statistiche ricercatore

Continente	#
NA - Nord America	957
AS - Asia	404
EU - Europa	289
SA - Sud America	50
AF - Africa	7
Continente sconosciuto - Info sul continente non disponibili	2
OC - Oceania	1
Totale	1.710

Nazione	#
US - Stati Uniti d'America	938
SG - Singapore	200
CN - Cina	76
DE - Germania	71
HK - Hong Kong	45
UA - Ucraina	43
BR - Brasile	40
IT - Italia	38
RU - Federazione Russa	34
SE - Svezia	31
IN - India	19
TR - Turchia	18
FI - Finlandia	16
GB - Regno Unito	14
VN - Vietnam	14
CA - Canada	11
IE - Irlanda	10
IR - Iran	7
AR - Argentina	5
BE - Belgio	5
ES - Italia	5
IQ - Iraq	5
MX - Messico	5
PL - Polonia	5
ZA - Sudafrica	5
AT - Austria	4
FR - Francia	4
JP - Giappone	4
KR - Corea	4
BD - Bangladesh	3
NL - Olanda	3
SA - Arabia Saudita	3
CO - Colombia	2
CZ - Repubblica Ceca	2
UY - Uruguay	2
BG - Bulgaria	1
BZ - Belize	1
DK - Danimarca	1
DM - Dominica	1
EU - Europa	1
GY - Guiana	1
HR - Croazia	1
ID - Indonesia	1
IL - Israele	1
LA - Repubblica Popolare Democratica del Laos	1
LK - Sri Lanka	1
MR - Mauritania	1
NZ - Nuova Zelanda	1
PA - Panama	1
PK - Pakistan	1
SK - Slovacchia (Repubblica Slovacca)	1
SY - Repubblica araba siriana	1
TN - Tunisia	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	1.710

Nome	#
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder	177
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells	171
Somatic amplifications and deletions in genome of papillary thyroid carcinomas	168
Histone post-translational modifications associated to BAALC expression in leukemic cells.	163
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches	153
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers	138
Microdeletion 15q26.2qter and Microduplication 18q23 in a patient with prader-willi-like syndrome: Clinical findings	136
ANALISI DI CARCINOMI PAPILLIFERI TIROIDEI MEDIANTE CGH-ARRAY	120
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype	97
Quantitative PCR evaluation of deletions/duplications identified by array CGH	84
Using the AlphaFold system to the interpretation of variants of uncertain significance	77
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases	71
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance	66
null	65
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation	62
Totale	1.748

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	116	0	0	0	0	0	31	6	16	12	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	381	76	62	32	70	124	17	0	0	0	0	0	0
Totale													1.748