Leena Kinnunen

Helsinki, Finland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 35 publications

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

Journal: Journal of human immunity

Published: April 15, 2026

Donor-matched iPSC model reveals context-dependent T2D genetic signals in fibro-adipogenic progenitors.

Donor-matched iPSC model reveals context-dependent T2D genetic signals in fibro-adipogenic progenitors.

Journal: bioRxiv : the preprint server for biology

Published: February 12, 2026

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

Journal: medRxiv : the preprint server for health sciences

Published: September 19, 2025

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

Journal: Wellcome open research

Published: October 02, 2023

Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Journal: Nature communications

Published: February 09, 2021

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Journal: Nature communications

Published: January 23, 2020

Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle.

Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: May 12, 2019

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

Journal: Scientific data

Published: January 24, 2018

Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

Journal: PLoS genetics

Published: August 24, 2017

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

Journal: Scientific data

Published: May 31, 2017

Interactions between genetic variation and cellular environment in skeletal muscle gene expression.

Interactions between genetic variation and cellular environment in skeletal muscle gene expression.

Journal: PloS one

Published: May 16, 2017

The effect of age and gender on the genetic regulation of serum 25-hydroxyvitamin D - the FIN-D2D population-based study.

The effect of age and gender on the genetic regulation of serum 25-hydroxyvitamin D - the FIN-D2D population-based study.

Journal: The Journal of steroid biochemistry and molecular biology

Published: April 25, 2017

Showing 1-12 of 35

Last Updated: 09/26/2026