Search Results - "Bryzgalov, Leonid O"

  • Showing 1 - 11 results of 11
Refine Results
  1. 1

    Exploring the Genetic Predisposition to Epigenetic Changes in Alzheimer's Disease by Bryzgalov, Leonid O, Korbolina, Elena E, Merkulova, Tatiana I

    “…Alzheimer's disease (AD) is a prevalent type of dementia in elderly populations with a significant genetic component. The accumulating evidence suggests that…”
    Get full text
    Journal Article
  2. 2
  3. 3

    Novel functional variants at the GWAS-implicated loci might confer risk to major depressive disorder, bipolar affective disorder and schizophrenia by Bryzgalov, Leonid O, Korbolina, Elena E, Brusentsov, Ilja I, Leberfarb, Elena Y, Bondar, Natalia P, Merkulova, Tatiana I

    Published in BMC neuroscience (19-04-2018)
    “…A challenge of understanding the mechanisms underlying cognition including neurodevelopmental and neuropsychiatric disorders is mainly given by the potential…”
    Get full text
    Journal Article
  4. 4

    Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data by Bryzgalov, Leonid O, Antontseva, Elena V, Matveeva, Marina Yu, Shilov, Alexander G, Kashina, Elena V, Mordvinov, Viatcheslav A, Merkulova, Tatyana I

    Published in PloS one (29-10-2013)
    “…A vast amount of SNPs derived from genome-wide association studies are represented by non-coding ones, therefore exacerbating the need for effective…”
    Get full text
    Journal Article
  5. 5

    Novel approach to functional SNPs discovery from genome‐wide data reveals promising variants for colon cancer risk by Korbolina, Elena E., Brusentsov, Ilja I., Bryzgalov, Leonid O., Leberfarb, Elena Yu, Degtyareva, Arina O., Merkulova, Tatyana I.

    Published in Human mutation (01-06-2018)
    “…In the majority of colorectal cancer (CRC) cases, the genetic basis of predisposition remains unexplained. The goal of the study was to assess the regulatory…”
    Get full text
    Journal Article
  6. 6
  7. 7

    Application of quantitative trait locus mapping and transcriptomics to studies of the senescence-accelerated phenotype in rats by Korbolina, Elena E, Ershov, Nikita I, Bryzgalov, Leonid O, Kolosova, Natalia G

    Published in BMC genomics (19-12-2014)
    “…Etiology of complex disorders, such as cataract and neurodegenerative diseases including age-related macular degeneration (AMD), remains poorly understood due…”
    Get full text
    Journal Article
  8. 8

    Regulatory single nucleotide polymorphisms at the beginning of intron 2 of the human KRAS gene by Antontseva, Elena V, Matveeva, Marina Yu, Bondar, Natalia P, Kashina, Elena V, Leberfarb, Elena Yu, Bryzgalov, Leonid O, Gervas, Polina A, Ponomareva, Anastasia A, Cherdyntseva, Nadezhda V, Orlov, Yury L, Merkulova, Tatiana I

    Published in Journal of biosciences (01-12-2015)
    “…There are two regulatory single nucleotide polymorphisms (rSNPs) at the beginning of the second intron of the mouse K-ras gene that are strongly associated…”
    Get full text
    Journal Article
  9. 9
  10. 10

    Regulatory single nucleotide polymorphisms (rSNPs) at the promoters 1A and 1B of the human APC gene by Matveeva, Marina Yu, Kashina, Elena V, Reshetnikov, Vasily V, Bryzgalov, Leonid O, Antontseva, Elena V, Bondar, Natalia P, Merkulova, Tatiana I

    Published in BMC genetics (22-12-2016)
    “…Germline mutations in the coding sequence of the tumour suppressor APC gene give rise to familial adenomatous polyposis (which leads to colorectal cancer) and…”
    Get full text
    Journal Article
  11. 11

    Regulatory single nucleotide polymorphisms by Matveeva, Marina Yu, Kashina, Elena V, Reshetnikov, Vasily V, Bryzgalov, Leonid O, Antontseva, Elena V, Bondar, Natalia P, Merkulova, Tatiana I

    Published in BMC genetics (22-12-2016)
    “…Germline mutations in the coding sequence of the tumour suppressor APC gene give rise to familial adenomatous polyposis (which leads to colorectal cancer) and…”
    Get full text
    Journal Article