Issue |
Section |
Title |
File |
Vol 52, No 3 (2016) |
Human Genetics |
Role of allelic genes of matrix metalloproteinases and their tissue inhibitors in the risk of peptic ulcer disease development |
|
Vol 52, No 6 (2016) |
Human Genetics |
Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia |
|
Vol 52, No 9 (2016) |
Short Communications |
Mutational landscape of prostate tumors revealed by whole-exome sequencing |
|
Vol 52, No 10 (2016) |
Short Communications |
The search for new candidate genes involved in ovarian cancer pathogenesis by exome sequencing |
|
Vol 53, No 5 (2017) |
Review and Theoretical Articles |
Genetic aspects of keratoconus development |
|
Vol 53, No 6 (2017) |
Human Genetics |
Analysis of GJB6 (Сx30) and GJB3 (Сx31) genes in deaf patients with monoallelic mutations in GJB2 (Сx26) gene in the Sakha Republic (Yakutia) |
|
Vol 53, No 7 (2017) |
Human Genetics |
Search for osteoarthritis genetic markers in women with undifferentiated connective tissue dysplasia |
|
Vol 53, No 8 (2017) |
Medical Genetics |
The carrier rate of the phenylalanine hydoxylase gene (PAH) mutations p.Arg408Trp, pArg261Gln, and p.Arg261X in the populations of Eurasia |
|
Vol 53, No 8 (2017) |
Short Communications |
Reconstruction of SNP haplotypes with mutation c.-23+1G>A in human gene GJB2 (Chromosome 13) in some populations of Eurasia |
|
Vol 53, No 10 (2017) |
Human Genetics |
Genetic characterization of Balkars and Karachays according to the variability of the Y chromosome |
|
Vol 54, No 11 (2018) |
Mathematical Models and Methods |
Evaluation of Prioritization Methods of Extrinsic Apoptotic Signaling Pathway Genes for Retrieval of the New Candidates Associated with Major Depressive Disorder |
|
Vol 54, No 12 (2018) |
Reviews and Theoretical Articles |
The Role of Epigenetic Factors in the Development of Depressive Disorders |
|
Vol 54, No 2 (2018) |
Medical Genetics |
Ethnic Features of Genetic Susceptibility to Breast Cancer |
|
Vol 54, No 5 (2018) |
Human Genetics |
Marital Structure, Genetic Fitness, and the GJB2 Gene Mutations among Deaf People in Yakutia (Eastern Siberia, Russia) |
|
Vol 54, No 5 (2018) |
Human Genetics |
MicroRNA Biogenesis Pathway Gene Polymorphisms Are Associated with Breast Cancer Risk |
|
Vol 54, No 6 (2018) |
Reviews and Theoretical Articles |
Schizophrenia Genetics |
|
Vol 55, No 1 (2019) |
Human Genetics |
Genetic Characterization of Balkars and Karachays Using mtDNA Data |
|
Vol 55, No 2 (2019) |
Short Communications |
Major Mutation in the SPAST Gene in Patients with Autosomal Dominant Spastic Paraplegia from the Republic of Bashkortostan |
|
Vol 55, No 3 (2019) |
Human Genetics |
The Role of Allelic Variants of Several Genes of Cytokines in the Development of Gastric Cancer |
|
Vol 55, No 7 (2019) |
Reviews and Theoretical Articles |
Molecular Genetic Studies of Cognitive Ability |
|
Vol 55, No 7 (2019) |
Human Genetics |
A WRN Nonsense Mutation, p.R1406X, is Not a Risk Factor of Breast Cancer |
|
Vol 55, No 9 (2019) |
Reviews and Theoretical Articles |
Epigenetics of Aggressive Behavior |
|
Vol 55, No 12 (2019) |
Human Genetics |
Association between Allelic Variants of the Genes Involved in Glucocorticoids Metabolism and Asthma |
|