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I curricula dei dirigenti/consulenti del Policlinico

I Curricula pubblicati nel formato elettronico e resi disponibili attraverso il seguente motore di ricerca, contengono le informazioni previste dal D.Lgs. 33/2013, anche se non tutti sono strettamente in formato europeo.


Curriculum Vitae Europeo



INFORMAZIONI PERSONALI PIPPUCCI TOMMASO

Email: tommaso.pippucci@aosp.bo.it
Telefono: 051/2088387
Sesso Male | Data di nascita 28/5/1977


ESPERIENZA PROFESSIONALE
 
12/2017 - 12/2018
AZIENDA OSPEDALIERA -UNIVERSITARIA "POLICLINICO S.ORSOLA-MALPIGHI"DI BOLOGNA (BO
BIOLOGO -
1/2017 - 12/2017
AZIENDA OSPEDALIERA -UNIVERSITARIA "POLICLINICO S.ORSOLA-MALPIGHI"DI BOLOGNA (BO
BIOLOGO -
1/2016 - 1/2017
AZIENDA OSPEDALIERA -UNIVERSITARIA "POLICLINICO S.ORSOLA-MALPIGHI"DI BOLOGNA (BO
BIOLOGO -
1/2015 - 1/2016
AZIENDA OSPEDALIERA -UNIVERSITARIA "POLICLINICO S.ORSOLA-MALPIGHI"DI BOLOGNA (BO
BIOLOGO -
6/2012 - 11/2014
AZIENDA OSPEDALIERA -UNIVERSITARIA "POLICLINICO S.ORSOLA-MALPIGHI"DI BOLOGNA (BO
BIOLOGO -

ISTRUZIONE E FORMAZIONE
 
10/2007 - 3/2012
Università di Firenze
Specializzazione in Genetica Medica, 70/70 e lode
1/2004 - 6/2007
Università di Bologna
Dottorato di Ricerca in Biochimica
10/1996 - 6/2003
Università di Firenze
Laurea in Scienze Biologiche, 110/110 con lode

COMPETENZE PERSONALI
 
Lingua Madre:it

Altre lingue:
COMPRENSIONE PARLATO PRODUZIONE SCRITTA
Ascolto Lettura Interazione Produzione orale  
en inglese
A1 A1 A1 A1 A1
Competenze comunicative
Competenze organizzative
Competenze informatiche Bioinformatica, Genomica computazionale, Analisi dati genetici, Analisi dati NGS, Whole Exome Sequencing, Whole Genome Sequencing, Analisi clinica di dati WES/WGS
Patente di guida B

ULTERIORI INFORMAZIONI
 
Pubblicazioni
Presentazioni
Progetti
Conferenze
Seminari
Riconoscimenti e premi
Appartenenza a gruppi / associazioni
Referenze
Menzioni
Corsi
Certificazioni
https://www.ncbi.nlm.nih.gov/pubmed/?term=pippucci+t
Italian Ministry of Research PRIN 2006 Call ¿ Title: ¿Linkage studies in families with recurrence of a recessive form of hereditary spastic paraplegia and thin corpus callosum: analysis of the locus on chromosome 15q13-q15 and search for new disease loci¿ (Role: Staff Member) Italian Ministry of Health, Strategic Program 2009, Project RFPS-4-631972 ¿ Title: ¿Genetic Bases of Birth Defects¿ (Role: Staff Member) Italian Ministry of Health 2009 Call Young Investigator Project GR-2009-1574072 - Title: ¿Classical and innovative strategies for the identification of genetic defects at the basis of rare forms of partial epilepsy¿ (Role: Coordinator) Telethon Foundation 2010 Call Project GP10121 ¿ Title: "A new gene for inherited thrombocytopenias: clinical, pathogenetic and pharmacological studies¿ (Role: Staff Member) Telethon Foundation 2010 Call Project GP10089B ¿ Title: "Identification of new disease-causing genes in hereditary spastic paraplegia"(Role: Staff Member) Telethon Project 2013 Call GP13200A ¿ Title: ¿In‐depth clinical and genetic study of familial and sporadic patients with Nocturnal Frontal Lobe Epilepsy (NFLE): identification of new genes by WES in 192 cases negative for mutations in the neuronal nicotinic acetylcholine receptor subunits genes¿ (Role: Partner) Italian Ministry of Health 2018 ¿Ricerca Finalizzata¿ Project RF-2018-12366314 - Title: ¿Whole Genome Sequencing into the diagnostic workflow of rare diseases: a cost-effectiveness evaluation in a heterogeneous population of patients with inconclusive Whole Exome Sequencing¿ (Role: Staff Member)
Co-director of the "Corso di Alta Formazione in Elementi di Bioinformatica per l'Analisi di Dati NGS" (Advanced Course in Bioinformatic Elements for NGS Data Analysis) sponsored by Azienda Ospedaliero-Universitaria Careggi, Regione Toscana: Editions I to IX, Years: 2011 to 2015 Co-director of the annual European School of Genetic Medicine (ESGM) course in ¿Next Generation Sequencing¿ supported by the European Society of Human Genetics (ESHG): Editions III to V, Years 2013 to 2016 Co-director of the annual European School of Genetic Medicine (ESGM) course in ¿NGS and Clinical Genomics¿ supported by the European Society of Human Genetics (ESHG): Editions I, Years 2017 to 2018 Director of the Italian Society of Human Genetics (SIGU) course in ¿Data Analysis for Clinical Genomics¿, Years 2018-2019
Selected communications at congresses European Society of Human Genetics (ESHG) Conference, 2011: ¿Mutations in the 5' UTR of ANKRD26, the Ankirin Repeat Domain 26 Gene, cause an Autosomal-Dominant form of inherited Thrombocytopenia, THC2¿ Italian Society of Human Genetics (SIGU) Conference, 2011: ¿X-chromosome exome in ultrarare disorders¿ Italian Society of Human Genetics (SIGU) Conference, 2012: ¿Mendelian inheritance as a filtering strategy¿ Italian Society of Human Genetics (SIGU) Conference, 2013: ¿H3M2: an algorithm for the detection of biologically meaningful ROHs from NGS data¿ VIII International Congress on Vascular Dementia, 2013: ¿A homozygous truncating NOTCH3 gene mutation is associated with arteriopathy and cavitating leukoencephalopathy¿ European Society of Human Genetics (ESHG) Conference, 2019: ¿SSBP1 mutations cause a complex optic atrophy spectrum disorder with mitochondrial depletion¿ Invited communications at congresses European Biotechnology Thematic Network Association (EBTNA) Congress, 2011: ¿EX-HOM: exome sequencing in small consanguineous pedigrees¿ EBTNA Congress, 2014: ¿Whole exome sequencing, homozygosity, autozygosity¿ Italian Society of Human Genetics (SIGU) Conference, 2014: ¿Sequenziamento esomico per la ricerca di nuovi geni-malattia: resa diagnostica e criteri di inclusione dei pazienti¿ Italian Society of Human Genetics (SIGU) Conference, 2015: ¿Strategie d¿analisi per le malattie autosomiche recessive e X-linked¿
EMBO Short Term Fellowiship awarded for 3 months visit to Dr. E. Heinzen Lab, Institute for Genomic Medicine, Columbia University, New York, USA on the identification of brain-specific mosaic mutations in malformations of cortical development and epilepsy, June-September 2017 Member of the Scientific Committee of the XX National Congress of the Italian Society of Human Genetics (SIGU) in Napoli, 2017 Member of the Poster Jury of the European Society of Human Genetics (ESHG) meeting in Milan, 2018 Abstract Evaluator for the European Society of Human Genetics (ESHG) meeting in Goteborg, 2019 Member of the Genetic Commission of the Italian League Against Epilepsy (LICE) Italian National Scientific Qualification as Associate Professor in Academic Disciplines Genetica Medica (06/A1) (Medical Genetics), Genetica (05/I1) (Genetics), Biologia Applicata (05/F1) (Applied Biology) Enrolment in the national biologist registry from January 2016 Member of the Italian Society of Human Genetics (SIGU) Member of the Italian League Against Epilepsy (LICE) Member of the European Society of Human Genetics (ESHG)