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Giulietta M. Riboldi, MD, completed a post-doctoral movement disorders fellowship at NYU Langone's Fresco Institute for Parkinson's and Movement Disorders in 2020. She also holds a position with the Affiliated Faculty Center for Human Genetics & Genomics.
Genetic discoveries are rapidly changing our understanding of neurodegenerative diseases and opening the way to targeted therapeutic approaches. Through the study of genetics and functional genomics, my research focuses on the discovery of new genetic variants associated with Parkinson’s Disease and rare Movement Disorders to better understand how known and new genetic mutations contribute to disease mechanisms.
Genetic discoveries are rapidly changing our understanding of neurodegenerative diseases and opening the way to targeted therapeutic approaches. Through the study of genetics and functional genomics, my research focuses on the discovery of new genetic variants associated with Parkinson’s Disease and rare Movement Disorders to better understand how known and new genetic mutations contribute to disease mechanisms.
研究兴趣
论文共 90 篇作者统计合作学者相似作者
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Kristen Watkins, Julia Greenberg, Kelly Astudillo, Charalambos Argyrou,John Crary,Steven Frucht,Towfique Raj,Giulietta Riboldi
Clinical Parkinsonism & Related Disorderspp.100251, (2024)
MOVEMENT DISORDERS (2023): S475-S476
npj Parkinson's diseaseno. 1 (2023)
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FRONTIERS IN NEUROLOGY (2023)
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Kristen Whitney,Won-Min Song,Abhijeet Sharma, Diana K Dangoor,Kurt Farrell, Margaret M Krassner, Hadley W Ressler, Thomas D Christie,Ruth H Walker,Melissa J Nirenberg,Bin Zhang,Steven J Frucht,
bioRxiv (Cold Spring Harbor Laboratory) (2023)
International journal of molecular sciencesno. 10 (2023): 8995-8995
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Frontiers in neurology (2023): 1280958-1280958
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