IRIS Institutional Research Information System - OPENBS Open Archive UniBS

GARDELLA, Rita
 Distribuzione geografica
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Continente #
NA - Nord America 3.991
EU - Europa 2.261
AS - Asia 2.047
SA - Sud America 296
AF - Africa 42
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 2
AN - Antartide 1
Totale 8.660
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Nazione #
US - Stati Uniti d'America 3.934
CN - Cina 814
PL - Polonia 637
SG - Singapore 627
UA - Ucraina 400
IT - Italia 366
BR - Brasile 243
DE - Germania 202
HK - Hong Kong 184
FR - Francia 171
GB - Regno Unito 138
VN - Vietnam 132
FI - Finlandia 131
IN - India 77
TR - Turchia 66
RU - Federazione Russa 62
IE - Irlanda 59
BD - Bangladesh 33
CA - Canada 29
BE - Belgio 20
KR - Corea 20
AU - Australia 18
AR - Argentina 17
ID - Indonesia 16
ZA - Sudafrica 15
MX - Messico 14
SA - Arabia Saudita 13
CZ - Repubblica Ceca 12
ES - Italia 12
NL - Olanda 12
SE - Svezia 12
JP - Giappone 10
AT - Austria 9
IQ - Iraq 9
EC - Ecuador 8
VE - Venezuela 7
KE - Kenya 6
NG - Nigeria 6
UZ - Uzbekistan 6
AE - Emirati Arabi Uniti 5
CO - Colombia 5
IR - Iran 5
LT - Lituania 5
PE - Perù 5
CH - Svizzera 4
CL - Cile 4
JM - Giamaica 4
MA - Marocco 4
PH - Filippine 4
TW - Taiwan 4
MU - Mauritius 3
MY - Malesia 3
PA - Panama 3
PK - Pakistan 3
TT - Trinidad e Tobago 3
UY - Uruguay 3
BO - Bolivia 2
EU - Europa 2
HN - Honduras 2
JO - Giordania 2
LK - Sri Lanka 2
NZ - Nuova Zelanda 2
SI - Slovenia 2
TN - Tunisia 2
AL - Albania 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
CG - Congo 1
CR - Costa Rica 1
CU - Cuba 1
CY - Cipro 1
DZ - Algeria 1
EG - Egitto 1
ET - Etiopia 1
FK - Isole Falkland (Malvinas) 1
GE - Georgia 1
GS - Georgia del Sud e Isole Sandwich Australi 1
HU - Ungheria 1
IL - Israele 1
KW - Kuwait 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
NP - Nepal 1
PS - Palestinian Territory 1
PT - Portogallo 1
PY - Paraguay 1
RO - Romania 1
SC - Seychelles 1
SN - Senegal 1
SY - Repubblica araba siriana 1
Totale 8.660
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Città #
Warsaw 636
Fairfield 435
Ashburn 372
Singapore 367
Woodbridge 323
Jacksonville 287
Houston 253
Seattle 189
Hong Kong 183
Ann Arbor 165
Cambridge 161
Beijing 159
Wilmington 152
San Jose 145
Brescia 137
Chandler 132
Nanjing 112
Princeton 112
New York 109
The Dalles 100
Dearborn 88
Helsinki 70
Dublin 59
Los Angeles 57
Nanchang 55
Lauterbourg 52
Istanbul 47
Des Moines 42
Jinan 38
Shenyang 36
Hebei 32
Ho Chi Minh City 31
Lancaster 31
Milan 30
Munich 30
Changsha 28
Orem 27
Moscow 26
Hanoi 25
Buffalo 23
San Diego 23
Dong Ket 22
Santa Clara 20
São Paulo 20
Chicago 19
Dallas 19
Shanghai 19
Tianjin 19
Redondo Beach 18
San Francisco 18
Kunming 17
Brussels 16
Chennai 16
Hangzhou 16
Jiaxing 16
London 16
Council Bluffs 14
Frankfurt am Main 14
Guangzhou 14
Ningbo 14
Rome 14
San Mateo 14
Zhengzhou 12
Naples 11
Seongnam 11
Boardman 10
Boston 10
Denver 10
Jakarta 10
Paris 10
Washington 10
Brooklyn 9
Mumbai 9
Phoenix 9
Tokyo 9
Turku 9
Atlanta 8
Brno 8
Hefei 8
Lanzhou 8
Leawood 8
Manchester 8
Poplar 8
Rio de Janeiro 8
Toronto 8
Verona 8
Fuzhou 7
Haikou 7
Monmouth Junction 7
Norwalk 7
Riyadh 7
Abuja 6
Bela-Bela 6
Charlotte 6
Dhaka 6
Johannesburg 6
Nuremberg 6
Stockholm 6
Tashkent 6
Belo Horizonte 5
Totale 6.041
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Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 383
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 318
New Copy Number Variations in Schizophrenia 315
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 296
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure 239
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 223
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 218
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 185
Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia 184
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 183
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 181
The type III-9 repeat of human fibronectin is encoded by a single exon which is not alternatively spliced. 181
Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: analysis of transcript levels in dermal fibroblasts 179
A frequent HaeIII RFLP of the human fibronectin gene 171
Analysis of Copy Number Variations in Schizophrenia Italian Patients 170
A common MspI RFLP of the human fibronectin gene (FN1) 169
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 163
A -96C-T mutation in the promoter of the collagen type VII gene (COL7A1) abolishing transcription in a patient affected by recessive dystrophic epidermolys bullosa 161
RT-PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: molecular markers for hepatocellular carcinoma 156
A Taq RFLP for the human fibronectin (FN1) gene 153
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 148
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 146
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 143
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. 143
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 138
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients 137
Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample 135
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 135
Exclusion of candidate genes in a family with arterial tortuosity syndrome 133
Phenotypic correction of the defective fibronectin extracellular matrix of Ehlers-Danlos syndrome fibroblasts. 133
Reconstructing the genetic history of Italians: new insights from a male (Y-chromosome) perspective 133
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 131
Polymorphic CA repeat in IGF-I gene: lack of association with schizophrenia. 131
A new Taq RFLP of the human fibronecin gene (FN1) 129
Cerebellar ataxia in a family with recurrent epidermolysis bullosa dystrophica 127
Detection of high level of autozygosity in a group of Italian schizophrenia patients 127
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 127
Effect of dexamethasone on the assembly of the matrix of fibronectin and its receptors organization in Ehlers-Danlos syndrome skin fibroblasts. 125
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 125
New Copy Number Variations in Schizophrenia Italian Patients 123
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 121
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 120
A frequent Hind RFLP of the human fibronectin) gene (FN1) 118
Identification of two splicing mutations in the collagen type VII gene (COL7A1) of a patient affected by the localisata variant of recessive dystrophic epidermolysis bullosa 115
Genome wide study of Italian schizophrenia patients 115
Ricerca del gene malattia in una famiglia affetta da una forma di atassia cerebellare a difetto molecolare sconosciuto 113
Human fibronectin gene (FN1) RFLPs: mapping and linkage disequilibrium analysis 112
Mitochondrial DNA haplogroups and age at onset of schizophrenia 111
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 109
The Italian Registry of Hereditary Epidermolysis Bullosa 108
In vitro Glutamate treatments modify AMPA RNA editing and ADARs activity 106
Modulation of RNA editing by FMRP in mammals 105
RT-PCR detection of EDA+ fibronectin mRNA isoforms as hepatocarcinoma markers. 103
Analysis of the (TA) repeat polymorphism of the UGT1A1 (UDP-Glucuronosyltransferase) gene in schizophrenia 102
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 98
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 93
Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mithocondrial DNA 81
Human fibroblasts with mutations in COL5A1 and COL3A1 genes do not organize collagens and fibronectin in the extracellular matrix, down-regulate alpha2beta1 integrin and recruit alphavbeta3 instead of alpha5beta1 integrin 75
null 60
Totale 8.862
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Categoria #
all - tutte 36.090
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 36.090
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021258 0 0 0 0 0 0 0 0 0 84 130 44
2021/2022543 30 137 9 9 9 18 33 20 21 65 70 122
2022/2023389 62 6 9 32 39 111 1 30 57 3 18 21
2023/2024505 29 11 37 41 30 112 23 19 111 17 3 72
2024/2025970 13 15 4 152 114 82 84 22 112 45 182 145
2025/20261.956 204 236 128 281 235 162 367 56 129 158 0 0
Totale 8.862