statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	801
VN - Vietnam	226
IT - Italia	162
SG - Singapore	155
CN - Cina	141
GB - Regno Unito	81
SE - Svezia	59
DE - Germania	53
FR - Francia	34
HK - Hong Kong	32
RU - Federazione Russa	27
IE - Irlanda	23
IN - India	23
CI - Costa d'Avorio	22
BR - Brasile	20
FI - Finlandia	20
NL - Olanda	16
KR - Corea	13
TG - Togo	8
ZA - Sudafrica	8
AR - Argentina	7
BE - Belgio	7
SC - Seychelles	7
TH - Thailandia	7
CH - Svizzera	6
EE - Estonia	6
ID - Indonesia	6
JO - Giordania	5
JP - Giappone	5
PH - Filippine	5
BD - Bangladesh	4
BG - Bulgaria	4
CA - Canada	4
ES - Italia	4
IR - Iran	4
UA - Ucraina	4
AT - Austria	3
EC - Ecuador	3
PL - Polonia	3
AL - Albania	2
AU - Australia	2
CZ - Repubblica Ceca	2
HR - Croazia	2
KE - Kenya	2
LT - Lituania	2
SA - Arabia Saudita	2
TR - Turchia	2
TW - Taiwan	2
VE - Venezuela	2
AZ - Azerbaigian	1
CY - Cipro	1
IQ - Iraq	1
JM - Giamaica	1
KZ - Kazakistan	1
LK - Sri Lanka	1
MA - Marocco	1
MX - Messico	1
MY - Malesia	1
NG - Nigeria	1
PA - Panama	1
PE - Perù	1
PT - Portogallo	1
SK - Slovacchia (Repubblica Slovacca)	1
TN - Tunisia	1
Totale	2.053

Nome	#
Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2	290
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism	262
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy	247
Collagen VI–NG2 axis in human tendon fibroblasts under conditions mimicking injury response	206
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome (Scientific Reports, (2020), 10, 1, (4785), 10.1038/s41598-020-61735-3)	191
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder	186
Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models	183
PI-PLCβ1b affects Akt activation, cyclin E expression, and caspase cleavage, promoting cell survival in pro-B-lymphoblastic cells exposed to oxidative stress	161
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions	145
First TMEM126A missense mutation in an Italian proband with optic atrophy and deafness	133
Dominant ACO2 mutations are a frequent cause of isolated optic atrophy	94
Totale	2.098

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	56	0	0	0	0	0	0	0	0	0	0	6	50
2021/2022	246	10	8	11	14	24	13	15	21	18	22	55	35
2022/2023	309	28	42	21	34	22	26	6	19	54	7	26	24
2023/2024	95	5	13	7	6	5	24	7	3	5	8	4	8
2024/2025	249	22	31	17	19	31	8	20	16	6	29	12	38
2025/2026	717	66	53	51	63	86	34	139	23	145	53	4	0
Totale													2.098

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