CONTINI, ELISA
 Distribuzione geografica
Continente #
NA - Nord America 531
EU - Europa 215
AS - Asia 85
Totale 831
Nazione #
US - Stati Uniti d'America 531
IT - Italia 69
IE - Irlanda 48
SE - Svezia 38
CN - Cina 32
PL - Polonia 24
HK - Hong Kong 21
JO - Giordania 19
CH - Svizzera 10
AT - Austria 9
DE - Germania 9
PH - Filippine 6
VN - Vietnam 4
FR - Francia 3
SG - Singapore 3
RU - Federazione Russa 2
UA - Ucraina 2
GB - Regno Unito 1
Totale 831
Città #
Fairfield 87
Chandler 66
Ashburn 50
Dublin 48
Woodbridge 45
Seattle 40
Cambridge 39
Wilmington 34
Houston 25
Warsaw 24
Beijing 19
Florence 18
Hong Kong 14
Lawrence 14
Altamura 11
Ann Arbor 11
Buffalo 11
Princeton 11
Bern 10
New York 10
Boston 7
Vienna 7
Pian di Scò 6
Bremen 4
Dong Ket 4
Hillsboro 4
Medford 4
San Diego 4
Siena 4
Falls Church 3
Liberty 3
Norwalk 3
Quezon City 3
Shanghai 3
Ameno 2
Dearborn 2
Melito Di Napoli 2
Milan 2
Moscow 2
Paris 2
Redwood City 2
Singapore 2
Villa Minozzo 2
Washington 2
Andover 1
Arezzo 1
Azzano Decimo 1
Boardman 1
Brescia 1
Chengdu 1
Duncan 1
Fiesole 1
Fuzhou 1
Hefei 1
Inverigo 1
Landshut 1
Laurel 1
Leawood 1
Nanjing 1
Pavia 1
Redmond 1
Rome 1
Saviano 1
Scuola 1
Sesto Fiorentino 1
Shenyang 1
Torre Del Lago 1
Wuhan 1
Totale 690
Nome #
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center 155
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency 97
Mutated ASXL1 and number of somatic mutations as possible indicators of progression to chronic myelomonocytic leukemia of myelodysplastic syndromes with single or multilineage dysplasia 86
Mutation landscape in patients with myelofibrosis receiving ruxolitinib or hydroxyurea 86
Involvement of RUNX1 Pathway Is a Common Event in the Leukemic Transformation of Chronic Myeloproliferative Neoplasms (MPNs) 80
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome Sequencing 76
Fundus phenotype in retinitis pigmentosa associated with EYS mutations 73
THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS 63
Germline Mutation in KIF1Bβ Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma 55
Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest. 48
Characteristics and clinical correlates of NFE2 mutations in chronic Myeloproliferative neoplasms 35
Totale 854
Categoria #
all - tutte 2.422
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 2.422


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201946 0 0 0 0 0 0 0 0 1 9 20 16
2019/2020171 8 4 1 13 16 26 25 23 23 15 13 4
2020/2021160 4 5 23 28 3 10 5 11 13 33 17 8
2021/202287 13 4 3 1 1 9 4 1 6 6 15 24
2022/2023278 20 52 22 25 15 38 34 18 35 1 6 12
2023/202498 9 12 14 5 16 18 4 20 0 0 0 0
Totale 854