IRIS Institutional Research Information System - OPENBS Open Archive UniBS

GARDELLA, Rita
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 4.104
EU - Europa 2.278
AS - Asia 2.060
SA - Sud America 296
AF - Africa 42
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 2
AN - Antartide 1
Totale 8.803
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.037
CN - Cina 818
PL - Polonia 637
SG - Singapore 630
UA - Ucraina 400
IT - Italia 380
BR - Brasile 243
DE - Germania 203
HK - Hong Kong 185
FR - Francia 171
GB - Regno Unito 140
VN - Vietnam 132
FI - Finlandia 131
IN - India 77
TR - Turchia 66
RU - Federazione Russa 62
IE - Irlanda 59
BD - Bangladesh 38
CA - Canada 36
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
JM - Giamaica 5
LT - Lituania 5
PE - Perù 5
CH - Svizzera 4
CL - Cile 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
CR - Costa Rica 2
EU - Europa 2
HN - Honduras 2
JO - Giordania 2
LK - Sri Lanka 2
NZ - Nuova Zelanda 2
SI - Slovenia 2
TN - Tunisia 2
AG - Antigua e Barbuda 1
AL - Albania 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
CG - Congo 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 8.803
Salva come PNG Salva come JPEG
Città #
Warsaw 636
Fairfield 435
Ashburn 374
Singapore 368
Woodbridge 323
Jacksonville 287
Houston 253
Seattle 189
Hong Kong 184
San Jose 180
Ann Arbor 165
Cambridge 161
Beijing 160
Wilmington 152
Brescia 137
Chandler 132
New York 113
Nanjing 112
Princeton 112
The Dalles 100
Dearborn 89
Helsinki 70
Dublin 59
Los Angeles 58
Nanchang 55
Lauterbourg 52
Istanbul 47
Des Moines 42
Jinan 38
Shenyang 36
Hebei 32
Ho Chi Minh City 31
Lancaster 31
Milan 31
Munich 30
Changsha 28
Orem 27
Moscow 26
Dallas 25
Hanoi 25
Buffalo 24
San Diego 24
Santa Clara 24
Dong Ket 22
San Francisco 21
São Paulo 20
Chicago 19
Shanghai 19
Tianjin 19
Redondo Beach 18
Kunming 17
Brussels 16
Chennai 16
Council Bluffs 16
Hangzhou 16
Jiaxing 16
London 16
Frankfurt am Main 15
Guangzhou 14
Ningbo 14
Rome 14
San Mateo 14
Naples 12
Zhengzhou 12
Denver 11
Seongnam 11
Boardman 10
Boston 10
Brooklyn 10
Jakarta 10
Paris 10
Phoenix 10
Washington 10
Mumbai 9
Tokyo 9
Toronto 9
Turku 9
Atlanta 8
Brno 8
Hefei 8
Lanzhou 8
Leawood 8
Manchester 8
Poplar 8
Rio de Janeiro 8
Verona 8
Charlotte 7
Fuzhou 7
Haikou 7
Monmouth Junction 7
Norwalk 7
Riyadh 7
Abuja 6
Bela-Bela 6
Dhaka 6
Johannesburg 6
Montreal 6
Nuremberg 6
Stockholm 6
Tashkent 6
Totale 6.113
Salva come PNG Salva come JPEG
Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 397
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 320
New Copy Number Variations in Schizophrenia 318
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 301
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure 241
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 226
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 221
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 187
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 186
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 185
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 183
The type III-9 repeat of human fibronectin is encoded by a single exon which is not alternatively spliced. 182
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 181
A frequent HaeIII RFLP of the human fibronectin gene 175
Analysis of Copy Number Variations in Schizophrenia Italian Patients 173
A Taq RFLP for the human fibronectin (FN1) gene 172
A common MspI RFLP of the human fibronectin gene (FN1) 170
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 164
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 162
RT-PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: molecular markers for hepatocellular carcinoma 158
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 150
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 148
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 145
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. 145
Reconstructing the genetic history of Italians: new insights from a male (Y-chromosome) perspective 143
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients 142
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 139
Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample 136
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 136
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 134
Exclusion of candidate genes in a family with arterial tortuosity syndrome 134
A new Taq RFLP of the human fibronecin gene (FN1) 133
Phenotypic correction of the defective fibronectin extracellular matrix of Ehlers-Danlos syndrome fibroblasts. 133
Cerebellar ataxia in a family with recurrent epidermolysis bullosa dystrophica 131
Polymorphic CA repeat in IGF-I gene: lack of association with schizophrenia. 131
Detection of high level of autozygosity in a group of Italian schizophrenia patients 130
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 128
Effect of dexamethasone on the assembly of the matrix of fibronectin and its receptors organization in Ehlers-Danlos syndrome skin fibroblasts. 126
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 126
New Copy Number Variations in Schizophrenia Italian Patients 123
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 123
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 121
A frequent Hind RFLP of the human fibronectin) gene (FN1) 120
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 117
Ricerca del gene malattia in una famiglia affetta da una forma di atassia cerebellare a difetto molecolare sconosciuto 117
Genome wide study of Italian schizophrenia patients 116
Mitochondrial DNA haplogroups and age at onset of schizophrenia 114
Human fibronectin gene (FN1) RFLPs: mapping and linkage disequilibrium analysis 112
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 109
In vitro Glutamate treatments modify AMPA RNA editing and ADARs activity 109
The Italian Registry of Hereditary Epidermolysis Bullosa 108
Modulation of RNA editing by FMRP in mammals 107
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 103
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 99
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 94
Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mithocondrial DNA 82
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 76
null 60
Totale 9.005
Salva come PNG Salva come JPEG
Categoria #
all - tutte 37.802
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 37.802
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202144 0 0 0 0 0 0 0 0 0 0 0 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
2025/20262.099 204 236 128 281 235 162 367 56 129 205 61 35
Totale 9.005