Claes Ladenvall

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

Accumulation of high-risk genetic features after chemoimmunotherapy: A longitudinal study in mantle cell lymphoma

Nikkarinen, Anna; Almlöf, Jonas; Österroos, Albin; Ladenvall, Claes et al.

Ingår i Leukemia, s. 681-684, 2026

• DOI för Accumulation of high-risk genetic features after chemoimmunotherapy: A longitudinal study in mantle cell lymphoma

RAB3GAP2 is a regulator of skeletal muscle endothelial cell proliferation and associated with capillary-to-fiber ratio

Ström, Kristoffer; Oskolkov, Nikolay; Karaderi, Tugce; Kalamajski, Sebastian et al.

Ingår i Cell Reports, 2026

• DOI för RAB3GAP2 is a regulator of skeletal muscle endothelial cell proliferation and associated with capillary-to-fiber ratio
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Twist-ONT: Combining nanopore sequencing with the twist comprehensive viral research panel

Haars, Jonathan; Cumlin, Tomas; Ladenvall, Claes; Lennerstrand, Johan et al.

Ingår i Virology, 2026

• DOI för Twist-ONT: Combining nanopore sequencing with the twist comprehensive viral research panel

A novel PML germline variant as a candidate predisposing genetic aberration in familial acute myeloid leukaemia.

Soussi, Thierry; Kundu, Snehangshu; Gerbaud, Pauline; Pandzic, Tatjana et al.

Ingår i British Journal of Haematology, s. 1118-1121, 2025

• DOI för A novel PML germline variant as a candidate predisposing genetic aberration in familial acute myeloid leukaemia.
• Ladda ner fulltext (pdf) av A novel PML germline variant as a candidate predisposing genetic aberration in familial acute myeloid leukaemia.

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

Accumulation of high-risk genetic features after chemoimmunotherapy: A longitudinal study in mantle cell lymphoma

Nikkarinen, Anna; Almlöf, Jonas; Österroos, Albin; Ladenvall, Claes et al.

Ingår i Leukemia, s. 681-684, 2026

• DOI för Accumulation of high-risk genetic features after chemoimmunotherapy: A longitudinal study in mantle cell lymphoma

RAB3GAP2 is a regulator of skeletal muscle endothelial cell proliferation and associated with capillary-to-fiber ratio

Ström, Kristoffer; Oskolkov, Nikolay; Karaderi, Tugce; Kalamajski, Sebastian et al.

Ingår i Cell Reports, 2026

• DOI för RAB3GAP2 is a regulator of skeletal muscle endothelial cell proliferation and associated with capillary-to-fiber ratio
• Ladda ner fulltext (pdf) av RAB3GAP2 is a regulator of skeletal muscle endothelial cell proliferation and associated with capillary-to-fiber ratio

Twist-ONT: Combining nanopore sequencing with the twist comprehensive viral research panel

Haars, Jonathan; Cumlin, Tomas; Ladenvall, Claes; Lennerstrand, Johan et al.

Ingår i Virology, 2026

• DOI för Twist-ONT: Combining nanopore sequencing with the twist comprehensive viral research panel

A novel PML germline variant as a candidate predisposing genetic aberration in familial acute myeloid leukaemia.

Soussi, Thierry; Kundu, Snehangshu; Gerbaud, Pauline; Pandzic, Tatjana et al.

Ingår i British Journal of Haematology, s. 1118-1121, 2025

• DOI för A novel PML germline variant as a candidate predisposing genetic aberration in familial acute myeloid leukaemia.
• Ladda ner fulltext (pdf) av A novel PML germline variant as a candidate predisposing genetic aberration in familial acute myeloid leukaemia.

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

Single-cell sequencing reveals shared clonal signatures in nonmalignant B and tumor cells in T-prolymphocytic leukemia

Hesselager, Caroline; Thörn, Ingrid; Marincevic, Millaray; Ladenvall, Claes et al.

Ingår i Blood neoplasia, 2025

• DOI för Single-cell sequencing reveals shared clonal signatures in nonmalignant B and tumor cells in T-prolymphocytic leukemia
• Ladda ner fulltext (pdf) av Single-cell sequencing reveals shared clonal signatures in nonmalignant B and tumor cells in T-prolymphocytic leukemia

Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition: Results from a Prospective Cohort Study

Tesi, Bianca; Robelius, Anna; Baskin, Berivan; Lazarevic, Vladimir et al.

Ingår i Clinical Cancer Research, s. 3062-3071, 2025

• DOI för Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition: Results from a Prospective Cohort Study
• Ladda ner fulltext (pdf) av Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition: Results from a Prospective Cohort Study

Visualization using NIPTviewer support the clinical interpretation of noninvasive prenatal testing results

Smeds, Patrik; Baranowska Körberg, Izabella; Melin, Malin; Ladenvall, Claes

Ingår i BMC Medical Genomics, 2025

• DOI för Visualization using NIPTviewer support the clinical interpretation of noninvasive prenatal testing results
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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
• 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

From SARS-CoV-2 to Global Preparedness: A Graphical Interface for Standardised High-Throughput Bioinformatics Analysis in Pandemic Scenarios and Surveillance of Drug Resistance

Cumlin, Tomas; Karlsson, Ida; Haars, Jonathan; Rosengren, Maria et al.

Ingår i International Journal of Molecular Sciences, 2024

• DOI för From SARS-CoV-2 to Global Preparedness: A Graphical Interface for Standardised High-Throughput Bioinformatics Analysis in Pandemic Scenarios and Surveillance of Drug Resistance
• Ladda ner fulltext (pdf) av From SARS-CoV-2 to Global Preparedness: A Graphical Interface for Standardised High-Throughput Bioinformatics Analysis in Pandemic Scenarios and Surveillance of Drug Resistance

Novel pathological variants of NHP2 affect N-terminal domain flexibility, protein stability, H/ACA Ribonucleoprotein (RNP) complex formation and telomerase activity

Maliński, Bartosz; Vertemara, Jacopo; Faustini, Elena; Ladenvall, Claes et al.

Ingår i Human Molecular Genetics, s. 2901-2912, 2023

• DOI för Novel pathological variants of NHP2 affect N-terminal domain flexibility, protein stability, H/ACA Ribonucleoprotein (RNP) complex formation and telomerase activity
• Ladda ner fulltext (pdf) av Novel pathological variants of NHP2 affect N-terminal domain flexibility, protein stability, H/ACA Ribonucleoprotein (RNP) complex formation and telomerase activity

Genetic insights into resting heart rate and its role in cardiovascular disease

van de Vegte, Yordi; Eppinga, Ruben P.; van der Ende, M. Yldau; Hagemeijer, Yanick et al.

Ingår i Nature Communications, 2023

• DOI för Genetic insights into resting heart rate and its role in cardiovascular disease
• Ladda ner fulltext (pdf) av Genetic insights into resting heart rate and its role in cardiovascular disease

Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia

Eriksson, Anna; Engvall, Marie; Mathot, Lucy; Österroos, Albin et al.

Ingår i Clinical Cancer Research, s. 2826-2834, 2023

• DOI för Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia

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

Pandzic, Tatjana; Ladenvall, Claes; Engvall, Marie; Mattsson, Mattias et al.

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
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Arteria: An automation system for a sequencing core facility

Dahlberg, Johan; Hermansson, Johan; Sturlaugsson, Steinar; Lysenkova, Mariya et al.

Ingår i GigaScience, 2019

• DOI för Arteria: An automation system for a sequencing core facility
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Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis

Wheeler, Eleanor; Leong, Aaron; Liu, Ching-Ti; Hivert, Marie-France et al.

Ingår i PLoS Medicine, 2017

• DOI för Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
• Ladda ner fulltext (pdf) av Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis

A Gene-by-Environment Analysis of 184,428 Subjects Reveals a Role for Adaptive and Innate Immunity in Coronary Artery Disease in Subjects with Type 2 Diabetes

van Zuydam, Natalie R.; Voight, Benjamin F.; Ladenvall, Claes; Fernandez, Juan et al.

Ingår i Genetic Epidemiology, s. 668-668, 2016

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

Walford, Geoffrey A.; Gustafsson, Stefan; Rybin, Denis; Stancakova, Alena et al.

Ingår i Diabetes, s. 3200-3211, 2016

• DOI för Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

Molecular Profiling In A Population Based Cohort Of Nordic Myelodysplastic Syndrome Patients

Karimi, M.; Ljungström, Viktor; Hansen, J. Werner; Kittang, A. Olsnes et al.

Ingår i Haematologica, s. 72-72, 2016

Genome wide meta-analysis identifies novel regulators of circulating serum progranulin

Krueger, J.; Scholz, M.; Marzi, C.; Grallert, H. et al.

Ingår i Diabetologia, 2016

Accumulation of High-Risk Genetic Features after Chemoimmunotherapy: A Longitudinal Study in Mantle Cell Lymphoma

Nikkarinen, Anna; Almlöf, Jonas; Österroos, Albin; Ladenvall, Claes et al.

Impact of Clonal Hematopoiesis on Hematological Treatment Toxicity in Mantle Cell Lymphoma Patients

Nikkarinen, Anna; Selvin, Tove; Almlöf, Jonas; Österroos, Albin et al.