FINI, Sergio
 Distribuzione geografica
Continente #
NA - Nord America 858
EU - Europa 227
AS - Asia 136
AF - Africa 4
SA - Sud America 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.228
Nazione #
US - Stati Uniti d'America 852
CN - Cina 70
IT - Italia 66
DE - Germania 49
SG - Singapore 47
UA - Ucraina 31
GB - Regno Unito 30
SE - Svezia 13
FI - Finlandia 11
BE - Belgio 9
TR - Turchia 8
CA - Canada 6
DZ - Algeria 4
ID - Indonesia 4
CZ - Repubblica Ceca 3
NL - Olanda 3
SI - Slovenia 3
LT - Lituania 2
VN - Vietnam 2
AE - Emirati Arabi Uniti 1
BD - Bangladesh 1
BR - Brasile 1
BY - Bielorussia 1
CH - Svizzera 1
CL - Cile 1
ES - Italia 1
EU - Europa 1
FR - Francia 1
GR - Grecia 1
HU - Ungheria 1
IN - India 1
IR - Iran 1
LV - Lettonia 1
SA - Arabia Saudita 1
Totale 1.228
Città #
Fairfield 123
Chandler 82
Woodbridge 82
Ashburn 57
Houston 55
Ann Arbor 49
Seattle 48
Singapore 42
Cambridge 38
Santa Clara 38
Jacksonville 33
Wilmington 30
Beijing 25
New York 22
Munich 21
Ferrara 16
Los Angeles 13
Milan 12
Nanjing 12
Princeton 12
Shanghai 12
Brussels 9
Bremen 8
San Diego 8
Boardman 7
Dearborn 7
Izmir 7
Bologna 6
Helsinki 6
London 6
Jakarta 4
Ottawa 4
Pisa 4
Mcallen 3
Padova 3
San Mateo 3
Zhengzhou 3
Algiers 2
Brno 2
Des Moines 2
Dong Ket 2
Falls Church 2
Guangzhou 2
Kunming 2
Norwalk 2
Orange 2
Redwood City 2
Shenyang 2
Tianjin 2
Trento 2
Argenta 1
Athens 1
Augusta 1
Budapest 1
Changsha 1
Dubai 1
Falkenstein 1
Frankfurt am Main 1
Hebei 1
Jiaxing 1
Lowell 1
Minsk 1
Modena 1
Montreal 1
Montréal 1
Mountain View 1
Nanchang 1
Ningbo 1
Philadelphia 1
Pingdingshan 1
Prague 1
Riga 1
Riyadh 1
São Paulo 1
Tappahannock 1
Washington 1
Yellow Springs 1
Zurich 1
Totale 964
Nome #
Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay 131
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies 129
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome 128
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders. 126
Transcriptional behavior of DMD gene duplications in DMD/BMD males 121
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 121
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 119
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies 107
A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature 98
DMD gene molecular genetic characterization in Eastern Europe and non European countries 84
Workload measurement for molecular genetics laboratory: A survey study 71
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotype 17
Totale 1.252
Categoria #
all - tutte 6.697
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.697


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020176 0 0 0 0 0 36 34 31 30 29 11 5
2020/2021157 14 8 14 9 16 17 6 16 3 18 23 13
2021/2022157 8 6 3 4 21 10 8 13 12 14 10 48
2022/2023183 17 24 5 24 29 18 13 14 33 1 3 2
2023/2024101 8 12 4 0 5 30 4 7 1 2 6 22
2024/2025159 4 11 26 19 59 40 0 0 0 0 0 0
Totale 1.252