Elena V. Shakhtshneider

Novosibirsk, NVS 630090, Russian Federation

Last Updated: 09/26/2026

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Found 31 publications

Comorbidities and Molecular Genetics Status in Familial and Nonfamilial Hypercholesterolemia: A Single-Center Study.

Comorbidities and Molecular Genetics Status in Familial and Nonfamilial Hypercholesterolemia: A Single-Center Study.

Journal: International journal of molecular sciences

Published: November 09, 2025

Materials of the 2nd Conference with International Participation "Basic Research in Endocrinology: A Modern Strategy for the Development and Technologies of Personalized Medicine".

Materials of the 2nd Conference with International Participation "Basic Research in Endocrinology: A Modern Strategy for the Development and Technologies of Personalized Medicine".

Journal: Journal of personalized medicine

Published: March 21, 2025

Diagnosis of Familial Hypercholesterolemia in Children and Young Adults.

Diagnosis of Familial Hypercholesterolemia in Children and Young Adults.

Journal: International journal of molecular sciences

Published: November 09, 2023

Rare Variants of Obesity-Associated Genes in Young Adults with Abdominal Obesity.

Rare Variants of Obesity-Associated Genes in Young Adults with Abdominal Obesity.

Journal: Journal of personalized medicine

Published: September 05, 2023

Association of the APOE Gene Polymorphism with Depression in White Adults in the WHO "MONICA-Psychosocial" Program.

Association of the APOE Gene Polymorphism with Depression in White Adults in the WHO "MONICA-Psychosocial" Program.

Journal: Journal of personalized medicine

Published: July 18, 2023

Association of Common Variants of APOE, CETP, and the 9p21.3 Chromosomal Region with the Risk of Myocardial Infarction: A Prospective Study.

Association of Common Variants of APOE, CETP, and the 9p21.3 Chromosomal Region with the Risk of Myocardial Infarction: A Prospective Study.

Journal: International journal of molecular sciences

Published: May 30, 2023

Functionally Significant Variants in Genes Associated with Abdominal Obesity: A Review.

Functionally Significant Variants in Genes Associated with Abdominal Obesity: A Review.

Journal: Journal of personalized medicine

Published: December 15, 2022

Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning.

Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: December 13, 2022

The Mutation Spectrum of Rare Variants in the Gene of Adenosine Triphosphate (ATP)-Binding Cassette Subfamily C Member 8 in Patients with a MODY Phenotype in Western Siberia.

The Mutation Spectrum of Rare Variants in the Gene of Adenosine Triphosphate (ATP)-Binding Cassette Subfamily C Member 8 in Patients with a MODY Phenotype in Western Siberia.

Journal: Journal of personalized medicine

Published: December 09, 2022

Associations of APOE Gene Variants rs429358 and rs7412 with Parameters of the Blood Lipid Profile and the Risk of Myocardial Infarction and Death in a White Population of Western Siberia.

Associations of APOE Gene Variants rs429358 and rs7412 with Parameters of the Blood Lipid Profile and the Risk of Myocardial Infarction and Death in a White Population of Western Siberia.

Journal: Current issues in molecular biology

Published: March 22, 2022

Basic Research in Atherosclerosis: Technologies of Personalized Medicine.

Basic Research in Atherosclerosis: Technologies of Personalized Medicine.

Journal: Journal of personalized medicine

Published: February 24, 2022

Analysis of Rare Variants in Genes Related to Lipid Metabolism in Patients with Familial Hypercholesterolemia in Western Siberia (Russia).

Analysis of Rare Variants in Genes Related to Lipid Metabolism in Patients with Familial Hypercholesterolemia in Western Siberia (Russia).

Journal: Journal of personalized medicine

Published: October 31, 2021

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Last Updated: 09/26/2026