statistiche ricercatore

Continente	#
NA - Nord America	429
AS - Asia	357
EU - Europa	223
SA - Sud America	75
Continente sconosciuto - Info sul continente non disponibili	11
AF - Africa	6
AN - Antartide	1
Totale	1.102

Nazione	#
US - Stati Uniti d'America	403
SG - Singapore	145
IT - Italia	99
CN - Cina	70
BR - Brasile	66
HK - Hong Kong	43
BD - Bangladesh	32
DE - Germania	27
VN - Vietnam	27
GB - Regno Unito	18
FI - Finlandia	16
CA - Canada	15
RU - Federazione Russa	15
TR - Turchia	13
FR - Francia	12
IN - India	12
UA - Ucraina	10
MX - Messico	7
PL - Polonia	6
AR - Argentina	3
NL - Olanda	3
PT - Portogallo	3
AT - Austria	2
CO - Colombia	2
EC - Ecuador	2
ID - Indonesia	2
JP - Giappone	2
LT - Lituania	2
PY - Paraguay	2
SA - Arabia Saudita	2
SE - Svezia	2
TH - Thailandia	2
ZA - Sudafrica	2
AE - Emirati Arabi Uniti	1
AO - Angola	1
AQ - Antartide	1
AZ - Azerbaigian	1
BB - Barbados	1
CH - Svizzera	1
CR - Costa Rica	1
CZ - Repubblica Ceca	1
DK - Danimarca	1
ES - Italia	1
ET - Etiopia	1
GT - Guatemala	1
HU - Ungheria	1
IE - Irlanda	1
IL - Israele	1
JM - Giamaica	1
JO - Giordania	1
LA - Repubblica Popolare Democratica del Laos	1
LV - Lettonia	1
MY - Malesia	1
PS - Palestinian Territory	1
RO - Romania	1
SN - Senegal	1
YT - Mayotte	1
Totale	1.091

Nome	#
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome	158
ACOX1 gain‐of‐function variation in a 10‐years‐old patient responsive to immunomodulating therapy	141
Family History in Parkinson's Disease: A National Cross-Sectional Study	128
Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro	110
Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report	101
Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract	97
Benign Hereditary Chorea as a Manifestation of HPCA Mutation	91
Establishment of three Joubert syndrome-derived induced pluripotent stem cell (iPSC) lines harbouring compound heterozygous mutations in CC2D2A gene	84
Expanding the spectrum of clinical severity of AICA-ribosiduria: Report of two siblings with mild phenotype caused by a novel pathogenic variant in ATIC gene	75
Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature review	67
Letter to the Editors: Concerning “SSR4-CDG, an ultra-rare X-linked congenital disorder of glycosylation affecting the TRAP complex: Review of 22 affected individuals including the first adult patient” by Johnsen et al	50
Totale	1.102

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	4	0	0	0	0	0	0	1	0	0	0	1	2
2022/2023	26	1	0	1	2	0	5	8	3	4	0	2	0
2023/2024	54	3	2	1	6	1	5	2	0	8	0	15	11
2024/2025	255	5	10	7	31	19	16	28	17	20	18	32	52
2025/2026	572	50	63	34	71	57	51	72	35	32	54	32	21
2026/2027	145	28	19	43	55	0	0	0	0	0	0	0	0
Totale													1.102