Jaakko T. Leinonen
Espoo, Finland
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 22 publications
Introducing the Y-chromosomal Ancestral-like Reference Sequence-Improving the Capture of Human Evolutionary Information.
Journal: Molecular biology and evolution
Published: April 30, 2025
The Federated European Genome-Phenome Archive as a global network for sharing human genomics data.
Journal: Nature genetics
Published: March 03, 2025
Early establishment and life course stability of sex biases in the human brain transcriptome.
Journal: Cell genomics
Published: October 07, 2024
Author Correction: Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes.
Journal: Genome biology
Published: May 22, 2024
Y chromosome sequencing data suggest dual paths of haplogroup N1a1 into Finland.
Journal: European journal of human genetics : EJHG
Published: February 27, 2024
Disentangling the link between maternal influences on birth weight and disease risk in 36,211 genotyped mother-child pairs.
Journal: Communications biology
Published: October 18, 2023
Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes.
Journal: Genome biology
Published: February 19, 2023
Altered acylcarnitine metabolism and inflexible mitochondrial fuel utilization characterize the loss of neonatal myocardial regeneration capacity.
Journal: Experimental & molecular medicine
Published: May 22, 2022
Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.
Journal: Communications biology
Published: February 18, 2022
Genetic analyses implicate complex links between adult testosterone levels and health and disease.
Journal: Communications medicine
Published: September 17, 2021
GA4GH Passport standard for digital identity and access permissions.
Journal: Cell genomics
Published: March 18, 2021
Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation.
Journal: PloS one
Published: June 16, 2020
Last Updated: 09/26/2026