statistiche ricercatore

Continente	#
NA - Nord America	1.091
AS - Asia	490
EU - Europa	321
SA - Sud America	63
AF - Africa	13
Continente sconosciuto - Info sul continente non disponibili	2
OC - Oceania	1
Totale	1.981

Nazione	#
US - Stati Uniti d'America	1.066
SG - Singapore	234
CN - Cina	88
DE - Germania	71
HK - Hong Kong	49
BR - Brasile	46
IT - Italia	46
UA - Ucraina	45
RU - Federazione Russa	34
SE - Svezia	31
VN - Vietnam	30
IN - India	24
FR - Francia	20
TR - Turchia	19
FI - Finlandia	17
CA - Canada	16
GB - Regno Unito	16
IE - Irlanda	10
IQ - Iraq	8
AR - Argentina	7
IR - Iran	7
BD - Bangladesh	6
ES - Italia	6
ZA - Sudafrica	6
BE - Belgio	5
JP - Giappone	5
MX - Messico	5
PL - Polonia	5
AT - Austria	4
KR - Corea	4
SA - Arabia Saudita	4
CL - Cile	3
CZ - Repubblica Ceca	3
NL - Olanda	3
PK - Pakistan	3
BG - Bulgaria	2
CO - Colombia	2
EG - Egitto	2
LB - Libano	2
UY - Uruguay	2
BZ - Belize	1
DK - Danimarca	1
DM - Dominica	1
DZ - Algeria	1
EC - Ecuador	1
ET - Etiopia	1
EU - Europa	1
GA - Gabon	1
GY - Guiana	1
HR - Croazia	1
ID - Indonesia	1
IL - Israele	1
KZ - Kazakistan	1
LA - Repubblica Popolare Democratica del Laos	1
LK - Sri Lanka	1
MR - Mauritania	1
NP - Nepal	1
NZ - Nuova Zelanda	1
PA - Panama	1
PR - Porto Rico	1
SK - Slovacchia (Repubblica Slovacca)	1
SY - Repubblica araba siriana	1
TN - Tunisia	1
VE - Venezuela	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	1.981

Nome	#
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder	195
Somatic amplifications and deletions in genome of papillary thyroid carcinomas	189
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells	183
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches	174
Histone post-translational modifications associated to BAALC expression in leukemic cells.	173
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers	166
Microdeletion 15q26.2qter and Microduplication 18q23 in a patient with prader-willi-like syndrome: Clinical findings	157
ANALISI DI CARCINOMI PAPILLIFERI TIROIDEI MEDIANTE CGH-ARRAY	150
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype	114
Quantitative PCR evaluation of deletions/duplications identified by array CGH	100
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases	94
Using the AlphaFold system to the interpretation of variants of uncertain significance	91
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance	89
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation	79
null	65
Totale	2.019

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	51	0	0	0	0	0	0	0	0	0	11	26	14
2021/2022	129	6	6	9	7	4	6	7	3	3	15	49	14
2022/2023	133	13	22	2	17	19	23	0	14	17	0	4	2
2023/2024	133	8	5	8	5	29	30	2	8	15	3	1	19
2024/2025	416	12	13	21	69	18	14	30	21	49	28	62	79
2025/2026	652	76	62	32	70	124	71	92	8	70	47	0	0
Totale													2.019