statistiche ricercatore

Continente	#
NA - Nord America	425
EU - Europa	278
AS - Asia	226
SA - Sud America	32
AF - Africa	19
Continente sconosciuto - Info sul continente non disponibili	12
OC - Oceania	1
Totale	993

Nazione	#
US - Stati Uniti d'America	401
IT - Italia	106
SG - Singapore	78
CN - Cina	45
IE - Irlanda	40
RU - Federazione Russa	35
VN - Vietnam	35
DE - Germania	25
BR - Brasile	24
HK - Hong Kong	23
CA - Canada	14
GB - Regno Unito	14
ZA - Sudafrica	14
FI - Finlandia	13
FR - Francia	13
BD - Bangladesh	8
ES - Italia	6
IN - India	6
JP - Giappone	5
PK - Pakistan	5
NL - Olanda	4
PL - Polonia	4
AT - Austria	3
BE - Belgio	3
IQ - Iraq	3
MX - Messico	3
RO - Romania	3
SA - Arabia Saudita	3
SE - Svezia	3
AR - Argentina	2
CH - Svizzera	2
CO - Colombia	2
EC - Ecuador	2
HN - Honduras	2
ID - Indonesia	2
MY - Malesia	2
TR - Turchia	2
AE - Emirati Arabi Uniti	1
BH - Bahrain	1
BO - Bolivia	1
CG - Congo	1
CR - Costa Rica	1
EE - Estonia	1
ET - Etiopia	1
GT - Guatemala	1
IL - Israele	1
JM - Giamaica	1
KE - Kenya	1
KG - Kirghizistan	1
KR - Corea	1
KZ - Kazakistan	1
LA - Repubblica Popolare Democratica del Laos	1
LT - Lituania	1
LV - Lettonia	1
LY - Libia	1
MD - Moldavia	1
NP - Nepal	1
NR - Nauru	1
SV - El Salvador	1
TH - Thailandia	1
TN - Tunisia	1
TT - Trinidad e Tobago	1
VE - Venezuela	1
Totale	981

Nome	#
Pathogenic cryptic variants detectable through exome data reanalysis significantly increase the diagnostic yield in Joubert syndrome	145
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review	131
Case Report: Novel Compound Heterozygous RNASEH2B Mutations Cause Aicardi–Goutières Syndrome	116
Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis	111
Neuroradiologic, clinic and genetic characterization of cerebellar heterotopia: a pediatric multicentric study	101
Genetic and molecular mechanisms of Aicardi-Goutières Syndrome in RNASEH2 mutated patients	99
Ruxolitinib in Aicardi-Goutières syndrome	90
Cerebellar heterotopia in an 11-year-old child with KDM6B-related neurodevelopmental disorder: A case report and review of the literature	81
Clinical Characterization of a Multicenter International Cohort of Patients With Aicardi-Goutières Syndrome Homozygous for the RNASEH2B:p.Ala177Thr Variant: Early Clinical Markers of Disease Severity	61
Advancing Neuropediatric Rare Disease Diagnosis Through Clinical Genome Sequencing	40
Metformin Reduces Oxidative Damage in RNASEH2-Mutant Aicardi-Goutières Cells	18
Totale	993

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	26	0	0	0	0	1	1	1	2	2	2	2	15
2022/2023	100	11	8	3	5	6	8	0	6	45	0	8	0
2023/2024	58	2	7	3	6	7	13	0	4	0	1	7	8
2024/2025	158	2	9	1	1	3	10	12	14	44	4	20	38
2025/2026	443	31	19	32	40	51	23	75	33	59	33	35	12
2026/2027	202	16	80	42	61	3	0	0	0	0	0	0	0
Totale													993