Janet L. Lukacs
This is a likely match — the affiliation was inferred from OpenAlex, ORCID, and web sources but has not been fully confirmed. Treat with appropriate caution.
Researcher
Also affiliated: Arkansas Children's Hospital (1996–2004); Professional Services Group (United States) (1987); Phoenix Children's Hospital (1984–1987); College of Business Administration (1984)
Faculty Researcher
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: 14
- Publications: 52
- Citations: 854
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
- P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software
- P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software
- P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software
- P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software
- P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software
- P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software
- P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software
- P664: Comparative evaluation of an AI-based scanner-agnostic add-on utility versus conventional karyotyping software
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