Henrik Forsius

Mutations in KERA, encoding keratocan, cause cornea plana

Natalia S. Pellegata, José L. Dieguez-Lucena, Tarja Joensuu et al. · Nature Genetics · 2000 · 199 citations

Ophthalmology, Corneal Dystrophy, Genetics +5

Exfoliation syndrome: 
Frequency, gender distribution and association with climatically induced alterations of the cornea and conjunctiva

Henrik Forsius, Eva Forsman, Johan Fellman et al. · Acta Ophthalmologica Scandinavica · 2002 · 63 citations · Full text

Association of LOXL1 gene with Finnish exfoliation syndrome patients

Susanna Lemmelä, Eva Forsman, Päivi Onkamo et al. · Journal of Human Genetics · 2009 · 62 citations

Genetic Epidemiology, Dermatology, Loxl1 Gene +1

A Novel<i>CACNA1F</i>Gene Mutation Causes Aland Island Eye Disease

Reetta Jalkanen, N. Torben Bech‐Hansen, Rose Tobias et al. · Investigative Ophthalmology & Visual Science · 2007 · 58 citations

Exfoliation syndrome: prevalence and inheritance in a subisolate of the Finnish population

Eva Forsman, Rita M. Cantor, Ake T Lu et al. · Acta Ophthalmologica Scandinavica · 2007 · 52 citations