Automated Author ProfileBulavin, Leonid A.
Bulavin, Leonid A.
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets for this author
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the author's datasets
Total Mentions
Total mentions of the author's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 0.8 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
The geometries and molecular properties (DFT energies, dipole moments, traceless quadrupole moments, APT charges, RESP charges) of conformers of the four canonical 2'-deoxyribonucleotide-5'-monophosphates (namely, 613 conformers of dCMP, 660 of dTMP, 726 of dAMP and 745 of dGMP), taken from the following studies:
* Nikolaienko, T. Yu.; Hovorun D. M. Quantum-mechanical conformational analysis of 2'-deoxycytidilic acid molecule – the DNA structural unit. Dopov. Nac. akad. nauk Ukr. 2010, 9, 173–184.
* Nikolaienko, T. Yu.; Bulavin, L. A.; Hovorun D. M. Quantum-mechanical conformational analysis of the 5'-thymidilic acid molecule. Ukr. Biokhim. Zh. 2010, 82(6), 76–86.
* Nikolaienko, T. Yu.; Bulavin, L. A.; Hovorun D. M. The 5'-deoxyadenylic acid molecule con formational capacity : Quantum-mechanical investigation using density functional theory (DFT). Ukr. Biokhim. Zh. 2011, 83(4), 16–28.
* Nikolaienko, T. Yu.; Bulavin, L. A.; Hovorun D. M. Conformational capacity of 5'-deoxyguanylic acid molecule investigated by quantum-mechanical methods. Biopolym. Cell. 2011, 27(4), 291-299.
The structures are optimized at B3LYP/6-31G(d,p) level of theory.
Please, cite the mentioned original research papers in case if any data from this dataset is used.
Authors
- Tymofii Yu. Nikolaienko ;
- Bulavin, Leonid A. ;
- Hovorun, Dmytro M.
The geometries and molecular properties (DFT energies, dipole moments, traceless quadrupole moments, APT charges, RESP charges) of conformers of the four canonical 2'-deoxyribonucleotide-5'-monophosphates (namely, 613 conformers of dCMP, 660 of dTMP, 726 of dAMP and 745 of dGMP), taken from the following studies:
* Nikolaienko, T. Yu.; Hovorun D. M. Quantum-mechanical conformational analysis of 2'-deoxycytidilic acid molecule – the DNA structural unit. Dopov. Nac. akad. nauk Ukr. 2010, 9, 173–184.
* Nikolaienko, T. Yu.; Bulavin, L. A.; Hovorun D. M. Quantum-mechanical conformational analysis of the 5'-thymidilic acid molecule. Ukr. Biokhim. Zh. 2010, 82(6), 76–86.
* Nikolaienko, T. Yu.; Bulavin, L. A.; Hovorun D. M. The 5'-deoxyadenylic acid molecule con formational capacity : Quantum-mechanical investigation using density functional theory (DFT). Ukr. Biokhim. Zh. 2011, 83(4), 16–28.
* Nikolaienko, T. Yu.; Bulavin, L. A.; Hovorun D. M. Conformational capacity of 5'-deoxyguanylic acid molecule investigated by quantum-mechanical methods. Biopolym. Cell. 2011, 27(4), 291-299.
The structures are optimized at B3LYP/6-31G(d,p) level of theory.
Please, cite the mentioned original research papers in case if any data from this dataset is used.
Authors
- Tymofii Yu. Nikolaienko ;
- Bulavin, Leonid A. ;
- Hovorun, Dmytro M.