Lotte Moens

The FOCU.SE trial: a nationwide Swedish drug repurposing protocol and research framework

Abel, Edvard; Ostling, Paivi; Hult, Ebba Hallersjo; Kulbacka, Katarzyna et al.

Ingår i Acta Oncologica, s. 268-272, 2026

• DOI för The FOCU.SE trial: a nationwide Swedish drug repurposing protocol and research framework
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The evolutionary history of metastatic pancreatic neuroendocrine tumours reveals a therapy driven route to high-grade transformation

Backman, Samuel; Botling, Johan; Nord, Helena; Ghosal, Suman et al.

Ingår i Journal of Pathology, s. 357-370, 2024

• DOI för The evolutionary history of metastatic pancreatic neuroendocrine tumours reveals a therapy driven route to high-grade transformation
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Comparison of ROS1-rearrangement detection methods in a cohort of surgically resected non-small cell lung carcinomas

Thurfjell, Viktoria; Micke, Patrick; Yu, Hui; Krupar, Rosemarie et al.

Ingår i Translational Lung Cancer Research, s. 2477-2494, 2022

• DOI för Comparison of ROS1-rearrangement detection methods in a cohort of surgically resected non-small cell lung carcinomas
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Evaluation of NTRK immunohistochemistry as a screening method for NTRK gene fusion detection in non-small cell lung cancer

Elfving, Hedvig; Broström, Erika; Moens, Lotte N.J.; Almlöf, Jonas et al.

Ingår i Lung Cancer, s. 53-59, 2021

• DOI för Evaluation of NTRK immunohistochemistry as a screening method for NTRK gene fusion detection in non-small cell lung cancer

Mutation patterns in a population-based non-small cell lung cancer cohort and prognostic impact of concomitant mutations in KRAS and TP53 or STK11

La Fleur, Linnea; Falk-Sörqvist, Elin; Smeds, Patrik; Berglund, Anders et al.

Ingår i Lung Cancer, s. 50-58, 2019

• DOI för Mutation patterns in a population-based non-small cell lung cancer cohort and prognostic impact of concomitant mutations in KRAS and TP53 or STK11
• Ladda ner fulltext (pdf) av Mutation patterns in a population-based non-small cell lung cancer cohort and prognostic impact of concomitant mutations in KRAS and TP53 or STK11

The FOCU.SE trial: a nationwide Swedish drug repurposing protocol and research framework

Abel, Edvard; Ostling, Paivi; Hult, Ebba Hallersjo; Kulbacka, Katarzyna et al.

Ingår i Acta Oncologica, s. 268-272, 2026

• DOI för The FOCU.SE trial: a nationwide Swedish drug repurposing protocol and research framework
• Ladda ner fulltext (pdf) av The FOCU.SE trial: a nationwide Swedish drug repurposing protocol and research framework

The evolutionary history of metastatic pancreatic neuroendocrine tumours reveals a therapy driven route to high-grade transformation

Backman, Samuel; Botling, Johan; Nord, Helena; Ghosal, Suman et al.

Ingår i Journal of Pathology, s. 357-370, 2024

• DOI för The evolutionary history of metastatic pancreatic neuroendocrine tumours reveals a therapy driven route to high-grade transformation
• Ladda ner fulltext (pdf) av The evolutionary history of metastatic pancreatic neuroendocrine tumours reveals a therapy driven route to high-grade transformation

Comparison of ROS1-rearrangement detection methods in a cohort of surgically resected non-small cell lung carcinomas

Thurfjell, Viktoria; Micke, Patrick; Yu, Hui; Krupar, Rosemarie et al.

Ingår i Translational Lung Cancer Research, s. 2477-2494, 2022

• DOI för Comparison of ROS1-rearrangement detection methods in a cohort of surgically resected non-small cell lung carcinomas
• Ladda ner fulltext (pdf) av Comparison of ROS1-rearrangement detection methods in a cohort of surgically resected non-small cell lung carcinomas

Evaluation of NTRK immunohistochemistry as a screening method for NTRK gene fusion detection in non-small cell lung cancer

Elfving, Hedvig; Broström, Erika; Moens, Lotte N.J.; Almlöf, Jonas et al.

Ingår i Lung Cancer, s. 53-59, 2021

• DOI för Evaluation of NTRK immunohistochemistry as a screening method for NTRK gene fusion detection in non-small cell lung cancer

Mutation patterns in a population-based non-small cell lung cancer cohort and prognostic impact of concomitant mutations in KRAS and TP53 or STK11

La Fleur, Linnea; Falk-Sörqvist, Elin; Smeds, Patrik; Berglund, Anders et al.

Ingår i Lung Cancer, s. 50-58, 2019

• DOI för Mutation patterns in a population-based non-small cell lung cancer cohort and prognostic impact of concomitant mutations in KRAS and TP53 or STK11
• Ladda ner fulltext (pdf) av Mutation patterns in a population-based non-small cell lung cancer cohort and prognostic impact of concomitant mutations in KRAS and TP53 or STK11

Drug sensitivity testing on patient-derived sarcoma cells predicts patient response to treatment and identifies c-Sarc inhibitors as active drugs for translocation sarcomas

Brodin, Bertha A.; Wennerberg, Krister; Lidbrink, Elisabet; Brosjö, Otte et al.

Ingår i British Journal of Cancer, s. 435-443, 2019

• DOI för Drug sensitivity testing on patient-derived sarcoma cells predicts patient response to treatment and identifies c-Sarc inhibitors as active drugs for translocation sarcomas

Somatic Ephrin Receptor Mutations Are Associated with Metastasis in Primary Colorectal Cancer

Mathot, Lucy; Kundu, Snehangshu; Ljungström, Viktor; Svedlund, Jessica et al.

Ingår i Cancer Research, s. 1730-1740, 2017

• DOI för Somatic Ephrin Receptor Mutations Are Associated with Metastasis in Primary Colorectal Cancer

Mutation Profiling by Targeted Next Generation Sequencing of an Unselected NSCLC Cohort

La Fleur, Linnea; Falk-Sörqvist, Elin; Smeds, Patrik; Sundström, Magnus et al.

Ingår i Journal of Thoracic Oncology, 2017

• DOI för Mutation Profiling by Targeted Next Generation Sequencing of an Unselected NSCLC Cohort

Establishing Reflex NGS Testing in NSCLC in a Regional Network of County Hospitals in Central Sweden

Isaksson, Johan; Willen, Linda; La Fleur, Linnea; Mindus, Stephanie et al.

Ingår i Journal of Thoracic Oncology, 2017

• DOI för Establishing Reflex NGS Testing in NSCLC in a Regional Network of County Hospitals in Central Sweden

Mutation Profiling by Targeted Next-Generation Sequencing for Diagnostics and Patient Cohort Screening in FFPE NSCLC Samples

La Fleur, Linnea; Moens, Lotte; Falk-Sörqvist, Elin; Sundström, Magnus et al.

Ingår i Journal of Thoracic Oncology, 2015

HaloPlex Targeted Resequencing for Mutation Detection in Clinical Formalin-Fixed, Paraffin-Embedded Tumor Samples

Moens, Lotte N. J.; Falk-Sörqvist, Elin; Ljungström, Viktor; Mattsson, Johanna et al.

Ingår i Journal of Molecular Diagnostics, s. 729-739, 2015

• DOI för HaloPlex Targeted Resequencing for Mutation Detection in Clinical Formalin-Fixed, Paraffin-Embedded Tumor Samples

Clinical Validation of HaloPlex Targeted Resequencing in Formalin-Fixed, Paraffin-Embedded (FFPE) Cancer Biopsies

Moens, Lotte. N.; Falk-Sörqvist, Elin; La Fleur, Linnea; Mattsson, Johanna et al.

Ingår i Journal of Molecular Diagnostics, s. 822-822, 2015

Susceptibility to infections, without concomitant hyper-IgE, reported in 1976, is caused by hypomorphic mutation in the phosphoglucomutase 3 (PGM3) gene

Lundin, Karin E.; Hamasy, Abdulrahman; Backe, Paul Hoff; Moens, Lotte N. et al.

Ingår i Clinical Immunology, s. 366-372, 2015

• DOI för Susceptibility to infections, without concomitant hyper-IgE, reported in 1976, is caused by hypomorphic mutation in the phosphoglucomutase 3 (PGM3) gene
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Diagnostics of Primary Immunodeficiency Diseases: A Sequencing Capture Approach

Moens, Lotte N.; Falk-Sörqvist, Elin; Asplund, A. Charlotta; Bernatowska, Ewa et al.

Ingår i PLOS ONE, 2014

• DOI för Diagnostics of Primary Immunodeficiency Diseases: A Sequencing Capture Approach
• Ladda ner fulltext (pdf) av Diagnostics of Primary Immunodeficiency Diseases: A Sequencing Capture Approach

Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels

Sassi, Atfa; Lazaroski, Sandra; Wu, Gang; Haslam, Stuart M. et al.

Ingår i Journal of Allergy and Clinical Immunology, s. 1410-U681, 2014

• DOI för Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels

Targeted Resequencing of Formalin-Fixed, Paraffin-Embedded (FFPE) Specimens for Mutation Diagnostics in Solid Tumors

Botling, Johan; Moens, Lotte N.; Sorqvist, Elin Falk; Sundström, Magnus et al.

Ingår i Journal of Molecular Diagnostics, s. 916-916, 2013

Hypomorphic, Homozygous Mutations In Phosphoglucomutase-3 Impair Immunity And Increase Serum IgE Levels

Sassi, Atfa; Lazaroski, Sandra; Wu, Gang; Haslam, Stuart M. et al.

Ingår i Clinical and Experimental Immunology, s. 2-2, 2013

Automated Genotyping of Biobank Samples by Multiplex Amplification of Insertion/Deletion Polymorphisms

Mathot, Lucy; Falk Sörqvist, Elin; Moens, Lotte; Allen, Marie et al.

Ingår i PLOS ONE, 2012

• DOI för Automated Genotyping of Biobank Samples by Multiplex Amplification of Insertion/Deletion Polymorphisms
• Ladda ner fulltext (pdf) av Automated Genotyping of Biobank Samples by Multiplex Amplification of Insertion/Deletion Polymorphisms

Large-scale mutation analysis of primary immunodeficiency patients by next-generation sequencing

Asplund, A. C.; Falk, Elin; Moens, Lotte; Kumar, Y. et al.

Ingår i Journal of Clinical Immunology, s. 227-228, 2012

Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.

Moens, Lotte N; De Rijk, Peter; Reumers, Joke; Van den Bossche, Maarten J A et al.

Ingår i PLOS ONE, 2011

• DOI för Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.

PCM1 and schizophrenia: a replication study in the Northern Swedish population.

Moens, Lotte N; Ceulemans, Shana; Alaerts, Maaike; Van Den Bossche, Maarten J A et al.

Ingår i American Journal of Medical Genetics Part B, s. 1240-3, 2010

• DOI för PCM1 and schizophrenia: a replication study in the Northern Swedish population.

Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing.

Goossens, Dirk; Moens, Lotte N; Nelis, Eva; Lenaerts, An-Sofie et al.

Ingår i Human Mutation, s. 472-6, 2009

• DOI för Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing.

Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated population.

Alaerts, Maaike; Ceulemans, Shana; Forero, Diego; Moens, Lotte N et al.

Ingår i Archives of General Psychiatry, s. 828-37, 2009

• DOI för Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated population.

New technologies for DNA analysis: a review of the READNA Project

McGinn, Steven; Bauer, David; Brefort, Thomas; Dong, Liqin et al.

Ingår i New Biotechnology, s. 311-330, 2016

• DOI för New technologies for DNA analysis: a review of the READNA Project