statistiche ricercatore

Continente	#
NA - Nord America	1.034
EU - Europa	549
AS - Asia	378
SA - Sud America	33
AF - Africa	8
OC - Oceania	2
Continente sconosciuto - Info sul continente non disponibili	1
Totale	2.005

Nazione	#
US - Stati Uniti d'America	1.027
RU - Federazione Russa	245
SG - Singapore	102
CN - Cina	95
IT - Italia	88
HK - Hong Kong	49
IE - Irlanda	44
SE - Svezia	39
VN - Vietnam	38
BR - Brasile	26
PL - Polonia	26
FR - Francia	24
KR - Corea	24
DE - Germania	21
GB - Regno Unito	21
JO - Giordania	20
IN - India	19
FI - Finlandia	17
CH - Svizzera	10
PH - Filippine	8
CA - Canada	4
JP - Giappone	4
AR - Argentina	3
CI - Costa d'Avorio	3
ID - Indonesia	3
IQ - Iraq	3
SA - Arabia Saudita	3
UA - Ucraina	3
AU - Australia	2
AZ - Azerbaigian	2
ES - Italia	2
MX - Messico	2
NL - Olanda	2
TR - Turchia	2
AO - Angola	1
BD - Bangladesh	1
BO - Bolivia	1
CL - Cile	1
CO - Colombia	1
GR - Grecia	1
HR - Croazia	1
HU - Ungheria	1
IL - Israele	1
KE - Kenya	1
LT - Lituania	1
MA - Marocco	1
MT - Malta	1
NG - Nigeria	1
NP - Nepal	1
OM - Oman	1
PA - Panama	1
PK - Pakistan	1
PT - Portogallo	1
SI - Slovenia	1
TW - Taiwan	1
VE - Venezuela	1
XK - ???statistics.table.value.countryCode.XK???	1
ZA - Sudafrica	1
Totale	2.005

Nome	#
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center	260
Mutated ASXL1 and number of somatic mutations as possible indicators of progression to chronic myelomonocytic leukemia of myelodysplastic syndromes with single or multilineage dysplasia	211
Involvement of RUNX1 Pathway Is a Common Event in the Leukemic Transformation of Chronic Myeloproliferative Neoplasms (MPNs)	211
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency	203
Mutation landscape in patients with myelofibrosis receiving ruxolitinib or hydroxyurea	194
THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS	186
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome Sequencing	165
Fundus phenotype in retinitis pigmentosa associated with EYS mutations	162
Germline Mutation in KIF1Bβ Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma	159
Characteristics and clinical correlates of NFE2 mutations in chronic Myeloproliferative neoplasms	145
Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.	132
Totale	2.028

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	25	0	0	0	0	0	0	0	0	0	0	17	8
2021/2022	87	13	4	3	1	1	9	4	1	6	6	15	24
2022/2023	265	20	52	22	25	15	38	27	16	34	0	5	11
2023/2024	127	8	12	14	5	16	18	4	21	3	11	10	5
2024/2025	596	25	64	37	116	154	68	20	20	33	22	21	16
2025/2026	562	80	74	26	48	95	27	93	21	32	54	12	0
Totale													2.028