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Presence Current · Arkansas
Last published 2024
Sources OpenAlex · ORCID
Refreshed 2026-08-08

Regina Lichti Binz

Cytogenetic Specialist

Also affiliated: Arkansas Children's Hospital (2001–2004)

Faculty Researcher

11 h-index 25 pubs 456 cited

  • Humans
  • Chromosome Aberrations
  • In Situ Hybridization, Fluorescence
  • Translocation, Genetic
  • Chromosomes, Human, Pair 1
  • Female
  • Chromosome Banding
  • Male
  • Karyotyping
  • Middle Aged
  • Multiple Myeloma
  • Chromosome Deletion
  • Cytogenetic Analysis
  • Animals
  • Mice

Biography and Research Information

OverviewAI-generated summary

Regina Lichti Binz investigates cytogenetic and epigenetic alterations in human and murine cells. Her research includes studying the effects of dietary methionine deficiency on genetic instability in immune cells and evaluating the impact of simulated galactic cosmic rays on cognitive performance in mice. Binz has also examined cytogenetic and epigenetic aberrations in peripheral lymphocytes of the Marshallese population in northwest Arkansas. She has published protocols for chromosome preparation and staining for cytogenetic analysis, and her work has utilized molecular cytogenetics to identify mosaicism and novel translocations in human endothelial cells. Binz collaborates with several researchers at the University of Arkansas for Medical Sciences, including Rupak Pathak, Igor Koturbash, Martin Hauer‐Jensen, and Laura Ewing, with whom she shares multiple publications. Her work has a h-index of 11 with 451 total citations across 25 publications.

Metrics

  • h-index: 11
  • Publications: 25
  • Citations: 456

Selected Publications

  • G-Banding and Molecular Cytogenetics Detect Novel Translocations and Cryptic Aberrations in Human Immortal Endothelial Cells (2024)
    International Journal of Molecular Sciences DOI OpenAlex
  • Protocol for preparation and staining of chromosomes isolated from mouse and human tissues for conventional and molecular cytogenetic analysis (2024)
    STAR Protocols 4 citations DOI OpenAlex
  • Evaluating the effects of low-dose simulated galactic cosmic rays on murine hippocampal-dependent cognitive performance (2022)
    Frontiers in Neuroscience 7 citations DOI OpenAlex
  • Cytogenetic and epigenetic aberrations in peripheral lymphocytes of northwest Arkansas Marshallese (2022)
    International Journal of Radiation Biology 10 citations DOI OpenAlex
  • Molecular Cytogenetics Reveals Mosaicism in Human Umbilical Vein Endothelial Cells (2022)
    Genes 4 citations DOI OpenAlex
  • Dietary Methionine Deficiency Enhances Genetic Instability in Murine Immune Cells (2021)
    International Journal of Molecular Sciences 11 citations DOI OpenAlex
  • Identification of novel breakpoints for locus- and region-specific translocations in 293 cells by molecular cytogenetics before and after irradiation (2019)
    Scientific Reports 33 citations DOI OpenAlex
  • Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC (2016)
    Blood 2 citations DOI OpenAlex
  • The Vitamin E Analog Gamma-Tocotrienol (GT3) Suppresses Radiation-Induced Cytogenetic Damage (2016)
    Pharmaceutical Research 27 citations DOI OpenAlex
  • Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region (2015)
    Clinical Lymphoma Myeloma & Leukemia 1 citation DOI OpenAlex
  • Evidence of an Epigenetic Origin for High-Risk 1q21 Copy Number Aberrations in Multiple Myeloma (2014)
    Blood 1 citation DOI OpenAlex
  • Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification (2012)
    Blood 1 citation DOI OpenAlex
  • Jumping Translocations 1q12 Contribute to Copy Number (CN) Alterations in Multiple Myeloma (MM): Unexpected Focal Amplifications of Receptor Chromosomes (RC) (2011)
    Blood 1 citation DOI OpenAlex
  • Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon (2009)
    British Journal of Haematology 35 citations DOI OpenAlex
  • A Novel Mechanism for Intrachromosomal Gene Amplification in Multiple Myeloma: 1q12 Pericentromeric Heterochromatin Mediates Breakage- Fusion-Bridge Cycles of the 1q12~23 Amplicon (2008)
    Blood DOI OpenAlex

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Collaboration Network

21 Collaborators 2 Institutions 1 Country

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