David T. Miller

University of North Carolina at Chapel Hill — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

53h-index15.1kcitations194works4.72yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(38), Genomics and Rare Diseases(37), Neurofibromatosis and Schwannoma Cases(19), Congenital heart defects research(19), Nuclear physics research studies(15)

Publications189 total

Supplementary Figures 1-15 from Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA
2025Open Access
Supplementary Tables S1 and S2 from Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA
2025Open Access
Symposium report—ethical and social considerations regarding return of secondary findings in atomic bomb survivors
Carcinogenesis·2025· 2 citedOpen Access
Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation
UNC Libraries·2025Open Access
Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation
2025Open Access
ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2025· 24 cited
Long-read sequencing is required for precision diagnosis of incontinentia pigmenti
Human Genetics and Genomics Advances·2025Open Access
SAVANA: reliable analysis of somatic structural variants and copy number aberrations using long-read sequencing
Nature Methods·2025· 10 citedOpen Access
Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
UNC Libraries·2025Open Access
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
UNC Libraries·2025Open Access
Abstract 3888: Exploring intra-tumor heterogeneity in malignant peripheral nerve sheath tumors through single-cell multi-omics
Cancer Research·2025
Factors influencing readmission patterns following radical cystectomy: An analysis of social determinants and discharge outcomes
Urologic Oncology Seminars and Original Investigations·2024Open Access
SAVANA: reliable analysis of somatic structural variants and copy number aberrations in clinical samples using long-read sequencing
2024· 11 citedOpen Access
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders
Genetics in Medicine·2024· 13 citedOpen Access
Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2024· 10 citedOpen Access
FACTORS ASSOCIATED WITH RESTARTING ANDROGENIC ANABOLIC STEROIDS AFTER CESSATION IN MEN WITH INFERTILITY: A RETROSPECTIVE ANALYSIS
Fertility and Sterility·2023Open Access
A Multipronged Intervention to Reduce Readmissions and Readmission Intensity After Radical Cystectomy
Urology·2023
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria
JAMA Neurology·2023· 29 citedOpen Access
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine·2023· 366 citedOpen Access
Supplementary Tables S1 and S2 from Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA
2023Open Access
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Frequent Co-authors

Christa Lese Martin(9), Yiping Shen(9), Wendy K. Chung(7), Nicole J. Ullrich(6), Teri E. Klein(5), Bruce R. Korf(5), Douglas R. Stewart(5), Joan M. Stoler(5), Jonathan Picker(5), Michael S. Watson(4), David H. Ledbetter(4), C. Sue Richards(4), Kristy Lee(4), Allan Gordon(4), Laura M. Amendola(4), Michael H. Gollob(4), Steven M. Harrison(4), Ray E. Hershberger(4), David J. Harris(4), Robert R. Wolff(4)