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Allison Elizabeth Ashley-Koch

Professor in Medicine
Medicine, Nephrology
Duke Box 104775, Durham, NC 27701
300 N Duke St., Durham, NC 27701

Overview


My work focuses on the dissection of human traits using multi-omic technologies (genetics, epigenetics, metabolomics and proteomics).  I am investigating the basis of several neurological and psychiatric conditions such as neural tube defects and post-traumatic stress disorder. I also study modifiers of sickle cell disease.

Current Appointments & Affiliations


Professor in Medicine · 2021 - Present Medicine, Nephrology, Medicine
Research Professor in Molecular Genetics and Microbiology · 2014 - Present Molecular Genetics and Microbiology, Basic Science Departments
Professor in Biostatistics and Bioinformatics · 2021 - Present Biostatistics & Bioinformatics, Basic Science Departments
Faculty Network Member of the Duke Institute for Brain Sciences · 2009 - Present Duke Institute for Brain Sciences, University Institutes and Centers
Affiliate of the Center for Child and Family Policy · 2015 - Present Center for Child and Family Policy, Sanford School of Public Policy
Member of Duke Molecular Physiology Institute · 2016 - Present Duke Molecular Physiology Institute, Institutes and Centers

In the News


Published December 14, 2015
How the state is missing chances to find deadly birth defect’s cause

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Recent Publications


Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele.

Journal Article Nat Commun · April 11, 2025 Obesity is a major public health crisis associated with high mortality rates. Previous genome-wide association studies (GWAS) investigating body mass index (BMI) have largely relied on imputed data from European individuals. This study leveraged whole-geno ... Full text Link to item Cite

The contribution of de novo coding mutations to meningomyelocele.

Journal Article Nature · March 26, 2025 Meningomyelocele (also known as spina bifida) is considered to be a genetically complex disease resulting from a failure of the neural tube to close. Individuals with meningomyelocele display neuromotor disability and frequent hydrocephalus, requiring vent ... Full text Link to item Cite

Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.

Journal Article Int Psychogeriatr · November 2024 OBJECTIVE: This study sought to conduct a comprehensive search for genetic risk of cognitive decline in the context of geriatric depression. DESIGN: A genome-wide association study (GWAS) analysis in the Neurocognitive Outcomes of Depression in the Elderly ... Full text Link to item Cite
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Recent Grants


Identification of Host-Specific Determinants of APOL1-associated COVAN

ResearchAdvisor · Awarded by National Institute of Diabetes and Digestive and Kidney Diseases · 2024 - 2029

Establishing the Suicide Working Group of the Psychiatric Genomics Consortium to elucidate the genetics and biology of suicide outcomes

ResearchPrincipal Investigator · Awarded by Icahn School of Medicine at Mount Sinai · 2024 - 2028

U2C/TL1 NC KUH TRIO Professional Development Core

ResearchCore Lead · Awarded by University of North Carolina - Chapel Hill · 2023 - 2028

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Education, Training & Certifications


Emory University · 1997 Ph.D.