Wenche Sjursen
Trondheim, 7030, Norway
Last Updated: 09/26/2026
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Found 35 publications
Lynch syndrome caused by SINE-VNTR-Alu-F retrotransposon insert in MSH6 confirmed after 20 years of testing: a case report and literature review.
Journal: Hereditary cancer in clinical practice
Published: June 03, 2025
Merlin immunoreactivity fails to predict neurofibromatosis type 2 mutations in human meningiomas.
Journal: Journal of neuropathology and experimental neurology
Published: May 30, 2025
Clinical and genetic findings in 103 individuals in Norway with basal cell naevus syndrome.
Journal: The British journal of dermatology
Published: May 23, 2025
PMS2 mutation spectra in Norway and risk of cancer for carriers of pathogenic variants.
Journal: Hereditary cancer in clinical practice
Published: June 26, 2024
Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing.
Journal: European journal of human genetics : EJHG
Published: January 03, 2024
Comparison of the ABC and ACMG systems for variant classification.
Journal: European journal of human genetics : EJHG
Published: December 19, 2023
A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing.
Journal: European journal of human genetics : EJHG
Published: July 03, 2023
MTHFR C677T and A1298C polymorphism's effect on risk of colorectal cancer in Lynch syndrome.
Journal: Scientific reports
Published: March 11, 2023
Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing.
Journal: BMC medical genomics
Published: November 24, 2022
Characterization of POLE c.1373A > T p.(Tyr458Phe), causing high cancer risk.
Journal: Molecular genetics and genomics : MGG
Published: March 16, 2022
Last Updated: 09/26/2026