Match tier Listed
Presence Current · Arkansas
Last published 2020
Sources OpenAlex · ORCID
Refreshed 2026-08-08

Linda D. Murphy

Researcher

Also affiliated: Arkansas Children's Hospital (2020); University of Arkansas Medical Center (2020)

Unknown Researcher

2 h-index 2 pubs 53 cited

  • Genetic Markers
  • Humans
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • Congenital Abnormalities
  • Genetic Variation
  • High-Throughput Nucleotide Sequencing
  • Adolescent
  • DNA-Binding Proteins
  • Female
  • Immunohistochemistry
  • Magnetic Resonance Imaging
  • Sarcoma, Ewing
  • Skin Neoplasms
  • Transcription Factors

Biography and Research Information

OverviewAI-generated summary

Linda D. Murphy's research has focused on studies related to medical case reports and retrospective studies. Her most recent publication was in 2020. Murphy's work has contributed to the understanding of various medical conditions through detailed case analyses and historical data review.

Metrics

  • h-index: 2
  • Publications: 2
  • Citations: 53

Selected Publications

  • Primary superficial Ewing sarcoma: A unique entity? A case report including novel findings of <scp><i>ELF3</i></scp> and <scp><i>TNFRSF14</i></scp> copy number loss (2020)
    Journal of Cutaneous Pathology 7 citations DOI OpenAlex
  • Developments in our understanding of the genetic basis of birth defects (2015)
    Birth Defects Research Part A Clinical and Molecular Teratology 46 citations DOI OpenAlex

View all publications on OpenAlex →

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