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  1. Ansatte

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Wenche Sjursen

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Last ned pressefoto
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Wenche Sjursen

Professor

wenche.sjursen@ntnu.no
93666916 72573530 Laboratoriesenteret, 232.04.046, Øya, Erling Skjalgssons g 1
Om Publikasjoner Undervisning Formidling

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Publikasjoner

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  • Etter kategori
  • Se alle publikasjoner i Cristin

2025

  • Meta, Rahmina; Pettersen, Henrik Sahlin; Tollefsen, Sofie Eline; Ytterhus, Borgny; Salvesen, Øyvind Olav; Sjursen, Wenche. (2025) Tumour-associated macrophages in human meningiomas. PLOS ONE
    Vitenskapelig artikkel
  • Tollefsen, Sofie Eline; Meta, Rahmina; Solheim, Ole Skeidsvoll; Mjønes, Patricia Gjertrud; Vestrheim, Ingfrid; Sjursen, Wenche. (2025) Merlin immunoreactivity fails to predict neurofibromatosis type 2 mutations in human meningiomas. Journal of Neuropathology and Experimental Neurology
    Vitenskapelig artikkel

2024

  • Bjørnstad, Pål Marius; aaløkken, Ragnhild Margrethe; Åsheim, June; Sundaram, Arvind; Nangota Felde, Caroline; Østby, Gina Henriette. (2024) Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01494-7). European Journal of Human Genetics
    Errata
  • Meta, Rahmina; Pettersen, Henrik Sahlin; Tollefsen, Sofie Eline; Ytterhus, Borgny; Salvesen, Øyvind; Sjursen, Wenche. (2024) Clinicopathological aspects of tumour-associated macrophages in human meningiomas. Neuropathology and Applied Neurobiology
    Sammendrag/abstract
  • Meta, Rahmina; Dai, Hong Yan; Sjursen, Wenche; Torp, Sverre Helge. (2024) TERT promotor mutations in atypical meningiomas . Neuro-Oncology
    Sammendrag/abstract
  • Sjursen, Wenche; Hyldebrandt, Hanne Kjensli; Lavik, Liss Ane; Haukanes, Bjørn Ivar; Ariansen, Sarah Louise; Briskemyr, Siri. (2024) PMS2 mutation spectra in Norway and risk of cancer for carriers of pathogenic variants. Hereditary Cancer in Clinical Practice
    Vitenskapelig artikkel
  • Houge, Gunnar Douzgos; Bratland, Eirik; Aukrust, Ingvild; Tveten, Kristian; Žukauskaitė, Gabrielė; Sansovic, Ivona. (2024) Comparison of the ABC and ACMG systems for variant classification. European Journal of Human Genetics
    Vitenskapelig artikkel

2023

  • Bjørnstad, Pål Marius; Aaløkken, Ragnhild Margrethe; Åsheim, June; Sundaram, Arvind; Nangota Felde, Caroline; Østby, Gina Henriette. (2023) A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing. European Journal of Human Genetics
    Vitenskapelig artikkel
  • Hovland, Henrikke Nilsen; Mchaina, Eunice Kabanyana; Vetti, Hildegunn Høberg; Ariansen, Sarah Louise; Sjursen, Wenche; Van Ghelue, Marijke. (2023) Functional Analyses of Rare Germline Missense BRCA1 Variants Located within and outside Protein Domains with Known Functions. Genes
    Vitenskapelig artikkel
  • Torp, Sverre Helge; Meta, Rahmina; Tollefsen, Sofie Eline; Vestrheim, Ingfrid; Sjursen, Wenche. (2023) Merlin expression in human meningiomas - An immunohistochemical study. Journal of Neuropathology and Experimental Neurology
    Sammendrag/abstract
  • Rocque, Mariève; Leipart, Vilde; Singh, Ashish Kumar; Mur, Pilar; Olsen, Maren Fridtjofsen; Engebretsen, Lars Fredri. (2023) Characterization of POLE c.1373A > T p.(Tyr458Phe), causing high cancer risk. Molecular Genetics and Genomics
    Vitenskapelig artikkel
  • Singh, Ashish Kumar; Talseth-Palmer, Bente Anita; Xavier, Alexandre; Scott, Rodney J.; Drabløs, Finn Sverre; Sjursen, Wenche. (2023) Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing. BMC Medical Genomics
    Vitenskapelig artikkel
  • Wiik, Mariann Unhjem; Negline, Mia; Beisvag, Vidar; Clapham, Matthew; Holliday, Elizabeth; Dueñas, Nuria. (2023) MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome. Scientific Reports
    Vitenskapelig artikkel

2022

  • Hovland, Henrikke Nilsen; Al-Adhami, Rafal Isam Fatoohi; Ariansen, Sarah Louise; Van Ghelue, Marijke; Sjursen, Wenche; Anfinsen, Sigrid Lima. (2022) BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories. Familial Cancer
    Vitenskapelig artikkel

2021

  • Meta, Rahmina; Boldt, Henning B.; Kristensen, Bjarne W.; Sahm, Felix; Sjursen, Wenche; Torp, Sverre Helge. (2021) Methylation signature of atypical meningiomas. Clinical Neuropathology
    Sammendrag/abstract
  • Singh, Ashish Kumar; Olsen, Maren Fridtjofsen; Lavik, Liss Ane; Vold, Trine; Drabløs, Finn; Sjursen, Wenche. (2021) Detecting copy number variation in next generation sequencing data from diagnostic gene panels. BMC Medical Genomics
    Vitenskapelig artikkel
  • Meta, Rahmina; Boldt, Henning B.; Kristensen, Bjarne W.; Sahm, Felix; Sjursen, Wenche; Torp, Sverre Helge. (2021) The prognostic value of methylation signatures and NF2 mutations in atypical meningiomas . Cancers
    Vitenskapelig artikkel

2020

  • Singh, Ashish Kumar; Talseth-Palmer, Bente Anita; McPhillips, Mary; Lavik, Liss Ane; Xavier, Alexandre; Drabløs, Finn. (2020) Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer. PLOS ONE
    Vitenskapelig artikkel
  • Mjelle, Robin; Aass, Kristin Roseth; Sjursen, Wenche; Hofsli, Eva; Sætrom, Pål. (2020) sMETASeq: combined profiling of microbiota and host small RNAs. iScience
    Vitenskapelig artikkel

2019

  • Grolleman, Judith E.; de Voer, Richarda M.; Elsayed, Fadwa A.; Nielsen, Maartje; Weren, Robbert D.A.; Palles, Claire. (2019) Mutational signature analysis reveals NTHL1 deficiency to cause a multi-tumor phenotype. Cancer Cell
    Vitenskapelig artikkel
  • Valle, Laura; de Voer, Richarda M.; Goldberg, Yael; Sjursen, Wenche; Försti, Asta; Ruiz-Ponte, Clara. (2019) Update on genetic predisposition to colorectal cancer and polyposis. Molecular Aspects of Medicine
    Vitenskapelig oversiktsartikkel/review
  • Suerink, Manon; Rodriguez-Girondo, Mar; van der Klift, Heleen M.; Colas, Chrystelle; Brugieres, Laurence; Lavoine, Noémie. (2019) An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome. Genetics in Medicine
    Vitenskapelig artikkel
  • Mjelle, Robin; Sjursen, Wenche; Thommesen, Liv; Sætrom, Pål; Hofsli, Eva. (2019) Small RNA expression from viruses, bacteria and human miRNAs in colon cancer tissue and its association with microsatellite instability and tumor location. BMC Cancer
    Vitenskapelig artikkel
  • Xavier, Alexandre; Olsen, Maren Fridtjofsen; Lavik, Liss Ane; Johansen, Jostein; Singh, Ashish Kumar; Sjursen, Wenche. (2019) Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome. Molecular Genetics & Genomic Medicine
    Vitenskapelig artikkel
  • Sjursen, Wenche; Vetti, Hildegunn Høberg. (2019) NTHL1-mutasjoner gir ikke bare polypose. Best Practice Gastroenterology
    Populærvitenskapelig artikkel

2017

  • Hansen, Maren; Johansen, Jostein; Sylvander, Anna Elisabeth; Bjørnevoll, Inga; Talseth-Palmer, Bente Anita; Lavik, Liss Ane. (2017) Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome. Clinical Genetics
    Vitenskapelig artikkel
  • Mjelle, Robin; Sellæg, Kjersti; Sætrom, Pål; Thommesen, Liv; Sjursen, Wenche; Hofsli, Eva. (2017) Identification of metastasis-associated microRNAs in serum from rectal cancer patients. OncoTarget
    Vitenskapelig artikkel

2016

  • Sjursen, Wenche; McPhillips, Mary; Scott, Rodney J.; Talseth-Palmer, Bente. (2016) Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations. Molecular Genetics & Genomic Medicine
    Vitenskapelig artikkel
  • Talseth-Palmer, Bente; Bauer, Denis; Sjursen, Wenche; Evans, Tiffany-Jane; McPhillips, Mary; Proietto, Anthony. (2016) Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families. Cancer Medicine
    Vitenskapelig artikkel
  • Shirzadi, Maryam; Reimers, Arne; Helde, Grethe; Sjursen, Wenche; Brodtkorb, Eylert. (2016) No association between non-bullous skin reactions from lamotrigine and heterozygosity of UGT1A4 genetic variants *2(P24T) or *3(L48V) in Norwegian patients. Seizure
    Vitenskapelig artikkel

2015

  • Svaasand, Eva Kathrine; Engebretsen, Lars Fredri; Ludvigsen, Trond; Brechan, Wenche; Sjursen, Wenche. (2015) A Novel Deep Intronic Mutation Introducing a Cryptic Exon Causing Neurofibromatosis Type 1 in a Family with Highly Variable Phenotypes: A Case Study. Hereditary Genetics: Current Research
    Vitenskapelig artikkel
  • Hansen, Maren Fridtjofsen; Sjursen, Wenche. (2015) En ny POLE-mutasjon som årsak til økt risiko i en familie med høy forekomst av tykk- og endetarmskreft. Bestpractice Onkologi/Hematologi
    Populærvitenskapelig artikkel
  • Hansen, Maren Fridtjofsen; Johansen, Jostein; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Steinsbekk, Kristin Solum; Sætrom, Pål. (2015) A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine. Familial Cancer
    Vitenskapelig artikkel
  • Hansen, Maren Fridtjofsen; Johansen, Jostein; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Steinsbekk, Kristin Solum; Sætrom, Pål. (2015) A novel POLE variant, identified by exome sequencing, causes colorectal- and extra-colonic cancers. Familial Cancer
    Sammendrag/abstract

2014

  • Reimers, Arne; Sjursen, Wenche; Helde, Grethe; Brodtkorb, Eylert. (2014) Frequencies of UGT1A4*2 (P24T) and *3 (L48V) and their effects on serum concentrations of lamotrigine. European journal of drug metabolism and pharmacokinetics
    Vitenskapelig artikkel
  • Grindedal, Eli Marie; Aarset, Harald; Bjørnevoll, Inga; Røyset, Elin Synnøve; Mæhle, Lovise Olaug; Stormorken, Astrid T.. (2014) The Norwegian PMS2 founder mutation c.989-1G>T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry. Hereditary Cancer in Clinical Practice
    Vitenskapelig artikkel
  • Hansen, Maren Fridtjofsen; Neckmann, Ulrike; Lavik, Liss Anne; Vold, Trine; Gilde, Bodil; Toft, Ragnhild Karlgård. (2014) A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes. Molecular Genetics & Genomic Medicine
    Vitenskapelig artikkel

2013

  • Sjursen, Wenche; Halvorsen, Henrik; Hofsli, Eva; Bachke, Siri; Berge, Åsa; Engebretsen, Lars Fredri. (2013) Mutation screening in a Norwegian cohort with pheochromocytoma. Familial Cancer
    Vitenskapelig artikkel
  • Hofsli, Eva; Sjursen, Wenche; Prestvik, Wenche S; Johansen, Jostein; Rye, Morten Beck; Tranø, Gerd. (2013) Identification of serum microRNA profiles in colon cancer. British Journal of Cancer
    Vitenskapelig artikkel

2011

  • Jühlen, Ramona; Sjursen, Wenche. (2011) Colorectal Cancer in Norway; Identification of Hereditary and Non-Hereditary Subtypes - Establishment of Tissue Microarray for Molecular-Genetic Subclassification of Colorectal Cancer. LBK - DMF - NTNU
    Mastergradsoppgave
  • Tranø, Gerd; Wasmuth, Hans; Sjursen, Wenche; Vatten, Lars Johan. (2011) Patient and tumor characteristics may raise clinicians' awareness of familial colorectal cancer: A Norwegian population-based study. Scandinavian Journal of Gastroenterology
    Vitenskapelig artikkel

2010

  • Sjursen, Wenche; Haukanes, Bjørn Ivar; Grindedal, Eli Marie; Aarset, Harald; Stormorken, Astrid T.; Engebretsen, Lars Fredri. (2010) Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers. Journal of Medical Genetics
    Vitenskapelig artikkel
  • Tessem, May-Britt; Selnæs, Kirsten Margrete; Sjursen, Wenche; Tranø, Gerd; Giskeødegård, Guro F.; Bathen, Tone Frost. (2010) Discrimination of Patients with Microsatellite Instability Colon Cancer using H-1 HR MAS MR Spectroscopy and Chemometric Analysis. Journal of Proteome Research
    Vitenskapelig artikkel
  • Tranø, Gerd; Sjursen, Wenche; Wasmuth, Hans; Hofsli, Eva; Vatten, Lars Johan. (2010) Performance of clinical guidelines compared with molecular tumour screening methods in identifying possible Lynch syndrome among colorectal cancer patients: a Norwegian population-based study. British Journal of Cancer
    Vitenskapelig artikkel

2009

  • Sjursen, Wenche; Bjørnevoll, Inga; Engebretsen, Lars; Fjelland, Kristine; Halvorsen, Tore Bøhmer; Myrvold, Helge Elliot. (2009) A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts. Familial Cancer
    Vitenskapelig artikkel
  • Tranø, G; Wasmuth, HH; Sjursen, Wenche; Hofsli, E; Vatten, Lars Johan. (2009) Awareness of heredity in colorectal cancer patients is insufficient among clinicians: a Norwegian population-based study. Colorectal Disease
    Vitenskapelig artikkel

2002

  • Prestvik, Wenche S.; Sjursen, Wenche; Svaasand, Eva K; Eftedal, Ingrid. (2002) Diagnostikk av numeriske kromosomavvik ved hjelp av fluorescerende mikrosatelitt-analyser. Bioingeniøren
    Fagartikkel
  • Prestvik, Wenche Slettahjell; Sjursen, Wenche; Svaasand, Eva; Eftedal, Ingrid. (2002) Diagnostikk av numeriske kromosomavvik ved hjelp av fluorescerende mikrosatelitt-analyser Detection of numerical abnormalities by fluorescent microsatellite analysis. Bioingeniøren
    Fagartikkel

2000

  • Sjursen, Wenche; Brekke, Ole Lars; Johansen, Berit. (2000) Secretory and cytosolic phospholipase A2 regulate the long term cytokine induced eicosanoid production in human keratinocytes. Cytokine
    Vitenskapelig artikkel
  • Sjursen, Wenche; Brekke, Ole Lars; Johansen, Berit. (2000) Secretory and cytosolic phospholipase A2 regulate the long term cytokine induced eicosanoid production in human keratinocytes. Cytokine
    Vitenskapelig artikkel

1998

  • Thommesen, Liv; Sjursen, Wenche; Gåsvik, Kathrine; Hanssen, Wenche; Brekke, Ole-Lars; Skattebøl, Lars. (1998) Selective inhibitors of cytosolic or secretory phospholipase A2 block TNF-induced activation of transcription factor nuclear factor-kappa B and expression of ICAM-1. Journal of Immunology
    Vitenskapelig artikkel

1997

  • Frøyland, Livar; Madsen, Lise; Sjursen, W.; Garras, Alexis; Lie, Ø.; Songstad, Jon. (1997) Effect of 3-thia fatty acids on the lipid composition of rat liver, lipoproteins, and heart. Journal of Lipid Research
    Vitenskapelig artikkel
  • Johansen, Berit; Andersen, Sonja Benedikte; Sjursen, Wenche; Gundersen, Pia; Selbo, Pål Kristian. (1997) Phospholipase A2 in psoriasis. Progress in surgery
    Vitenskapelig artikkel
  • Frøyland, Livar; Madsen, Lise; Sjursen, Wenche; Garras, Alexis; Lie, Øyvind; Songstad, Jon. (1997) Effects of 3-thia fatty acids on the lipid composition of rat liver, lipoproteins, and heart. Journal of Lipid Research
    Vitenskapelig artikkel

1994

  • Andersen, S; Sjursen, W; Lægreid, A; Austgulen, Rigmor; Johansen, B. (1994) Immunohistologic detection of non-pancreatic phospholipase A2 (type II) in human placenta and its possible involvement in normal parturition at term. Prostaglandins, Leukotrienes and Essential Fatty Acids
    Vitenskapelig artikkel

Tidsskriftspublikasjoner

  • Meta, Rahmina; Pettersen, Henrik Sahlin; Tollefsen, Sofie Eline; Ytterhus, Borgny; Salvesen, Øyvind Olav; Sjursen, Wenche. (2025) Tumour-associated macrophages in human meningiomas. PLOS ONE
    Vitenskapelig artikkel
  • Tollefsen, Sofie Eline; Meta, Rahmina; Solheim, Ole Skeidsvoll; Mjønes, Patricia Gjertrud; Vestrheim, Ingfrid; Sjursen, Wenche. (2025) Merlin immunoreactivity fails to predict neurofibromatosis type 2 mutations in human meningiomas. Journal of Neuropathology and Experimental Neurology
    Vitenskapelig artikkel
  • Bjørnstad, Pål Marius; aaløkken, Ragnhild Margrethe; Åsheim, June; Sundaram, Arvind; Nangota Felde, Caroline; Østby, Gina Henriette. (2024) Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01494-7). European Journal of Human Genetics
    Errata
  • Meta, Rahmina; Pettersen, Henrik Sahlin; Tollefsen, Sofie Eline; Ytterhus, Borgny; Salvesen, Øyvind; Sjursen, Wenche. (2024) Clinicopathological aspects of tumour-associated macrophages in human meningiomas. Neuropathology and Applied Neurobiology
    Sammendrag/abstract
  • Meta, Rahmina; Dai, Hong Yan; Sjursen, Wenche; Torp, Sverre Helge. (2024) TERT promotor mutations in atypical meningiomas . Neuro-Oncology
    Sammendrag/abstract
  • Sjursen, Wenche; Hyldebrandt, Hanne Kjensli; Lavik, Liss Ane; Haukanes, Bjørn Ivar; Ariansen, Sarah Louise; Briskemyr, Siri. (2024) PMS2 mutation spectra in Norway and risk of cancer for carriers of pathogenic variants. Hereditary Cancer in Clinical Practice
    Vitenskapelig artikkel
  • Houge, Gunnar Douzgos; Bratland, Eirik; Aukrust, Ingvild; Tveten, Kristian; Žukauskaitė, Gabrielė; Sansovic, Ivona. (2024) Comparison of the ABC and ACMG systems for variant classification. European Journal of Human Genetics
    Vitenskapelig artikkel
  • Bjørnstad, Pål Marius; Aaløkken, Ragnhild Margrethe; Åsheim, June; Sundaram, Arvind; Nangota Felde, Caroline; Østby, Gina Henriette. (2023) A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing. European Journal of Human Genetics
    Vitenskapelig artikkel
  • Hovland, Henrikke Nilsen; Mchaina, Eunice Kabanyana; Vetti, Hildegunn Høberg; Ariansen, Sarah Louise; Sjursen, Wenche; Van Ghelue, Marijke. (2023) Functional Analyses of Rare Germline Missense BRCA1 Variants Located within and outside Protein Domains with Known Functions. Genes
    Vitenskapelig artikkel
  • Torp, Sverre Helge; Meta, Rahmina; Tollefsen, Sofie Eline; Vestrheim, Ingfrid; Sjursen, Wenche. (2023) Merlin expression in human meningiomas - An immunohistochemical study. Journal of Neuropathology and Experimental Neurology
    Sammendrag/abstract
  • Rocque, Mariève; Leipart, Vilde; Singh, Ashish Kumar; Mur, Pilar; Olsen, Maren Fridtjofsen; Engebretsen, Lars Fredri. (2023) Characterization of POLE c.1373A > T p.(Tyr458Phe), causing high cancer risk. Molecular Genetics and Genomics
    Vitenskapelig artikkel
  • Singh, Ashish Kumar; Talseth-Palmer, Bente Anita; Xavier, Alexandre; Scott, Rodney J.; Drabløs, Finn Sverre; Sjursen, Wenche. (2023) Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing. BMC Medical Genomics
    Vitenskapelig artikkel
  • Wiik, Mariann Unhjem; Negline, Mia; Beisvag, Vidar; Clapham, Matthew; Holliday, Elizabeth; Dueñas, Nuria. (2023) MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome. Scientific Reports
    Vitenskapelig artikkel
  • Hovland, Henrikke Nilsen; Al-Adhami, Rafal Isam Fatoohi; Ariansen, Sarah Louise; Van Ghelue, Marijke; Sjursen, Wenche; Anfinsen, Sigrid Lima. (2022) BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories. Familial Cancer
    Vitenskapelig artikkel
  • Meta, Rahmina; Boldt, Henning B.; Kristensen, Bjarne W.; Sahm, Felix; Sjursen, Wenche; Torp, Sverre Helge. (2021) Methylation signature of atypical meningiomas. Clinical Neuropathology
    Sammendrag/abstract
  • Singh, Ashish Kumar; Olsen, Maren Fridtjofsen; Lavik, Liss Ane; Vold, Trine; Drabløs, Finn; Sjursen, Wenche. (2021) Detecting copy number variation in next generation sequencing data from diagnostic gene panels. BMC Medical Genomics
    Vitenskapelig artikkel
  • Meta, Rahmina; Boldt, Henning B.; Kristensen, Bjarne W.; Sahm, Felix; Sjursen, Wenche; Torp, Sverre Helge. (2021) The prognostic value of methylation signatures and NF2 mutations in atypical meningiomas . Cancers
    Vitenskapelig artikkel
  • Singh, Ashish Kumar; Talseth-Palmer, Bente Anita; McPhillips, Mary; Lavik, Liss Ane; Xavier, Alexandre; Drabløs, Finn. (2020) Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer. PLOS ONE
    Vitenskapelig artikkel
  • Mjelle, Robin; Aass, Kristin Roseth; Sjursen, Wenche; Hofsli, Eva; Sætrom, Pål. (2020) sMETASeq: combined profiling of microbiota and host small RNAs. iScience
    Vitenskapelig artikkel
  • Grolleman, Judith E.; de Voer, Richarda M.; Elsayed, Fadwa A.; Nielsen, Maartje; Weren, Robbert D.A.; Palles, Claire. (2019) Mutational signature analysis reveals NTHL1 deficiency to cause a multi-tumor phenotype. Cancer Cell
    Vitenskapelig artikkel
  • Valle, Laura; de Voer, Richarda M.; Goldberg, Yael; Sjursen, Wenche; Försti, Asta; Ruiz-Ponte, Clara. (2019) Update on genetic predisposition to colorectal cancer and polyposis. Molecular Aspects of Medicine
    Vitenskapelig oversiktsartikkel/review
  • Suerink, Manon; Rodriguez-Girondo, Mar; van der Klift, Heleen M.; Colas, Chrystelle; Brugieres, Laurence; Lavoine, Noémie. (2019) An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome. Genetics in Medicine
    Vitenskapelig artikkel
  • Mjelle, Robin; Sjursen, Wenche; Thommesen, Liv; Sætrom, Pål; Hofsli, Eva. (2019) Small RNA expression from viruses, bacteria and human miRNAs in colon cancer tissue and its association with microsatellite instability and tumor location. BMC Cancer
    Vitenskapelig artikkel
  • Xavier, Alexandre; Olsen, Maren Fridtjofsen; Lavik, Liss Ane; Johansen, Jostein; Singh, Ashish Kumar; Sjursen, Wenche. (2019) Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome. Molecular Genetics & Genomic Medicine
    Vitenskapelig artikkel
  • Sjursen, Wenche; Vetti, Hildegunn Høberg. (2019) NTHL1-mutasjoner gir ikke bare polypose. Best Practice Gastroenterology
    Populærvitenskapelig artikkel
  • Hansen, Maren; Johansen, Jostein; Sylvander, Anna Elisabeth; Bjørnevoll, Inga; Talseth-Palmer, Bente Anita; Lavik, Liss Ane. (2017) Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome. Clinical Genetics
    Vitenskapelig artikkel
  • Mjelle, Robin; Sellæg, Kjersti; Sætrom, Pål; Thommesen, Liv; Sjursen, Wenche; Hofsli, Eva. (2017) Identification of metastasis-associated microRNAs in serum from rectal cancer patients. OncoTarget
    Vitenskapelig artikkel
  • Sjursen, Wenche; McPhillips, Mary; Scott, Rodney J.; Talseth-Palmer, Bente. (2016) Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations. Molecular Genetics & Genomic Medicine
    Vitenskapelig artikkel
  • Talseth-Palmer, Bente; Bauer, Denis; Sjursen, Wenche; Evans, Tiffany-Jane; McPhillips, Mary; Proietto, Anthony. (2016) Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families. Cancer Medicine
    Vitenskapelig artikkel
  • Shirzadi, Maryam; Reimers, Arne; Helde, Grethe; Sjursen, Wenche; Brodtkorb, Eylert. (2016) No association between non-bullous skin reactions from lamotrigine and heterozygosity of UGT1A4 genetic variants *2(P24T) or *3(L48V) in Norwegian patients. Seizure
    Vitenskapelig artikkel
  • Svaasand, Eva Kathrine; Engebretsen, Lars Fredri; Ludvigsen, Trond; Brechan, Wenche; Sjursen, Wenche. (2015) A Novel Deep Intronic Mutation Introducing a Cryptic Exon Causing Neurofibromatosis Type 1 in a Family with Highly Variable Phenotypes: A Case Study. Hereditary Genetics: Current Research
    Vitenskapelig artikkel
  • Hansen, Maren Fridtjofsen; Sjursen, Wenche. (2015) En ny POLE-mutasjon som årsak til økt risiko i en familie med høy forekomst av tykk- og endetarmskreft. Bestpractice Onkologi/Hematologi
    Populærvitenskapelig artikkel
  • Hansen, Maren Fridtjofsen; Johansen, Jostein; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Steinsbekk, Kristin Solum; Sætrom, Pål. (2015) A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine. Familial Cancer
    Vitenskapelig artikkel
  • Hansen, Maren Fridtjofsen; Johansen, Jostein; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Steinsbekk, Kristin Solum; Sætrom, Pål. (2015) A novel POLE variant, identified by exome sequencing, causes colorectal- and extra-colonic cancers. Familial Cancer
    Sammendrag/abstract
  • Reimers, Arne; Sjursen, Wenche; Helde, Grethe; Brodtkorb, Eylert. (2014) Frequencies of UGT1A4*2 (P24T) and *3 (L48V) and their effects on serum concentrations of lamotrigine. European journal of drug metabolism and pharmacokinetics
    Vitenskapelig artikkel
  • Grindedal, Eli Marie; Aarset, Harald; Bjørnevoll, Inga; Røyset, Elin Synnøve; Mæhle, Lovise Olaug; Stormorken, Astrid T.. (2014) The Norwegian PMS2 founder mutation c.989-1G>T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry. Hereditary Cancer in Clinical Practice
    Vitenskapelig artikkel
  • Hansen, Maren Fridtjofsen; Neckmann, Ulrike; Lavik, Liss Anne; Vold, Trine; Gilde, Bodil; Toft, Ragnhild Karlgård. (2014) A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes. Molecular Genetics & Genomic Medicine
    Vitenskapelig artikkel
  • Sjursen, Wenche; Halvorsen, Henrik; Hofsli, Eva; Bachke, Siri; Berge, Åsa; Engebretsen, Lars Fredri. (2013) Mutation screening in a Norwegian cohort with pheochromocytoma. Familial Cancer
    Vitenskapelig artikkel
  • Hofsli, Eva; Sjursen, Wenche; Prestvik, Wenche S; Johansen, Jostein; Rye, Morten Beck; Tranø, Gerd. (2013) Identification of serum microRNA profiles in colon cancer. British Journal of Cancer
    Vitenskapelig artikkel
  • Tranø, Gerd; Wasmuth, Hans; Sjursen, Wenche; Vatten, Lars Johan. (2011) Patient and tumor characteristics may raise clinicians' awareness of familial colorectal cancer: A Norwegian population-based study. Scandinavian Journal of Gastroenterology
    Vitenskapelig artikkel
  • Sjursen, Wenche; Haukanes, Bjørn Ivar; Grindedal, Eli Marie; Aarset, Harald; Stormorken, Astrid T.; Engebretsen, Lars Fredri. (2010) Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers. Journal of Medical Genetics
    Vitenskapelig artikkel
  • Tessem, May-Britt; Selnæs, Kirsten Margrete; Sjursen, Wenche; Tranø, Gerd; Giskeødegård, Guro F.; Bathen, Tone Frost. (2010) Discrimination of Patients with Microsatellite Instability Colon Cancer using H-1 HR MAS MR Spectroscopy and Chemometric Analysis. Journal of Proteome Research
    Vitenskapelig artikkel
  • Tranø, Gerd; Sjursen, Wenche; Wasmuth, Hans; Hofsli, Eva; Vatten, Lars Johan. (2010) Performance of clinical guidelines compared with molecular tumour screening methods in identifying possible Lynch syndrome among colorectal cancer patients: a Norwegian population-based study. British Journal of Cancer
    Vitenskapelig artikkel
  • Sjursen, Wenche; Bjørnevoll, Inga; Engebretsen, Lars; Fjelland, Kristine; Halvorsen, Tore Bøhmer; Myrvold, Helge Elliot. (2009) A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts. Familial Cancer
    Vitenskapelig artikkel
  • Tranø, G; Wasmuth, HH; Sjursen, Wenche; Hofsli, E; Vatten, Lars Johan. (2009) Awareness of heredity in colorectal cancer patients is insufficient among clinicians: a Norwegian population-based study. Colorectal Disease
    Vitenskapelig artikkel
  • Prestvik, Wenche S.; Sjursen, Wenche; Svaasand, Eva K; Eftedal, Ingrid. (2002) Diagnostikk av numeriske kromosomavvik ved hjelp av fluorescerende mikrosatelitt-analyser. Bioingeniøren
    Fagartikkel
  • Prestvik, Wenche Slettahjell; Sjursen, Wenche; Svaasand, Eva; Eftedal, Ingrid. (2002) Diagnostikk av numeriske kromosomavvik ved hjelp av fluorescerende mikrosatelitt-analyser Detection of numerical abnormalities by fluorescent microsatellite analysis. Bioingeniøren
    Fagartikkel
  • Sjursen, Wenche; Brekke, Ole Lars; Johansen, Berit. (2000) Secretory and cytosolic phospholipase A2 regulate the long term cytokine induced eicosanoid production in human keratinocytes. Cytokine
    Vitenskapelig artikkel
  • Sjursen, Wenche; Brekke, Ole Lars; Johansen, Berit. (2000) Secretory and cytosolic phospholipase A2 regulate the long term cytokine induced eicosanoid production in human keratinocytes. Cytokine
    Vitenskapelig artikkel
  • Thommesen, Liv; Sjursen, Wenche; Gåsvik, Kathrine; Hanssen, Wenche; Brekke, Ole-Lars; Skattebøl, Lars. (1998) Selective inhibitors of cytosolic or secretory phospholipase A2 block TNF-induced activation of transcription factor nuclear factor-kappa B and expression of ICAM-1. Journal of Immunology
    Vitenskapelig artikkel
  • Frøyland, Livar; Madsen, Lise; Sjursen, W.; Garras, Alexis; Lie, Ø.; Songstad, Jon. (1997) Effect of 3-thia fatty acids on the lipid composition of rat liver, lipoproteins, and heart. Journal of Lipid Research
    Vitenskapelig artikkel
  • Johansen, Berit; Andersen, Sonja Benedikte; Sjursen, Wenche; Gundersen, Pia; Selbo, Pål Kristian. (1997) Phospholipase A2 in psoriasis. Progress in surgery
    Vitenskapelig artikkel
  • Frøyland, Livar; Madsen, Lise; Sjursen, Wenche; Garras, Alexis; Lie, Øyvind; Songstad, Jon. (1997) Effects of 3-thia fatty acids on the lipid composition of rat liver, lipoproteins, and heart. Journal of Lipid Research
    Vitenskapelig artikkel
  • Andersen, S; Sjursen, W; Lægreid, A; Austgulen, Rigmor; Johansen, B. (1994) Immunohistologic detection of non-pancreatic phospholipase A2 (type II) in human placenta and its possible involvement in normal parturition at term. Prostaglandins, Leukotrienes and Essential Fatty Acids
    Vitenskapelig artikkel

Rapport

  • Jühlen, Ramona; Sjursen, Wenche. (2011) Colorectal Cancer in Norway; Identification of Hereditary and Non-Hereditary Subtypes - Establishment of Tissue Microarray for Molecular-Genetic Subclassification of Colorectal Cancer. LBK - DMF - NTNU
    Mastergradsoppgave

Undervisning

Emner

  • MOL3001 - Medical Genetics

Formidling

2024

  • Poster
    Meta, Rahmina; Pettersen, Henrik Sahlin; Tollefsen, Sofie Eline; Ytterhus, Borgny; Salvesen, Øyvind Olav; Sjursen, Wenche. (2024) The clinicopathological role of tumour-associated macrophages in human meningiomas. SNOG SYMPOSIUM 2024 – Multidisciplinary Neuro-Oncology Meeting , Gøteborg 2024-04-25 - 2024-04-27
  • Faglig foredrag
    Meta, Rahmina; Pettersen, Henrik Sahlin; Tollefsen, Sofie Eline; Ytterhus, Borgny; Salvesen, Øyvind Olav; Sjursen, Wenche. (2024) Tumorassosierte makrofager i meningeomer. Den norske patologforening Årsmøte i Den norske patologforening , Britannia Hotell, Trondheim, Norge 2024-04-11 -
  • Poster
    Meta, Rahmina; Pettersen, Henrik Sahlin; Tollefsen, Sofie Eline; Ytterhus, Borgny; Salvesen, Øyvind; Sjursen, Wenche. (2024) Clinicopathological aspects of tumour-associated macrophages in human meningiomas. 125TH Meeting of the British Neuropathological Society , London 2024-01-31 - 2024-02-02
  • Poster
    Meta, Rahmina; Dai, Hong Yan; Sjursen, Wenche; Torp, Sverre Helge. (2024) TERT promotor mutations in atypical meningiomas . 19th Meeting of the European Association of Neuro-Oncology (EANO 2024) , Glasgow 2024-10-17 - 2024-10-20

2023

  • Poster
    Torp, Sverre Helge; Meta, Rahmina; Tollefsen, Sofie Eline; Vestrheim, Ingfrid; Sjursen, Wenche. (2023) Merlin expression in human meningiomas - An immunohistochemical study. American Association of Neuropathologists 99th Annual Meeting of the American Association of Neuropathologists , Monterey, CA 2023-06-11 - 2023-06-11

2021

  • Poster
    Meta, Rahmina; Boldt, Henning B.; Kristensen, Bjarne W.; Sahm, Felix; Sjursen, Wenche; Torp, Sverre Helge. (2021) Methylation signature of atypical meningiomas. Euro-CNS 12th European Congress of Neuropathology , Odense 2021-05-31 - 2021-06-03

2019

  • Faglig foredrag
    Steinsbekk, Kristin Solum; Kjøbli, Eli; Kristiansen, Kine H; Prestvik, Wenche Slettahjell; Sjursen, Wenche; Bjørnevoll, Inga. (2019) Høykapasitetsanalyser innen medisinsk genetikk; Nye tider – Nye kunnskapsbehov! SAMGen: Studentaktiv undervisning innen medisinsk bruk av genomsekvensering. . Norsk selskap for human genetikk NSHG Fagmøte 2019 , Trondheim 2019-11-06 - 2019-11-07

2016

  • Poster
    Shirzadi, Maryam; Reimers, Arne; Helde, Grethe; Sjursen, Wenche; Brodtkorb, Eylert. (2016) No association between non-bullous skin reactions from lamotrigine and heterozygosity of UGT1A4 genetic variants *2(P24T) or *3(L48V). Internatioal League Against Epilepsy 12th European Congress on Epilepsy , Praha 2016-09-11 - 2016-09-20

2014

  • Vitenskapelig foredrag
    Hansen, Maren Fridtjofsen; Johansen, Jostein; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Steinsbekk, Kristin Solum; Sætrom, Pål. (2014) Using exome sequencing for identification of high-risk genetic variants in a family predisposed for colorectal cancer. COST Action BM1206 Meeting , Leiden 2014-09-04 - 2014-09-04
  • Poster
    Hansen, Maren Fridtjofsen; Steinsbekk, Kristin Solum; Bjørnevoll, Inga; Sylvander, Anna Elisabeth; Sjursen, Wenche; Drabløs, Finn. (2014) Using exome sequencing for identification of high-risk genetic variants in a family predisposed for colorectal cancer. Translational genomics in biomedicine , Barcelona 2014-03-13 - 2014-03-14
  • Vitenskapelig foredrag
    Drabløs, Finn; Sjursen, Wenche. (2014) A medical research infrastructure. COST Action BM1206 Meeting , Barcelona 2014-03-12 - 2014-03-12

2013

  • Poster
    Hansen, Maren Fridtjofsen; Lavik, Liss Anne; Gilde, Bodil; Vold, Trine; Neckmann, Ulrike; Bye, Kristin. (2013) Massive parallel sequencing in Molecular Diagnostics: Universal Tailed Amplicon Sequencing of Lynch Syndrome genes. European Society of Human Genetics (ESHG) European Human Genetics Conference 2013 , Palais des Congrès, 2 Place de la Porte Maillot, 75017 Paris 2013-06-08 - 2013-06-11
  • Poster
    Hansen, Maren Fridtjofsen; Lavik, Liss Anne; Gilde, Bodil; Vold, Trine; Neckmann, Ulrike; Bye, Kristin. (2013) A Massive Parallel Sequencing Workflow for Routine Clinical Diagnostics of Lynch Syndrome. International Society for Gastrointestinal Hereditary Tumou InSiGHT 2013 , Cairns 2013-08-28 - 2013-08-31
  • Faglig foredrag
    Hansen, Maren Fridtjofsen; Lavik, Liss Anne; Vold, Trine; Neckmann, Ulrike; Gilde, Bodil; Sjursen, Wenche. (2013) Høykapasitetsekvensering møter humangenetikk: Amplicon Sekvensering av Lynch Syndrom Gener. St. Olavs Hospita, APMG Årlig seminar innen molekylærmedisin , Trondheim 2013-01-23 -

2012

  • Faglig foredrag
    Hansen, Maren Fridtjofsen; Lavik, Liss Anne; Vold, Trine; Neckmann, Ulrike; Gilde, Bodil; Sjursen, Wenche. (2012) From Sanger- to High-Throughput Sequencing in Molecular Diagnostics: Universal Tailed Amplicon Sequencing of Lynch Synrome Genes. NSHG/NFMG Fagmøte i medisinsk genetikk , Oslo 2012-11-28 - 2012-11-29

2009

  • Vitenskapelig foredrag
    Tessem, May-Britt; Selnæs, Kirsten Margrete; Sjursen, Wenche; Tranø, Gerd; Gribbestad, Ingrid S; Hofsli, Eva. (2009) Characterization and evaluation of metabolic biomarkers for human colon adenocarcinomas by 1H HR MAS. ISMRM International Society for Magnetic Resonance in Medicine (ISMRM) annual meeting , Hawaii 2009-04-18 - 2009-04-24

2002

  • Poster
    Svaasand, Eva K; Sjursen, Wenche; Eftedal, Ingrid; Prestvik, Wenche S.. (2002) Detection of numerical chromosomal abnormalities by fluorescent microsatellite analysis. Norsk Biokjemisk Selskap Biokjemisk kontaktmøte 2002 , Røros 2002-01-17 - 2002-01-20
  • Poster
    Svaasand, Eva; Sjursen, Wenche; Eftedal, Ingrid; Prestvik, Wenche Slettahjell. (2002) Detection of numerical chromosomal abnormalities by fluorescent microsatellite analysis. Biokjemisk kontaktmøte 2002 , Røros 2002-01-17 - 2002-01-20
  • Poster
    Gilde, B; Sjursen, Wenche. (2002) Molecular diagnosis of hereditary non-polyposis colorectal cancer (HNPCC). 38. Biokjemiske kontaktmøte Functinal genomics - the mosaics of life , Røros 2002-01-17 - 2002-01-20

1998

  • Populærvitenskapelig foredrag
    Johansen, Berit; Lægreid, Astrid; Sjursen, Wenche; Thommesen, Liv; Anthonsen, Marit Walbye. (1998) A role of both secretory and cytosolic phospholipase A2 in TNF mediated nuclear translocation of NFkB and ICAM expression in keratinocytes?. NBS Kontaktmøte 98 , Lillehammer, Norge
  • Vitenskapelig foredrag
    Johansen, Berit; Lægreid, Astrid; Sjursen, Wenche; Thommesen, Liv; Anthonsen, Marit Walbye. (1998) A role for both secretory and cytosolic phospholipase A2 in TNF mediated nuclear translocation of NFkB and ICAM expression in keratinocytes?. NBS Kontaktmøte 98 , Lillehammer, Norge

1997

  • Vitenskapelig foredrag
    Johansen, Berit; Lægreid, Astrid; Sjursen, Wenche; Thommesen, Liv. (1997) A role for both secretory and cytosolic phospholipase A2 in TNF mediated nuclear translocation of NFkB and ICAM expression in keratinocytes. FEBS Special Meetintg on Signal Transduction , Amsterdam, Nederland

1996

  • Vitenskapelig foredrag
    Thommesen, Liv; Sjursen, Wenche; Gåsvik, Katrine; Johansen, Berit; Lægreid, Astrid. (1996) The role of phospholipases A2 in the activation of NFkB in human keratinocytes. 32. Biokjemiske kontaktmøte , Geilo

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