BOARETTO, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 2.313
EU - Europa 442
AS - Asia 352
OC - Oceania 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 3.112
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Nazione #
US - Stati Uniti d'America 2.309
CN - Cina 196
IT - Italia 133
FI - Finlandia 117
SG - Singapore 94
VN - Vietnam 54
SE - Svezia 40
DE - Germania 33
FR - Francia 33
GB - Regno Unito 33
UA - Ucraina 22
NL - Olanda 10
BE - Belgio 4
IN - India 4
CA - Canada 3
LU - Lussemburgo 3
AU - Australia 2
CH - Svizzera 2
DK - Danimarca 2
ES - Italia 2
HU - Ungheria 2
IE - Irlanda 2
IL - Israele 2
AF - Afghanistan, Repubblica islamica di 1
AT - Austria 1
AZ - Azerbaigian 1
CL - Cile 1
CZ - Repubblica Ceca 1
EG - Egitto 1
EU - Europa 1
LT - Lituania 1
MX - Messico 1
PL - Polonia 1
Totale 3.112
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Città #
Fairfield 336
Woodbridge 265
Chandler 255
Houston 203
Ashburn 170
Ann Arbor 151
Wilmington 120
Seattle 109
Jacksonville 100
Cambridge 98
Helsinki 85
Singapore 79
Dong Ket 54
Princeton 42
Beijing 38
Columbus 37
Des Moines 32
Padova 28
San Diego 27
Medford 26
Boardman 24
Nanjing 23
Roxbury 22
Jinan 15
Shenyang 14
Nanchang 12
New York 11
Hebei 9
Chicago 8
Changsha 7
Hangzhou 7
Cagliari 6
Dearborn 6
Haikou 6
Jiaxing 6
Santa Clara 6
Tianjin 6
Giarre 5
Hefei 5
Kunming 5
Milan 5
Norwalk 5
Guangzhou 4
Taizhou 4
Villavesco 4
Casier 3
Cepagatti 3
Frankfurt am Main 3
Lanzhou 3
Luxembourg 3
Ogden 3
Toronto 3
Zhengzhou 3
Bologna 2
Brussels 2
Budapest 2
Castelbuono 2
Catania 2
Chengdu 2
Comun Nuovo 2
Copenhagen 2
Cosenza 2
Dublin 2
Edinburgh 2
Foligno 2
Fort Worth 2
Herzliya 2
Hounslow 2
Indiana 2
Las Vegas 2
London 2
Monticello Conte Otto 2
Naples 2
Newark 2
Ningbo 2
Paris 2
Perugia 2
Redwood City 2
Salerno 2
Trento 2
Treviso 2
Waanrode 2
Amsterdam 1
Antwerp 1
Atlanta 1
Azzano Decimo 1
Baiano 1
Baku 1
Barcelona 1
Belluno 1
Borås 1
Brno 1
Cairo 1
Cattolica 1
Chiswick 1
Ciampino 1
Dallas 1
Drancy 1
Fuzhou 1
Islington 1
Totale 2.580
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Nome #
Individuazione e caratterizzazione di geni implicati nelle paraparesi spastiche ereditarie 303
Von Hippel-Lindau disease: an evaluation of natural history and functional disability 178
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 153
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. 133
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum 129
A novel missense mutation in the L1CAM gene in a boy with L1 disease 122
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling 116
A new mutation in two siblings with cystinosis presenting with Bartter syndrome. 114
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 107
Novel mutations in the L1CAM gene support the complexity of L1 syndrome 107
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma. 105
Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation 95
A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype 95
The pheochromocytoma and paraganglioma syndrome: founder effects and the PGL 1 syndrome. 93
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 93
Individuation of new mutations in L1CAM gene in patients with L1 diseases. 87
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28. 87
Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas 86
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients 84
Novel mutation of the mitofusin 2 gene in a family with Charcot-Marie-Tooth disease type 2 (CMT2A). 83
Evaluation of linkage signals in a subset of families with high recurrence of schizophrenia and bipolar disorder originating from Chioggia 73
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. 70
c.1392+2T>C mutation in MFN2 gene affects splicing in Charcot-Marie-Tooth (CMT) 2A family. 68
Studio genetico pilota sulla popolazione di Chioggia: dati preliminari 66
Genetics of adrenal tumors. 63
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites 63
Genome scan for schizophrenia/bipolar disorder supports a susceptibility locus in 15q26 61
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia. 50
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. 49
Novel MFN2 mutations and phenotypic variability in patients with Charcot-Marie-Tooth disease type 2A. 46
NOVEL MUTATION OF THE MITOFUSIN 2 GENE IN A FAMILY WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 2A 45
CLINICAL AND ELECTROPHYSIOLOGICAL SPECTRUM IN A GROUP OF SPORADIC DISTAL MOTOR NEUROPATHIES 44
Localization of a new highly repeated DNA sequence of Lemur cafta (Lemuridae, Strepsirhini). 34
Quantitative in situ detection of high-risk human papillomavirus in cytological specimens by SYBR Green I fluorescent labeling. 28
Totale 3.130
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Categoria #
all - tutte 10.374
article - articoli 8.638
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 19.012
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020431 0 0 0 24 47 44 46 60 54 105 30 21
2020/2021486 12 23 7 24 72 16 7 36 62 73 67 87
2021/2022502 4 76 74 33 15 10 37 55 16 8 66 108
2022/2023570 88 59 35 76 123 58 4 42 38 6 33 8
2023/2024272 10 21 32 14 19 17 51 18 12 6 49 23
2024/2025136 1 85 50 0 0 0 0 0 0 0 0 0
Totale 3.130