CALZOLARI, Elisa
 Distribuzione geografica
Continente #
NA - Nord America 3.595
EU - Europa 2.652
AS - Asia 716
SA - Sud America 5
OC - Oceania 4
Totale 6.972
Nazione #
US - Stati Uniti d'America 3.572
IT - Italia 1.589
CN - Cina 373
DE - Germania 316
UA - Ucraina 288
SG - Singapore 155
GB - Regno Unito 141
TR - Turchia 127
SE - Svezia 89
FI - Finlandia 78
RU - Federazione Russa 43
BE - Belgio 33
FR - Francia 27
TH - Thailandia 25
CA - Canada 21
NL - Olanda 12
IR - Iran 11
HK - Hong Kong 9
CH - Svizzera 6
IN - India 6
BR - Brasile 5
CZ - Repubblica Ceca 5
IE - Irlanda 4
JP - Giappone 4
LT - Lituania 4
PL - Polonia 4
PT - Portogallo 4
AU - Australia 3
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 6.972
Città #
Woodbridge 461
Fairfield 439
Ashburn 271
Chandler 266
Houston 266
Jacksonville 263
Ann Arbor 258
Seattle 173
Milan 169
Cambridge 167
Wilmington 166
Singapore 123
Rome 101
Beijing 98
Izmir 82
Nanjing 79
Princeton 52
Boardman 43
Naples 43
Addison 37
San Diego 36
Shanghai 34
Brussels 31
New York 31
Los Angeles 29
Palermo 26
San Mateo 26
Bangkok 25
Bremen 25
Turin 24
Catania 23
Helsinki 23
Shenyang 23
Bari 22
Tianjin 21
Falls Church 19
Hebei 18
Brescia 17
Florence 17
Padova 16
Redwood City 16
Nanchang 15
Verona 15
Dearborn 14
London 14
Bologna 13
Munich 13
Ferrara 12
Philadelphia 11
Toronto 11
Venice 11
Changsha 10
Jiaxing 10
Messina 9
Carbonera 8
Hong Kong 8
Mountain View 8
Trieste 8
Vicenza 8
Washington 8
Auburn Hills 7
Genoa 7
Jinan 7
Kunming 7
Nola 7
Ottawa 7
Salerno 7
Sesto San Giovanni 7
Ardabil 6
Bergamo 6
Leawood 6
Molfetta 6
Zhengzhou 6
Alba 5
Cerignola 5
Des Moines 5
Frankfurt am Main 5
Guangzhou 5
Iesi 5
Indiana 5
Pescara 5
Santa Clara 5
Augusta 4
Bosisio Parini 4
Cagliari 4
Caserta 4
Casoria 4
Changchun 4
Cursi 4
Enna 4
Gravina di Catania 4
Haikou 4
Lamezia Terme 4
Lanzhou 4
Lucca 4
Lugagnano 4
Northolt 4
Norwalk 4
Ortona 4
Perugia 4
Totale 4.468
Nome #
Mutazione Q283P nel gene HFE in un eterozigote C282Y affetto da emocromatosi. 1.131
Genetica della labiopalatoschisi non sindromica: ruolo di polimorfismi del metabolismo dei folati e dell’omocisteina. 578
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis. 181
In vitro short-term test evaluation of catecholestrogens genotoxicity 162
Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele. 150
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. 142
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 138
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point. 134
null 131
Mole maker phenotype: possible narrowing of the candidate region. 131
Characterization of a deleted Y chromosome in a male with Turner stigmata 130
Associazione tra il polimorfismo c.66A>G del gene MTRR e la palatoschisi non-sindromica. 129
null 125
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 124
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey. 122
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females. 117
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 116
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 115
Epidemiology of cleft palate in Europe: implications for genetic research. 112
A two-locus model for non-syndromic congenital dysplasia of the hip (CDH) 111
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 110
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 110
EUROCAT and orofacial clefts: The epidemiology of orofacial clefts in 30 european regions 109
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: case report. 108
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 107
Comparison of two statistical techniques for the surveillance of birth defects through a Monte Carlo simulation 106
Exclusion of COL2A1 and VDR as Developmental Dysplasia of the Hip Genes 105
Analisi del polimorfismo IVS2+4T>C del gene HFE in soggetti con sovraccarico di ferro. 103
Progress in understanding GJB2-linked deafness 100
null 100
CHARACTERIZATION OF THE PSEUDOGENIC REGION OF VON WILLEBRAND FACTOR BY MOLECULAR CLONING AND "IN SITU" HYBRIDIZATION 99
null 99
Exploring the clinical and epidemiological complexity of GJB2-linked deafness. 95
Clinical anophthalmos in a family 94
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. 92
null 92
null 91
null 91
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion. 89
Localization of cloned human DNA sequences and analysis of chromosomal alterations by in situ hybridization. 79
null 78
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence 76
Association between the c.66A>G variant in the Methionine Synthase reductase and nonsyndromic cleft palate. 73
Schisi facciale e genetica dei folati 68
Cloning and chromosome localization of the gene for the methenyltratrahydrofolate-synthetase 68
Analisi dei genotipi ed aplotipi HFE nella popolazione Ferrarese 67
Genomic organization and expression of the MTHFS gene 65
Frequenze genotipiche ed aplotipiche HFE nella popolazione della Provincia di Ferrara 62
Una nuova mutazione del gene HFE in un eterozigote C282Y con emocromatosi. 61
Epidemiologia e genetica delle schisi orofacciali 52
Mental retardation (MR) and coagulation factor XI deficiency in two first cousins once removed: a new X-linked syndrome? 51
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype. 41
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR 34
CHARACTERIZATION OF THE PSEUDOGENIC AND GENIC HOMOLOGOUS REGIONS OF VON WILLEBRAND FACTOR 30
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate. 29
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 27
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 22
Congenital heart defects: 15 Years of experience of the Emilia-Romagna Registry (Italy) 19
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 16
Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT) 13
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 12
Totale 7.022
Categoria #
all - tutte 23.583
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 421
Totale 24.004


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020761 0 0 0 0 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
2023/2024949 80 69 53 32 65 116 70 59 56 92 94 163
2024/2025619 126 123 167 199 4 0 0 0 0 0 0 0
Totale 7.022