Author

Oleguer Plana‐Ripoll

Aarhus UniversityORCID 0000-0002-6470-7465Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 3 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Assay:GWAS summary statistics· 3 Research Focus:benchmarking· 2 Research Focus:GWAS / association mapping· 2 Research Focus:fine-mapping· 1

Frequent Co-Authors

Anders Dupont BørglumiD· 4 shared Bjarni Jóhann VilhjálmssoniD· 4 shared Esben AgerboiD· 4 shared Thomas Mears WergeiD· 4 shared Andrew Joseph SchorkiD· 3 shared DAVID MICHAEL HOUGAARDiD· 3 shared Florian PrivéiD· 3 shared John Joseph McGrathiD· 3 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Anders Dupont BørglumORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

As rates of ASD and ADHD rise, genetic contributions fall: Evidence for widening diagnostic criteria

Sonja LaBianca, Mette Lise Lousdal, Morten Dybdahl Krebs, Ole S Hansen, Kajsa-Lotta Georgii Hellberg, Mischa Lundberg, Johanne Østerby Sørensen, Jesper R. Gådin, Henrik Ohlsson, Anders Dupont Børglum, Esben Agerbo, Thomas Mears Werge, Clara Albiñana, Bjarni Jóhann Vilhjálmsson, Kenneth S. Kendler, , Andrew Joseph Schork

This study shows that as ASD and ADHD diagnoses have increased, the genetic risk associated with these conditions has decreased over time.

medRxiv · Nov 10, 2025 · PreprintGenetic & Genomic Medicine

ADuLT: An efficient and robust time-to-event GWAS

Emil M. Pedersen, Esben Agerbo, Oleguer Plana‐Ripoll, Jette Steinbach, Morten Dybdahl Krebs, DAVID MICHAEL HOUGAARD, Thomas Mears Werge, Merete Nordentoft, Anders Dupont Børglum, Katherine Louise Musliner, Andrea Ganna, Andrew Joseph Schork, Preben Bo Mortensen, John Joseph McGrath, Florian Privé, Bjarni Jóhann Vilhjálmsson

ADuLT is a time-to-event GWAS method that outperforms Cox regression in strongly ascertained studies, finding more genome-wide significant associations in psychiatric disorder analyses.

Nature Communications · Sep 9, 2023Peer-reviewedGenetic & Genomic Medicine

Genetic correlates of vitamin D-binding protein and 25 hydroxyvitamin D in neonatal dried blood spots

Clara Albiñana, Zhihong Zhu, Nis Borbye‐Lorenzen, Sanne Grundvad Boelt, Arieh Sierra Cohen, Kristin Skogstrand, Naomi R. Wray, Joana A. Revez, Florian Privé, Liselotte Vogdrup Petersen, Cynthia Marie Bulik, Oleguer Plana‐Ripoll, Katherine Louise Musliner, Esben Agerbo, Anders Dupont Børglum, , John Joseph McGrath

This study identifies genetic loci associated with vitamin D-binding protein and 25 hydroxyvitamin D in neonates and links DBP to vitamin D status and disease risk.

Nature Communications · Feb 15, 2023Peer-reviewedGenetic & Genomic Medicine

Accounting for age-of-onset and family history improves power in genome-wide association studies

Emil M. Pedersen, Esben Agerbo, Oleguer Plana‐Ripoll, Jakob Grove, Julie Werenberg Dreier, Katherine Louise Musliner, Marie Bækvad‐Hansen, Georgios I. Athanasiadis, Andrew Joseph Schork, Jonas Bybjerg‐Grauholm, DAVID MICHAEL HOUGAARD, Thomas Mears Werge, Merete Nordentoft, Ole N Mors, Søren Dalsgaard, , Bjarni Jóhann Vilhjálmsson

This paper introduces LT-FH++, a method that improves GWAS power by incorporating age-of-onset and family history, showing increased significant associations in psychiatric disorders and mortality data.

The American Journal of Human Genetics · Feb 8, 2022Peer-reviewedBioinformatics