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Voskanian A, Katsonis P, Lichtarge O, et al. (2019) Assessing the performance of in-silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancer. Human Mutation |
Peters B, Brenner SE, Wang E, et al. (2018) Putting benchmarks in their rightful place: The heart of computational biology. Plos Computational Biology. 14: e1006494 |
Cirincione AG, Clark KL, Kann MG. (2018) Pathway networks generated from human disease phenome. Bmc Medical Genomics. 11: 75 |
Gauran IIM, Park J, Lim J, et al. (2017) Empirical null estimation using zero-inflated discrete mixture distributions and its application to protein domain data. Biometrics |
Peterson TA, Gauran IIM, Park J, et al. (2017) Oncodomains: A protein domain-centric framework for analyzing rare variants in tumor samples. Plos Computational Biology. 13: e1005428 |
Peterson TA, Mort M, Cooper DN, et al. (2016) Regulatory Single Nucleotide Variant Predictor (RSVP) Increases Predictive Performance of Functional Regulatory Variants. Human Mutation |
Burger JD, Doughty E, Khare R, et al. (2014) Hybrid curation of gene-mutation relations combining automated extraction and crowdsourcing. Database : the Journal of Biological Databases and Curation. 2014 |
Peterson TA, Doughty E, Kann MG. (2013) Towards precision medicine: advances in computational approaches for the analysis of human variants. Journal of Molecular Biology. 425: 4047-63 |
Peterson TA, Park D, Kann MG. (2013) A protein domain-centric approach for the comparative analysis of human and yeast phenotypically relevant mutations. Bmc Genomics. 14: S5 |
Gonzalez MW, Kann MG. (2012) Chapter 4: Protein interactions and disease. Plos Computational Biology. 8: e1002819 |