IRIS UniCatt

Sangiorgi, Eugenio
 Distribuzione geografica
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Continente #
NA - Nord America 1.644
AS - Asia 1.600
EU - Europa 1.213
SA - Sud America 266
AF - Africa 35
AN - Antartide 1
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 4.761
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Nazione #
US - Stati Uniti d'America 1.599
SG - Singapore 601
CN - Cina 575
SE - Svezia 267
IT - Italia 244
BR - Brasile 222
DE - Germania 197
VN - Vietnam 127
UA - Ucraina 109
FR - Francia 99
HK - Hong Kong 52
IE - Irlanda 48
PL - Polonia 47
FI - Finlandia 46
IN - India 46
JP - Giappone 43
ID - Indonesia 38
RU - Federazione Russa 36
GB - Regno Unito 35
TR - Turchia 26
CA - Canada 19
AR - Argentina 18
IQ - Iraq 18
CI - Costa d'Avorio 17
NL - Olanda 16
MX - Messico 15
BE - Belgio 14
KR - Corea 13
CZ - Repubblica Ceca 11
AT - Austria 10
BD - Bangladesh 10
IR - Iran 10
ZA - Sudafrica 9
CH - Svizzera 7
EC - Ecuador 7
PK - Pakistan 7
AE - Emirati Arabi Uniti 5
UZ - Uzbekistan 5
VE - Venezuela 5
CR - Costa Rica 4
ES - Italia 4
SA - Arabia Saudita 4
AL - Albania 3
BB - Barbados 3
CL - Cile 3
CO - Colombia 3
EG - Egitto 3
HU - Ungheria 3
JO - Giordania 3
MY - Malesia 3
PY - Paraguay 3
AM - Armenia 2
EE - Estonia 2
GR - Grecia 2
HR - Croazia 2
LT - Lituania 2
PE - Perù 2
PH - Filippine 2
RS - Serbia 2
UY - Uruguay 2
AQ - Antartide 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BO - Bolivia 1
CD - Congo 1
DK - Danimarca 1
DZ - Algeria 1
EU - Europa 1
GA - Gabon 1
HN - Honduras 1
IL - Israele 1
KE - Kenya 1
KG - Kirghizistan 1
KI - Kiribati 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
MD - Moldavia 1
MK - Macedonia 1
MZ - Mozambico 1
NI - Nicaragua 1
NP - Nepal 1
PA - Panama 1
PS - Palestinian Territory 1
PT - Portogallo 1
QA - Qatar 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
TW - Taiwan 1
Totale 4.761
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Città #
Singapore 344
Chandler 234
Ashburn 202
Hangzhou 200
San Jose 166
Beijing 90
Dublin 48
Ho Chi Minh City 46
San Mateo 46
Hong Kong 45
Nanjing 45
Rome 44
Tokyo 42
Los Angeles 39
Hefei 38
Ann Arbor 37
Jakarta 37
Lauterbourg 33
New York 31
Warsaw 31
Boston 30
Jacksonville 30
Munich 27
Hanoi 24
The Dalles 24
Wilmington 23
Moscow 22
Cattolica 20
Milan 20
São Paulo 20
Dearborn 19
Frankfurt am Main 19
Izmir 19
Santa Clara 19
Abidjan 17
Dallas 17
Helsinki 16
Nanchang 16
Chicago 15
Redmond 15
Brussels 14
Council Bluffs 14
Lawrence 14
Woodbridge 13
Kent 12
Kraków 12
Seattle 12
Houston 11
Paris 11
Princeton 11
Seoul 11
Tianjin 11
Augusta 10
Buffalo 10
Da Nang 10
Nuremberg 10
Shanghai 10
Brno 9
Hyderabad 9
Kish 9
North Bergen 9
Redwood City 9
Andover 8
Baghdad 8
Marseille 8
Stockholm 8
Brooklyn 7
Chennai 7
Curitiba 7
Florence 7
Lappeenranta 7
San Francisco 7
Turku 7
Contagem 6
Montreal 6
Philadelphia 6
Rio de Janeiro 6
Shenyang 6
Zhengzhou 6
Amsterdam 5
Boardman 5
Changsha 5
Charlotte 5
Fairfield 5
Guangzhou 5
Jinan 5
Johannesburg 5
Mexico City 5
Orem 5
Phoenix 5
Poplar 5
Salò 5
University Park 5
Atlanta 4
Bremen 4
Brunswick 4
Bắc Ninh 4
Dhaka 4
Edinburgh 4
Fortaleza 4
Totale 2.666
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Nome #
Bmi1 is expressed in vivo in intestinal stem cells 350
Applicazioni dell'ingegneria genetica in medicina 248
Difetti genetici dello sviluppo embrionale 219
A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy. 206
DNA Methylation in the Diagnosis of Monogenic Diseases. 206
Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. 159
Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome. 150
The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populations 148
A split hand-split foot (SHFM3) gene is located at 10q24-->25 139
Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. 137
In vivo evaluation of PhiC31 recombinase activity using a self-excision cassette 136
Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome 134
Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura 133
Sustained in vitro intestinal epithelial culture within a Wnt-dependent stem cell niche 131
Identification of new candidate genes for spina bifida through exome sequencing 130
Results of a gene panel approach in a cohort of patients with incomplete distal renal tubular acidosis and nephrolithiasis 129
Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitalia 128
BMI1 represses Ink4a/Arf and Hox genes to regulate stem cells in the rodent incisor 125
Phenotypic effects of chronic and acute use of methiopropamine in a mouse model 124
Bmi1 lineage tracing identifies a self-renewing pancreatic acinar cell subpopulation capable of maintaining pancreatic organ homeostasis 120
Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schonlein purpura 118
Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13 115
Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome 112
Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitalia 109
RADX Gene Variant May Predispose to Familial Asperger Syndrome 109
Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers 95
A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy 95
Clinical and molecular features of familial chronic lymphocytic leukemia: a pilot monocentric study 91
Clinical and molecular features of familial chronic lymphocytic leukemia: a pilot monocentric study 88
Advances in the genetics of progressive myoclonus epilepsy 87
Base-Excision Repair Mutational Signature in Two Sebaceous Carcinomas of the Eyelid 86
The clinical chameleon of autoinflammatory diseases in children 80
Kinetics of lymphocytosis in naïve chronic lymphocytic leukemia patients treated with covalent Bruton's tyrosine kinase inhibitors: An Italian multicenter real-life experience 79
From Churchill to Elephants: The Role of Protective Genes against Cancer 70
Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects 69
Severe chronic primary neutropenia: findings from a patient who underwent exstensive evaluation including adenosine deaminase 2 gene variant assessment 58
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome 53
Familial forms of chronic lymphocytic leukemia have a worse prognosis than sporadic forms: an Italian case-control study 47
Totale 4.813
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Categoria #
all - tutte 18.926
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 18.926
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202144 0 0 0 0 0 0 0 0 0 11 28 5
2021/2022320 16 21 5 14 30 17 7 59 10 17 53 71
2022/2023647 97 107 64 84 31 72 33 54 57 12 27 9
2023/2024361 10 76 13 37 11 34 29 17 5 24 47 58
2024/2025677 12 24 62 32 42 37 26 20 91 54 166 111
2025/20261.749 257 72 125 199 276 123 376 86 123 112 0 0
Totale 4.813