Author

Willehard Haaki

Broad InstituteORCID 0000-0002-2850-7650Unclaimed 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:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 2 shared Annamari Tuulio‐HenrikssoniD· 2 shared Ari Ahola‐OlliiD· 2 shared Asko WegeliusiD· 2 shared Erkki Tapio IsometsäiD· 2 shared Jaana SuvisaariiD· 2 shared Jari TiihoneniD· 2 shared Jarmo A. HietalaiD· 2 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aarno V. PalotieORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

The impact of rare protein coding genetic variation on adult cognitive function

Chia‐Yen Chen, Ruoyu Tian, Tian Ge, Max Lam, Gabriela Sánchez-Andrade, Tarjinder Singh, Lea Urpa, Jimmy Z. Liu, Mark Sanderson, Christine Rowley, Holly Ironfield, Terry Fang, Biogen Biobank Team, The SUPER-Finland study, Aija Kyttälä, , Heiko Runz

This study identifies eight genes associated with adult cognitive function through rare coding variants and shows how KDM5B dosage affects cognitive traits in mice and humans.

Nature Genetics · May 25, 2023Peer-reviewedGenetic & Genomic Medicine

Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

Katja Häkkinen, Johanna I. Kiiski, Markku Lähteenvuo, Tuomas Jukuri, Kimmo Suokas, Jussi Niemi-Pynttäri, Tuula Kieseppä, Teemu Männynsalo, Asko Wegelius, Willehard Haaki, Kaisla Lahdensuo, Risto Kajanne, Mari Anneli Kaunisto, Annamari Tuulio‐Henriksson, Olli Kampman, , Ari Ahola‐Olli

The paper constructs a CYP2D6 copy-number imputation panel and reports pharmacogenetic variant frequencies in Finnish individuals with psychosis, showing high imputation accuracy but limited clinical utility.

The Pharmacogenomics Journal · Feb 23, 2022Peer-reviewedGenetic & Genomic Medicine