Genomics and omics

Mutational signatures

10 papers and 6 abstracts co-authored by Raphael E. Szalat. Current lab members are shown in bold.

Papers 10

  1. 2026

    Genomically Smoldering Multiple Myeloma Is Not a Distinct Entity But a Collection of Monoclonal Gammopathy of Undetermined Significance or Multiple Myeloma

    Aktas Samur A, Corre J, Talluri S, …, Szalat R, …, Samur MK

    Journal of Clinical Oncology44(4):321-334DOI: Genomically Smoldering Multiple Myeloma Is Not a Distinct Entity But a Collection of Monoclonal Gammopathy of Undetermined Significance or Multiple MyelomaPubMed: Genomically Smoldering Multiple Myeloma Is Not a Distinct Entity But a Collection of Monoclonal Gammopathy of Undetermined Significance or Multiple Myeloma

  2. 2023

    High-dose melphalan treatment significantly increases mutational burden at relapse in multiple myeloma

    Samur MK, Roncador M, Aktas Samur A, …, Szalat R, …, Munshi NC

    Blood141(14):1724-1736DOI: High-dose melphalan treatment significantly increases mutational burden at relapse in multiple myelomaPubMed: High-dose melphalan treatment significantly increases mutational burden at relapse in multiple myeloma

  3. 2021

    Genetic Predictors of Mortality in Patients with Multiple Myeloma

    Hassan H, Szalat R

    The Application of Clinical GeneticsVolume 14:241-254DOI: Genetic Predictors of Mortality in Patients with Multiple MyelomaPubMed: Genetic Predictors of Mortality in Patients with Multiple Myeloma

  4. 2021

    IgM-MM is predominantly a pre–germinal center disorder and has a distinct genomic and transcriptomic signature from WM

    Bazarbachi AH, Avet-Loiseau H, Szalat R, …, Samur MK

    Blood138(20):1980-1985DOI: IgM-MM is predominantly a pre–germinal center disorder and has a distinct genomic and transcriptomic signature from WMPubMed: IgM-MM is predominantly a pre–germinal center disorder and has a distinct genomic and transcriptomic signature from WM

  5. 2020

    Genome-Wide Somatic Alterations in Multiple Myeloma Reveal a Superior Outcome Group

    Samur MK, Aktas Samur A, Fulciniti M, Szalat R, …, Munshi NC

    Journal of Clinical Oncology38(27):3107-3118DOI: Genome-Wide Somatic Alterations in Multiple Myeloma Reveal a Superior Outcome GroupPubMed: Genome-Wide Somatic Alterations in Multiple Myeloma Reveal a Superior Outcome Group

  6. 2019

    Genomic landscape and chronological reconstruction of driver events in multiple myeloma

    Maura F, Bolli N, Angelopoulos N, …, Szalat R, …, Campbell PJ

    Nature Communications10(1)DOI: Genomic landscape and chronological reconstruction of driver events in multiple myelomaPubMed: Genomic landscape and chronological reconstruction of driver events in multiple myeloma

  7. 2018

    Genomic patterns of progression in smoldering multiple myeloma

    Bolli N, Maura F, Minvielle S, …, Szalat R, …, Munshi N

    Nature Communications9(1)DOI: Genomic patterns of progression in smoldering multiple myelomaPubMed: Genomic patterns of progression in smoldering multiple myeloma

  8. 2018

    Identification of novel mutational drivers reveals oncogene dependencies in multiple myeloma

    Walker BA, Mavrommatis K, Wardell CP, …, Szalat R, …, Morgan GJ

    Blood132(6):587-597DOI: Identification of novel mutational drivers reveals oncogene dependencies in multiple myelomaPubMed: Identification of novel mutational drivers reveals oncogene dependencies in multiple myeloma

  9. 2017

    Biological and prognostic impact of APOBEC-induced mutations in the spectrum of plasma cell dyscrasias and multiple myeloma cell lines

    Maura F, Petljak M, Lionetti M, …, Szalat R, …, Bolli N

    Leukemia32(4):1043-1047DOI: Biological and prognostic impact of APOBEC-induced mutations in the spectrum of plasma cell dyscrasias and multiple myeloma cell linesPubMed: Biological and prognostic impact of APOBEC-induced mutations in the spectrum of plasma cell dyscrasias and multiple myeloma cell lines

  10. 2015

    Genomic heterogeneity in multiple myeloma

    Szalat R, Munshi NC

    Current Opinion in Genetics & Development30:56-65DOI: Genomic heterogeneity in multiple myelomaPubMed: Genomic heterogeneity in multiple myeloma

Abstracts & posters 6

  1. 2020

    High-Dose Melphalan Significantly Increases Mutational Burden in Multiple Myeloma Cells at Relapse: Results from a Randomized Study in Multiple Myeloma

    Samur MK, Roncador M, Aktas-Samur A, …, Szalat R, …, Munshi NC

    Blood136(Supplement 1):4-5DOI: High-Dose Melphalan Significantly Increases Mutational Burden in Multiple Myeloma Cells at Relapse: Results from a Randomized Study in Multiple Myeloma

  2. 2018

    Analysis of mutations and structural variants to redefine the genomic landscape of multiple myeloma and its clinical implications

    Bolli N, Maura F, Dawson KJ, Angelopoulos N, Minvielle S, Martincorena I, et al.

    Haematologica103(S3):S51-S51

  3. 2018

    Landscape of Recurrent Mutations in Non-Coding Genome with Functional Implications in Newly-Diagnosed Multiple Myeloma

    Samur MK, Chakraborty C, Szalat R, …, Munshi N

    Blood132(Supplement 1):190-190DOI: Landscape of Recurrent Mutations in Non-Coding Genome with Functional Implications in Newly-Diagnosed Multiple Myeloma

  4. 2017

    The apobec mutational activity in multiple myeloma: from diagnosis to cell lines

    Maura F, Petljak M, Minvielle S, Szalat R, Lionetti M, Cifola I, Liang W, et al.

    haematologica102(suppl. 3):124-124

  5. 2016

    Analysis of Mutational Signatures Suggest That Aid Has an Early and Driver Role in Multiple Myeloma

    Maura F, Bolli N, Minvielle S, …, Szalat R, …, Munshi N

    Blood128(22):116-116DOI: Analysis of Mutational Signatures Suggest That Aid Has an Early and Driver Role in Multiple Myeloma

  6. 2016

    Global Genomic Analysis of Newly Diagnosed t(4 ;14) Multiple Myeloma Reveals a Specific Mutational Spectrum and Identifies PKD2 As a Potential Therapeutic Target

    Song XL, Szalat R, Talbot A, …, Bories JC

    Blood128(22):4462-4462DOI: Global Genomic Analysis of Newly Diagnosed t(4 ;14) Multiple Myeloma Reveals a Specific Mutational Spectrum and Identifies PKD2 As a Potential Therapeutic Target