statistiche ricercatore

Continente	#
EU - Europa	875
NA - Nord America	853
AS - Asia	667
SA - Sud America	39
AF - Africa	9
Continente sconosciuto - Info sul continente non disponibili	1
OC - Oceania	1
Totale	2.445

Nazione	#
US - Stati Uniti d'America	819
GB - Regno Unito	340
CN - Cina	243
SG - Singapore	222
DE - Germania	129
IT - Italia	86
SE - Svezia	82
NL - Olanda	51
RU - Federazione Russa	49
UA - Ucraina	45
HK - Hong Kong	43
IN - India	34
CA - Canada	28
KR - Corea	25
TR - Turchia	25
VN - Vietnam	25
FR - Francia	23
BD - Bangladesh	19
BR - Brasile	19
EU - Europa	19
IE - Irlanda	17
FI - Finlandia	15
CO - Colombia	13
SK - Slovacchia (Repubblica Slovacca)	13
BE - Belgio	12
JP - Giappone	9
CI - Costa d'Avorio	5
IL - Israele	4
CL - Cile	3
CZ - Repubblica Ceca	3
ES - Italia	3
PK - Pakistan	3
SA - Arabia Saudita	3
AR - Argentina	2
GR - Grecia	2
GT - Guatemala	2
IQ - Iraq	2
LV - Lettonia	2
NP - Nepal	2
PH - Filippine	2
PL - Polonia	2
ZA - Sudafrica	2
AU - Australia	1
BO - Bolivia	1
BZ - Belize	1
CH - Svizzera	1
EC - Ecuador	1
GH - Ghana	1
ID - Indonesia	1
IR - Iran	1
JM - Giamaica	1
JO - Giordania	1
KZ - Kazakistan	1
LK - Sri Lanka	1
MA - Marocco	1
MX - Messico	1
OM - Oman	1
SV - El Salvador	1
Totale	2.463

Nome	#
Activity and function of the nuclear factor kappaB pathway in human parathyroid tumors	275
Genetics and phenomics of hypothyroidism due to TSH resistance	249
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant	227
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma	224
Candidate gene analyses in Caucasian patients with Primary Ovarian Insufficiency (POI)	221
SCREENING OF SIX CANDIDATE GENES FOR PRIMARY OVARIAN INSUFFICIENCY (POI) IN A LARGE CAUCASIAN FEMALE POPULATION	221
Prevalence on inactivating TSH receptor (TSHR) mutations in a large series of pediatric subjects with non-autoimmune mild hyper-thyrotropinemia (hyperTSH)	214
RET genotypes comprising specific haplotypes of polymorphic variants are associated with sporadic medullary thyroid cancer	201
An in-frame complex mutation in the juxtamembarne intracellular domain causing RET activation in a familial medullary thyroid carcinoma	195
RET genotypes in sporadic medullary thyroid cancer : studies in a large Italian series	190
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia	187
The role of Ret genotypes as modifier loci for sporadic medullary cancer	172
Totale	2.576

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	48	0	0	0	0	0	0	0	0	0	0	39	9
2021/2022	181	13	11	8	11	22	9	17	5	26	12	7	40
2022/2023	221	25	39	24	34	20	39	1	11	19	0	8	1
2023/2024	147	2	11	6	12	39	20	10	6	6	17	10	8
2024/2025	270	6	18	1	41	48	15	0	19	3	35	23	61
2025/2026	675	78	52	54	45	84	59	70	32	56	80	65	0
Totale													2.576

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