statistiche ricercatore

Continente	#
EU - Europa	1.331
NA - Nord America	475
AS - Asia	298
SA - Sud America	62
AF - Africa	15
OC - Oceania	11
Continente sconosciuto - Info sul continente non disponibili	1
Totale	2.193

Nazione	#
IT - Italia	643
US - Stati Uniti d'America	464
RU - Federazione Russa	288
IE - Irlanda	140
SG - Singapore	101
CN - Cina	85
DE - Germania	56
BR - Brasile	53
HK - Hong Kong	35
SE - Svezia	35
NL - Olanda	32
FR - Francia	31
GB - Regno Unito	31
FI - Finlandia	30
KR - Corea	22
VN - Vietnam	14
CZ - Repubblica Ceca	9
ES - Italia	9
AU - Australia	8
TR - Turchia	8
IN - India	7
MA - Marocco	6
MX - Messico	6
PK - Pakistan	5
PL - Polonia	5
BD - Bangladesh	4
CI - Costa d'Avorio	4
SA - Arabia Saudita	4
AR - Argentina	3
AT - Austria	3
JP - Giappone	3
KZ - Kazakistan	3
UA - Ucraina	3
CH - Svizzera	2
DK - Danimarca	2
DZ - Algeria	2
EC - Ecuador	2
IQ - Iraq	2
JM - Giamaica	2
LT - Lituania	2
NR - Nauru	2
VE - Venezuela	2
ZA - Sudafrica	2
AL - Albania	1
BA - Bosnia-Erzegovina	1
BE - Belgio	1
BY - Bielorussia	1
CA - Canada	1
CO - Colombia	1
HN - Honduras	1
HR - Croazia	1
ID - Indonesia	1
IR - Iran	1
IS - Islanda	1
KH - Cambogia	1
LK - Sri Lanka	1
MD - Moldavia	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	2.193

Nome	#
VEXAS syndrome: a new paradigm for adult-onset monogenic autoinflammatory diseases	803
Private somatic mutations identified with liquid biopsy lead tumor progression in solid cancers	147
Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases	145
New candidates for autism/intellectual disability identified by whole-exome sequencing	143
Exome sequencing in 200 intellectual disability/autistic patients: new candidates and atypical presentations	139
Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes (Front. Oncol., (2021), 11, 10.3389/fonc.2021.649435)	137
PIK3CA-CDKN2A clonal evolution in metastatic breast cancer and multiple points cell-free DNA analysis	129
Spondyloocular Syndrome: a novel XYLT2 variant with description of the neonatal phenotype	117
SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures	114
Development and Implementation of the AIDA International Registry for Patients With VEXAS Syndrome	111
Specific clonal expansion at disease progression (PD) in solid cancers pinpointed by cell free DNA analysis	106
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD	99
Identification of a Novel SHANK2 Pathogenic Variant in a Patient with a Neurodevelopmental Disorder	55
Totale	2.245

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	27	0	0	0	0	0	1	5	7	2	4	1	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	690	84	120	91	160	223	12	0	0	0	0	0	0
Totale													2.245