C. J. Spellicy, J. Norris, R. Bend, C. Bupp, P. Mester, T. Reynolds, J. Dean, Y. Peng, E. Alexov, C. E. Schwartz, and others. Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects. European Journal of Human Genetics, Nature Publishing Group, volume 26, issue 3, pages 420-427, 2018.

Y. Peng, J. Norris, C. Schwartz, and E. Alexov. Revealing the effects of missense mutations causing Snyder-Robinson syndrome on the stability and dimerization of spermine synthase. International journal of molecular sciences, Multidisciplinary Digital Publishing Institute, volume 17, issue 1, pages 77, 2016.

K. Vaidyanathan, T. Niranjan, M. May, R. Rose, C. F. Teo, S. Prabakaran, R. Bridger, E. Alexov, T. Wang, C. Schwartz, and others. Characterizing a missense mutation in O-GlcNAc transferase that segregates with disease in a family with X-linked Intellectual Disability. GLYCOBIOLOGY, volume 23, issue 11, pages 1334-1335, 2013.

Z. Zhang, J. Norris, V. Kalscheuer, T. Wood, L. Wang, C. Schwartz, E. Alexov, and H. V. Esch. A Y328C missense mutation in spermine synthase causes a mild form of Snyder--Robinson syndrome. Human molecular genetics, Oxford University Press, volume 22, issue 18, pages 3789-3797, 2013.

K. Takano, D. Liu, P. Tarpey, E. Gallant, A. Lam, S. Witham, E. Alexov, A. Chaubey, R. E. Stevenson, C. E. Schwartz, and others. An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. Human molecular genetics, Oxford University Press, volume 21, issue 20, pages 4497-4507, 2012.

Z. Zhang, J. Norris, C. Schwartz, and E. Alexov. In Silico and In Vitro Investigations of the Mutability of Disease-Causing Missense Mutation Sites in. 2011.

Z. Zhang, C. Schwartz, and E. Alexov. In Silico Investigation of Mutability of Spermine Synthase. Biophysical Journal, Elsevier, volume 100, issue 3, pages 321a, 2011.

S. Witham, K. Takano, C. Schwartz, and E. Alexov. In Silico Investigation of a Missense Mutation in CLIC2 Associated with Intellectual Disability. Biophysical Journal, Elsevier, volume 100, issue 3, pages 611a, 2011.

S. Witham, K. Takano, C. Schwartz, and E. Alexov. A missense mutation in CLIC2 associated with intellectual disability is predicted by in silico modeling to affect protein stability and dynamics. Proteins: Structure, Function, and Bioinformatics, Wiley Subscription Services, Inc., A Wiley Company Hoboken, volume 79, issue 8, pages 2444-2454, 2011.

Z. Zhang, J. Norris, C. Schwartz, and E. Alexov. In silico and in vitro investigations of the mutability of disease-causing missense mutation sites in spermine synthase. PloS one, Public Library of Science, volume 6, issue 5, pages e20373, 2011.

A. Pittman, R. Saul, A. Chaubey, E. Alexov, M. Tiemeyer, R. Steet, C. Schwartz, M. B\'en\'eteau, J. Ricci, V. Desquiret-Dumas, and others. PMCID: PMC2695060. Int Immunol, volume 22, issue 7, pages 593-603, 2010.

S. Teng, A. K. Srivastava, C. E. Schwartz, E. Alexov, and L. Wang. Structural assessment of the effects of Amino Acid Substitutions on protein stability and protein? protein interaction. International journal of computational biology and drug design, Inderscience Publishers, volume 3, issue 4, pages 334-349, 2010.

Z. Zhang, S. Teng, L. Wang, C. E. Schwartz, and E. Alexov. Computational analysis of missense mutations causing Snyder-Robinson syndrome. Human mutation, Wiley Subscription Services, Inc., A Wiley Company Hoboken, volume 31, issue 9, pages 1043-1049, 2010.