Lokki A Inkeri

8PUBLICATIONS
18CO-AUTHORS
Major global burdens of diseaseGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Predictive and prognostic markersHaematology
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Publications (8)

|Jun 29, 2026
Regulation of RGS2 is an important piece to the puzzle of syncytiotrophoblast dysfunction in preeclampsia.

|Apr 03, 2026
Risk Haplotype of BTNL2 Predisposes Male Patients to NSTEMI: A Genetic and Functional Study.

A Inkeri Lokki, Juha Sinisalo, Kitty Aierken

|Nov 27, 2025
The Impact of Complement Factor H-Related Protein Gene Deletions on Kidney Transplantation.

Salla Markkinen, A Inkeri Lokki, Ilkka Helanterä

|Dec 17, 2024
Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia.

A Inkeri Lokki, Michael Triebwasser, Emma Daly

|Apr 22, 2024
Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia.

A Lokki, Michael Triebwasser, Emma Daly

|Dec 23, 2023
The Novel Ceramide- and Phosphatidylcholine-Based Risk Score for the Prediction of New-Onset of Hypertension.

Mohammadreza Shoghli, A Inkeri Lokki, Mitja Lääperi

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Frequent Collaborators

2 joint publications

Juha Sinisalo

2 joint publications

John P Atkinson

1 joint publications

Mohammadreza Shoghli

1 joint publications

Jaakko Tuomilehto