Meis Omran
Stockholm, AB, Sweden
Last Updated: 09/26/2026
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Found 10 publications
Surveillance adherence and clinical findings in children with confirmed or familial TP53 variants: the Swedish multicenter constitutional TP53 study (SWEP53).
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 14, 2025
The argument for screening programs in previvors with Li-Fraumeni syndrome.
Journal: Expert review of anticancer therapy
Published: June 21, 2025
Digital Health Tools Embedded in a Cancer Genetics Clinic: Observational Study.
Journal: JMIR formative research
Published: March 23, 2025
Limiting surveillance in individuals with the Palestinian TP53 p. R181C founder variant-is it too soon to draw conclusions?
Journal: Journal of the National Cancer Institute
Published: January 06, 2025
Characterisation of heritable TP53-related cancer syndrome in Sweden-a nationwide study of genotype-phenotype correlations in 90 families.
Journal: European journal of human genetics : EJHG
Published: February 28, 2024
Whole-Body MRI Surveillance-Baseline Findings in the Swedish Multicentre Hereditary TP53-Related Cancer Syndrome Study (SWEP53).
Journal: Cancers
Published: December 08, 2021
Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53.
Journal: Hereditary cancer in clinical practice
Published: October 19, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026