Author

Eric Marshall

Biogen (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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Genetic & Genomic Medicine· 4 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 5 Research Focus:GWAS / association mapping· 4 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Heiko RunziD· 5 shared Chia‐Yen CheniD· 4 shared Benjamin B. SuniD· 3 shared Biogen Biobank Team· 3 shared Ellen A. TsaiiD· 3 shared Helen McLaughlin· 3 shared Christopher D. WhelaniD· 2 shared Christopher N. FoleyiD· 2 shared

Activity by Year

2021-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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5 shared papersGenetic & Genomic Medicine

Heiko RunzORCID

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Author profile →

6 papers

Recent·Most cited

Spatial transcriptomics reveals heterogeneous cell-cell interactions among brain regions in a cuprizone model consistent with multiple sclerosis lesions

Hui‐Hsin Tsai, Sarbottam Piya, Jing Wang, Jing Zhu, Wenxing Hu, Andrew R. Gehrke, Shaolong Cao, Amanda J. Guise, Su Jing Chan, Mark J. Sheehan, Jenhwa Chu, Zhengyu Ouyang, Matthew M. Ryals, Michelle Lee, Wanli Wang, , Baohong Zhang

The paper uses spatial transcriptomics to analyze cell-cell interactions in a cuprizone model, finding region-specific changes and partial translatability to multiple sclerosis lesions.

Frontiers in Bioinformatics · Aug 6, 2026Peer-reviewedNeuroscience

Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK Biobank

Robert Francis Hillary, Danni A. Gadd, Zhana Kuncheva, Tasos Mangelis, Tin-Chi Lin, Kyle L. Ferber, Helen McLaughlin, Heiko Runz, Biogen Biobank Team, Eric Marshall, Riccardo Emilio Marioni, Christopher N. Foley, Benjamin B. Sun

This study identifies gene-environment interactions affecting plasma proteins in UK Biobank, discovering 683 vQTLs and over 1,400 GEIs across 571 proteins.

Nature Communications · Aug 26, 2024Peer-reviewedGenetic & Genomic Medicine

Rare genetic variants impact muscle strength

Yunfeng Huang, Dóra Bodnár, Chia‐Yen Chen, Gabriela Sánchez-Andrade, Mark Sanderson, Biogen Biobank Team, Christopher D. Whelan, Paola G. Bronson, David Sexton, Sally John, Eric Marshall, Mehool Patel, Saranya Duraisamy, Timothy Swan, Denis A. Baird, , Heiko Runz

This study identifies six genes associated with hand grip strength using rare protein-coding variants in 340,319 individuals and shows additive effects with common variants.

Nature Communications · Jun 10, 2023Peer-reviewedGenetic & Genomic Medicine

Brain expression quantitative trait locus and network analysis reveals downstream effects and putative drivers for brain-related diseases

Niek de Klein, Ellen A. Tsai, Martijn Vochteloo, Denis A. Baird, Yunfeng Huang, Chia‐Yen Chen, Sipko van Dam, Roy Oelen, Patrick Deelen, Olivier B. Bakker, Omar El Garwany, Zhengyu Ouyang, Eric Marshall, Maria I. Zavodszky, Wouter van Rheenen, , Harm-Jan Westra

The paper integrates brain RNA-seq and genotype data to identify eQTLs and their downstream effects on brain-related diseases.

Nature Genetics · Feb 23, 2023Peer-reviewedGenomics

Genetic associations of protein-coding variants in human disease

Benjamin B. Sun, Mitja Kurki, Christopher N. Foley, Asma Mechakra, Chia‐Yen Chen, Eric Marshall, Jemma B. Wilk, Biogen Biobank Team, Chia-Yen Ghen, Heiko Runz, Mohamed Chahine, Philippe Chevalier, Georges Christé, FinnGen, Aarno V. Palotie, Mark J. Daly

This study combines sequencing and genotyping data from two biobanks to identify 975 protein-coding variant associations across 744 disease endpoints, enhancing understanding of genetic disease mechanisms and drug targets.

Nature · Feb 23, 2022Peer-reviewedGenetic & Genomic Medicine

Advancing Human Genetics Research and Drug Discovery through Exome Sequencing of the UK Biobank

Joseph D. Szustakowski, Suganthi Balasubramanian, Erika M. Kvikstad, Shareef Khalid, Paola G. Bronson, Ariella Sasson, Emily Wong, Daren Liu, J. Wade Davis, Carolina Haefliger, A. Katrina Loomis, Rajesh Mikkilineni, Hyun Ji Noh, Samir Wadhawan, Xiaodong Bai, , Adam Platt

The paper describes exome sequencing of 200,643 UK Biobank participants, providing a rich resource of coding variants for genetic and drug discovery research.

Nature Genetics · Jun 28, 2021Peer-reviewedGenetic & Genomic Medicine