statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	1.230
CN - Cina	174
SG - Singapore	174
UA - Ucraina	96
PL - Polonia	75
BR - Brasile	70
IT - Italia	63
DE - Germania	52
GB - Regno Unito	37
FI - Finlandia	35
VN - Vietnam	34
FR - Francia	33
HK - Hong Kong	32
CA - Canada	19
TR - Turchia	17
IE - Irlanda	16
IN - India	14
RU - Federazione Russa	11
BD - Bangladesh	8
SE - Svezia	8
MX - Messico	7
AR - Argentina	5
JP - Giappone	5
ZA - Sudafrica	5
ES - Italia	4
IQ - Iraq	4
AT - Austria	3
BE - Belgio	3
ID - Indonesia	3
JO - Giordania	3
LT - Lituania	3
UZ - Uzbekistan	3
CO - Colombia	2
CZ - Repubblica Ceca	2
IR - Iran	2
NL - Olanda	2
PK - Pakistan	2
SA - Arabia Saudita	2
UY - Uruguay	2
AU - Australia	1
BA - Bosnia-Erzegovina	1
CH - Svizzera	1
DO - Repubblica Dominicana	1
DZ - Algeria	1
EE - Estonia	1
ET - Etiopia	1
GR - Grecia	1
HN - Honduras	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
NP - Nepal	1
PS - Palestinian Territory	1
SK - Slovacchia (Repubblica Slovacca)	1
TN - Tunisia	1
VE - Venezuela	1
Totale	2.282

Nome	#
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1)	263
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease	201
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients	197
BAFF-R mutations in Good's syndrome.	193
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation.	192
Allele *1 of HS1.2 enhancer associates with selective IgA deficiency and IgM concentration.	175
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease	173
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency.	152
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.	141
The tec kinase-regulated phosphoproteome reveals a mechanism for the regulation of inhibitory signals in murine macrophages	140
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency	135
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation.	134
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.	118
P85α is an intrinsic regulator of human natural killer cell effector functions	111
Totale	2.325

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	77	0	0	0	0	0	0	0	0	0	24	42	11
2021/2022	137	6	14	6	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	616	61	58	42	112	98	60	103	19	22	41	0	0
Totale													2.325