Ludmila Volozonoka

Riga, RIX, Latvia

Last Updated: 09/26/2026

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Found 13 publications

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Journal: American journal of human genetics

Published: February 06, 2026

Preterm birth in Latvia: Two-decade national trends, structure, and risk factors.

Preterm birth in Latvia: Two-decade national trends, structure, and risk factors.

Journal: Acta obstetricia et gynecologica Scandinavica

Published: April 03, 2025

Unravelling the genetic landscape of cervical insufficiency: Insights into connective tissue dysfunction and hormonal pathways.

Unravelling the genetic landscape of cervical insufficiency: Insights into connective tissue dysfunction and hormonal pathways.

Journal: PloS one

Published: February 29, 2024

Management of Pregnancy with Cervical Shortening: Real-Life Clinical Challenges.

Management of Pregnancy with Cervical Shortening: Real-Life Clinical Challenges.

Journal: Medicina (Kaunas, Lithuania)

Published: February 13, 2023

Whole Genome Amplification in Preimplantation Genetic Testing in the Era of Massively Parallel Sequencing.

Whole Genome Amplification in Preimplantation Genetic Testing in the Era of Massively Parallel Sequencing.

Journal: International journal of molecular sciences

Published: April 10, 2022

A systematic review and standardized clinical validity assessment of genes involved in female reproductive failure.

A systematic review and standardized clinical validity assessment of genes involved in female reproductive failure.

Journal: Reproduction (Cambridge, England)

Published: December 08, 2021

Reducing misdiagnosis caused by maternal cell contamination in genetic testing for early pregnancy loss.

Reducing misdiagnosis caused by maternal cell contamination in genetic testing for early pregnancy loss.

Journal: Systems biology in reproductive medicine

Published: October 16, 2020

Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.

Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.

Journal: Human reproduction (Oxford, England)

Published: August 14, 2020

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

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

Journal: PloS one

Published: January 28, 2020

Lack of evidence for a role of PIWIL1 variants in human male infertility.

Lack of evidence for a role of PIWIL1 variants in human male infertility.

Journal: Cell

Published: October 21, 2019

A systematic review and standardized clinical validity assessment of male infertility genes.

A systematic review and standardized clinical validity assessment of male infertility genes.

Journal: Human reproduction (Oxford, England)

Published: October 05, 2018

First preimplantation genetic testing case for monogenic disease in Latvia.

First preimplantation genetic testing case for monogenic disease in Latvia.

Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology

Published: December 22, 2017

Showing 1-12 of 13

Last Updated: 09/26/2026