Helena Nord

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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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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Mixed gangliocytoma-pituitary neuroendocrine tumour: clinical, immunohistochemical, and molecular genetic profiles in a series of four patients

Dalakas, Konstantinos; Edén Engström, Britt; Tebani, Abdellah; Bontell, Thomas Olsson et al.

Ingår i Acta neuropathologica communications, 2026

• DOI för Mixed gangliocytoma-pituitary neuroendocrine tumour: clinical, immunohistochemical, and molecular genetic profiles in a series of four patients
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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
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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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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

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

Mixed gangliocytoma-pituitary neuroendocrine tumour: clinical, immunohistochemical, and molecular genetic profiles in a series of four patients

Dalakas, Konstantinos; Edén Engström, Britt; Tebani, Abdellah; Bontell, Thomas Olsson et al.

Ingår i Acta neuropathologica communications, 2026

• DOI för Mixed gangliocytoma-pituitary neuroendocrine tumour: clinical, immunohistochemical, and molecular genetic profiles in a series of four patients
• Ladda ner fulltext (pdf) av Mixed gangliocytoma-pituitary neuroendocrine tumour: clinical, immunohistochemical, and molecular genetic profiles in a series of four patients

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

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

Matched Analyses of Brain Metastases versus Primary Non-Small Cell Lung Cancer Reveal a Unique microRNA Signature

Tsakonas, Georgios; Koulouris, Andreas; Kazmierczak, Dominika; Botling, Johan et al.

Ingår i International Journal of Molecular Sciences, 2023

• DOI för Matched Analyses of Brain Metastases versus Primary Non-Small Cell Lung Cancer Reveal a Unique microRNA Signature
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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

An immune gene expression signature distinguishes central nervous system metastases from primary tumours in non-small-cell lung cancer

Tsakonas, Georgios; Lewensohn, Rolf; Botling, Johan; Ortiz-Villalon, Cristian et al.

Ingår i European Journal of Cancer, s. 24-34, 2020

• DOI för An immune gene expression signature distinguishes central nervous system metastases from primary tumours in non-small-cell lung cancer
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Genetic prevention of hepatitis C virus-induced liver fibrosis by allele-specific downregulation of MERTK

Cavalli, Marco; Pan, Gang; Nord, Helena; Wallén Arzt, Emelie et al.

Ingår i Hepatology Research, s. 826-830, 2017

• DOI för Genetic prevention of hepatitis C virus-induced liver fibrosis by allele-specific downregulation of MERTK

PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c

Pan, Gang; Ameur, Adam; Enroth, Stefan; Bysani, Madhusudhan et al.

Ingår i Nucleic Acids Research, s. 2408-2422, 2017

• DOI för PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c

Novel regulatory variant detected on the VKORC1 haplotype that is associated with warfarin dose

Cavalli, Marco; Pan, Gang; Nord, Helena; Eriksson, Niclas et al.

Ingår i Pharmacogenomics (London), s. 1305-1314, 2016

• DOI för Novel regulatory variant detected on the VKORC1 haplotype that is associated with warfarin dose
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lobChIP: from cells to sequencing ready ChIP libraries in a single day

Wallerman, Ola; Nord, Helena; Bysani, Madhusudhan; Borghini, Lisa et al.

Ingår i Epigenetics & Chromatin, 2015

• DOI för lobChIP: from cells to sequencing ready ChIP libraries in a single day
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Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling

Nord, Helena; Pfeifer, Susan; Nilsson, Pelle; Sandgren, Johanna et al.

Ingår i Journal of Neuro-Oncology, s. 37-49, 2012

• DOI för Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling

Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma

Nord, Helena; Segersten, Ulrika; Sandgren, Johanna; Wester, Kenneth et al.

Ingår i International Journal of Cancer, s. 1390-1402, 2010

• DOI för Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma

Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis

Sandgren, Johanna; Diaz de Ståhl, Teresita; Andersson, Robin; Menzel, Uwe et al.

Ingår i Endocrine-Related Cancer, s. 561-579, 2010

• DOI för Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis

Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array

Nord, Helena; Hartmann, Christian; Andersson, Robin; Menzel, Uwe et al.

Ingår i Neuro-Oncology, s. 803-818, 2009

• DOI för Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

de Ståhl, Teresita Díaz; Sandgren, Johanna; Piotrowski, Arkadiusz; Nord, Helena et al.

Ingår i Human Mutation, s. 398-408, 2008

• DOI för Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

A Segmental Maximum A Posteriori Approach to Genome-wide Copy Number Profiling

Andersson, Robin; Bruder, Carl E G; Piotrowski, Arkadiusz; Menzel, Uwe et al.

Ingår i Bioinformatics, s. 751-758, 2008

• DOI för A Segmental Maximum A Posteriori Approach to Genome-wide Copy Number Profiling

Application of Genomic and Expression Arrays for Identification of new Cancer Genes

Nord, Helena

2010

• Ladda ner fulltext (pdf) av Application of Genomic and Expression Arrays for Identification of new Cancer Genes

Novel amplicons in pediatric medulloblastoma identified by high-resolution genomic analysis: Genetic aberrations in medulloblastoma

Nord, Helena; Pfeifer, Susan; Nilsson, Pelle; Strömberg, Bo et al.