Pia Alhopuro
Helsinki, Finland
Last Updated: 09/26/2026
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Found 8 publications
Updated ENIGMA recommendations for reporting germline variants in cancer susceptibility genes and their translation into twenty languages.
Journal: Journal of medical genetics
Published: January 13, 2026
Correction to: Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA.
Journal: Orphanet journal of rare diseases
Published: October 07, 2024
Comparison of the ABC and ACMG systems for variant classification.
Journal: European journal of human genetics : EJHG
Published: December 19, 2023
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA.
Journal: Orphanet journal of rare diseases
Published: December 12, 2023
Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group.
Journal: Journal of medical genetics
Published: January 10, 2022
Constitutional mosaicism for a BRCA2 mutation as a cause of early-onset breast cancer.
Journal: Familial cancer
Published: January 10, 2020
Loss of SUFU function in familial multiple meningioma.
Journal: American journal of human genetics
Published: March 28, 2012
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Last Updated: 09/26/2026