Search Results - "Ljungstrom, Viktor"
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Prognostic and Predictive Implications of Cytogenetics and Genomics
Published in Hematology/oncology clinics of North America (01-08-2021)“…Chronic lymphocytic leukemia (CLL) is characterized by extreme genomic heterogeneity. Numerous recurrent genetic abnormalities are associated with dismal…”
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Not so lost in translation: RPS15 mutations in CLL
Published in Blood (29-11-2018)“…In this issue of Blood, Bretones et al expand knowledge of the functional consequences of recurrent mutations in RPS15, a gene that encodes a ribosomal protein…”
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Accurate and sensitive mutational signature analysis with MuSiCal
Published in Nature genetics (01-03-2024)“…Mutational signature analysis is a recent computational approach for interpreting somatic mutations in the genome. Its application to cancer data has enhanced…”
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Tumor Vessel Up-Regulation of INSR Revealed by Single-Cell Expression Analysis of the Tyrosine Kinome and Phosphatome in Human Cancers
Published in The American journal of pathology (01-06-2015)“…The tyrosine kinome and phosphatome harbor oncogenes and tumor suppressor genes and important regulators of angiogenesis and tumor stroma formation. To provide…”
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Five Percent Variant Allele Frequency Is a Reliable Reporting Threshold for TP53 Variants Detected by Next Generation Sequencing in Chronic Lymphocytic Leukemia in the Clinical Setting
Published in HemaSphere (01-08-2022)“…The clinical significance of small TP53 clones detected with next generation sequencing (NGS) in chronic lymphocytic leukemia is an issue of active debate…”
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Bioinformatic Challenges in Clinical Diagnostic Application of Targeted Next Generation Sequencing: Experience from Pheochromocytoma
Published in PloS one (31-07-2015)“…Recent studies have demonstrated equal quality of targeted next generation sequencing (NGS) compared to Sanger Sequencing. Whereas these novel sequencing…”
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Clonal hematopoiesis in patients with high‐grade B‐cell lymphoma is associated with inferior outcome
Published in American journal of hematology (01-10-2020)Get full text
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BTK and PLCG2 remain unmutated in one-third of patients with CLL relapsing on ibrutinib
Published in Blood advances (27-06-2023)“…•One-third of patients with CLL relapsing on ibrutinib do not carry BTK/PLCG2 mutations, even with a 0.1% sensitivity.•Additional mechanisms, such as del(8p),…”
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Prognostic impact of epigenetic classification in chronic lymphocytic leukemia: The case of subset #2
Published in Epigenetics (02-06-2016)“…Based on the methylation status of 5 single CpG sites, a novel epigenetic classification of chronic lymphocytic leukemia (CLL) was recently proposed,…”
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Loss of Y and clonal hematopoiesis in blood—two sides of the same coin?
Published in Leukemia (01-03-2022)Get full text
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Whole-exome sequencing in relapsing chronic lymphocytic leukemia: clinical impact of recurrent RPS15 mutations
Published in Blood (25-02-2016)“…Fludarabine, cyclophosphamide, and rituximab (FCR) is first-line treatment of medically fit chronic lymphocytic leukemia (CLL) patients; however, despite good…”
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Genetics and Prognostication in Splenic Marginal Zone Lymphoma: Revelations from Deep Sequencing
Published in Clinical cancer research (15-09-2015)“…Mounting evidence supports the clinical significance of gene mutations and immunogenetic features in common mature B-cell malignancies. We undertook a detailed…”
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SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts
Published in Blood (09-07-2015)“…Refractory anemia with ring sideroblasts (RARS) is a myelodysplastic syndrome (MDS) characterized by isolated erythroid dysplasia and 15% or more bone marrow…”
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Highly similar genomic landscapes in monoclonal B-cell lymphocytosis and ultra-stable chronic lymphocytic leukemia with low frequency of driver mutations
Published in Haematologica (Roma) (01-05-2018)“…Despite the recent discovery of recurrent driver mutations in chronic lymphocytic leukemia, the genetic factors involved in disease onset remain largely…”
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Defining eligible patients for allele-selective chemotherapies targeting NAT2 in colorectal cancer
Published in Scientific reports (31-12-2020)“…Therapies targeting somatic bystander genetic events represent a new avenue for cancer treatment. We recently identified a subset of colorectal cancer (CRC)…”
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ERα-associated translocations underlie oncogene amplifications in breast cancer
Published in Nature (London) (29-06-2023)“…Focal copy-number amplification is an oncogenic event. Although recent studies have revealed the complex structure 1 – 3 and the evolutionary trajectories 4 of…”
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Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort
Published in Scientific reports (09-11-2020)“…Breast cancer (BC) is a genetically heterogeneous disease with high prevalence in Northern Europe. However, there has been no detailed investigation into the…”
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Molecular characterization of a large unselected cohort of metastatic colorectal cancers in relation to primary tumor location, rare metastatic sites and prognosis
Published in Acta oncologica (02-04-2020)“…We have reported that V600E mutations and microsatellite instability-high (MSI-H) are more prevalent in a population-based cohort of metastatic colorectal…”
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Comparative analysis of targeted next-generation sequencing panels for the detection of gene mutations in chronic lymphocytic leukemia: an ERIC multi-center study
Published in Haematologica (Roma) (01-03-2021)“…Next-generation sequencing (NGS) has transitioned from research to clinical routine, yet the comparability of different technologies for mutation profiling…”
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Somatic Ephrin Receptor Mutations Are Associated with Metastasis in Primary Colorectal Cancer
Published in Cancer research (Chicago, Ill.) (01-04-2017)“…The contribution of somatic mutations to metastasis of colorectal cancers is currently unknown. To find mutations involved in the colorectal cancer metastatic…”
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