Felicitas Lacbawan

Quest Diagnostics (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

28h-index3.0kcitations81works8.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(14), Hedgehog Signaling Pathway Studies(14), Cancer Genomics and Diagnostics(9), Acute Myeloid Leukemia Research(8), Ocular Disorders and Treatments(7)

Publications80 total

Biotinidase biochemical and molecular analyses: Experience at a large reference laboratory
Pediatrics International·2024· 8 citedOpen Access
NGS-defined measurable residual disease (MRD) after initial chemotherapy as a prognostic biomarker for acute myeloid leukemia
Blood Cancer Journal·2023· 21 citedOpen Access
NGS-defined measurable residual disease (MRD) after initial chemotherapy as a prognostic biomarker for acute myeloid leukemia
2022· 1 citedOpen Access
Rising to the Challenge: Shortages in Laboratory Medicine
Clinical Chemistry·2022· 11 citedOpen Access
Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratory
Scientific Reports·2022· 25 citedOpen Access
Development and Validation of a High-Throughput Next-Generation Sequencing Workflow for SARS-CoV-2 Whole Genome Sequencing: Results from Over 65,000 Clinical Cases
Research Square (Research Square)·2021Open Access
Analytical validation and performance characteristics of a 48-gene next-generation sequencing panel for detecting potentially actionable genomic alterations in myeloid neoplasms
PLoS ONE·2021· 8 citedOpen Access
Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemia
Molecular Genetics and Metabolism·2021· 1 cited
Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemia
Molecular Genetics and Metabolism Reports·2021· 10 citedOpen Access
Abstract PS16-02: Moving in the fast lane: Test design and validation to produce up-to-date hereditary breast and gynecologic cancer tests
Cancer Research·2021
Identification of eight SARS-CoV-2 ORF7a deletion variants in 2,726 clinical specimens
2020· 19 cited
Analytical validation and performance characteristics of a 48-gene next-generation sequencing panel for detecting potentially actionable genomic alterations in myeloid neoplasms
2020· 5 citedOpen Access
Abstract 5741: Highly specific copy number variant-flagging algorithm using next-generation sequencing in cancer-predisposition genes
Cancer Research·2020
Abstract 5742: Comparison of variants identified by next-generation sequencing panels: A 48-gene panel for myeloid neoplasms and a 35-gene panel for hematologic neoplasms
Cancer Research·2020
Development and Validation of a 34‐Gene Inherited Cancer Predisposition Panel Using Next‐Generation Sequencing
BioMed Research International·2020· 8 citedOpen Access
Evaluation of a 42-Gene Next-Generation Sequencing Panel for Detection of Acute Myeloid Leukemia Mutations for Clinical Use
American Journal of Clinical Pathology·2019Open Access
Abstract 4026: Assessment of microsatellite instability (MSI) status in colorectal cancer tissue using a next-generation sequencing-based tumor profiling assay
Clinical Research (Excluding Clinical Trials)·2019· 1 cited
Abstract 4026: Assessment of microsatellite instability (MSI) status in colorectal cancer tissue using a next-generation sequencing-based tumor profiling assay
Cancer Research·2019· 1 cited
Analytical validation of a 47-gene NGS panel for molecular profiling of myeloid neoplasms.
Journal of Clinical Oncology·2019
Clinical validation of long-range PCR assay for MLL partial tandem duplications for acute myeloid leukemia.
Journal of Clinical Oncology·2019
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Frequent Co-authors

Maximilian Muenke(19), Erich Roessler(12), Jorge I. Vélez(6), Sherri J. Bale(6), Maia V. Ouspenskaia(5), Benjamin D. Solomon(5), Kênia Balbi El-Jaick(5), Nancy J. Clegg(5), Mauricio R. Delgado(5), Ute Hehr(5), Renius Owen(5), Richard L. Davis(4), P D Holohan(4), George H. Collins(4), Daniel A. Lawrence(4), Donald W. Hadley(4), Aimée Paulussen(4), Jin S. Hahn(4), Christèle Dubourg(4), Daniel Pineda‐Alvarez(4)