Y. Yang, T. G. Kucukkal, J. Li, E. Alexov, and W. Cao. Binding analysis of methyl-CpG binding domain of MeCP2 and Rett syndrome mutations. ACS chemical biology, American Chemical Society, volume 11, issue 10, pages 2706-2715, 2016.

T. G. Kucukkal and E. Alexov. Structural, dynamical, and energetical consequences of Rett syndrome mutation R133C in MeCP2. Computational and mathematical methods in medicine, Hindawi, volume 2015, 2015.

T. G. Kucukkal, Y. Yang, O. Uvarov, W. Cao, and E. Alexov. Impact of rett syndrome mutations on MeCP2 MBD stability. Biochemistry, American Chemical Society, volume 54, issue 41, pages 6357-6368, 2015.

Y. Peng, J. Suryadi, Y. Yang, T. G. Kucukkal, W. Cao, and E. Alexov. Mutations in the KDM5C ARID domain and their plausible association with syndromic Claes-Jensen-Type disease. International journal of molecular sciences, Multidisciplinary Digital Publishing Institute, volume 16, issue 11, pages 27270-27287, 2015.

M. Petukh, T. G. Kucukkal, and E. Alexov. On human disease-causing amino acid variants: Statistical study of sequence and structural patterns. Human mutation, volume 36, issue 5, pages 524-534, 2015.

T. G. Kucukkal, M. Petukh, L. Li, and E. Alexov. Structural and physico-chemical effects of disease and non-disease nsSNPs on proteins. Current opinion in structural biology, Elsevier Current Trends, volume 32, pages 18-24, 2015.

T. G. Kucukkal, Y. Yang, S. C. Chapman, W. Cao, and E. Alexov. Computational and experimental approaches to reveal the effects of single nucleotide polymorphisms with respect to disease diagnostics. International journal of molecular sciences, Multidisciplinary Digital Publishing Institute, volume 15, issue 6, pages 9670-9717, 2014.