Author

Daniele Novarina

University Medical Center GroningenORCID 0000-0001-9526-0750Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Genetics· 1 Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:yeast· 3 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1 Organism:human· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Michael ChangiD· 4 shared Hinke G. KazemieriD· 2 shared Liesbeth M. VeenhoffiD· 2 shared Elizabeth C. Riquelme BarrientosiD· 1 shared Fernando Rodrigo Rosas BringasiD· 1 shared Georges E. JanssensiD· 1 shared Grant W. BrowniD· 1 shared Jessica A. Vaisica· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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4 shared papersCell Biology

Michael ChangORCID

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4 papers

Recent·Most cited

The role of the nuclear pore complex in the stability of disease-related short tandem DNA repeats

Sandra Ollivaud, Daniele Novarina, Elizabeth C. Riquelme Barrientos, Hinke G. Kazemier, Suzan Gonera, Maxime Kislanski, Liesbeth M. Veenhoff, Michael Chang

This study shows disease-related short tandem repeats relocate to nuclear pore complexes, with implications for genome stability and repeat dynamics.

Nucleic Acids Research · May 20, 2026Peer-reviewedCell Biology

Revisiting the role of the spindle assembly checkpoint in the formation of gross chromosomal rearrangements in Saccharomyces cerevisiae

Yue Yao, Ziqing Yin, Fernando Rodrigo Rosas Bringas, Jonathan Boudeman, Daniele Novarina, Michael Chang

The paper revisits the role of the spindle assembly checkpoint in promoting gross chromosomal rearrangements in yeast and finds no such role after correcting for experimental artifacts.

Genetics · Sep 12, 2024Peer-reviewedMolecular Biology

A genome-wide screen for genes affecting spontaneous direct-repeat recombination in Saccharomyces cerevisiae

Daniele Novarina, Ridhdhi Desai, Jessica A. Vaisica, Jiongwen Ou, Mohammed Bellaoui, Grant W. Brown, Michael Chang

The paper identifies 35 genes that, when deleted, cause hyper-recombination between direct repeats in yeast, including mismatch repair genes and DNA replication factors.

G3 Genes Genomes Genetics · Apr 7, 2020Peer-reviewedGenomics

A genome-wide screen identifies genes that suppress the accumulation of spontaneous mutations in young and aged yeast cells

Daniele Novarina, Georges E. Janssens, Koen Bokern, Tim Schut, Noor C. van Oerle, Hinke G. Kazemier, Liesbeth M. Veenhoff, Michael Chang

The paper identifies genes that suppress spontaneous mutation accumulation in yeast cells, finding PEX19 as an age-specific mutation suppressor.

Aging Cell · Dec 18, 2019Peer-reviewedGenetics