Dr. Duis is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.
- Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
- Read the latest clinical news, personalized to your specialty.
Office
RareDiseaseDoc
Aurora, CO 80016Phone+1 720-642-6110Fax+1 720-580-5613
Summary
- Dr. Jessica Duis is an accomplished and highly skilled board-certified geneticist and special care physician who has dedicated her career to the diagnosis and management of rare disorders throughout the lifespan. With a focus on neurodevelopmental disabilities, Dr. Duis has gained extensive expertise in a range of rare disorders, including Angelman syndrome, Prader Willi syndrome, Pitt Hopkins syndrome, Kabuki syndrome, and many others.
Her medical training at Johns Hopkins School of Medicine in Baltimore, MD, included pediatrics and genetics training, as well as a post-doctorate in the Department of Psychiatry focused on bench and translational research, and additional training in epigenetics and imprinting disorders. During this time, Dr. Duis gained additional expertise in the neurologic and psychiatric management of individuals with neurodevelopmental disabilities.
Dr. Duis is committed to providing compassionate, patient-centered care that emphasizes shared decision making, access to comprehensive cutting-edge care, and consideration of precision therapies.
Education & Training
- George Washington University School of Medicine and Health SciencesClass of 2011
Certifications & Licensure
- TN State Medical License 2016 - 2026
- UT State Medical License 2023 - 2026
- AZ State Medical License 2023 - 2025
- CO State Medical License 2019 - 2025
- SD State Medical License Active through 2025
- WY State Medical License 2021 - 2025
- GA State Medical License 2023 - 2024
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
- Join now to see all
Publications & Presentations
PubMed
- International Expert Opinion on Standard of Care for Patients With Schinzel-Giedion Syndrome: A Modified Delphi Study.Jessica Duis, Laura Agresta, William E Bennett Jr, Henry Chambers, Antonia Clarke
American Journal of Medical Genetics. Part A. 2025-02-19 - Germline de novo alterations of RUNX1T1 in individuals with neurodevelopmental and congenital anomalies.Erfan Aref-Eshghi, Katherine J Anderson, Lauren Boulay, Kathleen Brown, Jessica Duis
HGG Advances. 2025-01-09 - MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature.Remzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, Anoja Namasivayam, Jack Reilly
American Journal of Human Genetics. 2024-07-11
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence: