Thale Kristin Olsen

Somatic RUNX1 exonic deletions in myelodysplastic syndrome: A rare yet high-risk recurrent genetic aberration

Al-Djaber, Ahmed; Österroos, Albin; Baldi, Alessandro; Munters, Arielle R. et al.

Ingår i HemaSphere, 2026

• DOI för Somatic RUNX1 exonic deletions in myelodysplastic syndrome: A rare yet high-risk recurrent genetic aberration
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The Nordic ChiCaP Network: An interdisciplinary approach to childhood cancer predisposition

Taylan, Fulya; Janhonen, Joel; Ekholm, Katja; Bajalica-Lagercrantz, Svetlana et al.

Ingår i Rare, 2025

• DOI för The Nordic ChiCaP Network: An interdisciplinary approach to childhood cancer predisposition
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Low Rate of Germline Investigation for Variants of Suspected Germline Origin Detected During the Diagnostic Work-Up of Myeloid Neoplasms

Al-Djaber, Ahmed; Munters, Arielle; Cammenga, Jörg; Pandzic, Tatjana et al.

Ingår i eJHaem, 2025

• DOI för Low Rate of Germline Investigation for Variants of Suspected Germline Origin Detected During the Diagnostic Work-Up of Myeloid Neoplasms
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Comparative Single-Cell Transcriptomics of Human Neuroblastoma and Preclinical Models Reveals Conservation of an Adrenergic Cell State

Embaie, Bethel Tesfai; Sarkar, Hirak; Alchahin, Adele M.; Otte, Jorg et al.

Ingår i Cancer Research, s. 1015-1034, 2025

• DOI för Comparative Single-Cell Transcriptomics of Human Neuroblastoma and Preclinical Models Reveals Conservation of an Adrenergic Cell State
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Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression

Milosevic, Jelena; Fransson, Susanne; Svensson, Johanna; Otte, Jorg et al.

Ingår i Cancer Letters, 2025

• DOI för Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression
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Somatic RUNX1 exonic deletions in myelodysplastic syndrome: A rare yet high-risk recurrent genetic aberration

Al-Djaber, Ahmed; Österroos, Albin; Baldi, Alessandro; Munters, Arielle R. et al.

Ingår i HemaSphere, 2026

• DOI för Somatic RUNX1 exonic deletions in myelodysplastic syndrome: A rare yet high-risk recurrent genetic aberration
• Ladda ner fulltext (pdf) av Somatic RUNX1 exonic deletions in myelodysplastic syndrome: A rare yet high-risk recurrent genetic aberration

The Nordic ChiCaP Network: An interdisciplinary approach to childhood cancer predisposition

Taylan, Fulya; Janhonen, Joel; Ekholm, Katja; Bajalica-Lagercrantz, Svetlana et al.

Ingår i Rare, 2025

• DOI för The Nordic ChiCaP Network: An interdisciplinary approach to childhood cancer predisposition
• Ladda ner fulltext (pdf) av The Nordic ChiCaP Network: An interdisciplinary approach to childhood cancer predisposition

Low Rate of Germline Investigation for Variants of Suspected Germline Origin Detected During the Diagnostic Work-Up of Myeloid Neoplasms

Al-Djaber, Ahmed; Munters, Arielle; Cammenga, Jörg; Pandzic, Tatjana et al.

Ingår i eJHaem, 2025

• DOI för Low Rate of Germline Investigation for Variants of Suspected Germline Origin Detected During the Diagnostic Work-Up of Myeloid Neoplasms
• Ladda ner fulltext (pdf) av Low Rate of Germline Investigation for Variants of Suspected Germline Origin Detected During the Diagnostic Work-Up of Myeloid Neoplasms

Comparative Single-Cell Transcriptomics of Human Neuroblastoma and Preclinical Models Reveals Conservation of an Adrenergic Cell State

Embaie, Bethel Tesfai; Sarkar, Hirak; Alchahin, Adele M.; Otte, Jorg et al.

Ingår i Cancer Research, s. 1015-1034, 2025

• DOI för Comparative Single-Cell Transcriptomics of Human Neuroblastoma and Preclinical Models Reveals Conservation of an Adrenergic Cell State
• Ladda ner fulltext (pdf) av Comparative Single-Cell Transcriptomics of Human Neuroblastoma and Preclinical Models Reveals Conservation of an Adrenergic Cell State

Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression

Milosevic, Jelena; Fransson, Susanne; Svensson, Johanna; Otte, Jorg et al.

Ingår i Cancer Letters, 2025

• DOI för Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression
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DHODH Inhibition Suppresses MYC and Inhibits the Growth of Medulloblastoma in a Novel In Vivo Zebrafish Model

Tsea, Ioanna; Olsen, Thale Kristin; Polychronopoulos, Panagiotis Alkinoos; Tummler, Conny et al.

Ingår i Cancers, 2024

• DOI för DHODH Inhibition Suppresses MYC and Inhibits the Growth of Medulloblastoma in a Novel In Vivo Zebrafish Model
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Epigenetic regulation of cell state by H2AFY governs immunogenicity in high-risk neuroblastoma

Nagarajan, Divya; Parracho, Rebeca T.; Corujo, David; Xie, Minglu et al.

Ingår i Journal of Clinical Investigation, 2024

• DOI för Epigenetic regulation of cell state by H2AFY governs immunogenicity in high-risk neuroblastoma
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Joint single-cell genetic and transcriptomic analysis reveal pre-malignant SCP-like subclones in human neuroblastoma

Olsen, Thale K.; Otte, Jörg; Mei, Shenglin; Embaie, Bethel Tesfai et al.

Ingår i Molecular Cancer, 2024

• DOI för Joint single-cell genetic and transcriptomic analysis reveal pre-malignant SCP-like subclones in human neuroblastoma
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Dormant SOX9-Positive Cells Facilitate MYC-Driven Recurrence of Medulloblastoma

Borgenvik, Anna; Holmberg, Karl O.; Bolin, Sara; Zhao, Miao et al.

Ingår i Cancer Research, s. 4586-4603, 2022

• DOI för Dormant SOX9-Positive Cells Facilitate MYC-Driven Recurrence of Medulloblastoma
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DHODH is an independent prognostic marker and potent therapeutic target in neuroblastoma

Olsen, Thale Kristin; Dyberg, Cecilia; Embaie, Bethel Tesfai; Alchahin, Adele et al.

Ingår i JCI Insight, 2022

• DOI för DHODH is an independent prognostic marker and potent therapeutic target in neuroblastoma
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