statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	459
RU - Federazione Russa	189
SG - Singapore	177
VN - Vietnam	122
DE - Germania	111
IT - Italia	97
CN - Cina	81
BR - Brasile	40
HK - Hong Kong	28
ES - Italia	22
FR - Francia	19
CA - Canada	17
NL - Olanda	17
FI - Finlandia	13
GB - Regno Unito	13
AR - Argentina	10
CH - Svizzera	9
IN - India	7
BG - Bulgaria	6
CI - Costa d'Avorio	6
KR - Corea	6
MX - Messico	6
AT - Austria	4
ID - Indonesia	4
IQ - Iraq	4
PK - Pakistan	4
BD - Bangladesh	3
JP - Giappone	3
LT - Lituania	3
PL - Polonia	3
TH - Thailandia	3
ZA - Sudafrica	3
AU - Australia	2
AZ - Azerbaigian	2
EC - Ecuador	2
IE - Irlanda	2
KE - Kenya	2
MY - Malesia	2
PH - Filippine	2
SA - Arabia Saudita	2
TR - Turchia	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
BE - Belgio	1
CD - Congo	1
CL - Cile	1
CO - Colombia	1
CR - Costa Rica	1
DJ - Gibuti	1
DK - Danimarca	1
GA - Gabon	1
GY - Guiana	1
JO - Giordania	1
KH - Cambogia	1
LB - Libano	1
LV - Lettonia	1
MA - Marocco	1
MK - Macedonia	1
MN - Mongolia	1
MZ - Mozambico	1
NP - Nepal	1
PA - Panama	1
PY - Paraguay	1
SE - Svezia	1
SI - Slovenia	1
SK - Slovacchia (Repubblica Slovacca)	1
SV - El Salvador	1
TJ - Tagikistan	1
UA - Ucraina	1
VE - Venezuela	1
Totale	1.536

Nome	#
Portal vein thrombosis relevance on liver cirrhosis: Italian Venous Thrombotic Events Registry	227
Platelet count does not predict bleeding in cirrhotic patients: Results from the PRO-LIVER Study	184
Incidence of fatigue and low-dose corticosteroid use in prostate cancer patients receiving systemic treatment: a meta-analysis of randomized controlled trials	167
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency	163
M170. GENETIC CHARACTERIZATION OF A COHORT OF PATIENTS AFFECTED BY SCHIZOPHRENIA. THE ROLE FOR RARE STRUCTURAL VARIANTS IN MODULATING TREATMENT RESISTANT ENDOPHENOTYPES: PRELIMINARY DATA	161
Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor	141
Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus	136
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias	131
The evolving role of monoclonal antibodies in the treatment of patients with advanced renal cell carcinoma: a systematic review	126
The Pro12Ala polymorphism of PPARγ2 modulates beta cell function and failure to oral glucose-lowering drugs in patients with type 2 diabetes	122
Totale	1.558

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	12	0	0	0	0	0	0	0	0	0	2	2	8
2021/2022	85	0	0	1	6	0	0	0	4	16	16	22	20
2022/2023	205	9	6	6	5	11	12	2	17	110	16	10	1
2023/2024	72	3	11	15	6	3	8	0	9	3	2	9	3
2024/2025	361	11	6	2	4	11	14	30	25	17	33	163	45
2025/2026	730	84	49	98	64	139	29	86	29	98	54	0	0
Totale													1.558