Anna Syreeni

Helsinki, Finland

Last Updated: 09/26/2026

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Found 24 publications

Response to the Letter to the Editor Entitled "A Missing Genomic Dimension: The Small but Central Mitochondrial Genome in Diabetic Kidney Disease Genetics".

Response to the Letter to the Editor Entitled "A Missing Genomic Dimension: The Small but Central Mitochondrial Genome in Diabetic Kidney Disease Genetics".

Journal: Kidney international reports

Published: April 02, 2026

Blood DNA methylation markers are associated with diabetic kidney disease progression in type 1 diabetes.

Blood DNA methylation markers are associated with diabetic kidney disease progression in type 1 diabetes.

Journal: Diabetologia

Published: August 26, 2025

Exome-Wide Analysis Identifies a Rare EXD3 Missense Variant Associated With Diabetic Kidney Disease.

Exome-Wide Analysis Identifies a Rare EXD3 Missense Variant Associated With Diabetic Kidney Disease.

Journal: Kidney international reports

Published: May 30, 2025

Blood methylation biomarkers are associated with diabetic kidney disease progression in type 1 diabetes.

Blood methylation biomarkers are associated with diabetic kidney disease progression in type 1 diabetes.

Journal: medRxiv : the preprint server for health sciences

Published: December 09, 2024

Integrated analysis of blood DNA methylation, genetic variants, circulating proteins, microRNAs, and kidney failure in type 1 diabetes.

Integrated analysis of blood DNA methylation, genetic variants, circulating proteins, microRNAs, and kidney failure in type 1 diabetes.

Journal: Science translational medicine

Published: May 22, 2024

Whole-exome and whole-genome sequencing of 1064 individuals with type 1 diabetes reveals novel genes for diabetic kidney disease.

Whole-exome and whole-genome sequencing of 1064 individuals with type 1 diabetes reveals novel genes for diabetic kidney disease.

Journal: Diabetologia

Published: December 20, 2023

Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes.

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

Residual insulin secretion in individuals with type 1 diabetes in Finland: longitudinal and cross-sectional analyses.

Residual insulin secretion in individuals with type 1 diabetes in Finland: longitudinal and cross-sectional analyses.

Journal: The lancet. Diabetes & endocrinology

Published: February 03, 2023

Haptoglobin genotype and its relation to asymptomatic cerebral small-vessel disease in type 1 diabetes.

Haptoglobin genotype and its relation to asymptomatic cerebral small-vessel disease in type 1 diabetes.

Journal: Acta diabetologica

Published: December 12, 2022

Telomeres in clinical diabetes research - Moving towards precision medicine in diabetes care?

Telomeres in clinical diabetes research - Moving towards precision medicine in diabetes care?

Journal: Diabetes research and clinical practice

Published: October 27, 2022

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations.

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations.

Journal: Genome medicine

Published: August 02, 2022

Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease.

Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease.

Journal: Nature communications

Published: April 27, 2022

Showing 1-12 of 24

Last Updated: 09/26/2026