SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

CALZOLARI, Elisa
 Distribuzione geografica
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Continente #
NA - Nord America 3.808
EU - Europa 2.828
AS - Asia 776
OC - Oceania 5
SA - Sud America 5
Totale 7.422
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Nazione #
US - Stati Uniti d'America 3.775
IT - Italia 1.728
CN - Cina 379
DE - Germania 320
UA - Ucraina 288
SG - Singapore 209
GB - Regno Unito 151
TR - Turchia 127
SE - Svezia 89
FI - Finlandia 83
RU - Federazione Russa 43
BE - Belgio 35
CA - Canada 31
FR - Francia 27
NL - Olanda 27
TH - Thailandia 25
IR - Iran 11
HK - Hong Kong 9
CH - Svizzera 6
IN - India 6
BR - Brasile 5
CZ - Repubblica Ceca 5
LT - Lituania 5
AU - Australia 4
IE - Irlanda 4
JP - Giappone 4
PL - Polonia 4
PT - Portogallo 4
GR - Grecia 2
HU - Ungheria 2
ID - Indonesia 2
KZ - Kazakistan 2
MN - Mongolia 2
AT - Austria 1
ES - Italia 1
HN - Honduras 1
MD - Moldavia 1
MK - Macedonia 1
MX - Messico 1
NZ - Nuova Zelanda 1
RO - Romania 1
Totale 7.422
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Città #
Woodbridge 461
Fairfield 439
Ashburn 271
Chandler 266
Houston 266
Jacksonville 263
Ann Arbor 258
Milan 183
Santa Clara 180
Singapore 177
Seattle 173
Cambridge 167
Wilmington 166
Rome 110
Beijing 98
Izmir 82
Nanjing 79
Naples 54
Princeton 52
Boardman 43
Addison 37
San Diego 36
Shanghai 34
Brussels 33
New York 31
Los Angeles 29
Bari 28
Helsinki 28
Palermo 27
San Mateo 26
Turin 26
Bangkok 25
Bremen 25
Catania 23
Shenyang 23
Florence 22
Tianjin 21
Falls Church 19
Hebei 18
London 18
Brescia 17
Padova 16
Redwood City 16
Bologna 15
Nanchang 15
Verona 15
Carbonera 14
Dearborn 14
Toronto 14
Munich 13
Ottawa 13
Ferrara 12
Venice 12
Philadelphia 11
Changsha 10
Jiaxing 10
Messina 10
Iesi 9
Nola 9
Hong Kong 8
Mountain View 8
Trieste 8
Vicenza 8
Washington 8
Auburn Hills 7
Genoa 7
Jinan 7
Kunming 7
Salerno 7
Sesto San Giovanni 7
Ardabil 6
Bergamo 6
Frankfurt am Main 6
Guangzhou 6
Leawood 6
Molfetta 6
Zhengzhou 6
Alba 5
Caserta 5
Cerignola 5
Des Moines 5
Indiana 5
Pavia 5
Pescara 5
Augusta 4
Bosisio Parini 4
Cagliari 4
Casoria 4
Changchun 4
Cursi 4
Enna 4
Gravina di Catania 4
Haikou 4
Lamezia Terme 4
Lanzhou 4
Lucca 4
Lugagnano 4
Modena 4
Northolt 4
Norwalk 4
Totale 4.785
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Nome #
Mutazione Q283P nel gene HFE in un eterozigote C282Y affetto da emocromatosi. 1.217
Genetica della labiopalatoschisi non sindromica: ruolo di polimorfismi del metabolismo dei folati e dell’omocisteina. 619
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis 187
In vitro short-term test evaluation of catecholestrogens genotoxicity 170
Associazione tra il polimorfismo c.66A>G del gene MTRR e la palatoschisi non-sindromica. 162
Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele. 157
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. 149
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 142
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point. 141
Mole maker phenotype: possible narrowing of the candidate region. 136
Characterization of a deleted Y chromosome in a male with Turner stigmata 134
null 131
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey. 129
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 128
null 125
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females. 124
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 124
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 121
Epidemiology of cleft palate in Europe: implications for genetic research. 120
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 117
A two-locus model for non-syndromic congenital dysplasia of the hip (CDH) 115
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 115
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: case report. 113
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region 113
EUROCAT and orofacial clefts: The epidemiology of orofacial clefts in 30 european regions 113
Exclusion of COL2A1 and VDR as Developmental Dysplasia of the Hip Genes 113
Comparison of two statistical techniques for the surveillance of birth defects through a Monte Carlo simulation 112
Analisi del polimorfismo IVS2+4T>C del gene HFE in soggetti con sovraccarico di ferro. 108
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion 107
CHARACTERIZATION OF THE PSEUDOGENIC REGION OF VON WILLEBRAND FACTOR BY MOLECULAR CLONING AND "IN SITU" HYBRIDIZATION 105
Progress in understanding GJB2-linked deafness 103
Exploring the clinical and epidemiological complexity of GJB2-linked deafness. 101
null 100
null 99
Clinical anophthalmos in a family 99
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. 96
null 92
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Localization of cloned human DNA sequences and analysis of chromosomal alterations by in situ hybridization. 83
Association between the c.66A>G variant in the Methionine Synthase reductase and nonsyndromic cleft palate. 80
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence 79
null 78
Analisi dei genotipi ed aplotipi HFE nella popolazione Ferrarese 74
Cloning and chromosome localization of the gene for the methenyltratrahydrofolate-synthetase 72
Schisi facciale e genetica dei folati 71
Genomic organization and expression of the MTHFS gene 71
Frequenze genotipiche ed aplotipiche HFE nella popolazione della Provincia di Ferrara 69
Una nuova mutazione del gene HFE in un eterozigote C282Y con emocromatosi. 64
Epidemiologia e genetica delle schisi orofacciali 58
Mental retardation (MR) and coagulation factor XI deficiency in two first cousins once removed: a new X-linked syndrome? 54
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype. 49
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR 40
CHARACTERIZATION OF THE PSEUDOGENIC AND GENIC HOMOLOGOUS REGIONS OF VON WILLEBRAND FACTOR 36
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 34
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate. 34
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 27
Congenital heart defects: 15 Years of experience of the Emilia-Romagna Registry (Italy) 24
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 23
Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT) 17
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 16
Totale 7.472
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Categoria #
all - tutte 25.941
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 457
Totale 26.398
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020544 0 0 0 0 0 0 98 118 88 133 76 31
2020/2021753 71 72 38 85 31 68 28 78 11 86 129 56
2021/2022789 32 64 86 41 46 35 46 33 32 54 69 251
2022/2023858 63 89 34 96 119 97 57 81 99 22 57 44
2023/2024949 80 69 53 32 65 116 70 59 56 92 94 163
2024/20251.069 126 123 167 199 262 192 0 0 0 0 0 0
Totale 7.472