statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	1.148
SG - Singapore	179
CN - Cina	155
GB - Regno Unito	138
VN - Vietnam	98
IT - Italia	93
DE - Germania	81
HK - Hong Kong	75
IN - India	58
CA - Canada	48
KR - Corea	46
RU - Federazione Russa	41
SE - Svezia	36
FR - Francia	35
JP - Giappone	29
AU - Australia	26
BR - Brasile	26
CI - Costa d'Avorio	25
TG - Togo	25
IE - Irlanda	24
ZA - Sudafrica	23
TR - Turchia	22
ES - Italia	19
TW - Taiwan	19
NL - Olanda	15
SC - Seychelles	14
IL - Israele	13
EE - Estonia	10
PK - Pakistan	10
FI - Finlandia	8
PH - Filippine	8
CH - Svizzera	7
IR - Iran	7
BE - Belgio	6
IQ - Iraq	6
UA - Ucraina	6
AR - Argentina	5
TH - Thailandia	5
AT - Austria	4
DZ - Algeria	4
MY - Malesia	4
NO - Norvegia	4
RO - Romania	4
SA - Arabia Saudita	4
BD - Bangladesh	3
CY - Cipro	3
ET - Etiopia	3
HR - Croazia	3
MO - Macao, regione amministrativa speciale della Cina	3
PT - Portogallo	3
SI - Slovenia	3
CD - Congo	2
DK - Danimarca	2
EC - Ecuador	2
EG - Egitto	2
ID - Indonesia	2
LB - Libano	2
MX - Messico	2
PL - Polonia	2
UG - Uganda	2
CL - Cile	1
CO - Colombia	1
KH - Cambogia	1
KZ - Kazakistan	1
LT - Lituania	1
NA - Namibia	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
OM - Oman	1
PE - Perù	1
QA - Qatar	1
SY - Repubblica araba siriana	1
TN - Tunisia	1
VE - Venezuela	1
Totale	2.666

Nome	#
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods	1.075
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges	228
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI	169
Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges	157
Bioinformatics for personal genome interpretation	155
Collective judgment predicts disease-associated single nucleotide variants	154
SNP-SIG 2013: The state of the art of genomic variant interpretation	141
SNP-SIG 2013: From coding to non-coding - New approaches for genomic variant interpretation	127
SNP-SIG Meeting 2011: identification and annotation of SNPs in the context of structure, function, and disease	118
VarI-SIG 2015: Methods for personalized medicine - the role of variant interpretation in research and diagnostics	72
VarI-SIG 2014--From SNPs to variants: interpreting different types of genetic variants	72
null	67
Thoughts from SNP-SIG 2012: future challenges in the annotation of genetic variations	66
null	63
null	60
Totale	2.724

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	49	0	0	0	0	0	0	0	0	0	0	7	42
2021/2022	149	14	2	4	4	29	13	2	13	13	1	13	41
2022/2023	199	16	41	11	14	11	17	3	14	29	17	10	16
2023/2024	742	0	10	5	8	3	6	0	16	126	244	179	145
2024/2025	480	118	92	23	18	64	30	19	18	10	12	22	54
2025/2026	560	69	60	67	45	64	29	47	24	80	65	10	0
Totale													2.724

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