Match tier Listed
Presence Current · Arkansas
Last published 2021
Sources OpenAlex · ORCID
Refreshed 2026-08-08

Jill Kelsay

Researcher

Also affiliated: University of Arkansas Medical Center (2017); University of Cincinnati (2005)

Unknown Researcher

4 h-index 5 pubs 121 cited

  • Adult
  • Humans
  • Female
  • Male
  • Genetic Predisposition to Disease
  • Genetic Association Studies
  • Down Syndrome
  • Femur
  • Lumbar Vertebrae
  • Middle Aged
  • Osteogenesis
  • Osteoporosis
  • Peptide Fragments
  • Peptides
  • Procollagen

Biography and Research Information

OverviewAI-generated summary

Jill Kelsay's research investigates the genetic underpinnings of neurodevelopmental conditions. Her work has identified de novo variants in H3-3A and H3-3B genes as contributors to neurodevelopmental delay, dysmorphic features, and structural brain abnormalities. This research contributes to understanding the molecular basis of complex neurological disorders.

Metrics

  • h-index: 4
  • Publications: 5
  • Citations: 121

Selected Publications

  • De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities (2021)
    npj Genomic Medicine 28 citations DOI OpenAlex
  • Phelan‐McDermid syndrome and cancer predisposition: The value of a karyotype (2017)
    American Journal of Medical Genetics Part A 5 citations DOI OpenAlex
  • Low bone turnover and low bone density in a cohort of adults with Down syndrome (2012)
    Osteoporosis International 83 citations DOI OpenAlex
  • Male infertility associated with hereditary leiomyomatosis and renal cell carcinoma (2010)
    Fertility and Sterility 5 citations DOI OpenAlex

View all publications on OpenAlex →

Collaboration Network

25 Collaborators 20 Institutions 3 Countries

Top Collaborators

Similar Researchers

Based on overlapping research topics