Kirsi M. Maatta
Tampere, 33520, Finland
Last Updated: 09/26/2026
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Found 13 publications
Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families.
Journal: BMC cancer
Published: August 30, 2016
Decorin Genotypes, Serum Glucose, Heart Rate, and Cerebrovascular Events: The Tampere Adult Population Cardiovascular Risk Study.
Journal: Genetic testing and molecular biomarkers
Published: June 18, 2016
Glucuronic Acid Epimerase (GLCE) Variant rs3865014 (A>G) Is Associated with BMI, Blood Hemoglobin, Hypertension, and Cerebrovascular Events, the TAMRISK Study.
Journal: Annals of human genetics
Published: June 06, 2016
Whole-exome sequencing of Finnish hereditary breast cancer families.
Journal: European journal of human genetics : EJHG
Published: January 22, 2016
Genetic Polymorphisms of Transcription Factor NRF2 and of its Host Gene Sulfiredoxin (SRXN1) are Associated with Cerebrovascular Disease in a Finnish Cohort, the TAMRISK Study.
Journal: International journal of medical sciences
Published: December 30, 2015
Functional Inducible Nitric Oxide Synthase Gene Variants Associate With Hypertension: A Case-Control Study in a Finnish Population-The TAMRISK Study.
Journal: Medicine
Published: November 19, 2015
NLR family pyrin domain containing 3 (NLRP3) inflammasome gene polymorphism rs7512998 (C>T) predicts aging-related increase of blood pressure, the TAMRISK study.
Journal: Immunity & ageing : I & A
Published: August 17, 2015
A functional variant in the serine-threonine kinase coding gene is associated with hypertension: a case-control study in a Finnish population, the Tampere adult population cardiovascular risk study.
Journal: Journal of hypertension
Published: December 14, 2012
Contribution of SLC7A1 genetic variant to hypertension, the TAMRISK study.
Journal: BMC medical genetics
Published: November 12, 2012
Last Updated: 09/26/2026