statistiche ricercatore

Continente	#
NA - Nord America	502
AS - Asia	471
EU - Europa	278
SA - Sud America	64
AF - Africa	19
OC - Oceania	4
Continente sconosciuto - Info sul continente non disponibili	1
Totale	1.339

Nazione	#
US - Stati Uniti d'America	494
SG - Singapore	184
IT - Italia	100
CN - Cina	98
VN - Vietnam	76
HK - Hong Kong	46
BR - Brasile	41
IE - Irlanda	40
SE - Svezia	37
DE - Germania	22
FR - Francia	16
NL - Olanda	13
ZA - Sudafrica	12
ES - Italia	11
GB - Regno Unito	11
JP - Giappone	10
IN - India	7
BE - Belgio	6
EC - Ecuador	6
IQ - Iraq	6
AR - Argentina	5
BD - Bangladesh	5
CA - Canada	5
CH - Svizzera	5
PK - Pakistan	5
SA - Arabia Saudita	5
AU - Australia	4
CL - Cile	4
IR - Iran	4
NO - Norvegia	4
TR - Turchia	4
CO - Colombia	3
ID - Indonesia	3
AE - Emirati Arabi Uniti	2
CZ - Repubblica Ceca	2
FI - Finlandia	2
KE - Kenya	2
KR - Corea	2
LK - Sri Lanka	2
MA - Marocco	2
PA - Panama	2
PL - Polonia	2
RU - Federazione Russa	2
UA - Ucraina	2
VE - Venezuela	2
A2 - ???statistics.table.value.countryCode.A2???	1
AT - Austria	1
AZ - Azerbaigian	1
CY - Cipro	1
DK - Danimarca	1
EG - Egitto	1
ET - Etiopia	1
GE - Georgia	1
IL - Israele	1
JO - Giordania	1
KZ - Kazakistan	1
LB - Libano	1
MX - Messico	1
MY - Malesia	1
PE - Perù	1
PH - Filippine	1
PY - Paraguay	1
RO - Romania	1
SY - Repubblica araba siriana	1
TH - Thailandia	1
TN - Tunisia	1
TW - Taiwan	1
UY - Uruguay	1
Totale	1.339

Nome	#
Saccharomyces cerevisiae as a model to study the role of mutations in SDHA gene associated to hereditary optic neuropathies	358
Yeast, worm, patient’s fibroblasts and zebrafish as models for drug repositioning of molecules targeting POLG-related diseases	205
Saccharomyces cerevisiae as a model for the identification of beneficial molecules for mitochondrial diseases.	146
The power of yeast in modeling human mutations leading to mitochondrial disease:the case of ANT1, YARS2, DNM1L and LYRM7.	141
Mitochondrial aminoacyl‐trna synthetase and disease: The yeast contribution for functional analysis of novel variants	128
Modeling of pathogenic variants of mitochondrial DNA polymerase: insight into the replication defects and implication for human disease	127
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features	126
The absence of SNF8 in the yeast Saccharomyces cerevisiae leads to mitochondrial dysfunction	122
Studies on Saccharomyces cerevisiae demonstrate association between mutation in MECR gene and Hereditary Optic Neuropathies (HON)	87
Recessive MECR pathogenic variants cause a LHON-like optic neuropathy	86
Recessive MECR pathogenic variants cause an LHON-like optic neuropathy	84
Totale	1.610

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	16	0	0	0	0	0	0	0	0	0	0	10	6
2021/2022	60	4	2	0	5	1	9	14	4	1	3	1	16
2022/2023	162	18	16	13	10	3	14	2	8	59	5	9	5
2023/2024	119	14	9	9	5	13	18	3	14	5	7	7	15
2024/2025	340	5	13	21	8	39	54	21	19	54	29	32	45
2025/2026	554	46	39	70	45	103	29	85	10	69	42	16	0
Totale													1.610