statistiche ricercatore

Continente	#
NA - Nord America	587
AS - Asia	478
EU - Europa	292
Continente sconosciuto - Info sul continente non disponibili	273
SA - Sud America	68
AF - Africa	19
OC - Oceania	4
Totale	1.721

Nazione	#
US - Stati Uniti d'America	575
SG - Singapore	186
IT - Italia	112
CN - Cina	99
VN - Vietnam	76
HK - Hong Kong	46
BR - Brasile	43
IE - Irlanda	40
SE - Svezia	37
DE - Germania	23
FR - Francia	16
NL - Olanda	13
ZA - Sudafrica	12
ES - Italia	11
GB - Regno Unito	11
JP - Giappone	10
BD - Bangladesh	9
IN - India	7
AR - Argentina	6
BE - Belgio	6
CA - Canada	6
EC - Ecuador	6
IQ - Iraq	6
CH - Svizzera	5
PK - Pakistan	5
SA - Arabia Saudita	5
AU - Australia	4
CL - Cile	4
CO - Colombia	4
IR - Iran	4
NO - Norvegia	4
TR - Turchia	4
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
CR - Costa Rica	1
CY - Cipro	1
DK - Danimarca	1
EG - Egitto	1
ET - Etiopia	1
GE - Georgia	1
IL - Israele	1
JM - Giamaica	1
JO - Giordania	1
KZ - Kazakistan	1
LB - Libano	1
MK - Macedonia	1
MX - Messico	1
MY - Malesia	1
NI - Nicaragua	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	1.449

Nome	#
Saccharomyces cerevisiae as a model to study the role of mutations in SDHA gene associated to hereditary optic neuropathies	368
Yeast, worm, patient’s fibroblasts and zebrafish as models for drug repositioning of molecules targeting POLG-related diseases	227
Saccharomyces cerevisiae as a model for the identification of beneficial molecules for mitochondrial diseases.	152
The power of yeast in modeling human mutations leading to mitochondrial disease:the case of ANT1, YARS2, DNM1L and LYRM7.	147
Mitochondrial aminoacyl‐trna synthetase and disease: The yeast contribution for functional analysis of novel variants	137
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features	134
The absence of SNF8 in the yeast Saccharomyces cerevisiae leads to mitochondrial dysfunction	134
Modeling of pathogenic variants of mitochondrial DNA polymerase: insight into the replication defects and implication for human disease	133
Recessive MECR pathogenic variants cause an LHON-like optic neuropathy	94
Studies on Saccharomyces cerevisiae demonstrate association between mutation in MECR gene and Hereditary Optic Neuropathies (HON)	93
Recessive MECR pathogenic variants cause a LHON-like optic neuropathy	91
The yeast Saccharomyces cerevisiae: a helpful tool to study mutations in genes associated with Hereditary Optic Neuropathies (HON)	11
Totale	1.721

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	54	0	0	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	579	46	39	70	45	103	29	85	10	69	42	29	12
2026/2027	86	18	43	25	0	0	0	0	0	0	0	0	0
Totale													1.721