Reetta‐Stiina Järvinen

In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria from a Pathogenic Variant in NLRP3.

T. Kivelä, J. Turunen, A. Jaakkola, 2020, American journal of ophthalmology.

Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene.

T. Kivelä, J. Wedenoja, A. Riikonen, 2018, American journal of ophthalmology.

Population-based analysis of BAP1 germline variations in patients with uveal melanoma.

V. Raivio, T. Kivelä, J. Turunen, 2019, Human molecular genetics.

Germline Loss-of-function Variants in MBD4 are Rare in Finnish Patients with Uveal Melanoma.

V. Raivio, T. Kivelä, J. Turunen, 2020, Pigment cell & melanoma research.

A novel missense TGFBI variant p.(Ser591Phe) in a Finnish family with variant lattice corneal dystrophy

T. Kivelä, J. Turunen, A. Jaakkola, 2021, European journal of ophthalmology.

Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide

Ivana K. Kim, S. Puig, N. Hayward, 2018, Journal of the National Cancer Institute.