statistiche ricercatore

Continente	#
NA - Nord America	1.220
AS - Asia	507
EU - Europa	352
SA - Sud America	67
Continente sconosciuto - Info sul continente non disponibili	40
AF - Africa	13
OC - Oceania	1
Totale	2.200

Nazione	#
US - Stati Uniti d'America	1.190
SG - Singapore	237
CN - Cina	88
IT - Italia	73
DE - Germania	72
HK - Hong Kong	49
BR - Brasile	46
UA - Ucraina	45
RU - Federazione Russa	34
SE - Svezia	31
VN - Vietnam	31
IN - India	24
FR - Francia	20
CA - Canada	19
TR - Turchia	19
FI - Finlandia	18
GB - Regno Unito	16
BD - Bangladesh	15
IE - Irlanda	10
IQ - Iraq	8
AR - Argentina	7
IR - Iran	7
JP - Giappone	7
ES - Italia	6
ZA - Sudafrica	6
BE - Belgio	5
MX - Messico	5
PL - Polonia	5
SA - Arabia Saudita	5
AT - Austria	4
CO - Colombia	4
CZ - Repubblica Ceca	4
KR - Corea	4
CL - Cile	3
NL - Olanda	3
PK - Pakistan	3
BG - Bulgaria	2
DM - Dominica	2
EC - Ecuador	2
EG - Egitto	2
HR - Croazia	2
ID - Indonesia	2
LB - Libano	2
UY - Uruguay	2
VE - Venezuela	2
BZ - Belize	1
DK - Danimarca	1
DZ - Algeria	1
ET - Etiopia	1
EU - Europa	1
GA - Gabon	1
GY - Guiana	1
IL - Israele	1
JM - Giamaica	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
XK - ???statistics.table.value.countryCode.XK???	1
Totale	2.162

Nome	#
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder	207
Somatic amplifications and deletions in genome of papillary thyroid carcinomas	198
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells	195
Histone post-translational modifications associated to BAALC expression in leukemic cells.	186
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches	183
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers	178
Microdeletion 15q26.2qter and Microduplication 18q23 in a patient with prader-willi-like syndrome: Clinical findings	166
ANALISI DI CARCINOMI PAPILLIFERI TIROIDEI MEDIANTE CGH-ARRAY	166
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases	131
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype	124
Quantitative PCR evaluation of deletions/duplications identified by array CGH	110
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance	105
Using the AlphaFold system to the interpretation of variants of uncertain significance	100
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation	86
null	65
Totale	2.200

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	108	0	0	0	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	734	76	62	32	70	124	71	92	8	70	52	57	20
2026/2027	99	15	34	47	3	0	0	0	0	0	0	0	0
Totale													2.200