statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	752
IT - Italia	336
RU - Federazione Russa	213
SG - Singapore	146
CN - Cina	140
VN - Vietnam	121
BR - Brasile	66
HK - Hong Kong	55
IE - Irlanda	53
DE - Germania	52
KR - Corea	42
FI - Finlandia	36
FR - Francia	33
GB - Regno Unito	21
IN - India	21
ES - Italia	20
NL - Olanda	20
ZA - Sudafrica	16
CA - Canada	9
PL - Polonia	9
BD - Bangladesh	8
SE - Svezia	8
AT - Austria	7
CI - Costa d'Avorio	7
UA - Ucraina	5
AE - Emirati Arabi Uniti	4
IR - Iran	4
KE - Kenya	4
MX - Messico	4
AO - Angola	3
AR - Argentina	3
BW - Botswana	3
EC - Ecuador	3
IQ - Iraq	3
JP - Giappone	3
PE - Perù	3
PK - Pakistan	3
TN - Tunisia	3
TR - Turchia	3
UZ - Uzbekistan	3
AU - Australia	2
BE - Belgio	2
CH - Svizzera	2
CO - Colombia	2
MA - Marocco	2
PH - Filippine	2
PT - Portogallo	2
SA - Arabia Saudita	2
BF - Burkina Faso	1
BO - Bolivia	1
CL - Cile	1
CR - Costa Rica	1
CZ - Repubblica Ceca	1
DK - Danimarca	1
GR - Grecia	1
HU - Ungheria	1
ID - Indonesia	1
IM - Isola di Man	1
JO - Giordania	1
KG - Kirghizistan	1
KZ - Kazakistan	1
LK - Sri Lanka	1
LT - Lituania	1
LU - Lussemburgo	1
MD - Moldavia	1
MU - Mauritius	1
PA - Panama	1
PY - Paraguay	1
SK - Slovacchia (Repubblica Slovacca)	1
Totale	2.282

Nome	#
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death	506
Pathogen-sugar interactions revealed by universal saturation transfer analysis	323
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19	273
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes	242
Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder	213
Differential gene expression analysis pipelines and bioinformatic tools for the identification of specific biomarkers: A review	193
Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant	183
Expanding the Landscape of Breast Cancer-Associated Rare Variants and Combining with Polygenic Risk Score	161
Heterozygosity for Neuronal Ceroid Lipofuscinosis predisposes to Bipolar Disorder	159
Rare variants modulating phenotype in NF1 carriers	65
Totale	2.318

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2022/2023	94	0	0	0	0	0	0	51	21	8	4	8	2
2023/2024	197	7	10	21	19	10	35	46	15	2	10	13	9
2024/2025	556	41	21	39	33	57	47	43	27	61	35	48	104
2025/2026	1.471	71	226	277	177	212	61	242	46	72	87	0	0
Totale													2.318