Publikationer i DiVA – Viktor Ljungström
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Clonal haematopoiesis as a risk factor for therapy-related myeloid neoplasms in patients with chronic lymphocytic leukaemia treated with chemo-(immuno)therapy
Ingår i British Journal of Haematology, s. 103-113, 2022.
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Familial platelet disorder due to germline exonic deletions in RUNX1: a diagnostic challenge with distinct alterations of the transcript isoform equilibrium
Ingår i Leukemia and Lymphoma, s. 2311-2320, 2022.
DOI för Familial platelet disorder due to germline exonic deletions in RUNX1: a diagnostic challenge with distinct alterations of the transcript isoform equilibrium Ladda ner fulltext (pdf) av Familial platelet disorder due to germline exonic deletions in RUNX1: a diagnostic challenge with distinct alterations of the transcript isoform equilibrium
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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
Ingår i HemaSphere, 2022.
DOI för 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 Ladda ner fulltext (pdf) av 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
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A single-tube multiplex method for monitoring mutations in cysteine 481 of Bruton Tyrosine Kinase (BTK) gene in chronic lymphocytic leukemia patients treated with ibrutinib
Ingår i Leukemia and Lymphoma, s. 2018-2021, 2021.
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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
Ingår i Haematologica, s. 682-691, 2021.
DOI för Comparative analysis of targeted next-generation sequencing panels for the detection of gene mutations in chronic lymphocytic leukemia: an ERIC multi-center study Ladda ner fulltext (pdf) av Comparative analysis of targeted next-generation sequencing panels for the detection of gene mutations in chronic lymphocytic leukemia: an ERIC multi-center study
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Consistent B Cell Receptor Immunoglobulin Features Between Siblings in Familial Chronic Lymphocytic Leukemia
Ingår i Frontiers in Oncology, 2021.
DOI för Consistent B Cell Receptor Immunoglobulin Features Between Siblings in Familial Chronic Lymphocytic Leukemia Ladda ner fulltext (pdf) av Consistent B Cell Receptor Immunoglobulin Features Between Siblings in Familial Chronic Lymphocytic Leukemia
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Prognostic and Predictive Implications of Cytogenetics and Genomics
Ingår i Hematology/Oncology Clinics of North America, s. 703-713, 2021.
DOI för Prognostic and Predictive Implications of Cytogenetics and Genomics Ladda ner fulltext (pdf) av Prognostic and Predictive Implications of Cytogenetics and Genomics
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Clonal hematopoiesis in patients with high-grade B-cell lymphoma is associated with inferior outcome
Ingår i American Journal of Hematology, s. E287-E289, 2020.
DOI för Clonal hematopoiesis in patients with high-grade B-cell lymphoma is associated with inferior outcome Ladda ner fulltext (pdf) av Clonal hematopoiesis in patients with high-grade B-cell lymphoma is associated with inferior outcome
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Defining eligible patients for allele-selective chemotherapies targeting NAT2 in colorectal cancer
Ingår i Scientific Reports, 2020.
DOI för Defining eligible patients for allele-selective chemotherapies targeting NAT2 in colorectal cancer Ladda ner fulltext (pdf) av Defining eligible patients for allele-selective chemotherapies targeting NAT2 in colorectal cancer
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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
Ingår i Acta Oncologica, s. 417-426, 2020.
DOI för Molecular characterization of a large unselected cohort of metastatic colorectal cancers in relation to primary tumor location, rare metastatic sites and prognosis Ladda ner fulltext (pdf) av Molecular characterization of a large unselected cohort of metastatic colorectal cancers in relation to primary tumor location, rare metastatic sites and prognosis
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Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort
Ingår i Scientific Reports, 2020.
DOI för Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort Ladda ner fulltext (pdf) av Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort
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DNA methylation profiles in chronic lymphocytic leukemia patients treated with chemoimmunotherapy
Ingår i Clinical Epigenetics, 2019.
DOI för DNA methylation profiles in chronic lymphocytic leukemia patients treated with chemoimmunotherapy Ladda ner fulltext (pdf) av DNA methylation profiles in chronic lymphocytic leukemia patients treated with chemoimmunotherapy
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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
Ingår i Haematologica, s. 865-873, 2018.
DOI för Highly similar genomic landscapes in monoclonal B-cell lymphocytosis and ultra-stable chronic lymphocytic leukemia with low frequency of driver mutations Ladda ner fulltext (pdf) av Highly similar genomic landscapes in monoclonal B-cell lymphocytosis and ultra-stable chronic lymphocytic leukemia with low frequency of driver mutations
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Not so lost in translation: RPS15 mutations in CLL
Ingår i Blood, s. 2317-2319, 2018.
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Transcriptome sequencing provides novel insights into the biology of chronic lymphocytic leukemia: focus on major stereotyped subsets
Ingår i Leukemia and Lymphoma, s. 220-221, 2017.
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Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemia
Ingår i Leukemia, s. 2179-2186, 2016.
DOI för Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemia Ladda ner fulltext (pdf) av Genomic disruption of the histone methyltransferase SETD2 in chronic lymphocytic leukaemia
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Molecular Profiling In A Population Based Cohort Of Nordic Myelodysplastic Syndrome Patients
Ingår i Haematologica, s. 72-72, 2016.
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Transposon Mutagenesis Reveals Fludarabine Resistance Mechanisms in Chronic Lymphocytic Leukemia
Ingår i Clinical Cancer Research, s. 6217-6227, 2016.
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Bioinformatic Challenges in Clinical Diagnostic Application of Targeted Next Generation Sequencing: Experience from Pheochromocytoma
Ingår i PLOS ONE, 2015.
DOI för Bioinformatic Challenges in Clinical Diagnostic Application of Targeted Next Generation Sequencing: Experience from Pheochromocytoma Ladda ner fulltext (pdf) av Bioinformatic Challenges in Clinical Diagnostic Application of Targeted Next Generation Sequencing: Experience from Pheochromocytoma
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DISSECTING RESISTANCE MECHANISMS IN CHRONIC LYMPHOCYTIC LEUKEMIA USING WHOLE-EXOME SEQUENCING: IMPACT OF RECURRENT RPS15 MUTATIONS ON P53 DYSREGULATION
Ingår i Haematologica, s. 10-11, 2015.
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EGR2 Mutations in Chronic Lymphocytic Leukemia: A New Bad Player
Ingår i Blood, 2015.
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EGR2 mutations in chronic lymphocytic leukemiam - a new bad player?
Ingår i Leukemia and Lymphoma, s. 83-85, 2015.
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Functional loss of IκBε leads to NF-κB deregulation in aggressive chronic lymphocytic leukemia
Ingår i Journal of Experimental Medicine, s. 833-843, 2015.
DOI för Functional loss of IκBε leads to NF-κB deregulation in aggressive chronic lymphocytic leukemia Ladda ner fulltext (pdf) av Functional loss of IκBε leads to NF-κB deregulation in aggressive chronic lymphocytic leukemia
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Genetics and Prognostication in Splenic Marginal Zone Lymphoma: Revelations from Deep Sequencing
Ingår i Clinical Cancer Research, s. 4174-4183, 2015.
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HaloPlex Targeted Resequencing for Mutation Detection in Clinical Formalin-Fixed, Paraffin-Embedded Tumor Samples
Ingår i Journal of Molecular Diagnostics, s. 729-739, 2015.
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Targeted next-generation sequencing in chronic lymphocytic leukemia: a high-throughput yet tailored approach will facilitate implementation in a clinical setting
Ingår i Haematologica, s. 370-376, 2015.
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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
Ingår i American Journal of Pathology, s. 1600-1609, 2015.
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Hög tid att söka till nya MD/PhD-programmet vid Uppsala universitet: Tidig bro mellan preklinisk forskning och klinik
Ingår i Läkartidningen, s. 898-898, 2012.