Universitą degli studi di Pavia

 

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Cova's curriculum

Curriculum

PERSONAL INFORMATION

NAME: Giulia
SURNAME: Cova
DATE OF BIRTH: 05/03/1990
BORN IN: Voghera (PV) Italy
NATIONALITY: Italian
E-MAIL: giulia.cova01@ateneopv.it
DRIVING LICENCE: B, car owner
LINKEDIN PROFILE: Giulia Cova (it.linkedin.com/pub/giulia-cova/6a/253/1a1/)


EDUCATION AND TRAINING

2014 - Present
PhD in Genetics, Molecular and Cellular Biology
Universitą degli Studi di Pavia
I.R.C.C.S. Fondazione Casimiro Mondino

2012 – 2014
Master’s Degree in Medical and Pharmaceutical Biotechnology
Universitą degli Studi di Pavia
Vote: 110/110 cum Laude
Supervisor: Roberto Ciccone
Thesis: NEXT GENERATION SEQUENCING: IMPATTO DELL'INDAGINE MOLECOLARE NELLO STUDIO DELLE PATOLOGIE DEI PICCOLI VASI

2009 – 2012
Bachelor’s Degree in Biotechnology
Universitą degli Studi di Pavia
Vote: 100/110.
Supervisor: Cesare Danesino
Thesis: ANALISI DI MUTAZIONE IN PAZIENTE CON TELEANGECTASIA EMORRAGICA EREDITARIA E LESIONI POLMONARI

2004 – 2009
Classical High School Diploma
High School “G.Galilei” of Voghera
Votazione: 90/100.

PROFESSIONAL EXPERIENCE

2014 - Present
PhD in Genetics, Molecular and Cellular Biology
Universitą degli Studi di Pavia
I.R.C.C.S. Fondazione Casimiro Mondino

2014
Internship for Master’s Degree
Universitą degli Studi di Pavia
I.R.C.C.S. Fondazione Casimiro Mondino
GenTher Center Laboratory: Application of next generation sequencing techniques in the study of small vessels disease.

2012
Internship for Bachelor’s Degree
Universitą degli Studi di Pavia
Medical Genetics Laboratory: Analysis of mutations in patients with Hereditary Hemorrhagic Telangiectasia

LANGUAGE SKILLS

ITALIAN
Mother tongue

INGLESE
Medium-High
2007: PET (Preliminary English Test – Council of Europe Level B1)
2009: FCE (First Certificate in English – Council of Europe Level B2)

INFORMATIC SKILLS

Operating Systems
Windows Vista, Windows 7, Windows 8

Programs
Office (Word, Power Point, Excel) 2010, 2013
Internet Explorer, Mozilla Firefox, E-mail




Publications





Research project

INVESTIGATION OF THE MOLECULAR CAUSES OF NEUROLOGICAL DISORDERS THROUGH NEXT GENERATION SEQUENCING TECHNIQUES
Application of specific Next Generation Sequencing platforms to the analysis of panel of genes in order to identify new genetic variants that could be associated with neurological disorders, for example epilepsy in children, dementia and neurodegenerative diseases in adults.
The final end will be to understand the biological effects of these mutations in affected subjects and to define genotype-phenotype correlations.


















































 
 
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