Author

Amber Logemann

Translational Genomics Research Institute

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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Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Elizabeth D. HutchinsiD· 2 shared Eric B. AlsopiD· 2 shared Kendall R. Van Keuren‐JenseniD· 2 shared Alexandra G. BeilinaiD· 1 shared Amanda Courtright-LimiD· 1 shared Amanda McQuadeiD· 1 shared Anastasia IllarionovaiD· 1 shared Andrew SingletoniD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenomics

Elizabeth D. HutchinsORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

The Foundational data initiative for Parkinsons disease (FOUNDIN-PD): enabling efficient translation from genetic maps to mechanism

Elisângela Bressan, Xylena Reed, Vikas Bansal, Elizabeth D. Hutchins, Melanie M. Cobb, Michelle G. Webb, Eric B. Alsop, Francis P. Grenn, Anastasia Illarionova, Natalia Savytska, Ivo Violich, Stefanie Bröer, Noémia Fernandes, Ramiyapriya Sivakumar, Alexandra G. Beilina, , Cornelis Blauwendraat

The paper presents a multi-layered molecular dataset from iPSC-derived dopaminergic neurons to model Parkinson's disease genetic risk and provides a data browser for accessing these resources.

Cell Genomics · Feb 6, 2023Peer-reviewedGenomics

Cellular and molecular phenotypes of C9orf72 ALS/FTD patient derived iPSC-microglia mono-cultures

Ileana Lorenzini, Eric B. Alsop, Jennifer Levy, Lauren M. Gittings, Deepti Lall, Benjamin E. Rabichow, Stephen R. Moore, Ryan S. Pevey, Lynette M. Bustos, Camelia Burciu, Divya Bhatia, Mo Singer, Justin Saul, Amanda McQuade, Makis Tzioras, , Rita Sattler

This study examines C9orf72 ALS/FTD patient-derived iPSC-microglia mono-cultures, finding they form RNA foci, have reduced C9orf72 protein, and show endosomal-lysosomal dysfunction, but no significant microglial-enriched gene expression differences.

bioRxiv · Sep 3, 2020 · PreprintNeuroscience