De Bonis, Maria
 Distribuzione geografica
Continente #
NA - Nord America 328
EU - Europa 261
AS - Asia 129
AF - Africa 2
SA - Sud America 1
Totale 721
Nazione #
US - Stati Uniti d'America 326
DE - Germania 77
CN - Cina 63
SE - Svezia 59
IT - Italia 52
SG - Singapore 37
IE - Irlanda 15
UA - Ucraina 13
ID - Indonesia 10
RU - Federazione Russa 9
FI - Finlandia 8
FR - Francia 8
IN - India 8
NL - Olanda 5
TR - Turchia 5
BE - Belgio 4
GB - Regno Unito 4
IR - Iran 3
RO - Romania 3
CA - Canada 2
CI - Costa d'Avorio 2
AT - Austria 1
BR - Brasile 1
DK - Danimarca 1
HK - Hong Kong 1
KR - Corea 1
MY - Malesia 1
PL - Polonia 1
PT - Portogallo 1
Totale 721
Città #
Chandler 105
Singapore 28
Ashburn 24
San Mateo 17
Dublin 15
Nanjing 14
New York 12
Ann Arbor 11
Wilmington 11
Jakarta 10
Cattolica 9
Jacksonville 9
Milan 9
Bremen 7
Dearborn 7
Boston 6
Moscow 6
Princeton 5
Beijing 4
Boardman 4
Guangzhou 4
Helsinki 4
Izmir 4
Kunming 4
Lawrence 4
Rome 4
Caserta 3
Hebei 3
Houston 3
Jiaxing 3
Munich 3
Nürnberg 3
Shenyang 3
Tianjin 3
Abidjan 2
Aci Catena 2
Augusta 2
Brussels 2
Fairfield 2
Fremont 2
Lanzhou 2
Leawood 2
Napoli 2
Pune 2
Redwood City 2
Seattle 2
Seveso 2
Waanrode 2
Wuhan 2
Amsterdam 1
Andover 1
Ardabil 1
Berlin 1
Cambridge 1
Central 1
Centrale 1
Changchun 1
Cincinnati 1
Copenhagen 1
Detroit 1
Eden Prairie 1
Falkenstein 1
Foshan 1
Groningen 1
Hefei 1
Kemerovo 1
Kish 1
Kuala Lumpur 1
Lisbon 1
Miami 1
Monmouth Junction 1
Montespertoli 1
Mountain View 1
Nanchang 1
Norwalk 1
Novokuznetsk 1
Ottawa 1
Paese 1
Reggio Nell'emilia 1
Rio Saliceto 1
Sacramento 1
San Francisco 1
Shanghai 1
Suceava 1
São Paulo 1
Toronto 1
Torrance 1
Vienna 1
Yellow Springs 1
Totale 431
Nome #
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms? 105
Multidisciplinary team for elucidation of any new mutation and how this approach can be useful to individualize any genetic result: the case of BRCA2 c.631G > A/c.7008-2A > T genotype 105
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome 94
A rapid screening of a recurrent CYP24A1 pathogenic variant opens the way to molecular testing for Idiopathic Infantile Hypercalcemia (IIH) 80
Red blood cell PK deficiency: An update of PK-LR gene mutation database 78
A whole germline BRCA2 gene deletion: How to learn from CNV in silico analysis 78
Competitive PCR-High Resolution Melting Analysis (C-PCR-HRMA) for large genomic rearrangements (LGRs) detection: A new approach to assess quantitative status of BRCA1 gene in a reference laboratory 74
High Resolution Melting Analysis is Very Useful to Identify Breast Cancer Type 1 Susceptibility Protein (BRCA1) c.4964\_4982del19 (rs80359876) Founder Calabrian Pathogenic Variant on Peripheral Blood and Buccal Swab DNA 66
Identification and Characterization of a New BRCA2 Rearrangement in an Italian Family with Hereditary Breast and Ovarian Cancer Syndrome 53
Multiple Sclerosis Onset before and after COVID-19 Vaccination: Can HLA Haplotype Be Determinant? 9
Totale 742
Categoria #
all - tutte 3.354
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 3.354


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202049 0 0 0 0 0 3 17 2 6 3 11 7
2020/202143 4 4 2 5 3 1 4 0 5 2 12 1
2021/202296 5 3 0 0 6 4 0 23 5 5 18 27
2022/2023241 34 46 31 38 16 26 3 20 21 0 4 2
2023/202491 4 27 0 1 1 20 2 4 3 4 13 12
2024/202569 5 7 23 7 18 9 0 0 0 0 0 0
Totale 742