statistiche ricercatore

Continente	#
NA - Nord America	1.136
AS - Asia	462
EU - Europa	343
SA - Sud America	89
AF - Africa	16
Continente sconosciuto - Info sul continente non disponibili	1
OC - Oceania	1
Totale	2.048

Nazione	#
US - Stati Uniti d'America	1.115
SG - Singapore	217
CN - Cina	135
DE - Germania	80
IT - Italia	75
BR - Brasile	73
GB - Regno Unito	45
HK - Hong Kong	38
UA - Ucraina	33
VN - Vietnam	29
SE - Svezia	21
FI - Finlandia	17
RU - Federazione Russa	17
CA - Canada	10
MX - Messico	10
BE - Belgio	9
TR - Turchia	9
ZA - Sudafrica	8
AR - Argentina	7
JP - Giappone	6
NL - Olanda	6
PL - Polonia	6
BD - Bangladesh	5
ES - Italia	5
FR - Francia	5
ID - Indonesia	5
IN - India	5
DZ - Algeria	4
LT - Lituania	4
VE - Venezuela	4
CO - Colombia	3
CZ - Repubblica Ceca	3
IE - Irlanda	3
SI - Slovenia	3
AT - Austria	2
BY - Bielorussia	2
IQ - Iraq	2
MA - Marocco	2
NO - Norvegia	2
PH - Filippine	2
SA - Arabia Saudita	2
AE - Emirati Arabi Uniti	1
AL - Albania	1
AZ - Azerbaigian	1
CH - Svizzera	1
CL - Cile	1
CM - Camerun	1
CR - Costa Rica	1
CY - Cipro	1
EG - Egitto	1
EU - Europa	1
GR - Grecia	1
HU - Ungheria	1
IR - Iran	1
LA - Repubblica Popolare Democratica del Laos	1
LK - Sri Lanka	1
LV - Lettonia	1
PY - Paraguay	1
TV - Tuvalu	1
UZ - Uzbekistan	1
Totale	2.048

Nome	#
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies	206
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies	203
Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay	196
Genetic counseling for women referred for advanced maternal age: a telegenetic approach	195
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders	192
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies	189
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome	184
A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature	181
Transcriptional behavior of DMD gene duplications in DMD/BMD males	175
DMD gene molecular genetic characterization in Eastern Europe and non European countries	146
Workload measurement for molecular genetics laboratory: A survey study	125
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotype	82
Totale	2.074

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	96	0	0	0	0	0	17	6	16	3	18	23	13
2021/2022	157	8	6	3	4	21	10	8	13	12	14	10	48
2022/2023	183	17	24	5	24	29	18	13	14	33	1	3	2
2023/2024	101	8	12	4	0	5	30	4	7	1	2	6	22
2024/2025	413	4	11	26	19	59	40	19	14	83	39	46	53
2025/2026	568	117	33	84	131	165	38	0	0	0	0	0	0
Totale													2.074

SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara