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Caterina Garone

Professoressa associata

Dipartimento di Scienze Mediche e Chirurgiche

Settore scientifico disciplinare: MED/03 GENETICA MEDICA

Curriculum vitae

EDUCATION

2014.   PhD: Human Genetics, University of Turin - Turin, Italy

2010    Child Neurology and Psychiatry, University of Bologna - Bologna

2005    MD: Medical Doctor Degree, University of Bologna - Bologna

 

PREVIOUS POSITIONS

2014 - 2019 Postdoctoral Scientist -MRC Mitochondrial Biology Unit, University of Cambridge -UK

2015 - 2019 Honorary Consultant Pediatric Neurology, Cambridge University Hospital -UK

2010 - 2014 Research Scientist, Columbia University - New York, US

 

FELLOWSHIPS AND AWARDS

2019 - 2022 Rita Levi Montalcini Award- Rientro Cervelli (MED03/BIO12)

2019 - 2022 Charlie Gard Foundation Award Individual Fellowship on “Development of treatment strategies for mitochondrial dNTP unbalance-related disorders”(PI)

2021 - 2022 Bando Ricerca Traslazionale Carisbo

2020 - 2021 Bando Alta Tecnologia Carisbo

2016 - 2018 Marie Skłodowska-Curie Actions - Individual Fellowship - Reintegration Panel -Proposal 705560-MITOBIOPATH

2015  - in-year Special Award Scheme (SAS) - Medical Research Council Mitochondrial Biology Unit, Cambridge

2013  - Young Investigator at Neurolobiology and Disease in Children symposium: mitochondrial disease, US

2013 Travel Grant at 18th International World Muscle Society Congress, Asilomar (US)

2010 - 2011 Fellowship AMMeC (Associazione Malattie Metaboliche e congenite ereditarie)

 

SUPERVISION OF GRADUATE STUDENTS AND POSTDOCTORAL FELLOWS

2019 - present Supervisor for Postdoctorale Fellow (2), Master Students (5), Master Degree Fellow (1), Medical Doctor Student (2), Child Neurology Trainees (5), Medical Genetics Trainees (2), Department of Medical and Surgical Sciences, University of Bologna, Italy

2014 -2019 Supervisor for Master Students (2), PhD student (1)

 

TEACHING ACTIVITIES

2019 - present Professor in Medical Genetics, University of Bologna, Italy

2017 European School of Human Genetics, Faculty member (Bertinoro, Italy)

 

REVIEWING ACTIVITIES

2021 - present Associate Editor in Genetics of Common and Rare Diseases

2018 Guest Editor for “Essay in Biochemistry: Mitochondrial diseases”

2019 Guest Editor for Frontiers in Genetics Special Issue“Mitochondrial Genetics and Epigenetics”

2014 - present Referee for Journal of Pediatric Neurology, Brain, Gene, Gene Review, Archive of Diseases in childhood, EMBO Molecular Medicine, Clinical Neurology and Neuroscience, Frontiers in Genetics, Annals of Human Genetics

2016 Referee for Italian Minister of Health (grant application - PRIN), Insubria university (Italy), Rita Levi Montalcini program (Italy), Biotechnology and Biological Sciences Research Council Fellowship Scheme (UK)

 

MEMBERSHIPS OF SCIENTIFIC SOCIETIES

2016 - present 1000 Genome Project: GeCIP committee for mitochondrial disorders

2016 - present Italian Society of Human Genetics (Società Italiana di Genetica Umana) (SIGU)

2013 - present Purine and Pyrimidine Society, “Purine and Pyrimidine disorders”

2013 - present World Muscle Society, “Muscle diseases”

2012 - present Italian Society of inherited metabolic diseases and newborn screening- (Società Italiana di malattie metaboliche ereditare e screening neonatale) (SIMMEsN )

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