From deciphering underlying genetic factors of diseases to developing cutting-edge genome technology, our scientists are making impactful discoveries everyday.
Strength in Genetics and Genomics Research
The Department of Genetics has traditional strengths in computational biology and genome science, as well as model organism, evolutionary and human genetics. Recent specialties include neurological disorders, cellular bioenergetics, epigenomics, personalized medicine and genome technology development.
We have established leadership in the following flagship NIH genomic medicine themed projects:
- The Human Pangenome Project (NHGRI)
- The Impact of Genetic Variation on Function (NHGRI)
- The Long Life Family Study (NIA)
- Somatic Mosaicism across Human Tissues (NIH Common Fund)
- Multi-Omics for Health and Disease (NHGRI, NCI, NIEHS)
- The BRAIN (The Brain Research through Advancing Innovative Neurotechnologies) Initiative Cell Atlas Network (NIMH)
Within the close-knit research community of Washington University School of Medicine, our scientists are supported by a strong foundation. School of Medicine Facts & Figures
| #2 NIH Funding (2023) | $838.3 Million Research Funding 2022 | 19 Nobel Laureates |
Latest News
Saintilnord, Reynolds named exceptional early-career research fellows (Links to an external site)
WashU Medicine postdoctoral researchers Wesley Saintilnord, PhD, in the Department of Genetics (left) and Matthew Reynolds, PhD, in the Department of Biochemistry and Molecular Biophysics (right) have been named Jane Coffin Childs Fellows. The prestigious award supports early-career scientists conducting biomedical research that could inform the cause and treatment of human disease.
$12 million grant funds studies of role of genes in autism, similar diagnoses (Links to an external site)
Researchers at Washington University School of Medicine in St. Louis have received an $11.85 million grant to create a resource for the WashU and national research communities to study the growing number of neurodevelopmental and psychiatric disorders known to be caused by a single gene mutation.
Phillips-Cremins named BJC investigator (Links to an external site)
Jennifer E. Phillips-Cremins, PhD, an international leader in understanding 3D genome structure and how it affects brain development and neurological diseases, has been named a BJC Investigator at Washington University School of Medicine in St. Louis. Phillips-Cremins will join the Department of Genetics as the James McDonnell Professor and have a dual appointment in the Department of Neuroscience.