statistiche ricercatore

Continente	#
EU - Europa	932
NA - Nord America	909
AS - Asia	586
SA - Sud America	80
AF - Africa	42
Continente sconosciuto - Info sul continente non disponibili	36
OC - Oceania	2
Totale	2.587

Nazione	#
US - Stati Uniti d'America	887
IT - Italia	426
RU - Federazione Russa	213
SG - Singapore	147
CN - Cina	142
VN - Vietnam	121
BR - Brasile	66
HK - Hong Kong	57
DE - Germania	55
IE - Irlanda	53
KR - Corea	42
FI - Finlandia	36
FR - Francia	35
BD - Bangladesh	23
NL - Olanda	23
ES - Italia	22
IN - India	22
GB - Regno Unito	21
ZA - Sudafrica	16
CA - Canada	14
SE - Svezia	10
PL - Polonia	9
AT - Austria	8
CI - Costa d'Avorio	7
UA - Ucraina	6
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
SC - Seychelles	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
GT - Guatemala	1
HN - Honduras	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	2.551

Nome	#
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death	534
Pathogen-sugar interactions revealed by universal saturation transfer analysis	373
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19	302
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes	260
Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder	229
Differential gene expression analysis pipelines and bioinformatic tools for the identification of specific biomarkers: A review	220
Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant	205
Expanding the Landscape of Breast Cancer-Associated Rare Variants and Combining with Polygenic Risk Score	190
Heterozygosity for Neuronal Ceroid Lipofuscinosis predisposes to Bipolar Disorder	181
Rare variants modulating phenotype in NF1 carriers	93
Totale	2.587

	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	1.631	71	226	277	177	212	61	242	46	72	90	64	93
2026/2027	109	70	39	0	0	0	0	0	0	0	0	0	0
Totale													2.587