Sangiorgi, Eugenio
 Distribuzione geografica
Continente #
NA - Nord America 1.716
AS - Asia 1.629
EU - Europa 1.249
SA - Sud America 267
AF - Africa 35
AN - Antartide 1
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 4.899
Nazione #
US - Stati Uniti d'America 1.663
SG - Singapore 602
CN - Cina 578
IT - Italia 276
SE - Svezia 267
BR - Brasile 222
DE - Germania 200
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
BD - Bangladesh 35
GB - Regno Unito 35
TR - Turchia 26
CA - Canada 20
AR - Argentina 18
IQ - Iraq 18
CI - Costa d'Avorio 17
MX - Messico 16
NL - Olanda 16
BE - Belgio 14
KR - Corea 13
CZ - Repubblica Ceca 11
AT - Austria 10
IR - Iran 10
ZA - Sudafrica 9
CH - Svizzera 7
EC - Ecuador 7
PK - Pakistan 7
AE - Emirati Arabi Uniti 5
CR - Costa Rica 5
UZ - Uzbekistan 5
VE - Venezuela 5
CO - Colombia 4
ES - Italia 4
SA - Arabia Saudita 4
AL - Albania 3
BB - Barbados 3
CL - Cile 3
EG - Egitto 3
HN - Honduras 3
HU - Ungheria 3
JO - Giordania 3
LT - Lituania 3
MY - Malesia 3
PY - Paraguay 3
AM - Armenia 2
EE - Estonia 2
GR - Grecia 2
HR - Croazia 2
PE - Perù 2
PH - Filippine 2
RS - Serbia 2
TT - Trinidad e Tobago 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
GT - Guatemala 1
IL - Israele 1
KE - Kenya 1
KG - Kirghizistan 1
KI - Kiribati 1
KN - Saint Kitts e Nevis 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
TW - Taiwan 1
Totale 4.899
Città #
Singapore 344
Chandler 234
Ashburn 207
Hangzhou 200
San Jose 172
Beijing 90
Rome 49
Dublin 48
Ho Chi Minh City 46
San Mateo 46
Hong Kong 45
Nanjing 45
Los Angeles 42
Tokyo 42
Hefei 38
Ann Arbor 37
Jakarta 37
New York 35
Lauterbourg 33
Jacksonville 31
Warsaw 31
Boston 30
Munich 27
Hanoi 24
The Dalles 24
Wilmington 23
Moscow 22
Milan 21
Cattolica 20
Dallas 20
Santa Clara 20
São Paulo 20
Dearborn 19
Frankfurt am Main 19
Izmir 19
Abidjan 17
Chicago 16
Helsinki 16
Nanchang 16
Redmond 15
Brussels 14
Council Bluffs 14
Lawrence 14
Seattle 13
Woodbridge 13
Buffalo 12
Kent 12
Kraków 12
Houston 11
Paris 11
Princeton 11
Seoul 11
Tianjin 11
Augusta 10
Boardman 10
Da Nang 10
Nuremberg 10
Shanghai 10
Brno 9
Hyderabad 9
Kish 9
North Bergen 9
Redwood City 9
Andover 8
Baghdad 8
Brooklyn 8
Marseille 8
Stockholm 8
Chennai 7
Curitiba 7
Florence 7
Lappeenranta 7
Philadelphia 7
Phoenix 7
San Francisco 7
Turku 7
Contagem 6
Mexico City 6
Montreal 6
Rio de Janeiro 6
Shenyang 6
Zhengzhou 6
Amsterdam 5
Changsha 5
Charlotte 5
Fairfield 5
Guangzhou 5
Jinan 5
Johannesburg 5
Orem 5
Poplar 5
Salò 5
University Park 5
Atlanta 4
Berlin 4
Bologna 4
Bremen 4
Brunswick 4
Bắc Ninh 4
Dhaka 4
Totale 2.709
Nome #
Bmi1 is expressed in vivo in intestinal stem cells 351
Applicazioni dell'ingegneria genetica in medicina 254
Difetti genetici dello sviluppo embrionale 221
A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy. 208
DNA Methylation in the Diagnosis of Monogenic Diseases. 207
Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. 159
The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populations 152
Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome. 152
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. 138
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 137
In vivo evaluation of PhiC31 recombinase activity using a self-excision cassette 136
Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura 135
Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schonlein purpura 134
Sustained in vitro intestinal epithelial culture within a Wnt-dependent stem cell niche 133
Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitalia 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 130
BMI1 represses Ink4a/Arf and Hox genes to regulate stem cells in the rodent incisor 126
Phenotypic effects of chronic and acute use of methiopropamine in a mouse model 125
Bmi1 lineage tracing identifies a self-renewing pancreatic acinar cell subpopulation capable of maintaining pancreatic organ homeostasis 123
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 113
Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers 111
Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitalia 111
RADX Gene Variant May Predispose to Familial Asperger Syndrome 109
Kinetics of lymphocytosis in naïve chronic lymphocytic leukemia patients treated with covalent Bruton's tyrosine kinase inhibitors: An Italian multicenter real-life experience 107
A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy 97
Clinical and molecular features of familial chronic lymphocytic leukemia: a pilot monocentric study 92
Clinical and molecular features of familial chronic lymphocytic leukemia: a pilot monocentric study 90
Base-Excision Repair Mutational Signature in Two Sebaceous Carcinomas of the Eyelid 90
Advances in the genetics of progressive myoclonus epilepsy 87
Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects 82
The clinical chameleon of autoinflammatory diseases in children 82
From Churchill to Elephants: The Role of Protective Genes against Cancer 71
Severe chronic primary neutropenia: findings from a patient who underwent exstensive evaluation including adenosine deaminase 2 gene variant assessment 61
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome 55
Familial forms of chronic lymphocytic leukemia have a worse prognosis than sporadic forms: an Italian case-control study 51
NLRP12 as a regulator of inflammation: insights into the correlation with autoinflammatory disorders 7
Totale 4.952
Categoria #
all - tutte 20.066
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 20.066


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20215 0 0 0 0 0 0 0 0 0 0 0 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
2025/20261.888 257 72 125 199 276 123 376 86 123 115 67 69
Totale 4.952