statistiche ricercatore

Continente	#
EU - Europa	748
NA - Nord America	554
AS - Asia	203
SA - Sud America	13
Continente sconosciuto - Info sul continente non disponibili	1
Totale	1.519

Nazione	#
US - Stati Uniti d'America	530
GB - Regno Unito	332
CN - Cina	125
DE - Germania	118
SE - Svezia	81
IT - Italia	58
UA - Ucraina	45
TR - Turchia	25
CA - Canada	23
KR - Corea	23
NL - Olanda	23
EU - Europa	19
IE - Irlanda	17
IN - India	17
RU - Federazione Russa	16
FI - Finlandia	14
SK - Slovacchia (Repubblica Slovacca)	13
BE - Belgio	12
CO - Colombia	12
FR - Francia	11
HK - Hong Kong	4
CZ - Repubblica Ceca	2
ES - Italia	2
GR - Grecia	2
JP - Giappone	2
NP - Nepal	2
SG - Singapore	2
CH - Svizzera	1
CL - Cile	1
IR - Iran	1
LK - Sri Lanka	1
LV - Lettonia	1
MX - Messico	1
SA - Arabia Saudita	1
Totale	1.537

Nome	#
Activity and function of the nuclear factor kappaB pathway in human parathyroid tumors	179
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant	160
SCREENING OF SIX CANDIDATE GENES FOR PRIMARY OVARIAN INSUFFICIENCY (POI) IN A LARGE CAUCASIAN FEMALE POPULATION	153
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma	142
Candidate gene analyses in Caucasian patients with Primary Ovarian Insufficiency (POI)	142
Genetics and phenomics of hypothyroidism due to TSH resistance	133
RET genotypes comprising specific haplotypes of polymorphic variants are associated with sporadic medullary thyroid cancer	132
An in-frame complex mutation in the juxtamembarne intracellular domain causing RET activation in a familial medullary thyroid carcinoma	125
Prevalence on inactivating TSH receptor (TSHR) mutations in a large series of pediatric subjects with non-autoimmune mild hyper-thyrotropinemia (hyperTSH)	124
RET genotypes in sporadic medullary thyroid cancer : studies in a large Italian series	122
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia	104
The role of Ret genotypes as modifier loci for sporadic medullary cancer	97
Totale	1.613

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	60	0	0	0	0	0	0	0	0	0	17	21	22
2019/2020	223	30	13	12	20	15	17	26	11	28	33	9	9
2020/2021	189	3	19	21	1	13	13	15	13	33	10	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	129	2	11	6	12	39	20	10	6	6	17	0	0
Totale													1.613

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