Danny E. Miller, MD, PhD

Assistant Professor

Pronouns:

He, him

E-mail:

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Office Location:

I607-K

Mailing Address:

Box 356320
1959 NE Pacific St
Seattle, WA 98195‐7110

Research Lab

Miller Lab


Clinical and Research Background

​Dr. Miller’s laboratory uses long-read DNA and RNA sequencing to identify missing disease-causing genetic changes difficult to detect using standard genetic testing. These include complex changes difficult to detect or resolve with short-read sequencing, and variants in regions of the genome that were previously inaccessible to prior technologies. His group is interested in developing long-read sequencing-based clinical tests to simplify clinical genetic testing, increase the diagnostic rate, and shorten the time required to arrive at a genetic diagnosis. Clinically, he is an attending physician in the Department of Pediatrics, Division of Genetic medicine and sees patients in both general genetics and skeletal dysplasia clinics at Seattle Children’s Hospital.

Research Interests

Long-read genome sequencing

Unsolved genetic disorders

Clinical genetic testing

Academic and Medical Appointments

Academic Appointments

Assistant Professor, Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, WA, 2022-Present

Assistant Professor, Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 2022-Present

Medical Appointments

Attending Physician, Seattle Children’s Hospital 2022-Present

Education and Training

Combined Pediatrics and Medical Genetics Residency, University of Washington and Seattle Children’s Hospital, Seattle, WA, 2018-2022

MD and PhD in Physiology (with honors), University of Kansas Medical Center and The Stowers Institute for Medical Research, Kansas City, KS, 2010-2018

Publications

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