Author

Nicola H. Chapman

University of Washington

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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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ellen M. WijsmaniD· 2 shared Anita L. DeStefanoiD· 1 shared Cathy L. BarriD· 1 shared Elena L. GrigorenkoiD· 1 shared Elizabeth BlueiD· 1 shared Elizabeth Nellis KerriD· 1 shared Kaitlyn M. Price· 1 shared Karen G. Wigg· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetics

Ellen M. WijsmanORCID

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2 papers

Recent·Most cited

GeneticsThe American Journal of Human GeneticsPeer-reviewedFeb 17, 2026

Multiple-testing corrections in case-control studies using identity-by-descent segments

Seth D Temple, Nicola H. Chapman, Seung Hoan Choi…·Elizabeth Blue

This paper proposes a method to correct for multiple testing in IBD mapping for case-control studies, identifies six genome-wide significant AD risk loci, and shows positive selection can confound results.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsPLoS ONEPeer-reviewedMay 27, 2025

Targeted analysis of dyslexia-associated regions on chromosomes 6, 12 and 15 in large multigenerational cohorts

Nicola H. Chapman, Patrick A. Navas, Michael O. Dorschner…·Wendy H. Raskind

This study analyzes non-coding variants in five dyslexia candidate genes using targeted sequencing in large families, finding significant associations with reading and spelling traits but no large-effect coding variants.

4 citations

humanwhole-exome sequencing

𝕏 PostBluesky