Proyectos por año
Perfil personal
Research Interests
Dr. Ebbert studies neurodegenerative diseases using cutting-edge sequencing technologies and computational approaches (i.e., computational biology and bioinformatics), focusing primarily on Alzheimer’s disease and amyotrophic lateral sclerosis (ALS, or Lou Gehrig’s disease). He ultimately aims to discover disease etiology, and develop pre-symptomatic diagnostics and effective therapeutics through targeted “multi-omic” studies that combine gene expression, methylation, and long-read and single-cell sequencing technologies. Discovering the underlying etiology for Alzheimer’s disease and ALS will ultimately require discovering the mechanism at which genetics, epigenetics, and downstream processes intersect to drive disease.
Long-read sequencing is of special interest to Dr. Ebbert, because it can identify large DNA mutations (i.e., structural mutations) causing disease. Many individuals suffering from neurodegenerative diseases, including both Alzheimer’s disease and ALS, do not have a known genetic cause despite extensive efforts from medical and research communities. Most studies, to date, focus on short-read sequencing, overlooking disease-causing structural mutations. Dr. Ebbert is using long-read sequencing technologies to identify disease-causing structural mutations in families and diseases with no known genetic cause.
Focus areas
- Discovering inherited and somatic disease-causing structural mutations in ALS and Alzheimer’s disease. The genetic cause for most individuals suffering from ALS and Alzheimer’s disease is unknown, despite major short-read sequencing efforts. Structural mutations are known to cause numerous neurodegenerative diseases, but few studies have specifically targeted these large mutations. Dr. Ebbert hopes to identify both genetic and somatic (mutations arising during development or later) structural mutations causing disease using long-read sequencing technologies, including PacBio and Oxford Nanopore Technologies.
- Combine gene expression, methylation, and cutting-edge sequencing technologies to reveal underlying disease etiology. Humans are complex on every level, and human diseases are no exception. To truly understand a disease’s underlying etiology, Dr. Ebbert is combining gene expression, methylation, and cutting-edge sequencing technologies (e.g., long-read and single-cell sequencing) to understand how the genetics and all downstream processes work together to cause or prevent ALS and Alzheimer’s disease.
- Develop pre-symptomatic disease diagnostics. To meaningfully improve an ALS or Alzheimer’s disease patient’s life and outcome requires an effective therapy; equally important, however, is a pre-symptomatic diagnostic. Neurodegenerative diseases require pre-symptomatic intervention, because recovering lost neurons is not possible once clinical symptoms onset. Dr. Ebbert is applying his extensive experience in developing disease diagnostics to ALS and Alzheimer’s disease to identify disease before it’s too late.
Biography
Graduate Students & Trainees
- Grant Fox (Ph.D. student; May 2023-present)
- Patricia H. Doyle (Ph.D. student; October 2022-present)
- Mr. Bernardo Aguzzoli-Heberle (Ph.D. student; May 2022-present)
- Ms. Sabrina M. Krause (M.S.student; May 2021-2022)
Experiencia relacionada con los ODS de las Naciones Unidas
En 2015, los estados miembros de las Naciones Unidas acordaron 17 Objetivos de Desarrollo Sostenible (ODS) para erradicar la pobreza, proteger el planeta y garantizar la prosperidad para todos. El trabajo de esta persona contribuye al logro de los siguientes ODS:
Cuantificación de educación / académica
Doctor of Philosophy, Brigham Young University
2014
Master of Science, University Of Utah
2012
Bachelor of Science, Brigham Young University
2007
Huella digital
- 1 Perfiles similares
Colaboraciones y áreas de investigación principales de los últimos cinco años
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Resolving the full MAPT H2 inverted haplotype using optical genome mapping and ultra-long-read nanopore sequencing
Ebbert, M. T. W. (PI), Fardo, D. (CoI) & Nelson, P. (CoI)
University of Kentucky Neuroscience Research Priority Area
3/15/25 → …
Proyecto: Research project
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Fellowship for Bernardo Aguzzoli Heberle: Using Long-Read RNAseq to Find Targets for Alzheimer's Disease Treatment
Ebbert, M. T. W. (PI) & Norris, C. (CoI)
1/1/25 → 6/30/26
Proyecto: Research project
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Validating long-read single-cell PIPseq as a technology to study T Cell Variant Dynamics in Aging and Dementia in Women
Bachstetter, A. (PI), Nikolajczyk, B. (CoPI) & Ebbert, M. T. W. (CoPI)
University of Kentucky Neuroscience Research Priority Area
7/1/24 → …
Proyecto: Research project
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S'ORCe Collaborative Group (RENEWED)
Fardo, D. (PI), Ebbert, M. T. W. (CoPI), Katsumata, Y. (CoI), Miller, J. (CoI), Zhang, X. (CoI), O'Hara, B. (CoI), Messaoudi Powers, I. (CoI), Nikolajczyk, B. (CoI), Liu, J. (CoI), Jakubek Swartzlander, Y. (CoI) & Steely, C. (CoI)
University of Kentucky Neuroscience Research Priority Area
7/1/23 → …
Proyecto: Research project
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Genetic Architecture of Aging-Related TDP-43 and Mixed Pathology Dementia
Fardo, D. (PI), Ebbert, M. T. W. (CoI), Katsumata, Y. (CoI) & Nelson, P. (CoPI)
4/15/23 → 3/31/26
Proyecto: Research project
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Author Correction: GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia (Nature Genetics, (2024), 56, 11, (2407-2421), 10.1038/s41588-024-01939-9)
The National Alzheimer's Coordinating Center & The Alzheimer’s Disease Genetics Consortium, jul 2025, En: Nature Genetics. 57, 7, p. 1788 1 p.Producción científica: Comment/debate
Acceso abierto -
Mapping medically relevant RNA isoform diversity in the aged human frontal cortex with deep long-read RNA-seq
Aguzzoli Heberle, B., Brandon, J. A., Page, M. L., Nations, K. A., Dikobe, K. I., White, B. J., Gordon, L. A., Fox, G. A., Wadsworth, M. E., Doyle, P. H., Williams, B. A., Fox, E. J., Shantaraman, A., Ryten, M., Goodwin, S., Ghiban, E., Wappel, R., Mavruk-Eskipehlivan, S., Miller, J. B. & Seyfried, N. T. y 3 otros, , abr 2025, En: Nature Biotechnology. 43, 4, p. 635-646 12 p., 177.Producción científica: Article › revisión exhaustiva
Acceso abierto17 Citas (Scopus) -
Publisher Correction: GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia (Nature Genetics, (2024), 56, 11, (2407-2421), 10.1038/s41588-024-01939-9)
The National Alzheimer's Coordinating Center & The Alzheimer’s Disease Genetics Consortium, jul 2025, En: Nature Genetics. 57, 7, p. 1791 1 p.Producción científica: Comment/debate
Acceso abierto -
Ramp Sequence May Explain Synonymous Variant Association with Alzheimer’s Disease in the Paired Immunoglobulin-like Type 2 Receptor Alpha (PILRA)
Miller, J. B., Brandon, J. A., Harmon, L. M., Sabra, H. W., Lucido, C. C., Murcia, J. D. G., Nations, K. A., Payne, S. H., Ebbert, M. T. W., Kauwe, J. S. K. & Ridge, P. G., mar 2025, En: Biomedicines. 13, 3, 739.Producción científica: Article › revisión exhaustiva
Acceso abierto1 Cita (Scopus) -
RNApysoforms: fast rendering interactive visualization of RNA isoform structure and expression in Python
Aguzzoli Heberle, B., Page, M. L., Gustavsson, E. K., Ryten, M. & Ebbert, M. T. W., 2025, En: Bioinformatics Advances. 5, 1, vbaf057.Producción científica: Article › revisión exhaustiva
Acceso abierto