statistiche ricercatore

Continente	#
NA - Nord America	313
EU - Europa	244
AS - Asia	203
SA - Sud America	29
OC - Oceania	4
AF - Africa	2
Continente sconosciuto - Info sul continente non disponibili	1
Totale	796

Nazione	#
US - Stati Uniti d'America	310
IT - Italia	96
SG - Singapore	84
CN - Cina	59
IE - Irlanda	40
SE - Svezia	35
HK - Hong Kong	30
DE - Germania	22
BR - Brasile	21
NL - Olanda	12
ES - Italia	9
GB - Regno Unito	7
BE - Belgio	6
JP - Giappone	5
AU - Australia	4
FR - Francia	4
IR - Iran	4
NO - Norvegia	4
CL - Cile	3
CA - Canada	2
ID - Indonesia	2
IN - India	2
KR - Corea	2
LK - Sri Lanka	2
RU - Federazione Russa	2
TR - Turchia	2
VN - Vietnam	2
A2 - ???statistics.table.value.countryCode.A2???	1
AE - Emirati Arabi Uniti	1
AR - Argentina	1
AT - Austria	1
AZ - Azerbaigian	1
BD - Bangladesh	1
CH - Svizzera	1
CO - Colombia	1
CY - Cipro	1
CZ - Repubblica Ceca	1
DK - Danimarca	1
FI - Finlandia	1
GE - Georgia	1
IQ - Iraq	1
KZ - Kazakistan	1
MA - Marocco	1
PA - Panama	1
PE - Perù	1
PK - Pakistan	1
PY - Paraguay	1
RO - Romania	1
SA - Arabia Saudita	1
UA - Ucraina	1
VE - Venezuela	1
ZA - Sudafrica	1
Totale	796

Nome	#
Saccharomyces cerevisiae as a model to study the role of mutations in SDHA gene associated to hereditary optic neuropathies	315
Yeast, worm, patient’s fibroblasts and zebrafish as models for drug repositioning of molecules targeting POLG-related diseases	152
Saccharomyces cerevisiae as a model for the identification of beneficial molecules for mitochondrial diseases.	96
The power of yeast in modeling human mutations leading to mitochondrial disease:the case of ANT1, YARS2, DNM1L and LYRM7.	93
Modeling of pathogenic variants of mitochondrial DNA polymerase: insight into the replication defects and implication for human disease	91
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features	79
Mitochondrial aminoacyl‐trna synthetase and disease: The yeast contribution for functional analysis of novel variants	65
Recessive MECR pathogenic variants cause a LHON-like optic neuropathy	51
Studies on Saccharomyces cerevisiae demonstrate association between mutation in MECR gene and Hereditary Optic Neuropathies (HON)	48
The absence of SNF8 in the yeast Saccharomyces cerevisiae leads to mitochondrial dysfunction	40
Recessive MECR pathogenic variants cause an LHON-like optic neuropathy	37
Totale	1.067

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	63	1	0	2	2	13	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	11	11	0	0	0	0	0	0	0	0	0	0	0
Totale													1.067