statistiche ricercatore

Continente	#
EU - Europa	1.420
NA - Nord America	616
AS - Asia	419
SA - Sud America	73
AF - Africa	35
OC - Oceania	11
Continente sconosciuto - Info sul continente non disponibili	1
Totale	2.575

Nazione	#
IT - Italia	686
US - Stati Uniti d'America	602
RU - Federazione Russa	289
IE - Irlanda	141
SG - Singapore	122
CN - Cina	96
VN - Vietnam	62
DE - Germania	61
BR - Brasile	58
FR - Francia	46
GB - Regno Unito	38
HK - Hong Kong	37
SE - Svezia	35
NL - Olanda	34
FI - Finlandia	32
KR - Corea	22
BD - Bangladesh	19
IN - India	15
ZA - Sudafrica	15
ES - Italia	14
TR - Turchia	10
CZ - Repubblica Ceca	9
AU - Australia	8
MA - Marocco	6
MX - Messico	6
PL - Polonia	6
CI - Costa d'Avorio	5
PK - Pakistan	5
SA - Arabia Saudita	5
UZ - Uzbekistan	5
AR - Argentina	4
CA - Canada	4
JP - Giappone	4
UA - Ucraina	4
VE - Venezuela	4
AT - Austria	3
CH - Svizzera	3
DK - Danimarca	3
DZ - Algeria	3
EC - Ecuador	3
IQ - Iraq	3
KZ - Kazakistan	3
LT - Lituania	3
BA - Bosnia-Erzegovina	2
CO - Colombia	2
IL - Israele	2
JM - Giamaica	2
NG - Nigeria	2
NR - Nauru	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
AZ - Azerbaigian	1
BE - Belgio	1
BY - Bielorussia	1
CL - Cile	1
EG - Egitto	1
ET - Etiopia	1
GR - Grecia	1
HN - Honduras	1
HR - Croazia	1
ID - Indonesia	1
IR - Iran	1
IS - Islanda	1
KE - Kenya	1
KH - Cambogia	1
LK - Sri Lanka	1
MD - Moldavia	1
MT - Malta	1
MY - Malesia	1
NP - Nepal	1
NZ - Nuova Zelanda	1
PE - Perù	1
PT - Portogallo	1
RO - Romania	1
RS - Serbia	1
TM - Turkmenistan	1
TN - Tunisia	1
TT - Trinidad e Tobago	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	2.575

Nome	#
VEXAS syndrome: a new paradigm for adult-onset monogenic autoinflammatory diseases	883
New candidates for autism/intellectual disability identified by whole-exome sequencing	184
Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases	178
Private somatic mutations identified with liquid biopsy lead tumor progression in solid cancers	169
Exome sequencing in 200 intellectual disability/autistic patients: new candidates and atypical presentations	159
Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes (Front. Oncol., (2021), 11, 10.3389/fonc.2021.649435)	156
PIK3CA-CDKN2A clonal evolution in metastatic breast cancer and multiple points cell-free DNA analysis	147
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD	142
Development and Implementation of the AIDA International Registry for Patients With VEXAS Syndrome	139
Spondyloocular Syndrome: a novel XYLT2 variant with description of the neonatal phenotype	137
SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures	129
Specific clonal expansion at disease progression (PD) in solid cancers pinpointed by cell free DNA analysis	122
Identification of a Novel SHANK2 Pathogenic Variant in a Patient with a Neurodevelopmental Disorder	82
Totale	2.627

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	7	0	0	0	0	0	0	0	0	0	0	0	7
2021/2022	45	1	3	3	2	0	1	0	2	11	2	5	15
2022/2023	222	5	22	16	8	5	43	26	15	39	11	22	10
2023/2024	479	20	17	37	35	47	69	108	31	11	36	37	31
2024/2025	764	43	35	87	91	80	68	36	61	70	43	62	88
2025/2026	1.072	84	120	91	160	223	36	143	36	42	73	61	3
Totale													2.627