BOARETTO, FRANCESCA
 Distribuzione geografica
Continente #
NA - Nord America 2.275
EU - Europa 409
AS - Asia 288
OC - Oceania 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 2.977
Nazione #
US - Stati Uniti d'America 2.271
CN - Cina 193
IT - Italia 123
FI - Finlandia 117
VN - Vietnam 54
SE - Svezia 40
SG - Singapore 33
DE - Germania 32
GB - Regno Unito 32
UA - Ucraina 22
FR - Francia 12
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 2.977
Città #
Fairfield 336
Woodbridge 265
Chandler 255
Houston 203
Ashburn 169
Ann Arbor 151
Wilmington 120
Seattle 109
Jacksonville 100
Cambridge 98
Helsinki 85
Dong Ket 54
Princeton 42
Beijing 37
Columbus 37
Des Moines 32
Padova 28
San Diego 27
Medford 26
Boardman 24
Nanjing 23
Roxbury 22
Singapore 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
Tianjin 6
Giarre 5
Hefei 5
Kunming 5
Milan 5
Norwalk 5
Guangzhou 4
Taizhou 4
Villavesco 4
Casier 3
Cepagatti 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
Dublin 2
Edinburgh 2
Foligno 2
Fort Worth 2
Frankfurt am Main 2
Herzliya 2
Hounslow 2
Indiana 2
Las Vegas 2
London 2
Naples 2
Newark 2
Ningbo 2
Paris 2
Perugia 2
Redwood City 2
Salerno 2
Treviso 2
Waanrode 2
Amsterdam 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
Drancy 1
Fuzhou 1
Islington 1
Jinhua 1
Kabul 1
Kharkiv 1
Kilburn 1
Köln 1
Lancaster 1
Totale 2.512
Nome #
Individuazione e caratterizzazione di geni implicati nelle paraparesi spastiche ereditarie 282
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 150
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum 128
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. 126
A novel missense mutation in the L1CAM gene in a boy with L1 disease 120
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling 113
A new mutation in two siblings with cystinosis presenting with Bartter syndrome. 108
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 106
Novel mutations in the L1CAM gene support the complexity of L1 syndrome 103
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma. 101
The pheochromocytoma and paraganglioma syndrome: founder effects and the PGL 1 syndrome. 93
A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype 90
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 90
Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation 89
Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas 85
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28. 84
Individuation of new mutations in L1CAM gene in patients with L1 diseases. 80
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients 79
Novel mutation of the mitofusin 2 gene in a family with Charcot-Marie-Tooth disease type 2 (CMT2A). 78
Evaluation of linkage signals in a subset of families with high recurrence of schizophrenia and bipolar disorder originating from Chioggia 69
c.1392+2T>C mutation in MFN2 gene affects splicing in Charcot-Marie-Tooth (CMT) 2A family. 65
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. 65
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites 61
Studio genetico pilota sulla popolazione di Chioggia: dati preliminari 60
Genetics of adrenal tumors. 58
Genome scan for schizophrenia/bipolar disorder supports a susceptibility locus in 15q26 56
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia. 49
NOVEL MUTATION OF THE MITOFUSIN 2 GENE IN A FAMILY WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 2A 44
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. 44
Novel MFN2 mutations and phenotypic variability in patients with Charcot-Marie-Tooth disease type 2A. 44
CLINICAL AND ELECTROPHYSIOLOGICAL SPECTRUM IN A GROUP OF SPORADIC DISTAL MOTOR NEUROPATHIES 38
Localization of a new highly repeated DNA sequence of Lemur cafta (Lemuridae, Strepsirhini). 32
Quantitative in situ detection of high-risk human papillomavirus in cytological specimens by SYBR Green I fluorescent labeling. 27
Totale 2.995
Categoria #
all - tutte 9.481
article - articoli 7.923
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 17.404


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020529 72 16 10 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
2024/20251 1 0 0 0 0 0 0 0 0 0 0 0
Totale 2.995