Boris Eduardo Rebolledo Jaramillo
Researcher
Universidad del Desarrollo
Santiago, Chile
Rare diseases. Emphasis on mitochondrial genomics. FONDECYT #3170280 (2017-2020) "Contribution of mitochondrial DNA heteroplasmy to the phenotype of patients with maternally transmitted 22q11.2 deletion syndrome."
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Bioinformatics and Genomics, PENNSYLVANIA STATE UNIVERSITY. Estados Unidos, 2016
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Biochemistry and Bioinformatics, UNIVERSIDAD DE CONCEPCION. Chile, 2012
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Bioengineering, UNIVERSIDAD DE CONCEPCION. Chile, 2009
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Assistant professor Full Time
UNIVERSIDAD DEL DESARROLLO
Medicine
Santiago, Chile
2019 - At present
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Postdoctoral researcher Full Time
UNIVERSIDAD DEL DESARROLLO
Medicine
Santiago, Chile
2016 - 2019
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Research assistant Part Time
Universidad de Concepción
Chile
2008 - 2010
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Graduate research assistant
Pennsylvania State University
Estados Unidos
2010 - 2016
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Researcher Full Time
Universidad del Desarrollo
Santiago, Chile
2016 - At present
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Becas Chile Scholarship
COMISION NACIONAL DE INVESTIGACION CIENTIFICA Y TECNOLOGICA
Chile, 2009
Scholarship for doctoral studies abroad.
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Fulbright Scholarship
COMISION FULBRIGHT-CHILE
Chile, 2009
Fulbright scholarship for doctoral studies in the USA.
CONTRIBUTION OF MITOCHONDRIAL DNA HETEROPLASMY TO THE PHENOTYPE OF PATIENTS WITH MATERNALLY TRANSMITTED 22Q11.2 DELETION SYNDROME (VELOCARDIOFACIAL SYNDROME) |
Teneurins: An Integrative Molecular, Functional, and Biomedical Overview of Their Role in Cancer |