Nikolay N. Chekanov
Moscow, MOW 117437, Russian Federation
Last Updated: 09/26/2026
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Found 11 publications
An Endemic Region of Thiamine-Responsive Megaloblastic Anemia Caused by an SLC19A2 c.1223+1G>A Founder Mutation.
Journal: International journal of molecular sciences
Published: April 30, 2026
Carrier Frequencies of Medically Actionable Pathogenic Variants in the Russian Population.
Journal: International journal of molecular sciences
Published: April 21, 2026
Genetic Features of Albinism: A Comprehensive Analysis in the Russian Population.
Journal: Pigment cell & melanoma research
Published: June 19, 2025
The use of whole genome sequencing to study young patients with 100+ adenomas of the colon.
Journal: Frontiers in oncology
Published: April 22, 2025
GENA-LM: a family of open-source foundational DNA language models for long sequences.
Journal: Nucleic acids research
Published: September 16, 2024
Cell type-specific interpretation of noncoding variants using deep learning-based methods.
Journal: GigaScience
Published: May 01, 2022
Annotation of uORFs in the OMIM genes allows to reveal pathogenic variants in 5'UTRs.
Journal: Nucleic acids research
Published: February 07, 2022
Between Lake Baikal and the Baltic Sea: genomic history of the gateway to Europe.
Journal: BMC genetics
Published: January 04, 2018
Report on noninvasive prenatal testing: classical and alternative approaches.
Journal: F1000Research
Published: April 13, 2016
Study of Alzheimer family case reveals hemochromotosis-associated HFE mutation.
Journal: Human genome variation
Published: January 01, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026