IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

CRIPPA, MILENA
 Distribuzione geografica
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Continente #
NA - Nord America 3.867
EU - Europa 3.571
AS - Asia 2.857
Continente sconosciuto - Info sul continente non disponibili 376
SA - Sud America 271
OC - Oceania 89
AF - Africa 78
Totale 11.109
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Nazione #
US - Stati Uniti d'America 3.647
GB - Regno Unito 1.027
CN - Cina 856
IT - Italia 815
SG - Singapore 584
DE - Germania 376
BD - Bangladesh 352
VN - Vietnam 310
SE - Svezia 229
HK - Hong Kong 225
FR - Francia 203
BR - Brasile 196
CA - Canada 165
RU - Federazione Russa 160
IN - India 156
ES - Italia 107
PL - Polonia 97
NL - Olanda 96
TR - Turchia 92
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 38
UA - Ucraina 37
CI - Costa d'Avorio 34
IL - Israele 27
SI - Slovenia 21
AR - Argentina 19
CO - Colombia 18
ZA - Sudafrica 18
CZ - Repubblica Ceca 17
CH - Svizzera 16
HU - Ungheria 15
EC - Ecuador 14
EU - Europa 14
TH - Thailandia 14
AT - Austria 13
TW - Taiwan 13
UZ - Uzbekistan 13
GR - Grecia 12
EE - Estonia 11
NZ - Nuova Zelanda 10
CL - Cile 9
PT - Portogallo 9
NO - Norvegia 8
SA - Arabia Saudita 8
LV - Lettonia 7
MY - Malesia 7
RS - Serbia 7
VE - Venezuela 7
PH - Filippine 6
PK - Pakistan 6
IQ - Iraq 5
IR - Iran 5
LK - Sri Lanka 5
LT - Lituania 5
AL - Albania 4
HN - Honduras 4
KE - Kenya 4
MA - Marocco 4
RO - Romania 4
SK - Slovacchia (Repubblica Slovacca) 4
CY - Cipro 3
DZ - Algeria 3
JO - Giordania 3
PE - Perù 3
SN - Senegal 3
TN - Tunisia 3
BG - Bulgaria 2
BO - Bolivia 2
BY - Bielorussia 2
EG - Egitto 2
GE - Georgia 2
HR - Croazia 2
JM - Giamaica 2
KZ - Kazakistan 2
LB - Libano 2
NP - Nepal 2
PR - Porto Rico 2
PY - Paraguay 2
TT - Trinidad e Tobago 2
AO - Angola 1
BB - Barbados 1
BZ - Belize 1
DJ - Gibuti 1
DO - Repubblica Dominicana 1
GP - Guadalupe 1
GT - Guatemala 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
Totale 10.736
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Città #
Southend 843
Ashburn 379
Singapore 344
Chandler 274
Milan 214
Hong Kong 197
Fairfield 161
Ann Arbor 139
San Jose 135
Beijing 133
Wilmington 130
Dallas 125
Frankfurt am Main 123
Council Bluffs 110
Seattle 104
Ho Chi Minh City 102
Woodbridge 99
Los Angeles 97
Santa Clara 94
Redwood City 85
Dearborn 82
Hanoi 78
Dublin 68
Houston 65
Princeton 64
Toronto 58
Boardman 56
New York 56
Rome 55
Cambridge 54
Buffalo 44
Shanghai 42
Helsinki 41
Guangzhou 40
Phoenix 38
Chicago 36
Lauterbourg 36
Abidjan 34
Nanjing 34
Warsaw 34
Jinan 33
Paris 33
Bengaluru 32
Naples 31
Jakarta 30
Des Moines 29
Falls Church 29
Tokyo 29
Turin 29
Istanbul 28
Jacksonville 28
Da Nang 26
Delhi 26
Brussels 25
Moscow 25
Brisbane 24
São Paulo 24
Hangzhou 23
Munich 23
Minneapolis 22
Madrid 19
Ankara 18
Barcelona 18
Columbus 18
London 18
Mountain View 18
San Diego 18
Ljubljana 17
Hefei 16
Lexington 16
Melbourne 16
Montreal 16
Washington 16
Changsha 15
Fremont 15
Haiphong 15
Nanchang 15
Sydney 15
The Dalles 15
Cangzhou 14
Seoul 14
Tianjin 14
Genoa 13
Grafing 13
Hyderabad 13
Atlanta 12
Bangkok 12
Bogotá 12
Boston 12
Manchester 12
Redmond 12
Shenyang 12
Berlin 11
Fuzhou 11
Brooklyn 10
Edinburgh 10
Hebei 10
Shenzhen 10
Strasbourg 10
Tartu 10
Totale 6.013
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Nome #
9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression 2.350
From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients : New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks 398
High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function 380
SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome 349
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 326
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*) 324
Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype 317
Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein–Taybi syndrome : the interconnections of epigenetic machinery disorders 314
Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome 300
A balanced reciprocal translocation t(10;15)(q22.3;q26.1) interrupting ACAN gene in a family with proportionate short stature 300
Identification of rare CNVs involving genes acting in oocyte maturation and differentiation in a cohort of patients affected by Primary Ovarian Insufficiency 299
ATRX mutation in two adult brothers with non-specific moderate intellectual disability identified by exome sequencing 295
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors 295
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes 293
Fetal cell microchimerism : a protective role in autoimmune thyroid diseases 284
A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotype 276
Identification of balanced 4p16 paracentric inversions in three patients with Wolf-Hirschhorn phenotype not deleted for the WHS critical region 266
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. 261
Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes 257
Centa2 is expressed during heart development and is a candidate gene for CVMs 255
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 255
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 250
A new structural rearrangement associated to Wolfram syndrome in a child with a partial phenotype 247
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 246
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency 245
Nuova delezione intragenica in NSD1 in un paziente che presenta fenotipo composto Sotos/delezione subtelomerica 5q 239
Sindrome di Cornelia de Lange in un paziente portatore della Traslocazione t(5;15)(p13;q25.1): possibile effetto di posizione su NIPBL 221
Possible position effect on TRPS1 in a patient carrying t(2;8)(p16.1;q23.3) translocation with phenotype referring to trichorhinopahalangeal syndrome 217
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 211
Searching for centaurin-α2 interacting proteins: evidence of interaction with tubulin-β 202
A unique Smith-Magenis patient with a de novo intragenic deletion on the maternally inherited overexpressed RAI1 allele 177
Ricerca di interattori molecolari della centaurina-α2 : evidenze di associazione con la tubulina β 177
Central nervous system developmental disorder in Noonan syndrome: a genomic approach 175
A familial t(4;8) translocation segregates with epilepsy and migraine with aura 108
Totale 11.109
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Categoria #
all - tutte 26.484
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 26.484
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022715 0 0 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
2025/20262.921 262 166 207 197 234 147 453 88 231 190 423 323
2026/2027410 178 212 20 0 0 0 0 0 0 0 0 0
Totale 11.109