Elina Kilpelainen
Helsinki, Finland
Last Updated: 09/26/2026
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Found 9 publications
Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes.
Journal: Scientific reports
Published: September 25, 2023
High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases.
Journal: Laboratory investigation; a journal of technical methods and pathology
Published: August 10, 2023
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.
Journal: Nature
Published: February 24, 2023
Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations.
Journal: Genome medicine
Published: August 02, 2022
FinnGen provides genetic insights from a well-phenotyped isolated population.
Journal: Nature
Published: January 10, 2022
Dissecting the contribution of single nucleotide polymorphisms in CCR9 and CCL25 genomic regions to the celiac disease phenotype.
Journal: Journal of translational autoimmunity
Published: August 12, 2021
Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes.
Journal: Journal of human genetics
Published: June 30, 2020
Phenome-wide association studies across large population cohorts support drug target validation.
Journal: Nature communications
Published: October 27, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026