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Author Details

Predrag Radivojac
Indiana University
2002
131
43
Gloria M Sheynkman (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36540978Using Association Rules to Understand the Risk of Adverse Pregnancy Outcomes in a Diverse Population.Pac Symp Biocomput2023
37602697Searching and visualizing genetic associations of pregnancy traits by using GnuMoM2b.Genetics2023
37739408Learning from the unknown: exploring the range of bacterial functionality.Nucleic Acids Res2023
37333377Searching and visualizing genetic associations of pregnancy traits by using GnuMoM2b.medRxiv2023
36810564Non-Specific Signal Peptidase Processing of Extracellular Proteins in <i>Staphylococcus aureus</i> N315.Proteomes2023
36540991Exploiting Domain Knowledge as Causal Independencies in Modeling Gestational Diabetes.Pac Symp Biocomput2023
36540988Multi-objective prioritization of genes for high-throughput functional assays towards improved clinical variant classification.Pac Symp Biocomput2023
36540987An Approach to Identifying and Quantifying Bias in Biomedical Data.Pac Symp Biocomput2023
36540978Using Association Rules to Understand the Risk of Adverse Pregnancy Outcomes in a Diverse Population.Pac Symp Biocomput2023
37035530Active feature elicitation: An unified framework.Front Artif Intell2023
37739408Learning from the unknown: exploring the range of bacterial functionality.Nucleic Acids Res2023
37602697Searching and visualizing genetic associations of pregnancy traits by using GnuMoM2b.Genetics2023
37035530Active feature elicitation: An unified framework.Front Artif Intell2023
37333377Searching and visualizing genetic associations of pregnancy traits by using GnuMoM2b.medRxiv2023
36810564Non-Specific Signal Peptidase Processing of Extracellular Proteins in <i>Staphylococcus aureus</i> N315.Proteomes2023
36540991Exploiting Domain Knowledge as Causal Independencies in Modeling Gestational Diabetes.Pac Symp Biocomput2023
36540988Multi-objective prioritization of genes for high-throughput functional assays towards improved clinical variant classification.Pac Symp Biocomput2023
36540987An Approach to Identifying and Quantifying Bias in Biomedical Data.Pac Symp Biocomput2023
34549350Prioritizing de novo autism risk variants with calibrated gene- and variant-scoring models.Hum Genet2022
35709700Advancing remote homology detection: A step toward understanding and accurately predicting protein function.Cell Syst2022
36040739Association of Genetic Predisposition and Physical Activity With Risk of Gestational Diabetes in Nulliparous Women.JAMA Netw Open2022
35961013A roadmap for the functional annotation of protein families: a community perspective.Database (Oxford)2022
36149496Computational interpretation of human genetic variation.Hum Genet2022
36699361The field of protein function prediction as viewed by different domain scientists.Bioinform Adv2022
34549350Prioritizing de novo autism risk variants with calibrated gene- and variant-scoring models.Hum Genet2022
35709700Advancing remote homology detection: A step toward understanding and accurately predicting protein function.Cell Syst2022
36699361The field of protein function prediction as viewed by different domain scientists.Bioinform Adv2022
36149496Computational interpretation of human genetic variation.Hum Genet2022
36040739Association of Genetic Predisposition and Physical Activity With Risk of Gestational Diabetes in Nulliparous Women.JAMA Netw Open2022
35961013A roadmap for the functional annotation of protein families: a community perspective.Database (Oxford)2022
34258609A Probabilistic Approach to Extract Qualitative Knowledge for Early Prediction of Gestational Diabetes.Artif Intell Med Conf Artif Intell Med (2005-)2021
33683359Distinct error rates for reference and nonreference genotypes estimated by pedigree analysis.Genetics2021
34258609A Probabilistic Approach to Extract Qualitative Knowledge for Early Prediction of Gestational Diabetes.Artif Intell Med Conf Artif Intell Med (2005-)2021
33683359Distinct error rates for reference and nonreference genotypes estimated by pedigree analysis.Genetics2021
32657391The ortholog conjecture revisited: the value of orthologs and paralogs in function prediction.Bioinformatics2020
32016347An examination of citation-based impact of the computational biology conferences.Bioinformatics2020
33219223Inferring the molecular and phenotypic impact of amino acid variants with MutPred2.Nat Commun2020
32657391The ortholog conjecture revisited: the value of orthologs and paralogs in function prediction.Bioinformatics2020
32016347An examination of citation-based impact of the computational biology conferences.Bioinformatics2020
33219223Inferring the molecular and phenotypic impact of amino acid variants with MutPred2.Nat Commun2020
30463884New <i>Drosophila</i> Long-Term Memory Genes Revealed by Assessing Computational Function Prediction Methods.G3 (Bethesda)2019
31744546The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens.Genome Biol2019
30463884New <i>Drosophila</i> Long-Term Memory Genes Revealed by Assessing Computational Function Prediction Methods.G3 (Bethesda)2019
31144778Assessment of patient clinical descriptions and pathogenic variants from gene panel sequences in the CAGI-5 intellectual disability challenge.Hum Mutat2019
31301157Assessing computational predictions of the phenotypic effect of cystathionine-beta-synthase variants.Hum Mutat2019
31510708ISMB/ECCB 2019 Proceedings.Bioinformatics2019
31184403Assessment of methods for predicting the effects of PTEN and TPMT protein variants.Hum Mutat2019
31140652Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.Hum Mutat2019
30864324Precision Medicine: Improving health through high-resolution analysis of personal data.Pac Symp Biocomput2019
30864316Estimating classification accuracy in positive-unlabeled learning: characterization and correction strategies.Pac Symp Biocomput2019
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Collaborators

University of Washington
Co-authored papers 31
Center for Computational Biology, Indiana University School of Medicine
Co-authored papers 19
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Co-authored papers 17
Indiana University
Co-authored papers 17
Indiana University
Co-authored papers 16
Center for Data Analytics and Biomedical Informatics, Temple University
Co-authored papers 15
Iowa State University
Co-authored papers 12
Rutgers University
Co-authored papers 12
Morsani College of Medicine, University of South Florida
Co-authored papers 11
The Institute for Computational Medicine, The Johns Hopkins University
Co-authored papers 11
Institute of Medical Genetics, Cardiff University
Co-authored papers 11
Co-authored papers 11
BioMarin Pharmaceutical Inc.
Co-authored papers 11
Department of Pharmacy and Biotechnology, University of Bologna
Co-authored papers 10
Temple University
Co-authored papers 10
University of California berkeley
Co-authored papers 10
Baylor College of Medicine
Co-authored papers 9
Indiana University
Co-authored papers 9
The Buck Institute for Research on Aging
Co-authored papers 9
Department of Pharmacy and Biotechnology, University of Bologna
Co-authored papers 9
Department of Pharmacy and Biotechnology, University of Bologna
Co-authored papers 7
Institute for Bioscience and Biotechnology Research
Co-authored papers 6
Stanley Institute for Cognitive Genomics
Co-authored papers 6
Technical University of Munich (TUM)
Co-authored papers 5
University of Padova
Co-authored papers 5
University of Kent
Co-authored papers 5
University of Maryland
Co-authored papers 5
University of the Basque Country
Co-authored papers 4
Institute of Life Sciences, The Hebrew University of Jerusalem
Co-authored papers 4
University College London
Co-authored papers 4