Match tier
Likely match
Presence
Current · Arkansas
Last published
2026
Sources
OpenAlex · ORCID
Refreshed
2026-10-07
J
Janet L. Lukacs
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Also affiliated: Arkansas Children's Hospital (1996–2004); University of Arkansas Medical Center (2024)
13 h-index
27 pubs
822 cited
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Janet L. Lukacs investigates chromosomal abnormalities, particularly focusing on their impact on specific diseases. Her recent work includes an examination of how additional copies of chromosome 1q affect survival outcomes in patients with multiple myeloma. She also contributed to research evaluating the comparative performance of an AI-based utility versus conventional software for karyotyping analysis. Lukacs's research interests align with the study of genetic translocations and chromosome aberrations in humans, utilizing techniques such as fluorescence in situ hybridization and karyotyping. Her work has been recognized through a citation count of 852 and an h-index of 14 across 52 publications. She collaborates with researchers at the University of Arkansas for Medical Sciences, including Phillip Farmer, Jeffery R. Sawyer, Nishanth Thalambedu, and Marian Johnson.
Metrics
- h-index: 13
- Publications: 27
- Citations: 822
Selected Publications
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P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software (2026)
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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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Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping (1998)
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Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping (1998)
Collaboration Network
Top Collaborators
Gael Sammartino
University of Arkansas for Medical Sciences
9 shared publications
In database
- 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
Frits van Rhee
University of Arkansas for Medical Sciences
9 shared publications
In database
- 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
Jeffrey R. Sawyer
Arkansas Children's Hospital (US)
8 shared publications
- Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping
- Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- 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
Showing 5 of 8 shared publications
Charles M. Swanson
University of Arkansas for Medical Sciences (US)
7 shared publications
- 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
- 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
Maurizio Zangari
University of Arkansas for Medical Sciences
7 shared publications
In database
- 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
Bart Barlogie
Arkansas Children's Hospital
7 shared publications
In database
- Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping
- Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping
- An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome
- 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
Showing 5 of 7 shared publications
Erming Tian
University of Arkansas for Medical Sciences
7 shared publications
In database
- 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
- 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
Faith E. Davies
University of Arkansas for Medical Sciences (US)
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
Gareth J. Morgan
University of Arkansas for Medical Sciences (US)
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
Regina Lichti Binz
University of Arkansas for Medical Sciences
5 shared publications
In database
- 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)
- Evidence of an Epigenetic Origin for High-Risk 1q21 Copy Number Aberrations in Multiple Myeloma
Christoph Heuck
University of Arkansas for Medical Sciences (US)
4 shared publications
- 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
John D. Shaughnessy
Arkansas Children's Hospital
4 shared publications
In database
- Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping
- Identification of New Nonrandom Translocations in Multiple Myeloma With Multicolor Spectral Karyotyping
- Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
- Jumping Translocations 1q12 Contribute to Copy Number (CN) Alterations in Multiple Myeloma (MM): Unexpected Focal Amplifications of Receptor Chromosomes (RC)
Joshua Epstein
University of Arkansas for Medical Sciences (US)
4 shared publications
- 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
Clyde Bailey
University of Arkansas for Medical Sciences
4 shared publications
In database
- 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
Brian A. Walker
University of Arkansas for Medical Sciences (US)
4 shared publications
- 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
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