statistiche ricercatore

Continente	#
NA - Nord America	789
EU - Europa	718
AS - Asia	438
SA - Sud America	89
Continente sconosciuto - Info sul continente non disponibili	17
AF - Africa	9
OC - Oceania	8
Totale	2.068

Nazione	#
US - Stati Uniti d'America	763
DE - Germania	236
SG - Singapore	187
PL - Polonia	146
CN - Cina	142
SE - Svezia	80
BR - Brasile	67
IT - Italia	52
UA - Ucraina	52
FR - Francia	51
GB - Regno Unito	32
VN - Vietnam	29
IE - Irlanda	18
FI - Finlandia	17
CA - Canada	15
IN - India	12
ID - Indonesia	11
JP - Giappone	11
AR - Argentina	10
HK - Hong Kong	9
AU - Australia	8
BD - Bangladesh	8
NL - Olanda	7
IQ - Iraq	6
RU - Federazione Russa	6
TR - Turchia	6
ES - Italia	5
MX - Messico	5
BE - Belgio	4
BZ - Belize	4
AT - Austria	3
CI - Costa d'Avorio	3
CL - Cile	3
IR - Iran	3
JO - Giordania	3
SA - Arabia Saudita	3
VE - Venezuela	3
AE - Emirati Arabi Uniti	2
CO - Colombia	2
EC - Ecuador	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
CZ - Repubblica Ceca	1
EU - Europa	1
JM - Giamaica	1
KG - Kirghizistan	1
LA - Repubblica Popolare Democratica del Laos	1
LU - Lussemburgo	1
MK - Macedonia	1
MY - Malesia	1
NO - Norvegia	1
RO - Romania	1
SV - El Salvador	1
TH - Thailandia	1
TN - Tunisia	1
UY - Uruguay	1
Totale	2.052

Nome	#
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions	470
Mild beckwith-wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p.	273
A unique case of reversion to normal size of a maternal premutation FMR1 allele in a normal boy	194
Simpson–Golabi–Behmel syndrome in a female: A case report and an unsolved issue	159
A premature infant with Costello syndrome due to a rare G13C HRAS mutation	157
Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome.	152
The Simpson-Golabi-Behmel syndrome: a clinical case and a detective story	146
Unexpected finding of paternal premutation of the fragile X FMR1 gene in a female fetus of a premutation carrier mother	145
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.	130
A premature infant with Costello syndrome due to a rare G13C HRAS mutation.	123
Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1gene in fragile X cells treated with 5-aza-deoxycitidine	119
Totale	2.068

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	127	0	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	499	74	15	31	49	75	49	75	38	35	30	13	15
2026/2027	18	14	4	0	0	0	0	0	0	0	0	0	0
Totale													2.068

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