Author

Peter Nagy

Cornell University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Molecular Biology· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Organism:Drosophila· 1 Research Focus:drug response / drug discovery· 1 Research Focus:GWAS / association mapping· 1 Research Focus:host-pathogen & immune response· 1 Approach:statistical model· 1

Frequent Co-Authors

Alden Y Huang· 1 shared Alex Volkov· 1 shared Anastasios Konstantinidis· 1 shared Andreas HartmanniD· 1 shared Anna Bratek‐SkickiiD· 1 shared Cathy L Barr· 1 shared Cathy L Budman· 1 shared Chaker El KalamouniiD· 1 shared

Activity by Year

2016-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperGenetics

Alden Y Huang

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Comprehensive investigation of SARS-CoV-2 intestinal pathogenesis in Drosophila

Layla El Kamali, Peter Nagy, Justine Girard, Nicolas S. Buchon, Patrick Mavingui, Chaker El Kalamouni, Dani Osman

This study uses Drosophila midgut to investigate SARS-CoV-2-induced gastrointestinal pathogenesis, finding disrupted epithelial architecture, altered lipid homeostasis, and partial mitigation by Plitidepsin.

iScience · Apr 7, 2026Peer-reviewedPathology

Inhibiting toxicity of ALS-linked dipeptide repeat proteins by polystyrene sulfonate (PSS)

Anna Bratek‐Skicki, Junaid Ahmed, Joris Van Lindt, Karl Jonckheere, Eveline Peeters, Kara Heeren, Fatemeh Fakhri, Alex Volkov, Jelle Hendrix, Piotr Batys, Peter Nagy, Richard G. Pestell, Ludo Van Den Bosch, Péter Tompa

This study shows that polystyrene sulfonate (PSS) reduces toxicity of ALS-linked dipeptide repeat proteins in cellular and iPSC-derived motor neuron models.

bioRxiv · May 19, 2023 · PreprintMolecular Biology

Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

Alden Y Huang, Dongmei Yu, Lea K Davis, Jae-Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen, Lauren M McGrath, Cornelia Illmann, Paul Sandor, Cathy L Barr, Marco Grados, , Danielle C Cath

The paper identifies two rare copy number variants, NRXN1 and CNTN6, significantly increasing the risk of Tourette syndrome in a European ancestry sample.

bioRxiv · Jul 8, 2016Genetics