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Ilana Miller

TitleInstructor
InstitutionUniversity of Colorado Denver - Anschutz Medical Campus
DepartmentSOM-PEDS

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Fortin O, Christoffel K, Kousa Y, Miller I, Leon E, Donoho K, Mulkey SB, Anwar T. Pearls & Oy-sters: Delayed Response to Pyridoxine in Pyridoxine-Dependent Epilepsy. Neurology. 2023 10 31; 101(18):e1828-e1832. PMID: 37580162.
      View in: PubMed
    2. Miller IM, Yashar BM, Macnamara EF. Continuing a search for a diagnosis: the impact of adolescence and family dynamics. Orphanet J Rare Dis. 2023 01 09; 18(1):6. PMID: 36624503.
      View in: PubMed
    3. Turbitt E, Kohler JN, Angelo F, Miller IM, Lewis KL, Goddard KAB, Wilfond BS, Biesecker BB, Leo MC. The PrU: Development and validation of a measure to assess personal utility of genomic results. Genet Med. 2023 03; 25(3):100356. PMID: 36516964.
      View in: PubMed
    4. Berger SI, Miller I, Tochen L. Recessive GCH1 Deficiency Causing DOPA-Responsive Dystonia Diagnosed by Reported Negative Exome. Pediatrics. 2022 02 01; 149(2). PMID: 35083481.
      View in: PubMed
    5. Umstead KL, Han PKJ, Lewis KL, Miller IM, Hepler CL, Thompson LJ, Wolfsberg TG, Nguyen AD, Fredriksen MT, Gibney G, Turbitt E, Biesecker LG, Biesecker BB. Perceptions of uncertainties about carrier results identified by exome sequencing in a randomized controlled trial. Transl Behav Med. 2020 05 20; 10(2):441-450. PMID: 31505002.
      View in: PubMed
    6. Miller I, Greenberg S, Yashar BM, Marvin ML. Improving access to cancer genetic services: perspectives of high-risk clients in a community-based setting. J Community Genet. 2020 Jan; 11(1):119-123. PMID: 31020639.
      View in: PubMed
    7. Kumar N, Turbitt E, Biesecker BB, Miller IM, Cham B, Smith KC, Rimal RN. Managing the need to tell: Triggers and strategic disclosure of thalassemia major in Singapore. Am J Med Genet A. 2019 05; 179(5):762-769. PMID: 30821068.
      View in: PubMed
    8. Lewis KL, Heidlebaugh AR, Epps S, Han PKJ, Fishler KP, Klein WMP, Miller IM, Ng D, Hepler C, Biesecker BB, Biesecker LG. Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq® cohort. Genet Med. 2019 06; 21(6):1355-1362. PMID: 30382154.
      View in: PubMed
    9. Miller IM, Lewis KL, Lawal TA, Ng D, Johnston JJ, Biesecker BB, Biesecker LG. Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes. Genet Med. 2019 03; 21(3):748-752. PMID: 29997389.
      View in: PubMed
    10. Lewis KL, Umstead KL, Johnston JJ, Miller IM, Thompson LJ, Fishler KP, Biesecker LG, Biesecker BB. Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial. Am J Hum Genet. 2018 04 05; 102(4):540-546. PMID: 29526281.
      View in: PubMed
    11. Biesecker BB, Lewis KL, Umstead KL, Johnston JJ, Turbitt E, Fishler KP, Patton JH, Miller IM, Heidlebaugh AR, Biesecker LG. Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial. JAMA Intern Med. 2018 03 01; 178(3):338-346. PMID: 29356820.
      View in: PubMed
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