SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

CALZOLARI, Elisa
 Distribuzione geografica
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Continente #
NA - Nord America 3.503
EU - Europa 2.095
AS - Asia 531
SA - Sud America 5
OC - Oceania 4
Totale 6.138
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Nazione #
US - Stati Uniti d'America 3.491
IT - Italia 1.106
CN - Cina 348
DE - Germania 301
UA - Ucraina 288
GB - Regno Unito 130
TR - Turchia 127
SE - Svezia 89
FI - Finlandia 56
RU - Federazione Russa 43
BE - Belgio 29
FR - Francia 27
TH - Thailandia 25
CA - Canada 10
IR - Iran 10
HK - Hong Kong 9
NL - Olanda 7
IN - India 6
BR - Brasile 5
IE - Irlanda 4
JP - Giappone 4
PL - Polonia 4
AU - Australia 3
CH - Svizzera 2
HU - Ungheria 2
KZ - Kazakistan 2
AT - Austria 1
CZ - Repubblica Ceca 1
ES - Italia 1
HN - Honduras 1
MD - Moldavia 1
MK - Macedonia 1
MX - Messico 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
RO - Romania 1
Totale 6.138
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Città #
Woodbridge 461
Fairfield 439
Ashburn 267
Chandler 266
Houston 266
Jacksonville 263
Ann Arbor 258
Seattle 173
Cambridge 167
Wilmington 166
Milan 105
Beijing 98
Izmir 82
Nanjing 79
Rome 68
Princeton 52
Boardman 38
Addison 37
San Diego 36
New York 31
Brussels 27
San Mateo 26
Bangkok 25
Bremen 25
Naples 24
Palermo 23
Shenyang 23
Tianjin 21
Falls Church 19
Shanghai 19
Hebei 18
Turin 17
Redwood City 16
Catania 15
Nanchang 15
Bari 14
Dearborn 14
Brescia 13
Verona 13
Bologna 11
Ferrara 11
Philadelphia 11
Venice 11
Changsha 10
Jiaxing 10
Los Angeles 10
Hong Kong 8
Mountain View 8
Washington 8
Auburn Hills 7
Jinan 7
Kunming 7
Salerno 7
Sesto San Giovanni 7
Toronto 7
Ardabil 6
Bergamo 6
Florence 6
Leawood 6
London 6
Vicenza 6
Zhengzhou 6
Alba 5
Des Moines 5
Guangzhou 5
Indiana 5
Messina 5
Nola 5
Padova 5
Pescara 5
Casoria 4
Changchun 4
Cursi 4
Enna 4
Genoa 4
Gravina di Catania 4
Haikou 4
Helsinki 4
Lamezia Terme 4
Lanzhou 4
Molfetta 4
Northolt 4
Norwalk 4
Ortona 4
Reggio Calabria 4
Selvazzano Dentro 4
Torino 4
Trieste 4
Alessandria 3
Belmonte Mezzagno 3
Cagliari 3
Castagneto Carducci 3
Livorno 3
Manoppello Scalo 3
Montréal 3
Monza 3
Munich 3
Ningbo 3
Osasco 3
Pavia 3
Totale 4.049
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Nome #
Mutazione Q283P nel gene HFE in un eterozigote C282Y affetto da emocromatosi. 826
Genetica della labiopalatoschisi non sindromica: ruolo di polimorfismi del metabolismo dei folati e dell’omocisteina. 434
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis. 173
In vitro short-term test evaluation of catecholestrogens genotoxicity 155
Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele. 146
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. 138
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 133
null 131
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point. 129
Mole maker phenotype: possible narrowing of the candidate region. 128
null 125
Characterization of a deleted Y chromosome in a male with Turner stigmata 123
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 120
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey. 118
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females. 109
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 109
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 109
Epidemiology of cleft palate in Europe: implications for genetic research. 108
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 105
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 104
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: case report. 103
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 102
Comparison of two statistical techniques for the surveillance of birth defects through a Monte Carlo simulation 102
A two-locus model for non-syndromic congenital dysplasia of the hip (CDH) 101
null 100
null 99
Progress in understanding GJB2-linked deafness 98
Exclusion of COL2A1 and VDR as Developmental Dysplasia of the Hip Genes 98
CHARACTERIZATION OF THE PSEUDOGENIC REGION OF VON WILLEBRAND FACTOR BY MOLECULAR CLONING AND "IN SITU" HYBRIDIZATION 92
null 92
null 91
null 91
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. 90
Analisi del polimorfismo IVS2+4T>C del gene HFE in soggetti con sovraccarico di ferro. 89
Exploring the clinical and epidemiological complexity of GJB2-linked deafness. 88
EUROCAT and orofacial clefts: The epidemiology of orofacial clefts in 30 european regions 88
Clinical anophthalmos in a family 85
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion. 83
null 78
Localization of cloned human DNA sequences and analysis of chromosomal alterations by in situ hybridization. 77
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence 74
Schisi facciale e genetica dei folati 65
Association between the c.66A>G variant in the Methionine Synthase reductase and nonsyndromic cleft palate. 64
Associazione tra il polimorfismo c.66A>G del gene MTRR e la palatoschisi non-sindromica. 62
Genomic organization and expression of the MTHFS gene 61
Cloning and chromosome localization of the gene for the methenyltratrahydrofolate-synthetase 60
Analisi dei genotipi ed aplotipi HFE nella popolazione Ferrarese 58
Una nuova mutazione del gene HFE in un eterozigote C282Y con emocromatosi. 57
Frequenze genotipiche ed aplotipiche HFE nella popolazione della Provincia di Ferrara 50
Mental retardation (MR) and coagulation factor XI deficiency in two first cousins once removed: a new X-linked syndrome? 49
Epidemiologia e genetica delle schisi orofacciali 46
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype. 35
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 23
CHARACTERIZATION OF THE PSEUDOGENIC AND GENIC HOMOLOGOUS REGIONS OF VON WILLEBRAND FACTOR 22
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR 21
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate. 20
Congenital heart defects: 15 Years of experience of the Emilia-Romagna Registry (Italy) 14
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 11
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 11
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 9
Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT) 6
Totale 6.188
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Categoria #
all - tutte 17.504
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 286
Totale 17.790
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019436 0 0 0 0 0 0 0 0 0 0 169 267
2019/20201.212 181 47 50 173 87 130 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
2023/2024734 80 69 53 32 65 116 70 59 56 92 42 0
Totale 6.188