Dmitrijs Rots

6PUBLICATIONS
76CO-AUTHORS
Epidemiological modellingNeonatologyGene expression (incl. microarray and other genome-wide approaches)Cell and nuclear divisionGenetic immunology
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Publications (6)

|Jul 01, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity.

|Jan 29, 2026
A Novel PCK1 Gene Variant Associated With Cytosolic Phosphoenolpyruvate Carboxykinase Deficiency: Two Siblings With Different Clinical Presentations.

Lauma Vasiļevska, Ieva Puķīte, Madara Auzenbaha

|Oct 30, 2025
Novel GNB4 Gene Variant and the Spectrum of GNB4 Variants in Patients With Charcot-Marie-Tooth Disease.

Dace Pretkalnina, Marija Jurcenko, Marija Rozevska

|Oct 20, 2025
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making.

Daphne J Smits, Federico Ferraro, Mark Drost

|Mar 28, 2020
Genetic landscape of preterm birth due to cervical insufficiency: Comprehensive gene analysis and patient next-generation sequencing data interpretation.

Ludmila Volozonoka, Dmitrijs Rots, Inga Kempa

|Mar 13, 2018
Influence of IL15 gene variations on the clinical features, treatment response and risk of developing childhood acute lymphoblastic leukemia in Latvian population.

Dmitrijs Rots, Madara Kreile, Sergejs Nikulshin

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Frequent Collaborators

2 joint publications

Linda Gailite

1 joint publications

Ludmila Volozonoka

1 joint publications

Anna Miskova

1 joint publications

Daphne J Smits