statistiche ricercatore

Continente	#
EU - Europa	698
NA - Nord America	668
AS - Asia	365
SA - Sud America	83
AF - Africa	9
Continente sconosciuto - Info sul continente non disponibili	1
Totale	1.824

Nazione	#
US - Stati Uniti d'America	648
DE - Germania	233
SG - Singapore	154
PL - Polonia	146
CN - Cina	134
SE - Svezia	80
BR - Brasile	64
UA - Ucraina	52
IT - Italia	50
FR - Francia	43
GB - Regno Unito	32
FI - Finlandia	17
IE - Irlanda	17
VN - Vietnam	16
ID - Indonesia	11
CA - Canada	10
IN - India	10
AR - Argentina	9
BD - Bangladesh	6
NL - Olanda	6
RU - Federazione Russa	6
TR - Turchia	6
HK - Hong Kong	5
IQ - Iraq	5
JP - Giappone	5
MX - Messico	5
BE - Belgio	4
BZ - Belize	4
AT - Austria	3
CI - Costa d'Avorio	3
IR - Iran	3
JO - Giordania	3
VE - Venezuela	3
AE - Emirati Arabi Uniti	2
CL - Cile	2
EC - Ecuador	2
ES - Italia	2
KE - Kenya	2
LT - Lituania	2
PH - Filippine	2
ZA - Sudafrica	2
AO - Angola	1
BG - Bulgaria	1
BO - Bolivia	1
CH - Svizzera	1
CO - Colombia	1
CZ - Repubblica Ceca	1
EU - Europa	1
JM - Giamaica	1
KG - Kirghizistan	1
LA - Repubblica Popolare Democratica del Laos	1
LU - Lussemburgo	1
NO - Norvegia	1
SA - Arabia Saudita	1
TN - Tunisia	1
UY - Uruguay	1
Totale	1.824

Nome	#
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions	412
Mild beckwith-wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p.	250
A unique case of reversion to normal size of a maternal premutation FMR1 allele in a normal boy	172
Simpson–Golabi–Behmel syndrome in a female: A case report and an unsolved issue	142
A premature infant with Costello syndrome due to a rare G13C HRAS mutation	140
The Simpson-Golabi-Behmel syndrome: a clinical case and a detective story	135
Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome.	131
Unexpected finding of paternal premutation of the fragile X FMR1 gene in a female fetus of a premutation carrier mother	122
Simpson-Golabi-Behmel syndrome type 1 in a 27-week macrosomic preterm newborn: the diagnostic value of rib malformations and index nail and finger hypoplasia.	118
A premature infant with Costello syndrome due to a rare G13C HRAS mutation.	110
Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1gene in fragile X cells treated with 5-aza-deoxycitidine	103
Totale	1.835

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	79	0	0	0	0	0	5	26	1	18	10	16	3
2021/2022	148	21	15	2	6	12	8	7	22	8	9	15	23
2022/2023	277	40	50	26	48	15	34	10	20	26	0	5	3
2023/2024	93	9	30	3	7	2	11	4	2	4	2	12	7
2024/2025	241	8	10	13	9	24	1	0	19	45	25	42	45
2025/2026	284	74	15	31	49	75	40	0	0	0	0	0	0
Totale													1.835

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