statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	660
RU - Federazione Russa	488
DE - Germania	129
SG - Singapore	127
CN - Cina	114
BR - Brasile	109
IT - Italia	96
IE - Irlanda	85
SE - Svezia	71
FI - Finlandia	63
HK - Hong Kong	34
PL - Polonia	34
IN - India	22
FR - Francia	21
VN - Vietnam	19
GB - Regno Unito	15
CA - Canada	10
MX - Messico	10
MA - Marocco	7
AR - Argentina	6
CO - Colombia	5
ID - Indonesia	5
IQ - Iraq	5
BD - Bangladesh	4
BE - Belgio	4
CZ - Repubblica Ceca	4
EC - Ecuador	4
AT - Austria	3
AZ - Azerbaigian	3
LT - Lituania	3
PH - Filippine	3
VE - Venezuela	3
ZA - Sudafrica	3
CI - Costa d'Avorio	2
NL - Olanda	2
PK - Pakistan	2
SA - Arabia Saudita	2
TR - Turchia	2
UA - Ucraina	2
UY - Uruguay	2
UZ - Uzbekistan	2
AE - Emirati Arabi Uniti	1
BA - Bosnia-Erzegovina	1
CL - Cile	1
CY - Cipro	1
DO - Repubblica Dominicana	1
DZ - Algeria	1
EG - Egitto	1
ES - Italia	1
ET - Etiopia	1
FJ - Figi	1
HN - Honduras	1
HR - Croazia	1
KG - Kirghizistan	1
KR - Corea	1
KZ - Kazakistan	1
LA - Repubblica Popolare Democratica del Laos	1
ME - Montenegro	1
MU - Mauritius	1
MY - Malesia	1
NG - Nigeria	1
NP - Nepal	1
PA - Panama	1
PE - Perù	1
PS - Palestinian Territory	1
PT - Portogallo	1
PY - Paraguay	1
SN - Senegal	1
Totale	2.212

Nome	#
De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype	278
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment	231
A novel SLC1A4 homozygous mutation causing congenital microcephaly, epileptic encephalopathy and spastic tetraparesis: a video-EEG and tractography – case study	225
8q22.1 Microduplication Syndrome: Why the Brain Should Be Spared? A Literature Review and a Case Report	218
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease	189
Aripiprazole-induced Tardive Dyskinesia in 13 Years Old Girl Successfully Treated with Biperiden: A Case Report.	182
Electroclinical history of a five-year-old girl with GRIN1-related early-onset epileptic encephalopathy: a video-case study	159
A de novo truncating mutation in ASXL1 associated with segmental overgrowth	155
Il Parent Training in età evolutiva	149
Alstrom's Syndrome: Neurological Manifestations and Genetics	129
Bardet-Biedl Syndrome: A Brief Overview on Clinics and Genetics	107
Gender affects early psychomotor milestones and long-term neurodevelopment of preterm infants	88
CNTN2 gene: probabile causa di Encefalopatia Epilettica fenotipo Lennox-Gastaut like.	76
null	46
null	24
Totale	2.256

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	15	0	0	0	0	0	0	0	0	0	7	2	6
2021/2022	84	1	4	1	3	5	4	13	3	3	20	6	21
2022/2023	238	16	33	11	14	16	19	3	17	100	3	2	4
2023/2024	78	4	15	6	6	2	25	0	3	0	9	1	7
2024/2025	510	7	4	13	25	16	58	65	84	104	38	41	55
2025/2026	1.143	74	57	137	62	86	213	112	166	177	59	0	0
Totale													2.256