Author

Maarten Hoek

Merck & Co., Inc., Rahway, NJ, USA (United States)ORCID 0000-0002-5237-1626Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Maarten Hoek1 paper · Erasmus MC

Biology Disciplines

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Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:proteomics· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Abdulla al Shafi Majumder· 1 shared Abdullah Mesut ErzurumluogluiD· 1 shared Alex M. Tamburino· 1 shared Alex P. ReineriD· 1 shared Alison GoateiD· 1 shared Anders MälarstigiD· 1 shared Andrew C. HeathiD· 1 shared Andries R. van der Leij· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Abdulla al Shafi Majumder

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2 papers

Recent·Most cited

Identification of the Molecular Basis of Anti-fibrotic Effects of Soluble Guanylate Cyclase Activator Using the Human Lung Fibroblast Phosphoproteome

Sunhwa Kim, Ashmita Saigal, Weilong Zhao, Peyvand Amini, Alex M. Tamburino, Subharekha Raghavan, Maarten Hoek

This study identifies phosphorylation changes in human lung fibroblasts induced by an sGC activator, revealing potential molecular mechanisms of its anti-fibrotic effects.

bioRxiv · Jun 12, 2020 · PreprintMolecular Biology

Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior

David M. Brazel, Yu Jiang, Jordan M. Hughey, Valérie Turcot, Xiaowei Zhan, Jian Gong, Chiara Batini, J. Dylan Weissenkampen, Mengzhen Liu, Daniel R. Barnes, Sarah E. Bertelsen, Yi‐Ling Chou, Abdullah Mesut Erzurumluoglu, Jessica D. Faul, Jeff Haessler, , Jean Ferrières

The paper analyzes rare coding variants in smoking and drinking behavior using exome chip data, finding that they contribute to phenotypic variation but require larger samples for individual variant associations.

Biological Psychiatry · Dec 6, 2018Peer-reviewedGenetics