Marianna E. Weener
Moscow, MOW, Russian Federation
Last Updated: 09/26/2026
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Found 11 publications
Clinical and molecular features of PRCD-associated retinopathy.
Journal: Acta ophthalmologica
Published: May 07, 2026
Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations
Journal: Vestnik oftalmologii
Published: March 07, 2024
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction.
Journal: HGG advances
Published: October 11, 2022
Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease-associated genes.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 19, 2022
Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype.
Journal: NPJ genomic medicine
Published: May 19, 2022
Early audiological phenotype in patients with mutations in the USH2A gene.
Journal: International journal of pediatric otorhinolaryngology
Published: October 18, 2021
Combinatorial Approaches for Cancer Treatment Using Oncolytic Viruses: Projecting the Perspectives through Clinical Trials Outcomes.
Journal: Viruses
Published: May 29, 2021
A novel multi-omics-based highly accurate prediction of symptoms, comorbid conditions, and possible long-term complications of COVID-19.
Journal: Molecular omics
Published: March 08, 2021
The Spike of SARS-CoV-2: Uniqueness and Applications.
Journal: Frontiers in immunology
Published: February 04, 2021
Multi-omics-based identification of SARS-CoV-2 infection biology and candidate drugs against COVID-19.
Journal: Computers in biology and medicine
Published: August 11, 2020
Showing 1-11 of 11
Last Updated: 09/26/2026