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Author Details
Full Name
Michael L Tress
Affiliation
Spanish National Cancer Research Centre (CNIO)
ORCID
Career Start Year
1999
Papers
66
H Index
35
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36420896
GENCODE: reference annotation for the human and mouse genomes in 2023.
Nucleic Acids Res
2023
36420896
GENCODE: reference annotation for the human and mouse genomes in 2023.
Nucleic Acids Res
2023
37398104
Lost in the WASH. The functional human WASH complex 1 gene is on chromosome 20.
bioRxiv
2023
37398104
Lost in the WASH. The functional human WASH complex 1 gene is on chromosome 20.
bioRxiv
2023
34755885
APPRIS: selecting functionally important isoforms.
Nucleic Acids Res
2022
36346145
Origins and Evolution of Human Tandem Duplicated Exon Substitution Events.
Genome Biol Evol
2022
36083290
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants.
Genet Med
2022
36124785
APPRIS principal isoforms and MANE Select transcripts define reference splice variants.
Bioinformatics
2022
36257961
Clinical variant interpretation and biologically relevant reference transcripts.
NPJ Genom Med
2022
34755885
APPRIS: selecting functionally important isoforms.
Nucleic Acids Res
2022
36124785
APPRIS principal isoforms and MANE Select transcripts define reference splice variants.
Bioinformatics
2022
36257961
Clinical variant interpretation and biologically relevant reference transcripts.
NPJ Genom Med
2022
36346145
Origins and Evolution of Human Tandem Duplicated Exon Substitution Events.
Genome Biol Evol
2022
36083290
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants.
Genet Med
2022
33270111
GENCODE 2021.
Nucleic Acids Res
2021
34046593
Assessing the functional relevance of splice isoforms.
NAR Genom Bioinform
2021
34302486
The clinical importance of tandem exon duplication-derived substitutions.
Nucleic Acids Res
2021
33270111
GENCODE 2021.
Nucleic Acids Res
2021
34046593
Assessing the functional relevance of splice isoforms.
NAR Genom Bioinform
2021
34302486
The clinical importance of tandem exon duplication-derived substitutions.
Nucleic Acids Res
2021
33017396
An analysis of tissue-specific alternative splicing at the protein level.
PLoS Comput Biol
2020
31886458
Few SINEs of life: Alu elements have little evidence for biological relevance despite elevated translation.
NAR Genom Bioinform
2020
33017396
An analysis of tissue-specific alternative splicing at the protein level.
PLoS Comput Biol
2020
31886458
Few SINEs of life: Alu elements have little evidence for biological relevance despite elevated translation.
NAR Genom Bioinform
2020
30357393
GENCODE reference annotation for the human and mouse genomes.
Nucleic Acids Res
2019
31744546
The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens.
Genome Biol
2019
30357393
GENCODE reference annotation for the human and mouse genomes.
Nucleic Acids Res
2019
31744546
The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens.
Genome Biol
2019
29069475
APPRIS 2017: principal isoforms for multiple gene sets.
Nucleic Acids Res
2018
30395326
Corrigendum: Loose ends: almost one in five human genes still have unresolved coding status.
Nucleic Acids Res
2018
29967126
Corrigendum: SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification.
Genome Res
2018
29440222
SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification.
Genome Res
2018
29069475
APPRIS 2017: principal isoforms for multiple gene sets.
Nucleic Acids Res
2018
29967126
Corrigendum: SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification.
Genome Res
2018
30395326
Corrigendum: Loose ends: almost one in five human genes still have unresolved coding status.
Nucleic Acids Res
2018
29440222
SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification.
Genome Res
2018
27712956
Alternative Splicing May Not Be the Key to Proteome Complexity.
Trends Biochem Sci
2017
28483377
Most Alternative Isoforms Are Not Functionally Important.
Trends Biochem Sci
2017
27712956
Alternative Splicing May Not Be the Key to Proteome Complexity.
Trends Biochem Sci
2017
28483377
Most Alternative Isoforms Are Not Functionally Important.
Trends Biochem Sci
2017
27195705
Analysis of Paired Primary-Metastatic Hormone-Receptor Positive Breast Tumors (HRPBC) Uncovers Potential Novel Drivers of Hormonal Resistance.
PLoS One
2016
27195705
Analysis of Paired Primary-Metastatic Hormone-Receptor Positive Breast Tumors (HRPBC) Uncovers Potential Novel Drivers of Hormonal Resistance.
PLoS One
2016
27604469
An expanded evaluation of protein function prediction methods shows an improvement in accuracy.
Genome Biol
2016
27964752
Extreme genomic erosion after recurrent demographic bottlenecks in the highly endangered Iberian lynx.
Genome Biol
2016
27604469
An expanded evaluation of protein function prediction methods shows an improvement in accuracy.
Genome Biol
2016
27964752
Extreme genomic erosion after recurrent demographic bottlenecks in the highly endangered Iberian lynx.
Genome Biol
2016
25756922
Correction to "Analyzing the first drafts of the human proteome".
J Proteome Res
2015
25931610
The evolutionary fate of alternatively spliced homologous exons after gene duplication.
Genome Biol Evol
2015
25756922
Correction to "Analyzing the first drafts of the human proteome".
J Proteome Res
2015
25735770
Alternative splicing and co-option of transposable elements: the case of TMPO/LAP2α and ZNF451 in mammals.
Bioinformatics
2015
1 - 50 of 132
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Federico II University
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David T Jones
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