Michael L. Tress

Spanish National Cancer Research Centre — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

47h-index27.6kcitations109works28.02yr avg
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Research Topics

RNA and protein synthesis mechanisms(47), Genomics and Phylogenetic Studies(34), RNA modifications and cancer(30), Protein Structure and Dynamics(24), RNA Research and Splicing(20)

Publications101 total

The degradation of extended protein isoforms points to a misfiring translation initiation process
Molecular Genetics and Genomics·2025
An audit of the PeptideAtlas database uncovers evidence for repurposed pseudogenes and co-opted retroviral ORFs
BMC Genomics·2025Open Access
The state of the human coding gene catalogues
Database·2025· 2 citedOpen Access
More than 2,500 coding genes in the human reference gene set still have unsettled status
2024· 1 citedOpen Access
The rapid degradation of translated upstream regions points to an inefficient translation initiation process
2024Open Access
GENCODE 2025: reference gene annotation for human and mouse
Nucleic Acids Research·2024· 235 citedOpen Access
A deep audit of the PeptideAtlas database uncovers evidence for unannotated coding genes and aberrant translation
2024· 6 citedOpen Access
The GENCODE CLS project: massively expanding the lncRNA catalog through capture long-read RNA sequencing
2024· 22 citedOpen Access
Evidence for widespread translation of 5′ untranslated regions
Nucleic Acids Research·2024· 7 citedOpen Access
The T2T-CHM13 reference assembly uncovers essential WASH1 and GPRIN2 paralogues
Bioinformatics Advances·2024· 7 citedOpen Access
Lost in the WASH. The functional human WASH complex 1 gene is on chromosome 20
2023Open Access
The clinical importance of tandem exon duplication-derived substitutions
Faculty of 1000 Research Ltd·2023Open Access
GENCODE: reference annotation for the human and mouse genomes in 2023
Nucleic Acids Research·2022· 597 citedOpen Access
Origins and Evolution of Human Tandem Duplicated Exon Substitution Events
Genome Biology and Evolution·2022· 8 citedOpen Access
Clinical variant interpretation and biologically relevant reference transcripts
npj Genomic Medicine·2022· 16 citedOpen Access
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants
Genetics in Medicine·2022· 48 citedOpen Access
APPRIS principal isoforms and MANE Select transcripts define reference splice variants
Bioinformatics·2022· 21 citedOpen Access
APPRIS: selecting functionally important isoforms
Nucleic Acids Research·2021· 79 citedOpen Access
APPRIS principal isoforms and MANE Select transcripts in clinical variant interpretation
2021· 1 citedOpen Access
The clinical importance of tandem exon duplication-derived substitutions
Nucleic Acids Research·2021· 15 citedOpen Access
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Frequent Co-authors

Alfonso Valencia(29), Iakes Ezkurdia(18), José Manuel Rodrı́guez(14), Jesús Vázquez(12), Gonzalo López(10), Adam Frankish(9), Roderic Guigó(9), Fernando Campo del Pozo(7), José M. González(6), Mark Diekhans(6), Tim Hubbard(6), Tomás Di Domenico(6), Laura Martínez Gómez(6), Federico Abascal(6), Jennifer Harrow(5), If Barnes(5), Alexandra Bignell(5), Toby Hunt(5), Mark Gerstein(5), Rory Johnson(5)