statistiche ricercatore

Continente	#
NA - Nord America	1.285
EU - Europa	804
AS - Asia	387
SA - Sud America	57
Continente sconosciuto - Info sul continente non disponibili	26
AF - Africa	21
OC - Oceania	3
Totale	2.583

Nazione	#
US - Stati Uniti d'America	1.266
RU - Federazione Russa	216
GB - Regno Unito	130
CN - Cina	126
IE - Irlanda	114
SG - Singapore	114
IT - Italia	83
SE - Svezia	62
BR - Brasile	48
VN - Vietnam	47
UA - Ucraina	45
FR - Francia	41
DE - Germania	40
FI - Finlandia	27
HK - Hong Kong	26
IN - India	16
BD - Bangladesh	11
BE - Belgio	11
CA - Canada	10
ES - Italia	10
TR - Turchia	10
ZA - Sudafrica	10
KR - Corea	9
MX - Messico	7
NL - Olanda	7
PL - Polonia	7
CZ - Repubblica Ceca	6
CO - Colombia	4
IQ - Iraq	4
JP - Giappone	3
NG - Nigeria	3
PK - Pakistan	3
SA - Arabia Saudita	3
AR - Argentina	2
AT - Austria	2
AU - Australia	2
AZ - Azerbaigian	2
EG - Egitto	2
ID - Indonesia	2
JO - Giordania	2
TN - Tunisia	2
UZ - Uzbekistan	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
BG - Bulgaria	1
CY - Cipro	1
EC - Ecuador	1
GT - Guatemala	1
KE - Kenya	1
KG - Kirghizistan	1
KZ - Kazakistan	1
LA - Repubblica Popolare Democratica del Laos	1
LK - Sri Lanka	1
MA - Marocco	1
NE - Niger	1
NI - Nicaragua	1
NP - Nepal	1
NZ - Nuova Zelanda	1
PE - Perù	1
PY - Paraguay	1
RO - Romania	1
SC - Seychelles	1
Totale	2.557

Nome	#
A 2.6 Mb deletion of 6q24.3-25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears	345
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features	336
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome	322
2q24-q31 deletion: report of a case and review of the literature	315
Low-level TP53 mutational load antecedes clonal expansion in chronic lymphocytic leukaemia	298
Germline mosaicism in Rett syndrome identified by prenatal diagnosis	291
Private inherited microdeletion/microduplications: implications in clinical practice	279
Expanding the phenotype of 22q11 deletion syndrome: the MURCS association	251
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate	146
Totale	2.583

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	129	0	25	4	13	0	3	10	10	2	12	11	39
2022/2023	205	11	32	23	31	19	39	3	11	16	10	7	3
2023/2024	182	3	4	28	16	1	51	64	3	0	1	0	11
2024/2025	270	5	12	41	14	37	12	3	18	18	9	34	67
2025/2026	948	58	108	154	141	197	35	96	20	22	47	17	53
2026/2027	40	25	15	0	0	0	0	0	0	0	0	0	0
Totale													2.583