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Presence Current · Arkansas
Last published 2019
Sources OpenAlex · ORCID
Refreshed 2026-09-26

Gael Sammartino

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Also affiliated: Arkansas Children's Hospital (1993–2001)

10 h-index 19 pubs 419 cited

  • Humans
  • Translocation, Genetic
  • Karyotyping
  • Chromosome Aberrations
  • Chromosomes, Human, Pair 1
  • Multiple Myeloma
  • Female
  • Chromosome Deletion
  • In Situ Hybridization, Fluorescence
  • Chromosomes, Human, Pair 22
  • Chromosomes, Human, Pair 16
  • Disease Progression
  • Gene Dosage
  • Prognosis
  • Chromosomal Instability

Biography and Research Information

Metrics

  • h-index: 10
  • Publications: 19
  • Citations: 419

Selected Publications

  • An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome (2019)
    Blood Cancer Journal 39 citations DOI OpenAlex
  • An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome (2018)
    Blood 8 citations DOI OpenAlex
  • Chromosome 1q12 Instability Drives Both 1q21 Amplification and Arm-Length Deletions in Multiple Myeloma (2017)
    Blood DOI OpenAlex
  • Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC (2016)
    Blood 2 citations DOI OpenAlex
  • Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma (2016)
    Leukemia 32 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
  • A clonal reciprocal t(2;7)(p13;p13) in plantar fibromatosis (2005)
    Cancer Genetics and Cytogenetics 11 citations DOI OpenAlex
  • Constitutional t(16;22)(p13.3;q11.2∼12) in a primitive neuroectodermal tumor of the pineal region (2003)
    Cancer Genetics and Cytogenetics 6 citations DOI OpenAlex

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Collaboration Network

42 Collaborators 2 Institutions 1 Country

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