statistiche ricercatore

Continente	#
AS - Asia	427
NA - Nord America	407
EU - Europa	279
SA - Sud America	79
AF - Africa	28
Continente sconosciuto - Info sul continente non disponibili	1
OC - Oceania	1
Totale	1.222

Nazione	#
US - Stati Uniti d'America	393
SG - Singapore	174
IT - Italia	164
VN - Vietnam	83
CN - Cina	77
BR - Brasile	61
HK - Hong Kong	37
DE - Germania	21
NL - Olanda	15
RU - Federazione Russa	14
ZA - Sudafrica	14
FR - Francia	12
GB - Regno Unito	12
IN - India	12
AT - Austria	11
IQ - Iraq	7
BD - Bangladesh	6
CA - Canada	6
PL - Polonia	6
TR - Turchia	6
ES - Italia	5
PK - Pakistan	5
AR - Argentina	4
CO - Colombia	4
FI - Finlandia	4
JP - Giappone	4
MX - Messico	4
CI - Costa d'Avorio	3
IE - Irlanda	3
LT - Lituania	3
PY - Paraguay	3
SE - Svezia	3
VE - Venezuela	3
DO - Repubblica Dominicana	2
DZ - Algeria	2
HR - Croazia	2
KE - Kenya	2
KZ - Kazakistan	2
LV - Lettonia	2
PE - Perù	2
PH - Filippine	2
TN - Tunisia	2
TW - Taiwan	2
AZ - Azerbaigian	1
BS - Bahamas	1
CL - Cile	1
CM - Camerun	1
CY - Cipro	1
CZ - Repubblica Ceca	1
EC - Ecuador	1
EG - Egitto	1
ET - Etiopia	1
IL - Israele	1
IR - Iran	1
JO - Giordania	1
KR - Corea	1
MV - Maldive	1
NG - Nigeria	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
OM - Oman	1
PS - Palestinian Territory	1
PT - Portogallo	1
SN - Senegal	1
TH - Thailandia	1
XK - ???statistics.table.value.countryCode.XK???	1
Totale	1.222

Nome	#
Charcot-Marie-Tooth Disease with Myelin Protein Zero Mutation Presenting as Painful, Predominant Small-Fiber Neuropathy	159
Proof of Concept for Genome Profiling of the Neurofibroma/Sarcoma Sequence in Neurofibromatosis Type 1.	148
Genetic Basis of Breast and Ovarian Cancer: Approaches and Lessons Learnt from Three Decades of Inherited Predisposition Testing	144
Genetics of Darier’s Disease: New Insights into Pathogenic Mechanisms	141
Pure Parkinsonism as Possible Phenotype Expansion of THAP1-Related Disorders	118
Phenotypic Expansion of Autosomal Dominant LZTR1-Related Disorders with Special Emphasis on Adult-Onset Features	114
A case series of non-small cell lung cancer patients with EGFR or HER2 exon 20 insertion in Li Fraumeni syndrome	109
Mosaic derivative chromosomes at chorionic villi (CV) sampling are expression of genomic instability and precursors of cryptic disease-causing rearrangements: report of further four cases	106
Success and Pitfalls of Genetic Testing in Undiagnosed Diseases: Whole Exome Sequencing and Beyond	104
Reassessment of the NF1 variants of unknown significance found during the 20-year activity of a genetics diagnostic laboratory	91
Totale	1.234

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2023/2024	32	1	0	1	0	0	0	2	0	0	14	11	3
2024/2025	385	8	39	21	28	38	30	31	25	58	28	28	51
2025/2026	817	67	59	137	110	105	56	73	38	111	61	0	0
Totale													1.234