statistiche ricercatore

Continente	#
NA - Nord America	411
AS - Asia	370
EU - Europa	260
SA - Sud America	54
AF - Africa	16
OC - Oceania	4
Continente sconosciuto - Info sul continente non disponibili	1
Totale	1.116

Nazione	#
US - Stati Uniti d'America	405
SG - Singapore	162
IT - Italia	97
CN - Cina	93
IE - Irlanda	40
VN - Vietnam	40
SE - Svezia	37
BR - Brasile	35
HK - Hong Kong	32
DE - Germania	22
NL - Olanda	13
ZA - Sudafrica	12
ES - Italia	11
GB - Regno Unito	10
JP - Giappone	8
BE - Belgio	6
AR - Argentina	5
CA - Canada	5
CH - Svizzera	5
AU - Australia	4
CL - Cile	4
EC - Ecuador	4
FR - Francia	4
IN - India	4
IQ - Iraq	4
IR - Iran	4
NO - Norvegia	4
BD - Bangladesh	3
CO - Colombia	3
ID - Indonesia	3
AE - Emirati Arabi Uniti	2
CZ - Repubblica Ceca	2
KR - Corea	2
LK - Sri Lanka	2
PK - Pakistan	2
PL - Polonia	2
RU - Federazione Russa	2
TR - Turchia	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
FI - Finlandia	1
GE - Georgia	1
IL - Israele	1
KZ - Kazakistan	1
MA - Marocco	1
PA - Panama	1
PE - Perù	1
PY - Paraguay	1
RO - Romania	1
SA - Arabia Saudita	1
TH - Thailandia	1
TN - Tunisia	1
UA - Ucraina	1
VE - Venezuela	1
Totale	1.116

Nome	#
Saccharomyces cerevisiae as a model to study the role of mutations in SDHA gene associated to hereditary optic neuropathies	339
Yeast, worm, patient’s fibroblasts and zebrafish as models for drug repositioning of molecules targeting POLG-related diseases	180
Saccharomyces cerevisiae as a model for the identification of beneficial molecules for mitochondrial diseases.	122
Modeling of pathogenic variants of mitochondrial DNA polymerase: insight into the replication defects and implication for human disease	120
The power of yeast in modeling human mutations leading to mitochondrial disease:the case of ANT1, YARS2, DNM1L and LYRM7.	118
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features	107
Mitochondrial aminoacyl‐trna synthetase and disease: The yeast contribution for functional analysis of novel variants	103
The absence of SNF8 in the yeast Saccharomyces cerevisiae leads to mitochondrial dysfunction	91
Studies on Saccharomyces cerevisiae demonstrate association between mutation in MECR gene and Hereditary Optic Neuropathies (HON)	74
Recessive MECR pathogenic variants cause a LHON-like optic neuropathy	72
Recessive MECR pathogenic variants cause an LHON-like optic neuropathy	61
Totale	1.387

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	45	0	0	0	0	0	7	2	8	8	4	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	331	46	39	70	45	103	28	0	0	0	0	0	0
Totale													1.387