Anne Marie Jelsig

18PUBLICATIONS
48CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Haematological tumoursPredictive and prognostic markersInfant and child healthCancer genetics
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Publications (18)

|Dec 02, 2025
The c.1744G > C, p.(Glu582Gln) missense variant in coding exon 14 of APC increases skipping of a natural occurring isoform and causes Familial Adenomatous Polyposis.

Anne Marie Jelsig, Maria Bejerholm Boelman, Ulf Birkedal

|Oct 24, 2025
Exploring the spectrum of central nervous system tumours in carriers of germline POT1 variants.

Emilie Neerup Nielsen, Anne Marie Jelsig, Jon Foss-Skiftesvik

|May 03, 2025
The clinicopathological features of breast cancer in Peutz-Jeghers syndrome: results from an international survey.

Elizabeth Loehrer, Anja Wagner, Massiah Bahar

|Oct 29, 2024
Cancer Risks in Attenuated and Classical Familial Adenomatous Polyposis: A Nationwide Cohort With Matched, Nonexposed Individuals.

Søren Hammershøj Beck, John Gásdal Karstensen, Steffen Bülow

|Mar 17, 2024
Progress report: Peutz-Jeghers syndrome.

Anne Marie Jelsig, John Gásdal Karstensen, Thomas V Overeem Hansen

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