Nella Junna
Helsinki, 00290, Finland
Last Updated: 09/26/2026
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Found 9 publications
Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes.
Journal: Nature genetics
Published: March 04, 2023
Distinct and shared genetic architectures of Gestational diabetes mellitus and Type 2 Diabetes Mellitus.
Journal: medRxiv : the preprint server for health sciences
Published: March 03, 2023
Large registry-based analysis of genetic predisposition to tuberculosis identifies genetic risk factors at HLA.
Journal: Human molecular genetics
Published: February 25, 2022
How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study.
Journal: Circulation. Genomic and precision medicine
Published: February 07, 2022
LIN28B affects gene expression at the hypothalamic-pituitary axis and serum testosterone levels.
Journal: Scientific reports
Published: July 15, 2019
The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?
Journal: International journal of cardiology
Published: July 20, 2017
Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress.
Journal: BBA clinical
Published: January 13, 2015
De novo mutations in the motor domain of KIF1A cause cognitive impairment, spastic paraparesis, axonal neuropathy, and cerebellar atrophy.
Journal: Human mutation
Published: June 18, 2014
Showing 1-9 of 9
Last Updated: 09/26/2026