Author

Allan Daly

Wellcome Sanger Institute

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· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Jeffrey C. BarrettiD· 2 shared Vivek IyeriD· 2 shared Aarno V. PalotieiD· 1 shared Aaron Day-Williams· 1 shared Adam P. LevineiD· 1 shared Aileen Reghan FoleyiD· 1 shared Alain BittoniD· 1 shared Alejandro SifrimiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jeffrey C. BarrettORCID

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Author profile →

3 papers

Recent·Most cited

Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome study

Enrique Audain, Anna Wilsdon, Gregor Dombrowsky, Alejandro Sifrim, Jeroen Breckpot, Yasset Pérez‐Riverol, Siobhan Loughna, Allan Daly, Pavlos Antoniou, P. Hofmann, Amilcar Pérez-Riverol, Anne‐Karin Kahlert, Ulrike M. M. Bauer, Thomas Pickardt, Sabine Klaassen, , Marc‐Phillip Hitz

This study identifies rare variants and digenic interactions associated with congenital heart disease using a large-scale exome case-control analysis.

npj Genomic Medicine · Jun 2, 2026Peer-reviewedGenetic & Genomic Medicine

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

Aleksejs Sazonovs, Christine R. Stevens, Guhan Ram Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu, Tariq Ahmad, Matthieu Allez, Ashwin N. Ananthakrishnan, Gil Atzmon, Aris Baras, Jeffrey C. Barrett, Nir Barzilai, Laurent Beaugerie, Ashley Harris Beecham, , Rasha Shawky

The paper identifies ten new genes with coding variants linked to Crohn's disease risk using sequencing data from over 30,000 patients and 80,000 controls.

Nature Genetics · Aug 29, 2022Peer-reviewedGenetic & Genomic Medicine

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

Simon J. Haworth, Chin Yang Shapland, Caroline Hayward, Bram Peter Prins, Janine F. Felix, Carolina Medina‐Gómez, Fernando Rivadeneira, Carol A. Wang, Tarunveer S. Ahluwalia, Martine Vrijheid, Mònica Guxens, Jordi Sunyer, Ioanna Tachmazidou, Klaudia Walter, Valentina Iotchkova, , David K. Jackson

The paper identifies 9 novel genetic loci, including low-frequency variants in TP53, associated with head circumference and intracranial volume in up to 46,000 individuals.

Nature Communications · Jan 21, 2019Peer-reviewedGenetics