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Author Details

Michael L Tress
Spanish National Cancer Research Centre (CNIO)
1999
66
35
PMIDPaper TitleJournal TitlePublished Year
36420896GENCODE: reference annotation for the human and mouse genomes in 2023.Nucleic Acids Res2023
36420896GENCODE: reference annotation for the human and mouse genomes in 2023.Nucleic Acids Res2023
37398104Lost in the WASH. The functional human WASH complex 1 gene is on chromosome 20.bioRxiv2023
37398104Lost in the WASH. The functional human WASH complex 1 gene is on chromosome 20.bioRxiv2023
34755885APPRIS: selecting functionally important isoforms.Nucleic Acids Res2022
36346145Origins and Evolution of Human Tandem Duplicated Exon Substitution Events.Genome Biol Evol2022
36083290Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants.Genet Med2022
36124785APPRIS principal isoforms and MANE Select transcripts define reference splice variants.Bioinformatics2022
36257961Clinical variant interpretation and biologically relevant reference transcripts.NPJ Genom Med2022
34755885APPRIS: selecting functionally important isoforms.Nucleic Acids Res2022
36124785APPRIS principal isoforms and MANE Select transcripts define reference splice variants.Bioinformatics2022
36257961Clinical variant interpretation and biologically relevant reference transcripts.NPJ Genom Med2022
36346145Origins and Evolution of Human Tandem Duplicated Exon Substitution Events.Genome Biol Evol2022
36083290Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants.Genet Med2022
33270111GENCODE 2021.Nucleic Acids Res2021
34046593Assessing the functional relevance of splice isoforms.NAR Genom Bioinform2021
34302486The clinical importance of tandem exon duplication-derived substitutions.Nucleic Acids Res2021
33270111GENCODE 2021.Nucleic Acids Res2021
34046593Assessing the functional relevance of splice isoforms.NAR Genom Bioinform2021
34302486The clinical importance of tandem exon duplication-derived substitutions.Nucleic Acids Res2021
33017396An analysis of tissue-specific alternative splicing at the protein level.PLoS Comput Biol2020
31886458Few SINEs of life: Alu elements have little evidence for biological relevance despite elevated translation.NAR Genom Bioinform2020
33017396An analysis of tissue-specific alternative splicing at the protein level.PLoS Comput Biol2020
31886458Few SINEs of life: Alu elements have little evidence for biological relevance despite elevated translation.NAR Genom Bioinform2020
30357393GENCODE reference annotation for the human and mouse genomes.Nucleic Acids Res2019
31744546The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens.Genome Biol2019
30357393GENCODE reference annotation for the human and mouse genomes.Nucleic Acids Res2019
31744546The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens.Genome Biol2019
29069475APPRIS 2017: principal isoforms for multiple gene sets.Nucleic Acids Res2018
30395326Corrigendum: Loose ends: almost one in five human genes still have unresolved coding status.Nucleic Acids Res2018
29967126Corrigendum: SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification.Genome Res2018
29440222SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification.Genome Res2018
29069475APPRIS 2017: principal isoforms for multiple gene sets.Nucleic Acids Res2018
29967126Corrigendum: SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification.Genome Res2018
30395326Corrigendum: Loose ends: almost one in five human genes still have unresolved coding status.Nucleic Acids Res2018
29440222SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification.Genome Res2018
27712956Alternative Splicing May Not Be the Key to Proteome Complexity.Trends Biochem Sci2017
28483377Most Alternative Isoforms Are Not Functionally Important.Trends Biochem Sci2017
27712956Alternative Splicing May Not Be the Key to Proteome Complexity.Trends Biochem Sci2017
28483377Most Alternative Isoforms Are Not Functionally Important.Trends Biochem Sci2017
27195705Analysis of Paired Primary-Metastatic Hormone-Receptor Positive Breast Tumors (HRPBC) Uncovers Potential Novel Drivers of Hormonal Resistance.PLoS One2016
27195705Analysis of Paired Primary-Metastatic Hormone-Receptor Positive Breast Tumors (HRPBC) Uncovers Potential Novel Drivers of Hormonal Resistance.PLoS One2016
27604469An expanded evaluation of protein function prediction methods shows an improvement in accuracy.Genome Biol2016
27964752Extreme genomic erosion after recurrent demographic bottlenecks in the highly endangered Iberian lynx.Genome Biol2016
27604469An expanded evaluation of protein function prediction methods shows an improvement in accuracy.Genome Biol2016
27964752Extreme genomic erosion after recurrent demographic bottlenecks in the highly endangered Iberian lynx.Genome Biol2016
25756922Correction to "Analyzing the first drafts of the human proteome".J Proteome Res2015
25931610The evolutionary fate of alternatively spliced homologous exons after gene duplication.Genome Biol Evol2015
25756922Correction to "Analyzing the first drafts of the human proteome".J Proteome Res2015
25735770Alternative splicing and co-option of transposable elements: the case of TMPO/LAP2α and ZNF451 in mammals.Bioinformatics2015
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Collaborators

Josep Carreras Leukaemia Research Institute (IJC)
Co-authored papers 41
Campus Universitario
Co-authored papers 17
Children's Hospital of Philadelphia
Co-authored papers 12
Co-authored papers 10
Barcelona Institute of Science and Technology
Co-authored papers 7
Co-authored papers 7
Instituto de Genetica Medica y Molecular (INGEMM), Hospital Universitario La Paz
Co-authored papers 6
Co-authored papers 6
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Spanish National Cancer Research Centre-CNIO
Co-authored papers 6
Massachusetts Institute of Technology
Co-authored papers 6
Yale University
Co-authored papers 5
Genomics Institute, University of California Santa Cruz
Co-authored papers 5
Broad Institute of MIT and Harvard
Co-authored papers 5
Co-authored papers 5
Department of Pharmacy and Biotechnology, University of Bologna
Co-authored papers 5
Co-authored papers 4
Federico II University
Co-authored papers 4
European Bioinformatics Institute
Co-authored papers 4
Co-authored papers 4
University College London
Co-authored papers 4
UC Santa Cruz Genomics Institute, University of California
Co-authored papers 4
Imperial College London
Co-authored papers 3
Sapienza University of Rome
Co-authored papers 3
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University of Missouri
Co-authored papers 3
University College London, Institute of Structural and Molecular Biology
Co-authored papers 3
Department of Pharmacy and Biotechnology, University of Bologna
Co-authored papers 3
European Bioinformatics Institute
Co-authored papers 3
Technical University of Munich (TUM)
Co-authored papers 3