Author

Elias Pavlopoulos

Regeneron (United States)

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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Bioengineering· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Approach:statistical model· 1

Frequent Co-Authors

Shek Man ChimiD· 2 shared Alan R. ShuldineriD· 1 shared Alexandros G. KokkosisiD· 1 shared Andreja AvberšekiD· 1 shared Ariane H. Ayer· 1 shared Aris BarasiD· 1 shared Brian ZambrowicziD· 1 shared David J. LedereriD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersBioengineering

Shek Man ChimORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

A Human Brain-Chip for modelling brain pathologies and screening of BBB crossing therapeutic strategies

Shek Man Chim, Kristen Howell, Alexandros G. Kokkosis, Brian Zambrowicz, Katia P. Karalis, Elias Pavlopoulos

The paper develops a human Brain-Chip model to study brain pathologies and test BBB-crossing therapies, showing in vitro/in vivo correlation for drug screening.

Pharmaceutics · Oct 10, 2024Peer-reviewedBioengineering

Rare coding variants in CHRNB2 reduce the likelihood of smoking

Veera Manikandan Rajagopal, Kyoko Watanabe, Joelle S. Mbatchou, Ariane H. Ayer, Peter Quon, Deepika Sharma, Michael D. Kessler, Kavita Praveen, Sahar Gelfman, Neelroop Parikshak, Jacqueline M. Otto, Suying Bao, Shek Man Chim, Elias Pavlopoulos, Andreja Avberšek, , Giovanni Coppola

The paper identifies rare coding variants in CHRNB2 associated with reduced smoking likelihood and links them to downstream smoking-related phenotypes.

medRxiv · Oct 27, 2022 · PreprintGenetic & Genomic Medicine