IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

BESTETTI, ILARIA
 Distribuzione geografica
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Continente #
NA - Nord America 2.811
EU - Europa 2.720
AS - Asia 2.222
SA - Sud America 239
OC - Oceania 98
AF - Africa 66
Totale 8.156
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Nazione #
US - Stati Uniti d'America 2.635
CN - Cina 727
GB - Regno Unito 618
IT - Italia 550
SG - Singapore 483
DE - Germania 314
IN - India 205
FR - Francia 195
HK - Hong Kong 182
BR - Brasile 176
VN - Vietnam 167
SE - Svezia 143
RU - Federazione Russa 133
CA - Canada 125
NL - Olanda 120
ES - Italia 113
PL - Polonia 88
AU - Australia 84
BD - Bangladesh 74
DK - Danimarca 70
FI - Finlandia 64
TR - Turchia 64
JP - Giappone 63
IE - Irlanda 62
CZ - Repubblica Ceca 42
ID - Indonesia 41
MX - Messico 41
BE - Belgio 40
KR - Corea 40
IL - Israele 29
TW - Taiwan 27
CI - Costa d'Avorio 23
SI - Slovenia 22
AT - Austria 18
TH - Thailandia 17
ZA - Sudafrica 17
AR - Argentina 16
CH - Svizzera 16
GR - Grecia 15
HU - Ungheria 15
IR - Iran 14
NZ - Nuova Zelanda 14
CO - Colombia 13
EE - Estonia 13
PK - Pakistan 13
EC - Ecuador 11
MY - Malesia 10
PT - Portogallo 10
CL - Cile 9
HR - Croazia 9
NO - Norvegia 9
PH - Filippine 8
RS - Serbia 8
LV - Lettonia 7
SA - Arabia Saudita 7
SK - Slovacchia (Repubblica Slovacca) 7
UZ - Uzbekistan 7
IQ - Iraq 6
MA - Marocco 6
UA - Ucraina 6
VE - Venezuela 6
LT - Lituania 5
AE - Emirati Arabi Uniti 4
GE - Georgia 4
JO - Giordania 4
PS - Palestinian Territory 4
AL - Albania 3
EG - Egitto 3
LB - Libano 3
LK - Sri Lanka 3
PY - Paraguay 3
SN - Senegal 3
AZ - Azerbaigian 2
CR - Costa Rica 2
CY - Cipro 2
DZ - Algeria 2
HN - Honduras 2
KE - Kenya 2
LA - Repubblica Popolare Democratica del Laos 2
LU - Lussemburgo 2
NG - Nigeria 2
NI - Nicaragua 2
PE - Perù 2
QA - Qatar 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
AO - Angola 1
BG - Bulgaria 1
ET - Etiopia 1
GP - Guadalupe 1
GY - Guiana 1
KH - Cambogia 1
KZ - Kazakistan 1
MM - Myanmar 1
MN - Mongolia 1
MO - Macao, regione amministrativa speciale della Cina 1
MT - Malta 1
MU - Mauritius 1
MZ - Mozambico 1
Totale 8.149
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Città #
Southend 423
Singapore 293
Ashburn 263
Chandler 185
Hong Kong 141
Milan 129
Wilmington 119
Dallas 116
San Jose 110
Fairfield 103
Beijing 101
Frankfurt am Main 96
Ann Arbor 90
Redwood City 84
Seattle 74
Los Angeles 67
Ho Chi Minh City 65
Council Bluffs 61
Houston 59
Dublin 58
Delhi 56
Dearborn 54
Cambridge 52
Woodbridge 48
Santa Clara 47
Rome 45
Paris 42
Princeton 42
Guangzhou 41
Shanghai 41
Hanoi 34
Helsinki 33
Warsaw 33
Toronto 32
Moscow 30
Munich 30
Jakarta 29
Lauterbourg 29
Chicago 28
New York 28
Bengaluru 27
Boardman 27
Brisbane 27
Hefei 27
Chennai 26
Brussels 25
Tokyo 24
Abidjan 23
Buffalo 23
Madrid 23
Phoenix 23
Falls Church 22
Seoul 22
London 21
Minneapolis 21
Nanjing 21
São Paulo 21
Jinan 20
Melbourne 20
Montreal 20
Mumbai 20
Naples 20
Des Moines 19
Turin 19
Ankara 18
Barcelona 18
Ljubljana 17
San Diego 17
Berlin 16
Lexington 16
Pardubice 16
Hangzhou 15
Atlanta 14
Düsseldorf 14
Hyderabad 14
Nanchang 14
Oxford 14
Sydney 14
Washington 14
Manchester 13
The Dalles 13
Bangkok 12
Boston 12
Columbus 12
Fremont 12
Tartu 12
Changsha 11
Da Nang 11
Genoa 11
Grafing 11
Strasbourg 11
Taipei 11
Tianjin 11
Amsterdam 10
Cardiff 10
Istanbul 10
Shenzhen 10
Tel Aviv 10
Turku 10
Cangzhou 9
Totale 4.415
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Nome #
9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression 2.296
GENOME WIDE ANALYSIS IN A COHORT OF 46,XX PATIENTS AFFECTED BY AN EXTREME PHENOTYPE OF PRIMARY OVARIAN INSUFFICIENCY: AN EFFICIENT TOOL TO IDENTIFY NEW GENES INVOLVED IN OOCYTE MATURATION AND DIFFERENTIATION 512
Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency 429
High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function 348
SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome 304
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors 288
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome-case report and review of the literature 284
Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome 283
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes 278
Identification of rare CNVs involving genes acting in oocyte maturation and differentiation in a cohort of patients affected by Primary Ovarian Insufficiency 267
Regulatory element deletion cause a down-regulation of ZDHHC15 gene in a proband with Smith Magenis syndrome phenotype 264
A balanced reciprocal translocation t(10;15)(q22.3;q26.1) interrupting ACAN gene in a family with proportionate short stature 259
Submicroscopic genomic alterations detected by array CGH analysis in a cohort of patients with Silver Russell syndrome found negative to classical genetic and epigenetic tests 249
Complex de novo chromosomal rearrangement at 15q11-q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: Clinical report and review of the literature. 245
New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene 230
Microdeletion in two unrelated patients with intellectual disability 227
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency 221
DNA copy number variations in a cohort of 216 Italian women with premature ovarian failure 205
MBD5 molecular screening on Smith Magenis-like Syndrome patients without the typical 17p11.2 deletion 199
RAI1 intragenic deletion and concomitant overexpression in a syndromic patient: Smith-Magenis or Potocki-Lupski syndrome? 182
Central nervous system developmental disorder in Noonan syndrome: a genomic approach 168
A unique Smith-Magenis patient with a de novo intragenic deletion on the maternally inherited overexpressed RAI1 allele 159
Long-read sequencing reveals chromothripsis in a molecularly unsolved case of Cornelia de Lange syndrome 154
Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome 152
An intragenic duplication in the AFF2 gene associated with Cornelia de Lange syndrome phenotype 142
When alpha spectrin null alleles meet low expression alpha spectrin polymorphisms 51
Totale 8.396
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Categoria #
all - tutte 18.915
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 18.915
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021118 0 0 0 0 0 0 0 0 0 0 45 73
2021/2022682 55 45 59 56 55 51 30 57 57 70 31 116
2022/2023987 82 98 70 85 73 111 41 122 113 47 74 71
2023/20241.011 41 83 76 101 175 105 64 75 29 79 81 102
2024/20251.383 75 131 57 132 102 66 85 130 116 185 98 206
2025/20262.190 238 183 210 179 242 142 301 101 220 152 222 0
Totale 8.396