IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

CRIPPA, MILENA
 Distribuzione geografica
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Continente #
NA - Nord America 3.579
EU - Europa 3.492
AS - Asia 2.746
SA - Sud America 258
OC - Oceania 89
AF - Africa 77
Continente sconosciuto - Info sul continente non disponibili 3
Totale 10.244
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Nazione #
US - Stati Uniti d'America 3.386
GB - Regno Unito 1.025
CN - Cina 854
IT - Italia 750
SG - Singapore 567
DE - Germania 374
VN - Vietnam 310
BD - Bangladesh 263
SE - Svezia 228
HK - Hong Kong 225
FR - Francia 202
BR - Brasile 190
RU - Federazione Russa 160
IN - India 153
CA - Canada 147
ES - Italia 107
NL - Olanda 95
TR - Turchia 92
PL - Polonia 91
AU - Australia 79
DK - Danimarca 78
FI - Finlandia 77
IE - Irlanda 70
JP - Giappone 60
KR - Corea 51
BE - Belgio 39
ID - Indonesia 39
MX - Messico 37
UA - Ucraina 37
CI - Costa d'Avorio 34
IL - Israele 27
SI - Slovenia 21
AR - Argentina 19
ZA - Sudafrica 18
CZ - Repubblica Ceca 17
CH - Svizzera 16
CO - Colombia 16
HU - Ungheria 15
EU - Europa 14
TH - Thailandia 14
AT - Austria 13
EC - Ecuador 13
TW - Taiwan 13
UZ - Uzbekistan 13
GR - Grecia 12
EE - Estonia 11
NZ - Nuova Zelanda 10
PT - Portogallo 9
NO - Norvegia 8
SA - Arabia Saudita 8
CL - Cile 7
LV - Lettonia 7
MY - Malesia 7
RS - Serbia 7
PH - Filippine 6
PK - Pakistan 6
VE - Venezuela 6
IQ - Iraq 5
IR - Iran 5
LK - Sri Lanka 5
LT - Lituania 5
AL - Albania 4
MA - Marocco 4
SK - Slovacchia (Repubblica Slovacca) 4
CY - Cipro 3
DZ - Algeria 3
JO - Giordania 3
KE - Kenya 3
RO - Romania 3
SN - Senegal 3
TN - Tunisia 3
BG - Bulgaria 2
BO - Bolivia 2
BY - Bielorussia 2
EG - Egitto 2
GE - Georgia 2
HN - Honduras 2
HR - Croazia 2
KZ - Kazakistan 2
LB - Libano 2
NP - Nepal 2
PE - Perù 2
PY - Paraguay 2
TT - Trinidad e Tobago 2
AO - Angola 1
BZ - Belize 1
DJ - Gibuti 1
DO - Repubblica Dominicana 1
GP - Guadalupe 1
JM - Giamaica 1
KG - Kirghizistan 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
MM - Myanmar 1
MT - Malta 1
MZ - Mozambico 1
NG - Nigeria 1
NI - Nicaragua 1
OM - Oman 1
PS - Palestinian Territory 1
Totale 10.248
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Città #
Southend 843
Singapore 338
Ashburn 335
Chandler 274
Milan 202
Hong Kong 197
Fairfield 161
Ann Arbor 139
Beijing 133
Wilmington 130
San Jose 124
Frankfurt am Main 123
Dallas 116
Seattle 104
Ho Chi Minh City 102
Woodbridge 99
Council Bluffs 86
Los Angeles 85
Redwood City 85
Dearborn 82
Hanoi 78
Dublin 68
Houston 64
Princeton 64
Santa Clara 58
Boardman 56
Cambridge 54
Toronto 54
Rome 53
New York 50
Shanghai 42
Helsinki 41
Guangzhou 40
Buffalo 39
Phoenix 37
Lauterbourg 36
Abidjan 34
Nanjing 34
Jinan 33
Paris 33
Warsaw 33
Bengaluru 32
Jakarta 30
Chicago 29
Falls Church 29
Tokyo 29
Des Moines 28
Istanbul 28
Jacksonville 27
Naples 27
Da Nang 26
Delhi 26
Brussels 25
Moscow 25
Turin 25
Brisbane 24
São Paulo 24
Hangzhou 23
Munich 23
Minneapolis 22
Madrid 19
Ankara 18
Barcelona 18
Mountain View 18
San Diego 18
Columbus 17
Ljubljana 17
London 17
Hefei 16
Lexington 16
Melbourne 16
Changsha 15
Fremont 15
Haiphong 15
Montreal 15
Nanchang 15
The Dalles 15
Washington 15
Cangzhou 14
Seoul 14
Sydney 14
Tianjin 14
Grafing 13
Hyderabad 13
Bangkok 12
Manchester 12
Redmond 12
Shenyang 12
Atlanta 11
Bogotá 11
Boston 11
Fuzhou 11
Genoa 11
Edinburgh 10
Hebei 10
Shenzhen 10
Strasbourg 10
Tartu 10
Berlin 9
Birmingham 9
Totale 5.809
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Nome #
9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression 2.313
From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients : New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks 375
High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function 360
SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome 337
Generation of the Rubinstein-Taybi syndrome type 2 patient-derived induced pluripotent stem cell line (IAIi001-A) carrying the EP300 exon 23 stop mutation c.3829A > T, p.(Lys1277*) 313
Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein–Taybi syndrome : the interconnections of epigenetic machinery disorders 303
Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype 300
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 296
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors 290
Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome 289
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes 283
ATRX mutation in two adult brothers with non-specific moderate intellectual disability identified by exome sequencing 281
A balanced reciprocal translocation t(10;15)(q22.3;q26.1) interrupting ACAN gene in a family with proportionate short stature 277
Identification of rare CNVs involving genes acting in oocyte maturation and differentiation in a cohort of patients affected by Primary Ovarian Insufficiency 275
A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotype 262
Identification of balanced 4p16 paracentric inversions in three patients with Wolf-Hirschhorn phenotype not deleted for the WHS critical region 253
Centa2 is expressed during heart development and is a candidate gene for CVMs 250
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. 247
Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes 244
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 242
Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations 240
Nuova delezione intragenica in NSD1 in un paziente che presenta fenotipo composto Sotos/delezione subtelomerica 5q 235
A new structural rearrangement associated to Wolfram syndrome in a child with a partial phenotype 234
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency 227
Sindrome di Cornelia de Lange in un paziente portatore della Traslocazione t(5;15)(p13;q25.1): possibile effetto di posizione su NIPBL 216
Fetal cell microchimerism : a protective role in autoimmune thyroid diseases 208
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 206
Possible position effect on TRPS1 in a patient carrying t(2;8)(p16.1;q23.3) translocation with phenotype referring to trichorhinopahalangeal syndrome 203
Searching for centaurin-α2 interacting proteins: evidence of interaction with tubulin-β 197
Ricerca di interattori molecolari della centaurina-α2 : evidenze di associazione con la tubulina β 174
Central nervous system developmental disorder in Noonan syndrome: a genomic approach 169
A unique Smith-Magenis patient with a de novo intragenic deletion on the maternally inherited overexpressed RAI1 allele 163
A familial t(4;8) translocation segregates with epilepsy and migraine with aura 106
Totale 10.617
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Categoria #
all - tutte 25.261
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 25.261
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202170 0 0 0 0 0 0 0 0 0 0 0 70
2021/2022827 59 53 70 66 70 58 34 60 90 81 39 147
2022/20231.142 114 145 78 112 83 145 48 140 112 44 78 43
2023/20241.014 41 87 80 103 224 72 65 74 30 65 67 106
2024/20251.450 78 146 48 152 100 72 84 138 99 159 114 260
2025/20262.839 262 166 207 197 234 147 453 88 231 190 423 241
Totale 10.617