Danny Miller
 |
Clinical Fellow Office Phone: (206) 685-7336 Office Location: S413A Email: dm1 [AT] u.washington.edu |
Professional Experience
| Clinical Fellow |
Dept. Genome Sciences, U. Washington, Seattle, WA, USA |
2019-current |
| Pediatrics and Medical Genetics Resident |
Seattle Children's Hospital, Seattle, WA, USA |
2018-current |
Education
| M.D. |
University of Kansas Medical Center, Lawrence, KS, USA |
2018 |
| Ph.D., Physiology |
University of Kansas Medical Center and the Stowers Institute for Medical Research, Lawrence, KS, USA |
2016 |
Research Interests
| I am interested in using long-read sequencing to increase the rate of genetic diagnosis, shorten the time required to make a genetic diagnosis, and identify novel biological processes for further study in the laboratory. |
Selected Publications
Miller DE, Sulovari A, Wang T, Loucks L, Hoekzema K, Munson KM, Lewis AP, Almanza Fuerte EP, Paschal CR, Thies J, Bennett JT, Glass I, Dipple KM, Patterson K, Bonkowski ES, Nelson Z, Squire A, Sikes M, Beckman E, Bennett RL, Earl D, Lee W, Allikmets R, Perlman SJ, Chow P, Hing AV, Adam MP, Sun A, Lam C, Chang I, University of Washington Center for Mendelian Genomics, Cherry T, Chong JX, Bamshad MJ, Nickerson DA, Mefford HC, Doherty D, Eichler EE. Targeted long-read sequencing resolves complex structural variants and identifies missing disease-causing variants. American Journal of Human Genetics. July 2021. PMID: 34216551
Miller DE, Cook KR, Hawley RS. The joy of balancers. PLoS Genetics, November 2019. PMID: 31697682
Miller DE, Staber C, Zeitlinger J, Hawley RS. Highly contiguous genome assemblies of 15 Drosophila species generated using Nanopore sequencing. G3: Genes, Genomes, Genetics, August 2018. PMID: 30087105
Crown CN, Miller DE, Sekelsky J, Hawley RS. Local inversion heterozygosity alters recombination throughout the genome. Current Biology, September 2018. PMID: 30174188