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Computational Biophysics and Bioinformatics

Professor Emil Alexov Group

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Journal Articles by C. E. Schwartz


C. J. Spellicy, J. Norris, R. Bend, C. Bupp, P. Mester, T. Reynolds, J. Dean, Y. Peng, et al.
Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects
European Journal of Human Genetics, 26(3), 420-427, 2018
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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, 17(1), 77, 2016
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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, 22(18), 3789-3797, 2013
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K. Takano, D. Liu, P. Tarpey, E. Gallant, A. Lam, S. Witham, E. Alexov, A. Chaubey, et al.
An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity
Human molecular genetics, 21(20), 4497-4507, 2012
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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
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Z. Zhang, C. Schwartz, and E. Alexov
In Silico Investigation of Mutability of Spermine Synthase
Biophysical Journal, 100(3), 321a, 2011
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S. Witham, K. Takano, C. Schwartz, and E. Alexov
In Silico Investigation of a Missense Mutation in CLIC2 Associated with Intellectual Disability
Biophysical Journal, 100(3), 611a, 2011
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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, 79(8), 2444-2454, 2011
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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, 6(5), e20373, 2011
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A. Pittman, R. Saul, A. Chaubey, E. Alexov, M. Tiemeyer, R. Steet, C. Schwartz, M. B\'en\'eteau, et al.
PMCID: PMC2695060.
Int Immunol, 22(7), 593-603, 2010
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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, 3(4), 334-349, 2010
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Z. Zhang, S. Teng, L. Wang, C. E. Schwartz, and E. Alexov
Computational analysis of missense mutations causing Snyder-Robinson syndrome
Human mutation, 31(9), 1043-1049, 2010
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Conference Papers


K. Vaidyanathan, T. Niranjan, M. May, R. Rose, C. F. Teo, S. Prabakaran, R. Bridger, E. Alexov, et al.
Characterizing a missense mutation in O-GlcNAc transferase that segregates with disease in a family with X-linked Intellectual Disability
GLYCOBIOLOGY, 2013
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