: genotype-phenotype correlation in Italian patients with RPL5 and RPL11 mutations 134
Multiplex Ligation-dependent Probe Amplification (MLPA) enhances molecular diagnosis of Diamond Blackfan Anemia due to RPS19 deficiency 130
Analysis of seven ribosomal protein genes in Italian Diamond Blackfan anemia patients 119
High frequency of RPL5 and RPL11 gene mutation in Italians patients with Diamond-Blackfan anemia (DBA) 113
Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein 104
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia 99
MUTAZIONI IN PROTEINE RIBOSOMIALI IN PAZIENTI ITALIANI CON ANEMIA DI BLACKFAN DIAMOND 98
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. 93
AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndrome 92
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family 92
UN DATABASE PER L’ANEMIA DI DIAMOND-BLACKFAN 90
Somatic mosaicism and variable expressivity in Diamond Blackfan anemia (DBA): a gross deletion involving the 19q13 locus in a patient with transient anemia 89
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. 88
Neutropenie: considerazioni su una casistica monocentrica 88
Le basi genetiche di una ribosomopatia: un database per l'anemia di Diamond-Blackfan 86
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 82
HDR syndrome: a novel "de novo" mutation in GATA3 gene. 77
Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome. 75
Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations 73
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype. 70
RPS19 mutations in patients with Diamond-Blackfan anemia 64
Search for protein interactors of ribosomal protein S19, mutated in Diamond Blackfan Anemia 63
Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene. 62
The broad spectrum of autoimmune lymphoproliferative disease: molecular bases, clinical features and long-term follow-up in 31 patients 48
Totale 3.151
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Categoria #
all - tutte 8.877
article - articoli 0
book - libri 0
conference - conferenze 2.184
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.061
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020370 0 0 23 39 21 109 44 22 26 46 23 17
2020/2021517 37 34 55 32 49 41 39 24 59 41 55 51
2021/2022451 34 15 40 49 10 18 21 48 20 20 90 86
2022/2023712 45 39 20 100 86 182 34 62 96 16 17 15
2023/2024259 47 35 6 16 15 30 34 8 7 26 12 23
2024/202591 4 75 12 0 0 0 0 0 0 0 0 0
Totale 3.151