Small RNA expression from viruses, bacteria and human miRNAs in colon cancer tissue and its association with microsatellite instability and tumor location

por Mjelle, Robin, Sjursen, Wenche, Thommesen, Liv, Sætrom, Pål, Hofsli, Eva
Publicado 2019

sMETASeq: Combined Profiling of Microbiota and Host Small RNAs

por Mjelle, Robin, Aass, Kristin Roseth, Sjursen, Wenche, Hofsli, Eva, Sætrom, Pål
Publicado 2020

Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations

por Sjursen, Wenche, McPhillips, Mary, Scott, Rodney J., Talseth‐Palmer, Bente A.
Publicado 2016

Identification of metastasis-associated microRNAs in serum from rectal cancer patients

por Mjelle, Robin, Sellæg, Kjersti, Sætrom, Pål, Thommesen, Liv, Sjursen, Wenche, Hofsli, Eva
Publicado 2017

Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing

por Singh, Ashish Kumar, Talseth-Palmer, Bente, Xavier, Alexandre, Scott, Rodney J., Drabløs, Finn, Sjursen, Wenche
Publicado 2023

The Prognostic Value of Methylation Signatures and NF2 Mutations in Atypical Meningiomas

por Meta, Rahmina, Boldt, Henning B., Kristensen, Bjarne W., Sahm, Felix, Sjursen, Wenche, Torp, Sverre H.
Publicado 2021

Detecting copy number variation in next generation sequencing data from diagnostic gene panels

por Singh, Ashish Kumar, Olsen, Maren Fridtjofsen, Lavik, Liss Anne Solberg, Vold, Trine, Drabløs, Finn, Sjursen, Wenche
Publicado 2021

A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes

por Hansen, Maren F, Neckmann, Ulrike, Lavik, Liss A S, Vold, Trine, Gilde, Bodil, Toft, Ragnhild K, Sjursen, Wenche
Publicado 2014

Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer

por Singh, Ashish Kumar, Talseth-Palmer, Bente, McPhillips, Mary, Lavik, Liss Anne Solberg, Xavier, Alexandre, Drabløs, Finn, Sjursen, Wenche
Publicado 2020

The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry

por Grindedal, Eli Marie, Aarset, Harald, Bjørnevoll, Inga, Røyset, Elin, Mæhle, Lovise, Stormorken, Astrid, Heramb, Cecilie, Medvik, Heidi, Møller, Pål, Sjursen, Wenche
Publicado 2014

A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine

por Hansen, Maren F., Johansen, Jostein, Bjørnevoll, Inga, Sylvander, Anna E., Steinsbekk, Kristin S., Sætrom, Pål, Sandvik, Arne K., Drabløs, Finn, Sjursen, Wenche
Publicado 2015

Comprehensive mismatch repair gene panel identifies variants in patients with Lynch‐like syndrome

por Xavier, Alexandre, Olsen, Maren Fridtjofsen, Lavik, Liss A., Johansen, Jostein, Singh, Ashish Kumar, Sjursen, Wenche, Scott, Rodney J., Talseth‐Palmer, Bente A.
Publicado 2019

Targeted next‐generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families

por Talseth‐Palmer, Bente A., Bauer, Denis C., Sjursen, Wenche, Evans, Tiffany J., McPhillips, Mary, Proietto, Anthony, Otton, Geoffrey, Spigelman, Allan D., Scott, Rodney J.
Publicado 2016

Functional Analyses of Rare Germline Missense BRCA1 Variants Located within and outside Protein Domains with Known Functions

por Hovland, Henrikke Nilsen, Mchaina, Eunice Kabanyana, Høberg-Vetti, Hildegunn, Ariansen, Sarah Louise, Sjursen, Wenche, Van Ghelue, Marijke, Haukanes, Bjørn Ivar, Knappskog, Per Morten, Aukrust, Ingvild, Ognedal, Elisabet
Publicado 2023

Characterization of POLE c.1373A > T p.(Tyr458Phe), causing high cancer risk

por Rocque, Mariève J., Leipart, Vilde, Kumar Singh, Ashish, Mur, Pilar, Olsen, Maren F., Engebretsen, Lars F., Martin-Ramos, Edgar, Aligué, Rosa, Sætrom, Pål, Valle, Laura, Drabløs, Finn, Otterlei, Marit, Sjursen, Wenche
Publicado 2023

BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories

por Hovland, Henrikke N., Al-Adhami, Rafal, Ariansen, Sarah Louise, Van Ghelue, Marijke, Sjursen, Wenche, Lima, Sigrid, Bolstad, Marte, Berger, Amund H., Høberg-Vetti, Hildegunn, Knappskog, Per, Haukanes, Bjørn Ivar, Aukrust, Ingvild, Ognedal, Elisabet
Publicado 2022

Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers

por Sjursen, Wenche, Haukanes, Bjørn Ivar, Grindedal, Eli Marie, Aarset, Harald, Stormorken, Astrid, Engebretsen, Lars F, Jonsrud, Christoffer, Bjørnevoll, Inga, Andresen, Per Arne, Ariansen, Sarah, Lavik, Liss Anne S, Gilde, Bodil, Bowitz-Lothe, Inger Marie, Mæhle, Lovise, Møller, Pål
Publicado 2010

MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome

por Wiik, Mariann Unhjem, Negline, Mia, Beisvåg, Vidar, Clapham, Matthew, Holliday, Elizabeth, Dueñas, Nuria, Brunet, Joan, Pineda, Marta, Bonifaci, Nuria, Aretz, Stefan, Klinkhammer, Hannah, Spier, Isabel, Perne, Claudia, Mayr, Andreas, Valle, Laura, Lubinski, Jan, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.
Publicado 2023