Author

Claire C. Morgan

Imperial College LondonORCID 0000-0002-8191-3738Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:experimental assay· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:Hi-C· 1 Approach:statistical model· 1

Frequent Co-Authors

Allan R LinnebergiD· 2 shared Daniel R. WitteiD· 2 shared David TorrentsiD· 2 shared Emil V. R. AppeliD· 2 shared Goutham AtlaiD· 2 shared Ignasi MorániD· 2 shared Irene Miguel-EscaladaiD· 2 shared Jorge P. FerreriD· 2 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Allan R LinnebergORCID

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2 papers

Recent·Most cited

Human pancreatic islet 3D chromatin architecture provides insights into the genetics of type 2 diabetes

Irene Miguel-Escalada, Sílvia Bonàs‐Guarch, Inês Cebola, Joan Ponsa-Cobas, Julen Mendieta-Esteban, Goutham Atla, Biola M. Javierre, Delphine Rolando, Irene Farabella, Claire C. Morgan, Javier García-Hurtado, Anthony Beucher, Ignasi Morán, Lorenzo Pasquali, Mireia Ramos-Rodríguez, , Jorge P. Ferrer

The paper links diabetes-associated enhancers with their target genes using 3D chromatin architecture in human pancreatic islets, revealing genetic variants that impact insulin secretion heritability.

Nature Genetics · Jun 28, 2019Peer-reviewedGenomics

A Comprehensive Reanalysis Of Publicly Available GWAS Datasets Reveals An X Chromosome Rare Regulatory Variant Associated With High Risk For Type 2 Diabetes.

Sílvia Bonàs‐Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, Niels Grarup, David Sebastián, Elias Rodríguez-Fos, Friman Sánchez, Mercè Planas-Fèlix, Paula Cortés-Sánchez, Santiago González, Pascal N. Timshel, Tune H. Pers, Claire C. Morgan, Ignasi Morán, Goutham Atla, , David Torrents

The paper reanalyzes T2D GWAS data to identify a rare X chromosome variant associated with increased T2D risk in males.

Nature Communications · Jan 16, 2018Peer-reviewedGenetics