Our science

Research

The Miller Lab develops human-relevant experimental models to uncover disease mechanisms and accelerate therapeutic discovery for neurological and neurodegenerative disorders.

By combining patient-derived biology with mechanistic experimentation and therapeutic perturbation, we aim to bridge the gap between human disease discovery and preclinical drug development — identifying actionable pathways, validating therapeutic targets in human systems, and developing interventions with a clear path toward clinical translation.

Research areas

01

Neurodegeneration & Protein Aggregation

We investigate the molecular and cellular mechanisms driving neurodegeneration, with a focus on amyloid-β and α-synuclein pathology. Using human iPSC-derived neural organoids, primary human tissue, and proteomics, we identify how disease-associated protein aggregates disrupt neural function and explore therapeutic strategies to halt or reverse these processes.

iPSC-derived neural organoidsProteomicsSingle-cell transcriptomicsAdvanced microscopy
02

Infection-Triggered Neuropathology

A major focus of the lab is understanding how viral and immune-mediated insults trigger neurodegenerative cascades. Our work on SARS-CoV-2 and Long COVID has demonstrated that viral infection can induce Alzheimer's disease-related amyloid-β pathology in human retinal tissue and organoids, opening new avenues for biomarker discovery and therapeutic intervention.

Retinal organoidsEx vivo human tissueSpatial transcriptomicsImmunohistochemistry
03

Retinal Biomarkers & Ocular Disease

The retina offers a uniquely accessible window into CNS pathology. We use human retinal explants and organoids to model neurodegenerative and infection-triggered disease, identify retinal biomarkers of systemic neurological conditions, and characterize the cellular circuits underlying visual processing and their vulnerability to disease.

Retinal explantsElectrophysiologyOptical coherence tomographyOrganoid models
04

PANDAS & Neuroimmune Disorders

We are defining the neuropathological mechanisms underlying PANDAS using primary human brain tissue and cortical organoids. This work aims to identify the cellular and molecular substrates of autoimmune-driven neuropsychiatric disease and evaluate candidate therapeutic targets.

Cortical organoidsHuman brain tissueNeuroimmune profilingTranscriptomics

Grants & sponsored research

Principal InvestigatorAugust 2026–July 2029

Fellow-to-Faculty Award

Simons Foundation

Principal InvestigatorJune 2026–May 2028

Infection-Triggered Neurodegenerative Proteinopathy in Long COVID: Retinal Biomarkers and Human Organoid Models for Mechanistic Discovery and Therapeutic Development

PolyBio Research Foundation

Principal InvestigatorSeptember 2026–August 2027

Defining Neuropathological Mechanisms in PANDAS Using Human Brain Tissue and Cortical Organoids

The Alex Manfull Fund

Patents

Methods of treating or preventing conditions of dendritic and neural spine defects

Our approach

The Miller Lab is committed to human-relevant, mechanistic neuroscience. We integrate iPSC-derived neural and retinal organoids, primary human tissues, single-cell and spatial transcriptomics, proteomics, advanced microscopy, and functional electrophysiology to define how disease-associated molecular and cellular changes translate into neural dysfunction.

We place a strong emphasis on therapeutic translation: every mechanistic finding is evaluated for its potential as a drug target or biomarker, with the goal of developing interventions that have a clear path toward clinical application.

Miller Lab

Department of Physiology and BiophysicsJacobs School of Medicine & Biomedical Sciences, University at Buffalo-SUNY4th Floor, 955 Main StreetBuffalo, New York 14203

© 2026 Miller Lab. All rights reserved.

Recent Publications

Journal of Parkinson's Disease · 2026

The central cholinergic system as a therapeutic target in Parkinson's disease

Neuron · 2026

A hierarchical electrical synaptic circuit mechanism for integrative parallel visual processing in the retina

Alzheimer's & Dementia · 2026

Intracellular protein GBF1 displays significant associations with amyloid pathology in Alzheimer's disease

View all publications →