BOARETTO, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 2.860
AS - Asia 1.143
EU - Europa 797
SA - Sud America 218
AF - Africa 216
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 7
Totale 5.262
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Nazione #
US - Stati Uniti d'America 2.745
SG - Singapore 410
CN - Cina 283
IT - Italia 171
BR - Brasile 152
FI - Finlandia 140
HK - Hong Kong 122
VN - Vietnam 88
DE - Germania 56
GB - Regno Unito 46
SE - Svezia 43
FR - Francia 38
NL - Olanda 36
PL - Polonia 30
UA - Ucraina 28
RU - Federazione Russa 20
IN - India 17
BJ - Benin 15
TR - Turchia 14
CA - Canada 13
IQ - Iraq 13
AR - Argentina 12
JP - Giappone 12
AT - Austria 11
CY - Cipro 11
CZ - Repubblica Ceca 11
IL - Israele 11
JM - Giamaica 11
BE - Belgio 10
GM - Gambi 10
PY - Paraguay 10
CH - Svizzera 9
ES - Italia 9
LA - Repubblica Popolare Democratica del Laos 9
LU - Lussemburgo 9
UZ - Uzbekistan 9
DZ - Algeria 8
EC - Ecuador 8
EE - Estonia 8
GR - Grecia 8
HU - Ungheria 8
IR - Iran 8
KE - Kenya 8
KZ - Kazakistan 8
LV - Lettonia 8
MD - Moldavia 8
MX - Messico 8
MY - Malesia 8
PE - Perù 8
PK - Pakistan 8
TN - Tunisia 8
TT - Trinidad e Tobago 8
UG - Uganda 8
ZA - Sudafrica 8
BG - Bulgaria 7
BW - Botswana 7
BZ - Belize 7
CM - Camerun 7
CR - Costa Rica 7
DK - Danimarca 7
GA - Gabon 7
ID - Indonesia 7
JO - Giordania 7
LC - Santa Lucia 7
ME - Montenegro 7
PA - Panama 7
PT - Portogallo 7
RW - Ruanda 7
SI - Slovenia 7
TJ - Tagikistan 7
TW - Taiwan 7
VE - Venezuela 7
AU - Australia 6
BB - Barbados 6
CO - Colombia 6
EG - Egitto 6
GN - Guinea 6
IE - Irlanda 6
KR - Corea 6
MU - Mauritius 6
NP - Nepal 6
RS - Serbia 6
SN - Senegal 6
TZ - Tanzania 6
AF - Afghanistan, Repubblica islamica di 5
AL - Albania 5
AM - Armenia 5
AO - Angola 5
AZ - Azerbaigian 5
BO - Bolivia 5
BS - Bahamas 5
CV - Capo Verde 5
DJ - Gibuti 5
GF - Guiana Francese 5
GP - Guadalupe 5
HN - Honduras 5
KG - Kirghizistan 5
MA - Marocco 5
MK - Macedonia 5
MN - Mongolia 5
Totale 5.056
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Città #
Fairfield 336
Ashburn 271
Woodbridge 265
Chandler 255
Singapore 245
Houston 204
Ann Arbor 151
Hong Kong 121
Wilmington 121
Seattle 109
Jacksonville 100
Cambridge 98
Helsinki 89
Santa Clara 87
Beijing 73
Boardman 57
Dong Ket 54
Princeton 42
Columbus 37
Padova 37
Des Moines 32
San Diego 27
Medford 26
Nanjing 23
New York 23
Los Angeles 22
Roxbury 22
Bytom 17
Chicago 16
Cotonou 15
Ho Chi Minh City 15
Jinan 15
Turku 15
Shenyang 14
São Paulo 13
Nanchang 12
Milan 10
Hebei 9
Hefei 9
Kingston 9
Redondo Beach 9
Tashkent 9
Buffalo 8
Council Bluffs 8
Hanoi 8
Kampala 8
Luxembourg 8
Amman 7
Brooklyn 7
Castries 7
Changsha 7
Hangzhou 7
Kigali 7
Libreville 7
Munich 7
Nairobi 7
Nicosia 7
Nuremberg 7
Tokyo 7
Vientiane 7
Warsaw 7
Amsterdam 6
Baghdad 6
Belo Horizonte 6
Bridgetown 6
Cagliari 6
Conakry 6
Dakar 6
Dearborn 6
Dushanbe 6
Haikou 6
Jiaxing 6
Johannesburg 6
Ljubljana 6
Panama City 6
Riga 6
Tallinn 6
Tianjin 6
Baku 5
Bishkek 5
Brussels 5
Cayenne 5
Copenhagen 5
Dallas 5
Dar es Salaam 5
Djibouti 5
Dublin 5
Frankfurt am Main 5
Giarre 5
Istanbul 5
Kunming 5
Les Abymes 5
Mamoudzou 5
Managua 5
Naples 5
Nassau 5
Norwalk 5
Podgorica 5
Rio de Janeiro 5
San José 5
Totale 3.464
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Nome #
Individuazione e caratterizzazione di geni implicati nelle paraparesi spastiche ereditarie 422
Von Hippel-Lindau disease: an evaluation of natural history and functional disability 272
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 220
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. 208
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling 205
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum 188
A novel missense mutation in the L1CAM gene in a boy with L1 disease 186
A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype 186
Novel mutations in the L1CAM gene support the complexity of L1 syndrome 173
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma. 166
A new mutation in two siblings with cystinosis presenting with Bartter syndrome. 164
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 162
Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation 157
The pheochromocytoma and paraganglioma syndrome: founder effects and the PGL 1 syndrome. 155
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 155
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients 149
Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas 147
Novel mutation of the mitofusin 2 gene in a family with Charcot-Marie-Tooth disease type 2 (CMT2A). 143
Individuation of new mutations in L1CAM gene in patients with L1 diseases. 136
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28. 133
Evaluation of linkage signals in a subset of families with high recurrence of schizophrenia and bipolar disorder originating from Chioggia 131
Genome scan for schizophrenia/bipolar disorder supports a susceptibility locus in 15q26 131
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites 129
c.1392+2T>C mutation in MFN2 gene affects splicing in Charcot-Marie-Tooth (CMT) 2A family. 121
Genetics of adrenal tumors. 120
Studio genetico pilota sulla popolazione di Chioggia: dati preliminari 119
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. 118
CLINICAL AND ELECTROPHYSIOLOGICAL SPECTRUM IN A GROUP OF SPORADIC DISTAL MOTOR NEUROPATHIES 115
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia. 111
Novel MFN2 mutations and phenotypic variability in patients with Charcot-Marie-Tooth disease type 2A. 105
NOVEL MUTATION OF THE MITOFUSIN 2 GENE IN A FAMILY WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 2A 103
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. 96
Localization of a new highly repeated DNA sequence of Lemur cafta (Lemuridae, Strepsirhini). 78
Quantitative in situ detection of high-risk human papillomavirus in cytological specimens by SYBR Green I fluorescent labeling. 76
Totale 5.280
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Categoria #
all - tutte 16.144
article - articoli 13.140
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 29.284
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021420 0 0 0 0 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
2024/2025899 1 85 50 37 159 23 29 79 59 27 149 201
2025/20261.387 176 271 370 462 108 0 0 0 0 0 0 0
Totale 5.280