Curriculum Vitae

Curriculum Vitae
Elisa RUBINO Date of birth
03/06/1978
WORK ESPERIENCE
• Date
From 01/01/2010 • Name and address of
employer
• Type of business or sector
University of Torino
• Occupation or position held
PhD student in Clinical Neuroscience
• Main activities and
responsabilities
• Date
Department of Neuroscience, University of Torino
Research and clinical activity
From 08/02/2010 to date
• Name and address of
employer
• Type of business or sector
Ospedale Koelliker
• Occupation or position held
Physician Neurologist
• • Main activities and
responsabilities
Neurology
Neurological advice activity
EDUCATION AND TRAINING
• Date
• Name and type of
organisation providing
education and training
Principal
subjects/occupational skills
covered
• Date
• Name and type of
organisation providing
education and training
• Principal
subjects/occupational skills
covered
From 01/01/2010 XXV cycle, Doctoral School in Neuroscience, University of Torino
Research and clinic activity
From 01/01/2005 to 31/12/2009
Specialization School in Neurology, University of Torino
Knowledge of physiopathology of neurological diseases, diagnostic processes and algorithms, therapy and doctor­patient relation. • Title of qualification
awarded
• Score
• Date
• Name and type of
organisation providing
education and training
• Principal
subjects/occupational skills
covered
• Date
• Name and type of
organisation providing
education and training
• Principal
subjects/occupational skills
covered
• Date
• Name and type of
organisation providing
education and training
• Title of qualification
awarded
• Score
• Date
• Name and type of
organisation providing
education and training
• Principal
subjects/occupational skills
covered
• Date
• Name and type of
organisation and Title of
qualification awarded
Degree of Specialization in Neurology
70/70 cum laude
From 01/03/2007 to 01/09/2007
University of Toronto, Centre for Research in Neurodegenerative Diseases, (Prof. St­George Hyslop P) Post­doctoral fellowship in Neurology and Molecular Biology. The research activity was concerning Alzheimer’s disease and migraine. From October 2004 to March 2005
Department of Neuroscience, University of Torino
Medical School Research grant for “Valutation of polymorphisms in CLOCK gene and HFE gene in cluster headache patients” 16/07/2004
Medical School, University of Torino
Degree Certificate in Medicine
110/110 cum laude
From July 2003 to July 2004 University of Torino
Pre­doctoral fellowship in Genetics, concerning Molecular Biology
July 1997
Scientific High School, “I. Newton”, Chivasso (TO), Scientific school leaving certificate
PERSONAL SKILLS AND
COMPETENCES
MOTHER TONGUE
OTHER LANGUAGES
Italian
English • Reading skills
excellent • Writing skills
good • Verbal skills
good COMPUTER SKILLS AND
COMPETENCES
Knowledge of statistical analysis programs (SPSS, STAT, Sigmastat), main genetic programs (Haploview, Mutation Surveyor, Structure, Genepop, Allegro, etc.) most major office, graphic and web applications
GRANTS AND OTHER
Winner, of “Puca Grant”, promoted by the Italian Society for the Study of Headache (SISC) for the project: Migraine and Notch4 gene, in October 2007.
Finalist of the Young Researchers in Neurology, held in Rome in April 2009, promoted by Lilly.
MEMBERSHIP OF SCIENTIFIC
SOCIETIES
FELLOW OF: ­ Società Italiana di Neurologia (SIN) from 2005
­ Società Italiana per lo Studio delle Cefalee (SISC) from 2006
ATTENDEED COURSES,
CONGRESSES, SEMINARS, EVENTS
AND MEETINGS
Continuing education through participation in more than 6 monographic courses, conferences and conventions concerning neurological disorders.
Author and co­author of scientific papers presented to national and international meetings
I authorize the use of data provided in accordance with Italian legislative decree 196/03.
REFERENCES 1. Fontanella M, Rubino E, Crobeddu E, Gallone S, Gentile S, Garbossa D, Ducati A, Pinessi L, Rainero I. Brain Arteriovenous Malformations are associated with Interleukin­1 Cluster Gene Polymorphisms. Neurosurgery 2011 (accepted).
2. Rainero I, Rubino E, Gallone S, Fenoglio P, Picci LR, Giobbe L, Ostacoli L, Pinessi L. Evidence fora n association between migraine and the hypocretin receptor 1 gene. J Headache Pain 2011;12:193­9. 3. Rainero I, Ostacoli L, Rubino E, Gallone S, Rocco Picci L, Fenoglio P, Negro E, Rosso C, De Martino P, De Marchi M, Furlan PM, Pinessi L. Association between Major Mood Disorders and the hypocretin receptor 1 gene. J Affect Disord 2011;30:487­491. 4. Fontanella M, Rainero I, Gallone S, Rubino E, Fornaro R, Fenoglio P, Valfrè W, Vaula G, Benevello C, Ducati A, Pinessi L. Interleukin­1 Cluster Gene Polymorphisms and Aneurysmal Subarachnoid Hemorrhage. Neurosurgery 2010;66:1059­1063.
5. Bruni A, Bernardi L, Colao R, Rubino E, Smirne N, Frangipane F, Terni B, Curcio S, Mirabelli M, Clodomiro A, Di Lorenzo R, Maletta R, Anfossi M, Gallo M, Geracitano S, Tomaino C, Muraca MG, Leotta A, Lio SG, Pinessi L, Rainero I, Sorbi S, Nee L, Milan G, Pappatà S, Postiglione A, Abbamondi N, Forloni G, St. George Hyslop P, MD, Rogaeva, E, Bugiani O, Giaccone G, Foncin JF, Spillantini MG, Puccio G. Worldwide distribution of PSEN1 Met146Leu mutation: A large variability for a founder mutation. Neurology 2010:74;798­806.
6. Rainero I, Rubino E, Gallone S, Fenoglio P, Negro E, De Martino P, Savi L, Pinessi L. Cluster Headache is Associated With the Alcohol Dehydrogenase 4 (ADH4) Gene. Headache 2010:50;92­98.
7. Gallone S, Giordana MT, Scarpini E, Rainero I, Rubino E, Fenoglio P, Galimberti D, Grifoni S, Venturelli E, Acutis PL, Peletto S, Maniaci MG, Ferrero P, Zotta M, Pinessi L. Absence of TARDBP gene mutations in an italian series of patients with frontotemporal lobar degeneration. Dement Geriatr Cogn Disord 2009;28:239­43.
8. Rainero I, Rubino E, Cappa G, Rota E, Valfrè W, Ferrero P, Fenoglio P, Baci D, D'Amico G, Vaula G, Gallone S, Pinessi L. Pro­inflammatory cytokine genes influence the clinical features of frontotemporal lobar degeneration. Dement Geriatr Cogn Disord 2009;27:543­7. 9. Rubino E , Rainero I, Vaula G, Crasto F, Gravante E, Negro E, Brega F, Gallone S, Pinessi L. Investigating the genetic role of aquaporin4 gene in migraine. J Headache Pain 2009;10:111­4. 10. Rainero I, Gallone S, Rubino E, Ponzo P, Valfrè W, Binello E, Fenoglio P, Gentile S, Anodica M, Gasparini M, Pinessi L. Haplotype analysis confirms the association between the HCRTR2 gene and cluster headache. Headache 2008;48:1108­14. 11. Fontanella M, Rainero I, Gallone S, Rubino E, Fenoglio P, Valfrè W, Garbossa D, Benevello C, Ducati A, Pinessi L. Interleukin 6 gene polymorphisms are not associated with aneurysmal subarachnoid aemorrhage in an Italian population. J Neurol Neurosurg Psychiatry 2008;79:471­3.
12. Rubino E , Ferrero M, Rainero I, Binello E, Vaula G, Pinessi L. Association of the C677T .polymorphism in the MTHFR gene with migraine: a meta­analysis. Cephalalgia 2009;29:818­25.
13. Pinessi L, Binello E, De Martino P, Gallone S, Gentile S, Rainero I, Raivoiro C, Rubino E, Savi L, Valfrè W, Vaula G. The 1246G­­>A polymorphism of the HCRTR2 gene is not associated with migraine. Cephalalgia 2007;27:945­9.
14. Rainero I, Rubino E, Valfrè W, Gallone S, De Martino P, Zampella E, Pinessi L. Association between the G1246A polymorphism of the hypocretin receptor 2 gene and cluster headache: a meta­analysis. J Headache Pain 2007;8:152­6.
15. Fontanella M, Rainero I, Gallone S, Rubino E, Fenoglio P, Valfrè W, Garbossa D, Carlino C, Ducati A, Pinessi L. Tumor necrosis factor­alpha gene and cerebral aneurysms. Neurosurgery 2007;60:668­72.
16. Fontanella M, Rainero I, Gallone S, Rubino E, Rivoiro C, Valfrè W, Garbossa D, Nurisso C, Ducati A, Pinessi L. Lack of association between the apolipoprotein E gene and aneurysmal subarachnoid hemorrhage in an Italian population. J Neurosurg 2007;106:245­9.
17. Rainero I, Rubino E, Rivoiro C, Valfrè W, Binello E, Zampella E, De Martino P, Gentile S, Fenoglio P, Savi L, Gallone S, Pinessi L. Haemochromatosis gene (HFE) polymorphisms and migraine: an association study. Cephalalgia 2007;27:9­13. 18. Rainero I, Ferrero M, Rubino E, Valfrè W, Pellegrino M, Arvat E, Giordano R, Ghigo E, Limone P, Pinessi L. Endocrine function is altered in chronic migraine patients with medication­overuse. Headache 2006;46:597­603.
19. Gentile S, Fontanella M, Giudice RL, Rainero I, Rubino E, Pinessi L. Resolution of cluster headache after closure of an anterior communicating artery aneurysm: the role of pericarotid sympathetic fibres. Clin Neurol Neurosurg 2006;108:195­8. 20. Rainero I, Dall’Omo AM, Rubino E, Valfrè W, Fasano ME, Rivoiro C, Brancatello F, Savi L, Gallone S, Pinessi L. HLA­DRB1 genotyping in Italian migraine patients. Neurosci Lett 2006; 93:90­3.
21. Pinessi L, Rainero I, Rivoiro C, Rubino E, Gallone S. Genetics of cluster headache: an update.
J Headache Pain 2005; 6:234­6. 22. Rainero I, Rivoiro C, Gallone S, Valfrè W, Ferrero M, Angilella G, Rubino E, De Martino P, Savi L, Lo Giudice R, Pienssi L. Lack of association between the 3092 T­­>C Clock gene polymorphism and cluster headache. Cephalalgia 2005; 25:1078­81. 23. Rainero I, Rivoiro C, Rubino E, Milli V, Valfrè W, De Martino P, Lo giudice R, Angilellea G, Savi L, Gallone S, Pinessi L. Prevalence of HFE (hemochromatosis) gene mutations in patients with cluster headache. Headache 2005;45:1219­23.
24. Rainero I, Rivoiro C, Rubino E, Rivoiro C, Valfrè W, Gallone S, Savi L, Gentile S, Lo Giudice R, De Martino P, Dall’Omo AM, Pinessi L. Association between migraine and HLA­DRB1 gene polymorphisms. J Headache Pain 2005;6:185­187.
25. Rainero I, Limone P, Ferrero M, Valfre W, Pelissetto C, Rubino E, Gentile S, Lo Giudice R, Pinessi L. Insulin sensitivity is impaired in patients with migraine. Cephalalgia 2005; 25:593­7. 26. Rainero I, Gallone S, Valfre W, Ferrero M, Angilella G, Rivoiro C, Rubino E, De Martino P, Savi L, Ferrone M, Pinessi L. A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache. Neurology 2004; 63:1286­8. 27. Rebaudengo N, Rainero I, Parziale A, Rosina F, Pavanelli E, Rubino E, Mazza C, Ostacoli L, Furlna PM. Lack of interaction between a polymorphism in the dopamine D2 receptor gene and the clinical features of migraine. Cephalalgia 2004; 24:503­7.