statistiche ricercatore

Continente	#
NA - Nord America	846
AS - Asia	436
EU - Europa	414
SA - Sud America	41
OC - Oceania	12
AF - Africa	11
Continente sconosciuto - Info sul continente non disponibili	1
Totale	1.761

Nazione	#
US - Stati Uniti d'America	838
SG - Singapore	141
PL - Polonia	114
CN - Cina	97
IT - Italia	56
SE - Svezia	52
VN - Vietnam	43
HK - Hong Kong	38
DE - Germania	32
BR - Brasile	31
FR - Francia	24
BE - Belgio	18
FI - Finlandia	18
ES - Italia	17
UA - Ucraina	17
BD - Bangladesh	15
ID - Indonesia	15
IE - Irlanda	14
TH - Thailandia	14
IN - India	13
PH - Filippine	13
AU - Australia	12
KR - Corea	11
NL - Olanda	11
RU - Federazione Russa	11
TR - Turchia	10
GB - Regno Unito	9
BG - Bulgaria	6
MY - Malesia	6
CZ - Repubblica Ceca	4
JO - Giordania	4
ZA - Sudafrica	4
AR - Argentina	3
AT - Austria	3
CH - Svizzera	3
DK - Danimarca	3
IQ - Iraq	3
JP - Giappone	3
MX - Messico	3
SN - Senegal	3
CA - Canada	2
CO - Colombia	2
IL - Israele	2
MA - Marocco	2
NP - Nepal	2
UZ - Uzbekistan	2
VE - Venezuela	2
AF - Afghanistan, Repubblica islamica di	1
AZ - Azerbaigian	1
BN - Brunei Darussalam	1
BO - Bolivia	1
CL - Cile	1
DM - Dominica	1
EU - Europa	1
GT - Guatemala	1
KE - Kenya	1
KG - Kirghizistan	1
LT - Lituania	1
LV - Lettonia	1
PE - Perù	1
PR - Porto Rico	1
TN - Tunisia	1
Totale	1.761

Nome	#
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis	393
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations	359
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients	277
Short Communication Novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients	225
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss	224
Five new OTOF gene mutations and auditory neuropathy	157
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis	157
Totale	1.792

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	101	12	3	6	4	4	8	4	6	10	12	6	26
2022/2023	161	16	16	10	25	17	28	0	15	18	2	10	4
2023/2024	103	4	7	3	8	5	7	19	19	1	6	17	7
2024/2025	264	14	5	19	28	18	18	27	13	39	31	32	20
2025/2026	555	58	19	27	30	44	56	125	17	53	70	42	14
2026/2027	3	3	0	0	0	0	0	0	0	0	0	0	0
Totale													1.792

ArTS Archivio della ricerca di Trieste