Iris Casuga

Thermo Fisher Scientific (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

3h-index1.4kcitations13works0.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Cancer Genomics and Diagnostics(8), Molecular Biology Techniques and Applications(6), Genomic variations and chromosomal abnormalities(3), RNA modifications and cancer(3), Gene expression and cancer classification(2)

Publications13 total

Abstract 2944: Rapid and accurate variant calling of FFPE samples with the Genexus System
Cancer Research·2022· 2 cited
Abstract 42: High-throughput next-generation sequencing research solutions for detection of oncology variants, gene fusion events, and key oncology endpoints
Cancer Research·2022
Abstract 764: Fully automated sample-to-report NGS workflow for comprehensive genomic profiling for myeloid neoplasms
Cancer Research·2022· 2 cited
Abstract 2939: Automation meets reliability: Use of Oncomineprecision assay on the Genexussystem for accurate identification of cancer biomarkers in FFPE and liquid biopsy samples
Cancer Research·2022
Abstract 2282: Rapid and accurate variant calling of FFPE samples with the genexus system
Cancer Research·2021· 1 cited
Abstract 1330: Scalable single-day workflows for variant calling with the Genexus Integrated Sequencer
Cancer Research·2020
Abstract 1701: Improvement of tumor mutation burden measurement by removal of deaminated bases in FFPE DNA
Molecular and Cellular Biology / Genetics·2019· 1 cited
Abstract 1701: Improvement of tumor mutation burden measurement by removal of deaminated bases in FFPE DNA
Cancer Research·2019· 2 cited
Abstract 4218: Validation of the Ion AmpliSeq™ Comprehensive Cancer Panel (CCP) using castPCR™ technologies.
Cancer Research·2013· 5 cited
Abstract 3071: Accurate and sensitive detection of KRAS mutations in heterogeneous cancer specimens
Cancer Research·2011· 1 cited
Human Karyotyping Using TaqMan Copy Number Assays
PubMed Central·2010Open Access
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
New England Journal of Medicine·2008· 803 citedOpen Access
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
Nature Genetics·2008· 588 cited

Frequent Co-authors

Janice Au-Young(5), Frances Chan(4), Adam Broomer(3), Caifu Chen(3), Milton Huynh(3), Vinay Kumar Mittal(3), Dinesh Cyanam(3), Elaine Wong-Ho(3), Seth Sadis(3), Heather C. Mefford(2), Andrew J. Sharp(2), Carl Baker(2), Zhaoshi Jiang(2), Marco Fichera(2), Regina Regan(2), Cindy Skinner(2), Roger E. Stevenson(2), Giorgio Gimelli(2), Samantha J.L. Knight(2), Corrado Romano(2)