Laura Morsberger

Johns Hopkins University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

21h-index6.3kcitations75works3.02yr avg
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Research Topics

Cancer Genomics and Diagnostics(22), Acute Myeloid Leukemia Research(15), Pancreatic and Hepatic Oncology Research(13), Genomic variations and chromosomal abnormalities(13), Advanced biosensing and bioanalysis techniques(8)

Publications74 total

Optical Genome Mapping for Cytogenetic Analysis in Multiple Myeloma: Real‐World Evidence
American Journal of Hematology·2026Open Access
Racial Differences in the Molecular Genetic Biomarkers of Diffuse Large B-Cell Lymphoma
Biomedicines·2025Open Access
Hi-C Technology Reveals Actionable Gene Fusions and Rearrangements in Diffuse Large B-Cell Lymphoma Unidentified by Conventional FISH
Genes·2025Open Access
Ossifying Spindled and Epithelioid Tumor: A Novel Soft Tissue Tumor
Modern Pathology·2025· 2 cited
A Multi-Well Method for the CD138 and AML/MDS FISH Testing of Multiple Biomarkers on a Single Slide in Multiple Myeloma and AML/MDS Patients
DNA·2025Open Access
Chromoanagenesis in Osteosarcoma
Biomolecules·2025· 3 citedOpen Access
Abstract 471: CRISPR-Cas9 as a novel cancer gene therapy approach against pancreatic cancers
Cancer Research·2025
P123: Rapid detection of PML::RARA fusions in acute promyelocytic leukemia using CRISPR/Cas9-mediated nanopore sequencing with adaptive sampling
Genetics in Medicine Open·2025Open Access
Diagnostic and Prognostic/Therapeutic Significance of Comprehensive Analysis of Bone and Soft Tissue Tumors Using Optical Genome Mapping and Next-Generation Sequencing
Modern Pathology·2024· 12 cited
Rapid Detection of PML::RARA Fusions in Acute Promyelocytic Leukemia: CRISPR/Cas9 Nanopore Sequencing with Adaptive Sampling
Biomolecules·2024· 2 citedOpen Access
Optical Genome Mapping Reveals Complex and Cryptic Rearrangement Involving PML::RARA Fusion in Acute Promyelocytic Leukemia
Genes·2024· 6 citedOpen Access
1q jumping translocation as a biomarker in myeloid malignancy: frequently mutated genes associated with bad prognosis and low survival
Experimental Hematology and Oncology·2024· 2 citedOpen Access
A comprehensive approach to evaluate genetic abnormalities in multiple myeloma using optical genome mapping
Blood Cancer Journal·2024· 20 citedOpen Access
Abstract LB397: Simultaneous CRISPR-Cas9 induced double strand breaks causes chromosomal catastrophe in pancreatic cancers: A parallel comparison with ionizing radiation
Cancer Research·2024
An Integrated Approach Including CRISPR/Cas9-Mediated Nanopore Sequencing, Mate Pair Sequencing, and Cytogenomic Methods to Characterize Complex Structural Rearrangements in Acute Myeloid Leukemia
Biomedicines·2024· 1 citedOpen Access
P088: A comprehensive approach to evaluate genetic abnormalities in plasma cell neoplasms using optical genome mapping and next-generation sequencing
Genetics in Medicine Open·2024Open Access
Ring Chromosomes in Hematological Malignancies Are Associated with TP53 Gene Mutations and Characteristic Copy Number Variants
Cancers·2023· 7 citedOpen Access
Donor cell-derived genetic abnormalities after sex mismatched allogeneic cell transplantation: a unique challenge of donor cell leukemia
Blood Cancer Journal·2023· 1 citedOpen Access
Complex/cryptic EWSR1::FLI1/ERG Gene Fusions and 1q Jumping Translocation in Pediatric Ewing Sarcomas
Genes·2023· 10 citedOpen Access
Simultaneous CRISPR-Cas9-induced double strand breaks are lethal in cancers
2023· 4 citedOpen Access
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Frequent Co-authors

Constance A. Griffin(23), Ying Zou(18), Christopher D. Gocke(13), Victoria Stinnett(11), Raluca Yonescu(10), Ralph H. Hruban(10), Patty Long(10), Patricia P. Long(8), Aparna Pallavajjala(7), Melanie Hardy(7), Anita L. Hawkins(6), Lisa Haley(6), Melanie Klausner(6), Richard J. Jones(5), Pedram Argani(5), Charles J. Yeo(5), Denise Batista(5), Liqun Jiang(5), Emily Adams(5), Jen Ghabrial(5)