BOARETTO, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 3.640
AS - Asia 2.006
EU - Europa 999
SA - Sud America 283
AF - Africa 254
Continente sconosciuto - Info sul continente non disponibili 26
OC - Oceania 24
Totale 7.232
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Nazione #
US - Stati Uniti d'America 3.485
SG - Singapore 584
CN - Cina 416
VN - Vietnam 346
IT - Italia 248
HK - Hong Kong 196
BR - Brasile 190
FI - Finlandia 146
FR - Francia 81
BD - Bangladesh 72
DE - Germania 63
GB - Regno Unito 60
IN - India 60
NL - Olanda 51
SE - Svezia 47
PL - Polonia 33
UA - Ucraina 31
CA - Canada 29
JP - Giappone 27
IQ - Iraq 25
TR - Turchia 24
AR - Argentina 22
RU - Federazione Russa 22
SA - Arabia Saudita 20
BJ - Benin 16
ZA - Sudafrica 16
MX - Messico 15
AT - Austria 14
IL - Israele 14
JO - Giordania 14
KE - Kenya 14
PK - Pakistan 14
ES - Italia 13
ID - Indonesia 13
JM - Giamaica 13
CO - Colombia 12
PH - Filippine 12
PY - Paraguay 12
BE - Belgio 11
CY - Cipro 11
CZ - Repubblica Ceca 11
GR - Grecia 11
MD - Moldavia 11
UZ - Uzbekistan 11
CH - Svizzera 10
DZ - Algeria 10
EC - Ecuador 10
GM - Gambi 10
PS - Palestinian Territory 10
PT - Portogallo 10
TT - Trinidad e Tobago 10
VE - Venezuela 10
EG - Egitto 9
KR - Corea 9
LA - Repubblica Popolare Democratica del Laos 9
LU - Lussemburgo 9
LV - Lettonia 9
MY - Malesia 9
PE - Perù 9
TJ - Tagikistan 9
TN - Tunisia 9
AU - Australia 8
BG - Bulgaria 8
DK - Danimarca 8
EE - Estonia 8
GA - Gabon 8
HU - Ungheria 8
IE - Irlanda 8
IR - Iran 8
KZ - Kazakistan 8
ME - Montenegro 8
NP - Nepal 8
SI - Slovenia 8
TW - Taiwan 8
UG - Uganda 8
BB - Barbados 7
BW - Botswana 7
BZ - Belize 7
CM - Camerun 7
CR - Costa Rica 7
DO - Repubblica Dominicana 7
KG - Kirghizistan 7
LB - Libano 7
LC - Santa Lucia 7
MU - Mauritius 7
PA - Panama 7
RW - Ruanda 7
TZ - Tanzania 7
AF - Afghanistan, Repubblica islamica di 6
AL - Albania 6
AM - Armenia 6
AO - Angola 6
AZ - Azerbaigian 6
ET - Etiopia 6
GN - Guinea 6
HN - Honduras 6
NG - Nigeria 6
NI - Nicaragua 6
RS - Serbia 6
SN - Senegal 6
Totale 6.972
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Città #
Ashburn 400
Singapore 364
Fairfield 336
San Jose 279
Woodbridge 266
Chandler 255
Houston 204
Hong Kong 179
Ann Arbor 151
Wilmington 121
Seattle 110
Jacksonville 103
Cambridge 98
Helsinki 95
Santa Clara 95
Ho Chi Minh City 93
Beijing 91
Hanoi 77
Los Angeles 61
Boardman 58
Dong Ket 54
New York 42
Princeton 42
Columbus 37
Padova 37
Des Moines 33
Lauterbourg 27
San Diego 27
Medford 26
Nanjing 23
Chicago 22
Roxbury 22
Council Bluffs 20
Milan 19
Bytom 17
Da Nang 17
Cotonou 16
São Paulo 16
The Dalles 16
Jinan 15
Tokyo 15
Turku 15
Shenyang 14
Orem 13
Buffalo 12
Nairobi 12
Nanchang 12
Tashkent 11
Amman 10
Baghdad 10
Frankfurt am Main 10
Haiphong 10
Johannesburg 10
Kingston 10
London 10
Phoenix 10
Toronto 10
Amsterdam 9
Hebei 9
Hefei 9
Jeddah 9
Naples 9
Redondo Beach 9
Warsaw 9
Belo Horizonte 8
Changsha 8
Dushanbe 8
Kampala 8
Libreville 8
Luxembourg 8
Munich 8
Paris 8
Rome 8
Athens 7
Boston 7
Bridgetown 7
Brooklyn 7
Castries 7
Chennai 7
Denver 7
Guangzhou 7
Hangzhou 7
Istanbul 7
Kigali 7
Nicosia 7
Nuremberg 7
Riga 7
Vienna 7
Vientiane 7
Addis Ababa 6
Atlanta 6
Baku 6
Bishkek 6
Biên Hòa 6
Bologna 6
Cagliari 6
Conakry 6
Copenhagen 6
Dakar 6
Dallas 6
Totale 4.471
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Nome #
Individuazione e caratterizzazione di geni implicati nelle paraparesi spastiche ereditarie 534
Von Hippel-Lindau disease: an evaluation of natural history and functional disability 386
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling 386
A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype 289
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 277
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. 269
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum 256
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients 250
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 238
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma. 235
Novel mutations in the L1CAM gene support the complexity of L1 syndrome 230
Novel mutation of the mitofusin 2 gene in a family with Charcot-Marie-Tooth disease type 2 (CMT2A). 224
A novel missense mutation in the L1CAM gene in a boy with L1 disease 222
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 207
Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas 201
The pheochromocytoma and paraganglioma syndrome: founder effects and the PGL 1 syndrome. 196
A new mutation in two siblings with cystinosis presenting with Bartter syndrome. 192
c.1392+2T>C mutation in MFN2 gene affects splicing in Charcot-Marie-Tooth (CMT) 2A family. 187
Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation 185
Genetics of adrenal tumors. 181
Individuation of new mutations in L1CAM gene in patients with L1 diseases. 179
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites 179
Evaluation of linkage signals in a subset of families with high recurrence of schizophrenia and bipolar disorder originating from Chioggia 172
Studio genetico pilota sulla popolazione di Chioggia: dati preliminari 170
CLINICAL AND ELECTROPHYSIOLOGICAL SPECTRUM IN A GROUP OF SPORADIC DISTAL MOTOR NEUROPATHIES 167
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28. 163
NOVEL MUTATION OF THE MITOFUSIN 2 GENE IN A FAMILY WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 2A 158
Genome scan for schizophrenia/bipolar disorder supports a susceptibility locus in 15q26 158
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia. 152
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. 139
Novel MFN2 mutations and phenotypic variability in patients with Charcot-Marie-Tooth disease type 2A. 137
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. 117
Quantitative in situ detection of high-risk human papillomavirus in cytological specimens by SYBR Green I fluorescent labeling. 100
Localization of a new highly repeated DNA sequence of Lemur cafta (Lemuridae, Strepsirhini). 96
Totale 7.232
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Categoria #
all - tutte 20.129
article - articoli 16.415
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 36.544
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022498 0 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
2025/20263.216 176 271 370 462 322 139 499 249 350 164 117 97
2026/2027123 103 20 0 0 0 0 0 0 0 0 0 0
Totale 7.232