Molly Schroeder

Assistant Professor of Pathology and Immunology

    • 737 Citations
    20122020

    Research output per year

    If you made any changes in Pure these will be visible here soon.

    Personal profile

    Research interests

    Dr. Schroeder is a clinical laboratory geneticist with boards in molecular genetics and cytogenetics. She is experienced in genomics, clinical assay development, and translational research.

    Fingerprint Dive into the research topics where Molly Schroeder is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

    • 10 Similar Profiles

    Network Recent external collaboration on country level. Dive into details by clicking on the dots.

    Research Output

    • 737 Citations
    • 16 Article
    • 2 Review article
    • 1 Comment/debate

    Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

    on behalf of the ACMG Professional Practice and Guidelines Committee, Jun 1 2020, In : Genetics in Medicine. 22, 6, p. 986-1004 19 p.

    Research output: Contribution to journalArticle

    Open Access
  • 4 Scopus citations

    A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative

    Undiagnosed Diseases Network, Jan 1 2019, In : Genetics in Medicine. 21, 1, p. 161-172 12 p.

    Research output: Contribution to journalArticle

  • 18 Scopus citations

    Diagnostic Utility of Next-Generation Sequencing for Disorders of Somatic Mosaicism: A Five-Year Cumulative Cohort

    McNulty, S. N., Evenson, M. J., Corliss, M. M., Love-Gregory, L. D., Schroeder, M. C., Cao, Y., Lee, Y. S., Drolet, B. A., Neidich, J. A., Cottrell, C. E. & Heusel, J. W., Oct 3 2019, In : American journal of human genetics. 105, 4, p. 734-746 13 p.

    Research output: Contribution to journalArticle

  • 3 Scopus citations

    Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay

    Undiagnosed Diseases Network, Jan 3 2019, In : American journal of human genetics. 104, 1, p. 164-178 15 p.

    Research output: Contribution to journalArticle

  • 10 Scopus citations

    IgG4-related disease: Association with a rare gene variant expressed in cytotoxic T cells

    Undiagnosed Disease Network, Jun 2019, In : Molecular Genetics and Genomic Medicine. 7, 6, e686.

    Research output: Contribution to journalArticle

    Open Access
  • 2 Scopus citations