IRIS Institutional Research Information System - OPENBS Open Archive UniBS

GARDELLA, Rita
 Distribuzione geografica
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Continente #
NA - Nord America 3.115
EU - Europa 1.930
AS - Asia 965
AF - Africa 10
OC - Oceania 5
SA - Sud America 4
Continente sconosciuto - Info sul continente non disponibili 2
AN - Antartide 1
Totale 6.032
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Nazione #
US - Stati Uniti d'America 3.104
PL - Polonia 622
CN - Cina 556
UA - Ucraina 395
IT - Italia 322
DE - Germania 160
SG - Singapore 146
FI - Finlandia 111
FR - Francia 107
HK - Hong Kong 107
GB - Regno Unito 97
IE - Irlanda 59
TR - Turchia 57
IN - India 39
VN - Vietnam 22
BE - Belgio 20
KR - Corea 18
CA - Canada 11
CZ - Repubblica Ceca 10
ID - Indonesia 7
SE - Svezia 6
ZA - Sudafrica 6
NL - Olanda 5
RU - Federazione Russa 5
AU - Australia 4
TW - Taiwan 4
AT - Austria 3
ES - Italia 3
MU - Mauritius 3
CH - Svizzera 2
EU - Europa 2
IR - Iran 2
SA - Arabia Saudita 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
BR - Brasile 1
CY - Cipro 1
FK - Isole Falkland (Malvinas) 1
GE - Georgia 1
GS - Georgia del Sud e Isole Sandwich Australi 1
JP - Giappone 1
LT - Lituania 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
RO - Romania 1
SC - Seychelles 1
Totale 6.032
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Città #
Warsaw 622
Fairfield 435
Woodbridge 323
Jacksonville 285
Ashburn 257
Houston 249
Seattle 182
Ann Arbor 165
Cambridge 161
Wilmington 151
Brescia 135
Chandler 132
Singapore 115
Nanjing 112
Princeton 112
Hong Kong 106
Dearborn 88
Beijing 83
New York 82
Helsinki 60
Dublin 59
Nanchang 55
Istanbul 46
Des Moines 36
Jinan 35
Shenyang 34
Hebei 32
Lancaster 30
Changsha 27
San Diego 23
Dong Ket 22
Milan 20
Shanghai 19
Kunming 17
Brussels 16
Jiaxing 15
Tianjin 15
Hangzhou 14
Los Angeles 14
Ningbo 14
San Mateo 14
London 11
Seongnam 11
Zhengzhou 11
Boardman 10
Washington 9
Brno 8
Guangzhou 8
Lanzhou 8
Leawood 8
San Francisco 8
Verona 8
Haikou 7
Hefei 7
Jakarta 7
Monmouth Junction 7
Naples 7
Norwalk 7
Toronto 7
Bela-Bela 6
Fuzhou 6
Changchun 5
Frankfurt am Main 5
Kilburn 5
Mantova 5
Munich 5
Orange 5
Redwood City 5
Rome 5
Taizhou 5
Augusta 4
Council Bluffs 4
Kocaeli 4
Taipei 4
Mumbai 3
Phoenix 3
Santa Clara 3
Seoul 3
Taglio Di Po 3
Vienna 3
Alzano Lombardo 2
Ardabil 2
Cagliari 2
Canberra 2
Chengdu 2
Corridonia 2
Falkenstein 2
Gardone Val Trompia 2
Maccagno 2
Madrid 2
Modena 2
Moglia 2
New Delhi 2
Olomouc 2
Ottawa 2
Padova 2
Paris 2
Pignola 2
Prescot 2
Riyadh 2
Totale 4.692
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Nome #
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 296
New Copy Number Variations in Schizophrenia 268
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 264
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 216
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure 196
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 179
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 171
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 143
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 134
The type III-9 repeat of human fibronectin is encoded by a single exon which is not alternatively spliced. 132
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 131
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 131
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 125
RT-PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: molecular markers for hepatocellular carcinoma 123
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 123
A frequent HaeIII RFLP of the human fibronectin gene 106
Polymorphic CA repeat in IGF-I gene: lack of association with schizophrenia. 106
A common MspI RFLP of the human fibronectin gene (FN1) 105
Phenotypic correction of the defective fibronectin extracellular matrix of Ehlers-Danlos syndrome fibroblasts. 105
Reconstructing the genetic history of Italians: new insights from a male (Y-chromosome) perspective 105
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 101
Exclusion of candidate genes in a family with arterial tortuosity syndrome 99
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. 99
Effect of dexamethasone on the assembly of the matrix of fibronectin and its receptors organization in Ehlers-Danlos syndrome skin fibroblasts. 98
Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample 98
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 97
Analysis of Copy Number Variations in Schizophrenia Italian Patients 95
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 94
Human fibronectin gene (FN1) RFLPs: mapping and linkage disequilibrium analysis 94
Cerebellar ataxia in a family with recurrent epidermolysis bullosa dystrophica 93
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 93
New Copy Number Variations in Schizophrenia Italian Patients 89
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients 89
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 88
A Taq RFLP for the human fibronectin (FN1) gene 87
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 86
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 86
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 86
Mitochondrial DNA haplogroups and age at onset of schizophrenia 85
Detection of high level of autozygosity in a group of Italian schizophrenia patients 80
A new Taq RFLP of the human fibronecin gene (FN1) 78
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 77
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 76
RT-PCR detection of EDA+ fibronectin mRNA isoforms as hepatocarcinoma markers. 75
Genome wide study of Italian schizophrenia patients 74
The Italian Registry of Hereditary Epidermolysis Bullosa 71
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 71
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 70
A frequent Hind RFLP of the human fibronectin) gene (FN1) 69
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 68
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 68
Ricerca del gene malattia in una famiglia affetta da una forma di atassia cerebellare a difetto molecolare sconosciuto 66
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 63
Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mithocondrial DNA 60
null 60
In vitro Glutamate treatments modify AMPA RNA editing and ADARs activity 58
Modulation of RNA editing by FMRP in mammals 56
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 47
Analysis of the (TA) repeat polymorphism of the UGT1A1 (UDP-Glucuronosyltransferase) gene in schizophrenia 31
Totale 6.234
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Categoria #
all - tutte 26.203
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 26.203
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.244 0 0 0 0 106 201 194 187 120 246 98 92
2020/20211.091 25 111 26 122 66 146 63 110 164 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
2024/2025298 13 15 4 152 114 0 0 0 0 0 0 0
Totale 6.234