Gael Sammartino
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Also affiliated: Arkansas Children's Hospital (1993–2001)
Research Areas
Biomedical Subjects
Biography and Research Information
Metrics
- h-index: 10
- Publications: 19
- Citations: 419
Selected Publications
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An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome (2019)
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An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome (2018)
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Chromosome 1q12 Instability Drives Both 1q21 Amplification and Arm-Length Deletions in Multiple Myeloma (2017)
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Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC (2016)
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Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma (2016)
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Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region (2015)
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Evidence of an Epigenetic Origin for High-Risk 1q21 Copy Number Aberrations in Multiple Myeloma (2014)
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Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification (2012)
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Jumping Translocations 1q12 Contribute to Copy Number (CN) Alterations in Multiple Myeloma (MM): Unexpected Focal Amplifications of Receptor Chromosomes (RC) (2011)
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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)
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A Novel Mechanism for Intrachromosomal Gene Amplification in Multiple Myeloma: 1q12 Pericentromeric Heterochromatin Mediates Breakage- Fusion-Bridge Cycles of the 1q12~23 Amplicon (2008)
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A clonal reciprocal t(2;7)(p13;p13) in plantar fibromatosis (2005)
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Constitutional t(16;22)(p13.3;q11.2∼12) in a primitive neuroectodermal tumor of the pineal region (2003)
Collaboration Network
Top Collaborators
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- A clonal reciprocal t(2;7)(p13;p13) in plantar fibromatosis
- Constitutional t(16;22)(p13.3;q11.2∼12) in a primitive neuroectodermal tumor of the pineal region
Showing 5 of 10 shared publications
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification
Showing 5 of 9 shared publications
- Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
- Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification
Showing 5 of 9 shared publications
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
Showing 5 of 9 shared publications
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
Showing 5 of 9 shared publications
- Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
- Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification
- Jumping Translocations 1q12 Contribute to Copy Number (CN) Alterations in Multiple Myeloma (MM): Unexpected Focal Amplifications of Receptor Chromosomes (RC)
Showing 5 of 7 shared publications
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
- Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification
Showing 5 of 7 shared publications
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
Showing 5 of 7 shared publications
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
Showing 5 of 6 shared publications
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
Showing 5 of 6 shared publications
- Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage‐fusion‐bridge cycles of a 1q12∼23 amplicon
- Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification
- Jumping Translocations 1q12 Contribute to Copy Number (CN) Alterations in Multiple Myeloma (MM): Unexpected Focal Amplifications of Receptor Chromosomes (RC)
- A Novel Mechanism for Intrachromosomal Gene Amplification in Multiple Myeloma: 1q12 Pericentromeric Heterochromatin Mediates Breakage- Fusion-Bridge Cycles of the 1q12~23 Amplicon
- Jumping Translocations of 1q12 in Multiple Myeloma: Unexpected Intra-clonal Heterogeneity of Copy Number Aberrations in the 1q21-31 Region
- Hyperhaploid Multiple Myeloma (MM): A Rare Karyotypic Subgroup Retaining Disomy 18 and 1q12∼23 Amplification
- Jumping Translocations 1q12 Contribute to Copy Number (CN) Alterations in Multiple Myeloma (MM): Unexpected Focal Amplifications of Receptor Chromosomes (RC)
- Evidence of an Epigenetic Origin for High-Risk 1q21 Copy Number Aberrations in Multiple Myeloma
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Evidence of an Epigenetic Origin for High-Risk 1q21 Copy Number Aberrations in Multiple Myeloma
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Chromosome 1q12 Instability Drives Both 1q21 Amplification and Arm-Length Deletions in Multiple Myeloma
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- An Acquired High-Risk Chromosome Instability Phenotype in Multiple Myeloma: Jumping 1q Syndrome
- Concurrent Amplification of MYC and 1q21 in Multiple Myeloma: Focal and Segmental Jumping Translocations of MYC
- Chromosome 1q12 Instability Drives Both 1q21 Amplification and Arm-Length Deletions in Multiple Myeloma