statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	922
SG - Singapore	302
GB - Regno Unito	265
CN - Cina	258
IT - Italia	111
HK - Hong Kong	85
SE - Svezia	78
VN - Vietnam	66
BD - Bangladesh	60
BR - Brasile	54
DE - Germania	42
FR - Francia	37
RU - Federazione Russa	37
NL - Olanda	33
IN - India	27
CA - Canada	24
IE - Irlanda	21
DK - Danimarca	19
FI - Finlandia	16
CI - Costa d'Avorio	14
ID - Indonesia	12
TR - Turchia	11
BE - Belgio	10
UA - Ucraina	10
JP - Giappone	8
KR - Corea	6
PH - Filippine	4
PL - Polonia	4
AR - Argentina	3
CO - Colombia	3
CZ - Repubblica Ceca	3
ES - Italia	3
JM - Giamaica	3
MX - Messico	3
RO - Romania	3
UZ - Uzbekistan	3
ZA - Sudafrica	3
BG - Bulgaria	2
CH - Svizzera	2
IR - Iran	2
IS - Islanda	2
KE - Kenya	2
LV - Lettonia	2
PY - Paraguay	2
AE - Emirati Arabi Uniti	1
AF - Afghanistan, Repubblica islamica di	1
AO - Angola	1
AT - Austria	1
AU - Australia	1
CL - Cile	1
CM - Camerun	1
CR - Costa Rica	1
EC - Ecuador	1
EG - Egitto	1
HU - Ungheria	1
IQ - Iraq	1
LT - Lituania	1
MA - Marocco	1
MY - Malesia	1
PE - Perù	1
PK - Pakistan	1
PT - Portogallo	1
SA - Arabia Saudita	1
SN - Senegal	1
SV - El Salvador	1
TW - Taiwan	1
Totale	2.599

Nome	#
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome	268
Perthes disease : A new finding in Floating-Harbor syndrome	252
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth	252
Autoimmunity and cytokine imbalance in inherited epidermolysis bullosa	241
MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions	240
Olfactory Malformations in Mendelian Disorders of the Epigenetic Machinery	236
Progressive bone impairment with age and pubertal development in neurofibromatosis type I	223
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review	209
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation	201
The absence that makes the difference: choroidal abnormalities in Legius syndrome	189
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? : A case report and review of 62 cases	154
Response to "Characteristics of 2p15-p16.1 microdeletion syndrome : review and description of two additional patients"	132
Neurofibromatosis type I (NF1) and bone involvement in a pediatric setting: insights from FGF23 levels	102
Totale	2.699

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	12	0	0	0	0	0	0	0	0	0	0	0	12
2021/2022	171	27	8	10	11	5	6	10	6	30	16	7	35
2022/2023	233	28	28	31	23	23	44	3	22	25	2	2	2
2023/2024	107	2	13	12	7	26	9	0	3	4	4	8	19
2024/2025	411	10	53	13	36	26	11	11	34	23	48	42	104
2025/2026	1.022	95	59	114	86	122	59	168	33	69	56	118	43
Totale													2.699

IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca