Elena E. Baranova
Moscow, MOW 125993, Russian Federation
Last Updated: 09/26/2026
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Found 8 publications
CDKN2A Gene Mutations: Implications for Hereditary Cancer Syndromes.
Journal: Biomedicines
Published: November 12, 2023
The CFTR Gene Germline Heterozygous Pathogenic Variants in Russian Patients with Malignant Neoplasms and Healthy Carriers: 11,800 WGS Results.
Journal: International journal of molecular sciences
Published: March 17, 2023
A Unique Observation of a Patient with Vulto-van Silfhout-de Vries Syndrome.
Journal: Diagnostics (Basel, Switzerland)
Published: June 29, 2022
Whole genome non-invasive prenatal testing in prenatal screening algorithm: clinical experience from 12,700 pregnancies.
Journal: BMC pregnancy and childbirth
Published: March 10, 2022
Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 20, 2021
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
Journal: American journal of human genetics
Published: June 12, 2020
Hereditary cancer syndromes: a modern paradigm
Journal: Problemy endokrinologii
Published: March 23, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026