statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	558
IT - Italia	144
SG - Singapore	119
VN - Vietnam	74
HK - Hong Kong	64
CN - Cina	60
DE - Germania	35
BR - Brasile	34
IN - India	19
SE - Svezia	17
FI - Finlandia	16
ID - Indonesia	11
FR - Francia	10
KR - Corea	7
CA - Canada	6
JP - Giappone	6
RU - Federazione Russa	6
AT - Austria	5
GB - Regno Unito	5
BG - Bulgaria	4
IL - Israele	4
JO - Giordania	4
IQ - Iraq	3
IR - Iran	3
MX - Messico	3
PH - Filippine	3
UA - Ucraina	3
AE - Emirati Arabi Uniti	2
AZ - Azerbaigian	2
CI - Costa d'Avorio	2
CL - Cile	2
ES - Italia	2
KE - Kenya	2
MA - Marocco	2
MY - Malesia	2
PK - Pakistan	2
RO - Romania	2
TG - Togo	2
ZA - Sudafrica	2
AR - Argentina	1
AU - Australia	1
BE - Belgio	1
BY - Bielorussia	1
CH - Svizzera	1
EG - Egitto	1
GR - Grecia	1
IE - Irlanda	1
KG - Kirghizistan	1
LA - Repubblica Popolare Democratica del Laos	1
LT - Lituania	1
LY - Libia	1
NG - Nigeria	1
NL - Olanda	1
OM - Oman	1
PL - Polonia	1
RS - Serbia	1
SA - Arabia Saudita	1
SR - Suriname	1
SV - El Salvador	1
TN - Tunisia	1
UY - Uruguay	1
VE - Venezuela	1
Totale	1.270

Nome	#
3-Methylglutaconic Aciduria Type I Due to AUH Defect: The Case Report of a Diagnostic Odyssey and a Review of the Literature	197
Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage	177
Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7	176
Protein–protein interaction network analysis applied to DNA copy number profiling suggests new perspectives on the aetiology of Mayer–Rokitansky–Küster–Hauser syndrome	174
A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3	170
Epilepsy phenotype in patients with Xp22.31 microduplication	160
Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith–Magenis syndrome	149
Array-comparative genomic hybridization analysis in a cohort of 130 children with Autism Spectrum Disorders: A single Center Italian Study	119
Totale	1.322

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	7	0	0	0	0	0	0	0	0	0	0	7	0
2021/2022	95	2	6	8	3	8	6	6	6	2	2	33	13
2022/2023	88	18	17	5	11	8	7	5	5	8	2	2	0
2023/2024	71	3	6	3	11	8	6	1	5	10	9	6	3
2024/2025	236	3	13	11	20	5	7	19	16	38	35	18	51
2025/2026	575	64	26	44	47	65	26	150	23	50	44	36	0
Totale													1.322

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