Susanna Koivuluoma
Oulu, 90220, Finland
Last Updated: 09/26/2026
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Found 10 publications
Population-based study of recurrent DNA damage response gene variants in breast cancer cases.
Journal: Breast cancer research and treatment
Published: December 20, 2024
Evaluating the role of CHEK2 p.(Asp438Tyr) allele in inherited breast cancer predisposition.
Journal: Familial cancer
Published: November 22, 2022
Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility.
Journal: Familial cancer
Published: February 09, 2022
Novel Rare SORL1 Variants in Early-Onset Dementia.
Journal: Journal of Alzheimer's disease : JAD
Published: June 07, 2021
Exome sequencing identifies a recurrent variant in SERPINA3 associating with hereditary susceptibility to breast cancer.
Journal: European journal of cancer (Oxford, England : 1990)
Published: September 02, 2020
Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition.
Journal: Molecular genetics & genomic medicine
Published: June 15, 2020
Evaluating the role of MLH3 p.Ser1188Ter variant in inherited breast cancer predisposition.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 22, 2019
Tumor suppressor MCPH1 regulates gene expression profiles related to malignant conversion and chromosomal assembly.
Journal: International journal of cancer
Published: December 12, 2018
Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer.
Journal: International journal of cancer
Published: November 16, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026