Arielle Munters

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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Clonal hematopoiesis of indeterminate potential in high grade B-cell lymphomas: clinicobiological associations and further insight with single-cell multiomics analysis

Hesselager, Caroline; Hollander, Peter; Pettersson, Emma; Enblad, Gunilla et al.

Ingår i Blood Cancer Journal, 2026

• DOI för Clonal hematopoiesis of indeterminate potential in high grade B-cell lymphomas: clinicobiological associations and further insight with single-cell multiomics analysis
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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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Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel

Orsmark‐Pietras, Christina; Lyander, Anna; Ladenvall, Claes; Hallström, Björn et al.

Ingår i Genes, Chromosomes and Cancer, 2024

• DOI för Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel
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Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancer

Baliakas, Panagiotis; Munters, Arielle R; Kämpe, Anders; Tesi, Bianca et al.

Ingår i Journal of Medical Genetics, s. 150-154, 2024

• DOI för Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancer
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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

Clonal hematopoiesis of indeterminate potential in high grade B-cell lymphomas: clinicobiological associations and further insight with single-cell multiomics analysis

Hesselager, Caroline; Hollander, Peter; Pettersson, Emma; Enblad, Gunilla et al.

Ingår i Blood Cancer Journal, 2026

• DOI för Clonal hematopoiesis of indeterminate potential in high grade B-cell lymphomas: clinicobiological associations and further insight with single-cell multiomics analysis
• Ladda ner fulltext (pdf) av Clonal hematopoiesis of indeterminate potential in high grade B-cell lymphomas: clinicobiological associations and further insight with single-cell multiomics analysis

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

Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel

Orsmark‐Pietras, Christina; Lyander, Anna; Ladenvall, Claes; Hallström, Björn et al.

Ingår i Genes, Chromosomes and Cancer, 2024

• DOI för Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel
• Ladda ner fulltext (pdf) av Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel

Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancer

Baliakas, Panagiotis; Munters, Arielle R; Kämpe, Anders; Tesi, Bianca et al.

Ingår i Journal of Medical Genetics, s. 150-154, 2024

• DOI för Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancer
• Ladda ner fulltext (pdf) av Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancer

The genetic history of Scandinavia from the Roman Iron Age to the present

Rodríguez-Varela, Ricardo; Moore, Kristjan H.S.; Ebenesersdóttir, S. Sunna; Kilinc, Gulsah Merve et al.

Ingår i Cell, s. 32-460000000000000000000, 2023

• DOI för The genetic history of Scandinavia from the Roman Iron Age to the present
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Genome of Peştera Muierii skull shows high diversity and low mutational load in pre-glacial Europe

Svensson, Emma; Günther, Torsten; Hoischen, Alexander; Hervella, Montserrat et al.

Ingår i Current Biology, s. 2973-U21, 2021

• DOI för Genome of Peştera Muierii skull shows high diversity and low mutational load in pre-glacial Europe
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Variable kinship patterns in Neolithic Anatolia revealed by ancient genomes

Yaka, Reyhan; Mapelli, Igor; Kaptan, Damla; Dogu, Ayca et al.

Ingår i Current Biology, s. 2455-2.468e+21, 2021

• DOI för Variable kinship patterns in Neolithic Anatolia revealed by ancient genomes
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Competitive mapping allows for the identification and exclusion of human DNA contamination in ancient faunal genomic datasets

Feuerborn, Tatiana R.; Palkopoulou, Eleftheria; van der Valk, Tom; von Seth, Johanna et al.

Ingår i BMC Genomics, 2020

• DOI för Competitive mapping allows for the identification and exclusion of human DNA contamination in ancient faunal genomic datasets
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Illuminating Genetic Mysteries of the Dead Sea Scrolls

Anava, Sarit; Neuhof, Moran; Gingold, Hila; Sagy, Or et al.

Ingår i Cell, s. 1218-+, 2020

• DOI för Illuminating Genetic Mysteries of the Dead Sea Scrolls

The Neolithic Pitted Ware culture foragers were culturally but not genetically influenced by the Battle Axe culture herders

Coutinho, Alexandra; Günther, Torsten; Munters, Arielle R.; Svensson, Emma M. et al.

Ingår i American Journal of Physical Anthropology, s. 638-649, 2020

• DOI för The Neolithic Pitted Ware culture foragers were culturally but not genetically influenced by the Battle Axe culture herders
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The genomic ancestry of the Scandinavian Battle Axe Culture people and their relation to the broader Corded Ware horizon

Malmström, Helena; Günther, Torsten; Svensson, Emma M.; Juras, Anna et al.

Ingår i Proceedings of the Royal Society of London. Biological Sciences, 2019

• DOI för The genomic ancestry of the Scandinavian Battle Axe Culture people and their relation to the broader Corded Ware horizon
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Genetic data and radiocarbon dating question Plovers Lake as a Middle Stone Age hominin-bearing site

Lombard, Marlize; Malmström, Helena; Schlebusch, Carina; Svensson, Emma et al.

Ingår i Journal of Human Evolution, s. 203-209, 2019

• DOI för Genetic data and radiocarbon dating question Plovers Lake as a Middle Stone Age hominin-bearing site

Population genomics of Mesolithic Scandinavia: Investigating early postglacial migration routes and high-latitude adaptation

Günther, Torsten; Malmström, Helena; Svensson, Emma; Omrak, Ayca et al.

Ingår i PLoS biology, 2018

• DOI för Population genomics of Mesolithic Scandinavia: Investigating early postglacial migration routes and high-latitude adaptation
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Southern African ancient genomes estimate modern human divergence to 350,000 to 260,000 years ago

Schlebusch, Carina; Malmström, Helena; Günther, Torsten; Sjödin, Per et al.

Ingår i Science, s. 652-655, 2017

• DOI för Southern African ancient genomes estimate modern human divergence to 350,000 to 260,000 years ago

The mitogenome of a 35,000-year-old Homo sapiens from Europe supports a Palaeolithic back-migration to Africa

Hervella, M.; Svensson, Emma M.; Alberdi, A.; Günther, Torsten et al.

Ingår i Scientific Reports, 2016

• DOI för The mitogenome of a 35,000-year-old Homo sapiens from Europe supports a Palaeolithic back-migration to Africa
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