statistiche ricercatore

Continente	#
NA - Nord America	1.436
AS - Asia	497
EU - Europa	468
SA - Sud America	86
Continente sconosciuto - Info sul continente non disponibili	44
AF - Africa	12
OC - Oceania	1
Totale	2.544

Nazione	#
US - Stati Uniti d'America	1.389
CN - Cina	174
SG - Singapore	174
UA - Ucraina	96
IT - Italia	76
PL - Polonia	75
BR - Brasile	74
DE - Germania	52
GB - Regno Unito	38
FI - Finlandia	35
VN - Vietnam	34
FR - Francia	33
HK - Hong Kong	32
CA - Canada	28
BD - Bangladesh	21
IE - Irlanda	17
TR - Turchia	17
IN - India	15
RU - Federazione Russa	11
MX - Messico	8
SE - Svezia	8
AR - Argentina	5
JP - Giappone	5
LT - Lituania	5
ZA - Sudafrica	5
ES - Italia	4
IQ - Iraq	4
AT - Austria	3
BE - Belgio	3
CO - Colombia	3
GT - Guatemala	3
ID - Indonesia	3
JO - Giordania	3
NL - Olanda	3
UZ - Uzbekistan	3
CZ - Repubblica Ceca	2
IR - Iran	2
PK - Pakistan	2
SA - Arabia Saudita	2
SV - El Salvador	2
UY - Uruguay	2
AU - Australia	1
BA - Bosnia-Erzegovina	1
CH - Svizzera	1
CR - Costa Rica	1
CW - ???statistics.table.value.countryCode.CW???	1
DO - Repubblica Dominicana	1
DZ - Algeria	1
EC - Ecuador	1
EE - Estonia	1
ET - Etiopia	1
GR - Grecia	1
HN - Honduras	1
JM - Giamaica	1
KR - Corea	1
KZ - Kazakistan	1
LA - Repubblica Popolare Democratica del Laos	1
LV - Lettonia	1
MA - Marocco	1
MT - Malta	1
MU - Mauritius	1
MY - Malesia	1
NG - Nigeria	1
NI - Nicaragua	1
NP - Nepal	1
PS - Palestinian Territory	1
SC - Seychelles	1
SK - Slovacchia (Repubblica Slovacca)	1
TN - Tunisia	1
TT - Trinidad e Tobago	1
VE - Venezuela	1
Totale	2.501

Nome	#
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1)	277
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients	236
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease	219
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation.	205
BAFF-R mutations in Good's syndrome.	205
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration.	189
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease	189
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.	169
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency.	159
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency	150
The tec kinase-regulated phosphoproteome reveals a mechanism for the regulation of inhibitory signals in murine macrophages	149
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation.	146
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.	132
P85α is an intrinsic regulator of human natural killer cell effector functions	119
Totale	2.544

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	111	0	0	0	7	0	4	4	12	8	23	16	37
2022/2023	163	18	0	2	15	15	39	0	26	30	1	9	8
2023/2024	151	10	2	20	8	6	51	6	10	24	0	0	14
2024/2025	269	0	4	0	45	23	23	10	11	37	16	54	46
2025/2026	664	61	58	42	112	98	60	103	19	22	58	21	10
2026/2027	171	25	28	32	86	0	0	0	0	0	0	0	0
Totale													2.544