Lea M. Urpa

Helsinki, Finland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Population-scale molecular reconstruction of human circadian phase from blood biomarkers.

Population-scale molecular reconstruction of human circadian phase from blood biomarkers.

Journal: medRxiv : the preprint server for health sciences

Published: July 30, 2026

The genetic architecture of fibromyalgia across 2.5 million individuals.

The genetic architecture of fibromyalgia across 2.5 million individuals.

Journal: medRxiv : the preprint server for health sciences

Published: September 26, 2025

The genetic architecture of fibromyalgia across 2.5 million individuals.

The genetic architecture of fibromyalgia across 2.5 million individuals.

Journal: Nature medicine

Published: September 18, 2025

Genetic variants affect diurnal glucose levels throughout the day.

Genetic variants affect diurnal glucose levels throughout the day.

Journal: Nature communications

Published: May 07, 2025

Genetic variants affect diurnal glucose levels throughout the day.

Genetic variants affect diurnal glucose levels throughout the day.

Journal: bioRxiv : the preprint server for biology

Published: August 02, 2024

Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders.

Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders.

Journal: Molecular psychiatry

Published: July 21, 2023

Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability.

Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability.

Journal: European journal of human genetics : EJHG

Published: July 11, 2023

Functional Characterization of Six SLCO1B1 (OATP1B1) Variants Observed in Finnish Individuals with a Psychotic Disorder.

Functional Characterization of Six SLCO1B1 (OATP1B1) Variants Observed in Finnish Individuals with a Psychotic Disorder.

Journal: Molecular pharmaceutics

Published: February 13, 2023

The impact of rare protein coding genetic variation on adult cognitive function.

The impact of rare protein coding genetic variation on adult cognitive function.

Journal: Nature genetics

Published: June 22, 2022

A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development.

A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development.

Journal: European journal of human genetics : EJHG

Published: July 13, 2021

Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.

Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.

Journal: Molecular psychiatry

Published: March 19, 2020

The bradykinin system in stress and anxiety in humans and mice.

The bradykinin system in stress and anxiety in humans and mice.

Journal: Scientific reports

Published: September 22, 2019

Showing 1-12 of 15

Last Updated: 09/26/2026