statistiche ricercatore

Continente	#
NA - Nord America	435
AS - Asia	426
EU - Europa	340
SA - Sud America	55
Continente sconosciuto - Info sul continente non disponibili	21
AF - Africa	9
OC - Oceania	5
Totale	1.291

Nazione	#
US - Stati Uniti d'America	413
SG - Singapore	184
RU - Federazione Russa	169
VN - Vietnam	90
CN - Cina	87
IT - Italia	52
BR - Brasile	46
DE - Germania	28
HK - Hong Kong	26
NL - Olanda	21
GB - Regno Unito	16
CA - Canada	15
FI - Finlandia	13
FR - Francia	12
IN - India	9
JP - Giappone	9
IE - Irlanda	8
PL - Polonia	6
UA - Ucraina	6
AU - Australia	5
AR - Argentina	4
AT - Austria	3
BD - Bangladesh	3
IQ - Iraq	3
ZA - Sudafrica	3
CO - Colombia	2
CZ - Repubblica Ceca	2
JM - Giamaica	2
KR - Corea	2
MA - Marocco	2
PK - Pakistan	2
TH - Thailandia	2
BB - Barbados	1
CI - Costa d'Avorio	1
CR - Costa Rica	1
DZ - Algeria	1
EG - Egitto	1
ES - Italia	1
GP - Guadalupe	1
HN - Honduras	1
IL - Israele	1
IR - Iran	1
KE - Kenya	1
KH - Cambogia	1
MK - Macedonia	1
MX - Messico	1
MY - Malesia	1
PE - Perù	1
PH - Filippine	1
PT - Portogallo	1
PY - Paraguay	1
SA - Arabia Saudita	1
SK - Slovacchia (Repubblica Slovacca)	1
SY - Repubblica araba siriana	1
TR - Turchia	1
UY - Uruguay	1
UZ - Uzbekistan	1
Totale	1.270

Nome	#
Benign hereditary chorea: clinical and neuroimaging features in an Italian family.	161
Diagnostica, esame obiettivo e diagnosi bioumorale della tiroide	147
A Multicenter Epidemiological Study on Second Malignancy in Non-Syndromic Pheochromocytoma/Paraganglioma Patients in Italy	145
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis	137
Identification and functional characterization of a novel mutation in the NKX2-1 gene: Comparison with the data in the literature	128
Screening for mutations in the ISL1 gene in patients with thyroid dysgenesis	123
Identification and Functional Characterization of a Novel Mutation in theNKX2-1Gene: Comparison with the Data in the Literature	120
A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea.	117
A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementation.	117
Genetics of congenital hypothyroidism	96
Totale	1.291

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	51	0	0	0	0	0	0	0	4	8	7	11	21
2022/2023	76	9	9	0	1	7	7	3	5	10	20	5	0
2023/2024	75	6	3	8	10	3	16	0	14	0	3	10	2
2024/2025	335	10	5	2	1	11	24	29	27	22	25	148	31
2025/2026	644	67	36	77	64	130	31	77	25	65	45	16	11
2026/2027	11	9	2	0	0	0	0	0	0	0	0	0	0
Totale													1.291