Helena Kaariainen

Helsinki, Finland

Last Updated: 09/26/2026

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Found 33 publications

Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study.

Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study.

Journal: European journal of human genetics : EJHG

Published: October 14, 2025

Supplementing Disease Risk Information for Type 2 Diabetes and Coronary Heart Disease with Polygenic Risk Scores: Testing a Health Action Process Approach-Inspired Path Model to Predict Health Behavior.

Supplementing Disease Risk Information for Type 2 Diabetes and Coronary Heart Disease with Polygenic Risk Scores: Testing a Health Action Process Approach-Inspired Path Model to Predict Health Behavior.

Journal: International journal of behavioral medicine

Published: September 10, 2025

The impact of supplementing traditional risk information with polygenic risk score concerning type 2 diabetes and coronary heart disease on health behavior: a randomized controlled trial.

The impact of supplementing traditional risk information with polygenic risk score concerning type 2 diabetes and coronary heart disease on health behavior: a randomized controlled trial.

Journal: Journal of community genetics

Published: August 22, 2024

Infertility following trisomic pregnancies: A nationwide cohort study.

Infertility following trisomic pregnancies: A nationwide cohort study.

Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics

Published: June 06, 2024

The Finnish genetic heritage in 2022 - from diagnosis to translational research.

The Finnish genetic heritage in 2022 - from diagnosis to translational research.

Journal: Disease models & mechanisms

Published: October 26, 2022

Editorial: Can population health be personalized? Estonia and Finland as examples.

Editorial: Can population health be personalized? Estonia and Finland as examples.

Journal: Frontiers in genetics

Published: September 22, 2022

Opt-in for secondary findings as part of diagnostic whole-exome sequencing: Real-life experience from an international diagnostic laboratory.

Opt-in for secondary findings as part of diagnostic whole-exome sequencing: Real-life experience from an international diagnostic laboratory.

Journal: Molecular genetics & genomic medicine

Published: August 08, 2022

Psychosocial Effects of Receiving Genome-Wide Polygenic Risk Information Concerning Type 2 Diabetes and Coronary Heart Disease: A Randomized Controlled Trial.

Psychosocial Effects of Receiving Genome-Wide Polygenic Risk Information Concerning Type 2 Diabetes and Coronary Heart Disease: A Randomized Controlled Trial.

Journal: Frontiers in genetics

Published: February 22, 2022

A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use-The P5 Study.

A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use-The P5 Study.

Journal: Frontiers in genetics

Published: August 23, 2021

Simulating the Genetics Clinic of the Future - whether undergoing whole-genome sequencing shapes professional attitudes.

Simulating the Genetics Clinic of the Future - whether undergoing whole-genome sequencing shapes professional attitudes.

Journal: Journal of community genetics

Published: August 03, 2021

Rare diseases: past achievements and future prospects.

Rare diseases: past achievements and future prospects.

Journal: Journal of community genetics

Published: May 04, 2021

Clinical genetics in transition-a comparison of genetic services in Estonia, Finland, and the Netherlands.

Clinical genetics in transition-a comparison of genetic services in Estonia, Finland, and the Netherlands.

Journal: Journal of community genetics

Published: September 08, 2020

Showing 1-12 of 33

Last Updated: 09/26/2026