Author

Amanda Peterson

Oregon Health & Science 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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Genetic & Genomic Medicine· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:Drosophila· 1 Research Focus:drug response / drug discovery· 1 Research Focus:gene regulatory network inference· 1 Assay:metabolomics· 1

Frequent Co-Authors

Jillian G. BuchaniD· 2 shared Tania Attié‐BitachiD· 2 shared Alyssa L. RippertiD· 1 shared Amandine Smail· 1 shared Angus LindsayiD· 1 shared Ankita Tulangekar· 1 shared Anne GregoriD· 1 shared Antonio NovelliiD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jillian G. BuchanORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

ADSS1 is a suppressed metabolic control node in dystrophic skeletal muscle

Emma Rybalka, Stephanie Kourakis, Bo Qi, Dean G. Campelj, Ankita Tulangekar, Gretel S. Major, Nitika Kandhari, Amanda Peterson, Christos G. Stathis, Brunda Nijagal, Deanna Deveson Lucas, Dirk Fischer, Jeffrey J. Brault, Angus Lindsay, Hyung Jun Park, Cara A. Timpani

The paper identifies ADSS1 as a suppressed metabolic control node in dystrophic muscle, showing its role in purine metabolism and its impact on inflammatory and adipogenic remodelling.

bioRxiv · Jul 31, 2026 · PreprintMolecular Biology

De novo variants in LDB1 are linked to distinct neurodevelopmental phenotypes determined by variant location and differing pathomechanisms

Rebecca Fluri, Mireia Coll-Tané, Theresa Brunet, Benjamin Cogné, Solène Conrad, Mathilde Nizon, Francesco Nicita, Lorena Travaglini, Antonio Novelli, Margie Glissmeyer, Amanda Peterson, Jillian G. Buchan, Dan Serber, Kolja Meier, Jutta Gärtner, , Anne Gregor

The paper identifies de novo LDB1 variants linked to distinct neurodevelopmental phenotypes based on variant location and pathomechanisms, confirmed through in vitro and in vivo studies.

The American Journal of Human Genetics · Jun 19, 2026Peer-reviewedGenetic & Genomic Medicine

De novo MAP2K4 variants cause a novel neurodevelopmental syndrome with impaired JNK signaling in iPSC-derived neurons

Tomoki T. Nomakuchi, Alyssa L. Rippert, Sabrina A. Santos De Leon, Elizabeth M. Gonzalez, Dong Li, Rajesh Angireddy, Lívia Sertori Finoti, Flavio Faletra, Luciana Musante, Tuula Rinne, David J. Amor, Lydia von Wintzingerode, Rami Abou Jamra, Samantha R. Stover, Jillian G. Buchan, , Elizabeth J. K. Bhoj

medRxiv · Dec 27, 2025 · PreprintGenetic & Genomic Medicine