statistiche ricercatore

Continente	#
NA - Nord America	891
AS - Asia	445
EU - Europa	423
SA - Sud America	41
Continente sconosciuto - Info sul continente non disponibili	32
OC - Oceania	13
AF - Africa	11
Totale	1.856

Nazione	#
US - Stati Uniti d'America	879
SG - Singapore	142
PL - Polonia	115
CN - Cina	98
IT - Italia	60
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
IN - India	14
TH - Thailandia	14
AU - Australia	13
PH - Filippine	13
GB - Regno Unito	11
KR - Corea	11
NL - Olanda	11
RU - Federazione Russa	11
TR - Turchia	10
JP - Giappone	9
BG - Bulgaria	6
CZ - Repubblica Ceca	6
MY - Malesia	6
CA - Canada	4
JO - Giordania	4
ZA - Sudafrica	4
AR - Argentina	3
AT - Austria	3
CH - Svizzera	3
DK - Danimarca	3
IQ - Iraq	3
MX - Messico	3
SN - Senegal	3
CO - Colombia	2
GT - Guatemala	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
KE - Kenya	1
KG - Kirghizistan	1
LT - Lituania	1
LV - Lettonia	1
NI - Nicaragua	1
PE - Perù	1
PR - Porto Rico	1
TN - Tunisia	1
Totale	1.825

Nome	#
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis	416
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	362
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients	284
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss	239
Short Communication Novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients	227
Five new OTOF gene mutations and auditory neuropathy	164
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis	164
Totale	1.856

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	86	0	0	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	67	21	28	18	0	0	0	0	0	0	0	0	0
Totale													1.856

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