Annamari T Immonen

3PUBLICATIONS
8CO-AUTHORS
Neurology and neuromuscular diseasesForensic epidemiologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (3)

|Sep 16, 2026
A genetic and historical perspective on the origins of keratitis fugax hereditaria.

|Apr 21, 2026
Genetic risk factors in Finnish patients with Fuchs endothelial corneal dystrophy.

|Jun 08, 2023
Epithelial recurrent erosion dystrophy (ERED) from the splice site altering COL17A1 variant c.3156C>T in families of Finnish-Swedish ancestry.

Joni A Turunen, Ilpo S Tuisku, Pauliina Repo

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Frequent Collaborators

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Joni A Turunen

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Tero T Kivelä

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Pauliina Repo

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Sabita Kawan