Baiba Lace

8PUBLICATIONS
74CO-AUTHORS
Other European languagesOphthalmology and optometry not elsewhere classifiedMedical infection agents (incl. prions)Cancer geneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (8)

|Jun 15, 2026
Identifying barriers and policy priorities for rare disease research in underrepresented European countries.

|Jun 09, 2025
Describing the First Canadian Cohort of Oculogastrointestinal Neurodevelopmental Syndrome Caused by CAPN15 Pathogenic Variants.

Eric Lin, Tania Cruz-Marino, Nicolas Chrestian

|Nov 15, 2024
The phenotypic spectrum of PTCD3 deficiency.

Baiba Lace, Eissa Faqeih, Namik Kaya

|Apr 26, 2024
Unraveling the Pathogenetic Mechanisms Underlying the Association between Specific Mitochondrial DNA Haplogroups and Parkinson's Disease.

Min-Yu Lan, Tsu-Kung Lin, Baiba Lace

|Apr 08, 2024
The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy.

A Reghan Foley, Véronique Bolduc, Fady Guirguis

|Nov 16, 2022
Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia.

Baiba Lace, Ieva Micule, Viktorija Kenina

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Frequent Collaborators

1 joint publications

Magdalena Mroczek

1 joint publications

Inna Inashkina

1 joint publications

Janis Stavusis

1 joint publications

Andrey Khrunin