Author

Katherine Klinger

Sanofi (United States)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetic & Genomic Medicine· 4

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 3 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Clément ChatelainiD· 4 shared FinnGeniD· 3 shared Aarno V. PalotieiD· 2 shared Adam E. Ziemann· 2 shared Adriana Huertas‐Vázquez· 2 shared Anders MälarstigiD· 2 shared Anne Lehtonen· 2 shared Anne Marja Remes· 2 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Clément ChatelainORCID

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Author profile →

4 papers

Recent·Most cited

Genetic liability to psoriasis predicts severe disease outcomes

Jake R. Saklatvala, Samuel Lessard, Maris Teder‐Laving, Laurent F. Thomas, Ravi Ramessur, Jonas Zierer, Bjørn Olav Åsvold, Anne C Barton, David Baudry, John Bowes, Ben Michael Brumpton, Sandro Bruno, Vinod Chandran, Clément Chatelain, Emanuele de Rinaldis, , Kathy Sands

This study identifies genetic risk factors associated with severe psoriasis and shows that polygenic risk scores can predict severe disease outcomes better than traditional risk factors.

Genome Medicine · Dec 17, 2025Peer-reviewedGenetic & Genomic Medicine

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty

Jonathan K. L. Mak, Chenxi Qin, Moritz Krüger, Anna Kuukka, FinnGen, Aarno V. Palotie, Mark J. Daly, Bridget Riley-Gillis, Howard J. Jacob, Dirk S. Paul, Slavé Petrovski, Heiko Runz, Sally John, George Okafo, Robert M. Plenge, , Ekaterina A. Khramtsova

This study identifies 1,242 novel genetic variants and 31 novel genes associated with frailty through genome-wide association and proteomics integration.

Nature Aging · Aug 5, 2025Peer-reviewedGenetic & Genomic Medicine

Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations

Ville Salo, Juhani H. Määttä, Eeva Sliz, FinnGen, Aarno V. Palotie, Mark J. Daly, Bridget Riley-Gills, Howard J. Jacob, Dirk S. Paul, Slavé Petrovski, Heiko Runz, Sally John, George Okafo, Nathan Lawless, Heli Salminen‐Mankonen, , Jukka T. Koskela

This study conducts a genome-wide meta-analysis across three biobanks to identify new genetic loci associated with lumbar disc herniation, expanding the known genetic landscape.

Nature Communications · Nov 7, 2024Peer-reviewedGenetic & Genomic Medicine

Genetic analyses of inflammatory polyneuropathy and chronic inflammatory demyelinating polyradiculoneuropathy identified candidate genes.

Zhaohui Du, Samuel Lessard, Tejaswi Iyyanki, Michael J. Chao, FinnGen, Timothy Hammond, Dimitry Ofengeim, Katherine Klinger, Emanuele de Rinaldis, Khader Shameer, Clément Chatelain

This study identifies genetic risk loci and candidate genes for inflammatory polyneuropathy and CIDP through GWAS and functional analyses.

Human Genetics and Genomics Advances · Jun 8, 2024Peer-reviewedGenetic & Genomic Medicine