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Author Details

Gordana Raca
Children's Hospital Los Angeles
1997
87
25
PMIDPaper TitleJournal TitlePublished Year
37979304Diagnostic Yield of Epilepsy-Genes Sequencing and Chromosomal Microarray in Pediatric Epilepsy.Pediatr Neurol2024
38008288An Exome Capture-Based RNA-Sequencing Assay for Genome-Wide Identification and Prioritization of Clinically Important Fusions in Pediatric Tumors.J Mol Diagn2024
37992967Comparative Clinicopathologic and Genomic Analysis of Hepatocellular Neoplasm, Not Otherwise Specified, and Hepatoblastoma.Mod Pathol2024
37946548Pediatric Sertoli-Leydig Cell Tumors of the Ovary: An Integrated Study of Clinicopathological Features, Pan-cancer-Targeted Next-generation Sequencing and Chromosomal Microarray Analysis From a Single Institution.Am J Surg Pathol2024
37981088Transcriptome Sequencing Allows Comprehensive Genomic Characterization of Pediatric B-Acute Lymphoblastic Leukemia in an Academic Clinical Laboratory.J Mol Diagn2024
36373660CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.Nucleic Acids Res2023
38001730Cytogenetics Is a Science, Not a Technique! Why Optical Genome Mapping Is So Important to Clinical Genetic Laboratories.Cancers (Basel)2023
37149359Modern Classification and Management of Pediatric B-cell Leukemia and Lymphoma.Surg Pathol Clin2023
37129267Efficacy and safety of FLAG-IDA as front-line therapy in de novo paediatric acute myeloid leukaemia population.Br J Haematol2023
37261438Response to Spurdle et al.Genet Med2023
36507974Points to consider in the detection of germline structural variants using next-generation sequencing: A statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
34106024Primary Adrenal Malignant Rhabdoid Tumor in a 14-Year-Old Female: A Case Report and Literature Review.Int J Surg Pathol2022
35366592Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions.Cancer Genet2022
35624339A community approach to the cancer-variant-interpretation bottleneck.Nat Cancer2022
36063163Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).Genet Med2022
35101336Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).Genet Med2022
34915342Acute myeloid leukemia with t(X;6)9p11;q23);MYB-GATA1 and female sex: GATA1 insufficiency may be insufficient for pathogenesis.Cancer Genet2022
35245931Characterization of PAX5 intragenic tandem multiplication in pediatric B-lymphoblastic leukemia by optical genome mapping.Blood Adv2022
34907337Correction to: Recommendations for future extensions to the HGNC gene fusion nomenclature.Leukemia2022
35171727MUC4 expression by immunohistochemistry is a specific marker for <i>BCR-ABL1+</i> and <i>BCR-ABL1</i>-like B-lymphoblastic leukemia.Leuk Lymphoma2022
34488461Pediatric Metastatic Hepatoblastoma With an <i>ARID1A</i> Mutation and Rhabdoid Cells.Int J Surg Pathol2022
34601996PLAG1 Immunohistochemical Staining Is a Surrogate Marker for <i>PLAG1</i> Fusions in Lipoblastomas.Pediatr Dev Pathol2022
32886736Conventional Cytogenetic Analysis of Hematologic Neoplasms: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee.Arch Pathol Lab Med2021
33571894A multimodal genomics approach to diagnostic evaluation of pediatric hematologic malignancies.Cancer Genet2021
33876219Increased prevalence of CRLF2 rearrangements in obesity-associated acute lymphoblastic leukemia.Blood2021
33731880Correction: Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).Genet Med2021
33531655Increased Incidence of IKZF1 deletions and IGH-CRLF2 translocations in B-ALL of Hispanic/Latino children-a novel health disparity.Leukemia2021
34764425Recommendations for future extensions to the HGNC gene fusion nomenclature.Leukemia2021
33307280Dilated cardiomyopathy in a patient with autosomal dominant EEF1A2-related neurodevelopmental disorder.Eur J Med Genet2021
33470917Primary Knee Intra-articular Synovial Sarcoma in Pediatric and Adolescent Patients.Pediatr Dev Pathol2021
32296163Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG).Genet Med2020
31690835Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).Genet Med2020
32246132A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.Nat Genet2020
32302940Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia.Cancer Genet2020
30755392A semiautomated whole-exome sequencing workflow leads to increased diagnostic yield and identification of novel candidate variants.Cold Spring Harb Mol Case Stud2019
31779674Standard operating procedure for curation and clinical interpretation of variants in cancer.Genome Med2019
31138931Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consortium (CGC).Genet Med2019
29365323Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignancies.Blood Adv2018
30138724OncoKids: A Comprehensive Next-Generation Sequencing Panel for Pediatric Malignancies.J Mol Diagn2018
30377088Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.Cancer Genet2018
30344013Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.Cancer Genet2018
30311370Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.Hum Mutat2018
29797659Myeloid lineage switch following chimeric antigen receptor T-cell therapy in a patient with TCF3-ZNF384 fusion-positive B-lymphoblastic leukemia.Pediatr Blood Cancer2018
27855558Diagnostic evaluation of RNA sequencing for the detection of genetic abnormalities associated with Ph-like acute lymphoblastic leukemia (ALL).Leuk Lymphoma2017
29025601A neoplasm with FIP1L1-PDGFRA fusion presenting as pediatric T-cell lymphoblastic leukemia/lymphoma without eosinophilia.Cancer Genet2017
26864375Segmental Chromosomal Aberrations in Localized Neuroblastoma Can be Detected in Formalin-Fixed Paraffin-Embedded Tissue Samples and Are Associated With Recurrence.Pediatr Blood Cancer2016
27547725Congenital B-lymphoblastic leukemia with a cryptic MLL rearrangement and post-treatment evolution to mixed phenotype acute leukemia.Leuk Res Rep2016
25098428RCSD1-ABL2 fusion resulting from a complex chromosomal rearrangement in high-risk B-cell acute lymphoblastic leukemia.Leuk Lymphoma2015
26575169Cerdulatinib, a novel dual SYK/JAK kinase inhibitor, has broad anti-tumor activity in both ABC and GCB types of diffuse large B cell lymphoma.Oncotarget2015
26600955RCSD1-ABL1 Translocation Associated with IKZF1 Gene Deletion in B-Cell Acute Lymphoblastic Leukemia.Case Rep Hematol2015
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Collaborators

Children's Hospital Los Angeles
Co-authored papers 11
Baylor College of Medicine
Co-authored papers 11
Mayo Clinic
Co-authored papers 10
Iowa State University, Mayo Clinic, Nationwide Children's Hospital, The Ohio State University College of Medicine, University of Iowa, Washington University in Saint Louis
Co-authored papers 9
Washington University
Co-authored papers 8
Innovation Center for Biomedical Informatics, Georgetown University Medical Center
Co-authored papers 8
Washington University
Co-authored papers 8
McDonnell Genome Institute, Washington University in St Louis School of Medicine
Co-authored papers 7
Innovation Center for Biomedical Informatics, Georgetown University Medical Center
Co-authored papers 7
The University of Texas MD Anderson Cancer Center
Co-authored papers 7
Co-authored papers 7
Washington University School of Medicine
Co-authored papers 7
Co-authored papers 6
Autism and Developmental Medicine Institute
Co-authored papers 6
Association for Molecular Pathology
Co-authored papers 6
German Cancer Consortium and German Cancer Research Center
Co-authored papers 5
National Cancer Institute
Co-authored papers 5
Mayo Clinic
Co-authored papers 4
Children's Hospital of Los Angeles
Co-authored papers 4
Texas Children's Hospital and Baylor College of Medicine
Co-authored papers 4
Washington University
Co-authored papers 4
Washington University
Co-authored papers 4
Washington University
Co-authored papers 4
Geisinger Autism & Developmental Medicine Institute
Co-authored papers 4
McDonnell Genome Institute, Washington University in St Louis School of Medicine
Co-authored papers 4
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 4
German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT)
Co-authored papers 4
Memorial Sloan Kettering Cancer Center
Co-authored papers 3
University of Maryland School of Medicine, Institute for Genome Sciences
Co-authored papers 3
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 3