Author

Rebecca Kingdom

University of ExeterORCID 0009-0008-6168-0018Unclaimed 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:differential expression· 1 Assay:GWAS summary statistics· 1 Research Focus:polygenic risk· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Andrew R. WoodiD· 2 shared Caroline Fiona WrightiD· 2 shared Michael N. WeedoniD· 2 shared Robin N. BeaumontiD· 2 shared Marcus A. TukeiD· 1 shared Timothy M. FraylingiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 15 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Andrew R. WoodORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineNature GeneticsPeer-reviewedApr 18, 2024

Genetic modifiers of rare variants in monogenic developmental disorder loci

Rebecca Kingdom, Robin N. Beaumont, Andrew R. Wood…·Caroline Fiona Wright

The paper investigates how rare variants in monogenic developmental disorder genes interact with common variants to affect cognitive and socio-economic traits, finding that higher educational attainment polygenic scores can partially counterbalance adverse effects.

67 citationstop 1%

humanGWAS summary statistics

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Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedJun 13, 2022

Rare genetic variants in dominant developmental disorder loci cause milder related phenotypes in the general population

Rebecca Kingdom, Marcus A. Tuke, Andrew R. Wood…·Caroline Fiona Wright

The paper investigates the phenotypic effects of rare variants in developmental disorder genes in the general population, finding milder related traits in carriers.

59 citationstop 1%

humanwhole-exome sequencing

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