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个人简介
I started my career in Bio-Medical Sciences, and as a undergraduate student my first research experience were in biochemistry and human genetics. I fell in love with neuroscience early-on, and learned how to perform single-cell electrophysiological recordings as a Master's student.
During my PhD studies I investigated the molecular and cellular mechanisms behind impaired neural differentiation of human embryonic stem cells carrying the mutation for Fragile X Syndrome, a complex neurodevelopmental disorder that causes autism, mental retardation, epilepsy, attention deficit disorder, and more. My results were published in several peer-reviewed articles, including one in Developmental Biology that has become since a reference in the field, with more than 100 citations.
As a postdoc, my focus shifted to retinal degeneration in mice models, and the changes that the death of photoreceptors unleash on the downstream neurons that signal to the brain. Our findings have set in motion a new therapeutic approach to improve visual acuity in vision impairment and blindness, and are already being translated into the clinical world.
研究兴趣
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crossref(2024)
Science Advances (2021)
iPSCs for Modeling Central Nervous System Disorderspp.129-145, (2021)
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