O. Šterna

Phenylketonuria in the Latvian population: Molecular basis, phenylalanine levels, and patient compliance

L. Gailīte, M. Kreile, N. Proņina, 2020, Molecular genetics and metabolism reports.

Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia

Z. Krūmiņa, L. Gailīte, B. Lāce, 2022, Neurology: Genetics.

New-Born Screening for Spinal Muscular Atrophy: Results of a Latvian Pilot Study

L. Gailīte, I. Micule, O. Šterna, 2022, International journal of neonatal screening.

Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss

A. Krūmiņa, S. Kušķe, A. Petersons, 2009 .