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Fingerprint Dive into the research topics where Александр Артурович Канапин is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Mutation Биологические науки и медицина
Genome Биологические науки и медицина
Protein Databases Биологические науки и медицина
Proteins Биологические науки и медицина
Bacillus subtilis Биологические науки и медицина
motor development Биология и сельское хозяйство
Databases Биологические науки и медицина
Fish Proteins Биологические науки и медицина

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Research Output 1993 2019

  • 5346 Citations
  • 18 h-Index
  • 37 статья
  • 11 статья в сборнике материалов конференции
  • 1 глава/раздел
  • 1 Обзорная статья

Arginine methylation expands the regulatory mechanisms and extends the genomic landscape under E2F control

Roworth, A. P., Carr, S. M., Liu, G., Barczak, W., Miller, R. L., Munro, S., Kanapin, A. A., Samsonova, A. & La Thangué, N. B., Jun 2019, In : Science advances. 5, 6, eaaw4640.

Research output

Open Access

Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice

UK IBD Genetics Consortium and COLORS in IBD and Oxford IBD cohort study investigators and WGS500 Consortium, 2019, In : Human Molecular Genetics.

Research output

Open Access
23 Citations (Scopus)

Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project

Robbe, P., Popitsch, N., Knight, S. J. L., Antoniou, P., Becq, J., He, M., Kanapin, A., Samsonova, A., Vavoulis, D. V., Ross, M. T., Kingsbury, Z., Cabes, M., Ramos, S. D. C., Page, S., Dreau, H., Ridout, K., Jones, L. J., Tuff-Lacey, A., Henderson, S., Mason, J. & 14 others, Buffa, F. M., Verrill, C., Maldonado-Perez, D., Roxanis, I., Collantes, E., Browning, L., Dhar, S., Damato, S., Davies, S., Caulfield, M., Bentley, D. R., Taylor, J. C., Turnbull, C. & Schuh, A., 2018, In : Genetics in Medicine.

Research output

7 Citations (Scopus)
Genomic Segmental Duplications
18 Citations (Scopus)

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

UK IBD Genetics Consortium and COLORS in IBD and Oxford IBD cohort study investigators and WGS500 Consortium, 1 Mar 2018, In : Mucosal Immunology. 11, 2, p. 562-574 13 p.

Research output

Inflammatory Bowel Diseases
Reactive Oxygen Species