statistiche ricercatore

Continente	#
NA - Nord America	958
AS - Asia	429
EU - Europa	293
SA - Sud America	59
AF - Africa	15
Continente sconosciuto - Info sul continente non disponibili	2
Totale	1.756

Nazione	#
US - Stati Uniti d'America	938
SG - Singapore	202
CN - Cina	70
IT - Italia	60
UA - Ucraina	45
DE - Germania	43
VN - Vietnam	43
BR - Brasile	40
HK - Hong Kong	38
RU - Federazione Russa	33
FR - Francia	17
GB - Regno Unito	17
SE - Svezia	17
TR - Turchia	17
FI - Finlandia	16
CA - Canada	12
IE - Irlanda	12
IN - India	12
AR - Argentina	9
BE - Belgio	8
JP - Giappone	8
NL - Olanda	7
BD - Bangladesh	6
PK - Pakistan	6
ZA - Sudafrica	6
AT - Austria	5
IQ - Iraq	5
MX - Messico	5
IR - Iran	4
PL - Polonia	4
AE - Emirati Arabi Uniti	3
KR - Corea	3
MA - Marocco	3
SA - Arabia Saudita	3
UZ - Uzbekistan	3
CL - Cile	2
DZ - Algeria	2
EC - Ecuador	2
LT - Lituania	2
PY - Paraguay	2
UY - Uruguay	2
CO - Colombia	1
CZ - Repubblica Ceca	1
DM - Dominica	1
ES - Italia	1
ET - Etiopia	1
EU - Europa	1
GY - Guiana	1
HR - Croazia	1
ID - Indonesia	1
IL - Israele	1
IM - Isola di Man	1
KG - Kirghizistan	1
KZ - Kazakistan	1
LA - Repubblica Popolare Democratica del Laos	1
LV - Lettonia	1
MG - Madagascar	1
NI - Nicaragua	1
NP - Nepal	1
PA - Panama	1
PT - Portogallo	1
RS - Serbia	1
TG - Togo	1
TN - Tunisia	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	1.756

Nome	#
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder	195
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells	183
Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability	177
Histone post-translational modifications associated to BAALC expression in leukemic cells.	173
A polymorphic GGC repeat in the NPAS2 gene and its association with melanoma	170
A CGH array procedure to detect PAX6 gene structural defects	159
Meccanismi epigenetici alla base dell'espressione del gene BAALC nelle leucemie acute mieloidi	130
Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations	127
Plasma-Based Longitudinal Evaluation of ESR1 Epigenetic Status in Hormone Receptor-Positive HER2-Negative Metastatic Breast Cancer	127
Abstract PD10-01: Impact of ESR1 mutations on Selective Estrogen Receptor Degraders and Modulators: an integrated liquid-biopsy and pharmacodynamics approach	112
JAK2 V617F-mutated polycythemia vera developing in a patient with a 20-year-long chronic myeloid leukemia at the time of first molecular response	107
Using the AlphaFold system to the interpretation of variants of uncertain significance	90
A Prenatal Diagnosis of Verheij Syndrome in a Fetus Harboring a de novo PUF60 Variant.	40
Totale	1.790

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	44	0	0	0	0	0	0	0	0	0	11	13	20
2021/2022	117	6	7	7	6	2	4	8	2	1	17	40	17
2022/2023	146	16	21	3	16	17	30	0	13	16	7	4	3
2023/2024	88	8	8	4	2	9	22	0	11	7	3	0	14
2024/2025	335	4	11	26	26	16	15	43	24	46	17	42	65
2025/2026	597	69	58	30	81	128	73	59	12	50	37	0	0
Totale													1.790