Author

Jean-Christophe Debost

Aarhus UniversityORCID 0000-0001-6457-3148Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Esben AgerboiD· 2 shared John Joseph McGrathiD· 2 shared Liselotte Vogdrup PeterseniD· 2 shared Preben Bo MortenseniD· 2 shared Alex Bloemendal· 1 shared Allan F. McRaeiD· 1 shared Anders Dupont BørglumiD· 1 shared Beilei BianiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Esben AgerboORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineCell GenomicsPeer-reviewedDec 1, 2023

The genetic and phenotypic correlates of neonatal Complement Component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders

Nis Borbye‐Lorenzen, Zhihong Zhu, Esben Agerbo…·John Joseph McGrath

This study examines the genetic and phenotypic links between neonatal C3 and C4 protein concentrations and psychiatric and autoimmune disorders, finding no strong causal associations with mental disorders but evidence of lower autoimmune risk with higher C4 levels.

12 citations

humanbulk RNA-seq

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GeneticsNature CommunicationsPeer-reviewedJul 10, 2019

Paternal-age-related de novo mutations and risk for five disorders

Jacob L. Taylor, Jean-Christophe Debost, Sarah U. Morton…·Elise Robinson

The paper estimates the risk of five disorders from paternal-age-related de novo mutations using whole-exome-sequencing data and Danish registry data.

91 citationstop 2%

humanwhole-exome sequencing

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