Steven Finkbeiner and his lab study how brain cells learn and remember, and what causes them to malfunction or die in disease. The long-term goal is to understand how these normal functions go awry and cause neurological and psychiatric diseases. To this end, the lab has developed patient-derived models of several of them, including Huntington’s disease, Parkinson’s disease, amyotrophic lateral sclerosis (ALS), frontotemporal dementia, Alzheimer’s disease, autism and schizophrenia. The group has also developed state-of-the-art technologies to generate and analyze large troves of images and genetic data, including robotic microscopy and artificial intelligence.

Disease Areas

Huntington’s Disease
Parkinson’s Disease
Amyotrophic Lateral Sclerosis (ALS)
Frontotemporal Dementia
Alzheimer’s Disease
Autism
Schizophrenia
Neurodegenerative Diseases

Areas of Expertise

Stem Cells and iPS Cells
Disease Models
Robotic Microscopy
Artificial Intelligence
Data Science
Human Genetics
Genetic and Small Molecule Screening
Working in the Finkbeiner lab

Lab Focus

Understanding the basic mechanisms by which cells mitigate stresses such as the protein misfolding involved in aging and disease
Finding causes and treatments for Huntington’s, Parkinson’s and Alzheimer’s disease, ALS, frontotemporal dementia, autism and schizophrenia
Inventing and developing innovative technologies such as robotics and artificial intelligence to accelerate the pace of science and the discovery of cures

Research Impact

Finkbeiner’s lab strives to understand the neurobiology of disease well enough to design rational interventions and produce effective treatments. They bring human biology into the lab by combining human genomics and the creation of human models of disease based on iPS cells and other patient material. The limitations of conventional approaches led them to invent new tools such as robotic microscopy, and to adapt artificial intelligence to unravel cause and effect in complex mechanisms and gain insights from data that elude comprehension by the unaided human brain.

The work has led to seminal findings for the field and promising new therapeutic approaches. In one instance, robotic microscopy helped resolve a decade-old controversy about the pathogenesis of Huntington’s disease. In another, new biosensor technology helped design neuroprotective compounds that cause cells to destroy disease-causing proteins linked to Alzheimer’s, Parkinson’s and Huntington’s disease.

 

Lab Members

Monika Ahirwar, MA
Research Engineer III
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Noura Al Bistami, MS
Research Associate III
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Naufa Amirani, c
Software Engineer II
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Lise Barbe, PhD
Collaborator
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Una Chan
Research Associate II
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Beatrice Costa, PhD
Collaborator
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Zohreh Faghihmonzavi, MS
Research Scientist
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Vivek Gopal Ramaswamy, MS
Senior Software Engineer
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Austin Holub, MS
Research Engineer II
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Terry Huang, ,
Research Associate II
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Drew Linsley, PhD
Contractor
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Tiina Manninen, PhD
Visiting Scientist
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Brandy Mendoza
Student Intern
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Roma Moore
Research Engineer I
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Karen Sachs
Collaborator
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Kanchan Sarda, PhD
Staff Research Scientist I
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Kaushik Sridhar, MS
Research Engineer III
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Shijie Wang, PhD
Scientist
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Leela Wong
Research Associate I
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