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
• 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
• 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

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