Author

Alexys Knighton

University of Pennsylvania

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· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

David C. GlahniD· 1 shared Emma E. M. KnowlesiD· 1 shared Guillaume HuguetiD· 1 shared Josephine MolloniD· 1 shared Laura A. AlmasyiD· 1 shared Laura M. SchultziD· 1 shared Martineau Jean‐LouisiD· 1 shared Sébastien JacquemontiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

David C. GlahnORCID

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1 paper

Recent·Most cited

Copy number variants differ in frequency across genetic ancestry groups

Laura M. Schultz, Alexys Knighton, Guillaume Huguet, Zohra Saci, Martineau Jean‐Louis, Josephine Mollon, Emma E. M. Knowles, David C. Glahn, Sébastien Jacquemont, Laura A. Almasy

The paper examines CNV frequency differences across genetic ancestry groups and finds lower prevalence of deleterious CNVs in non-European ancestry groups.

Human Genetics and Genomics Advances · Aug 12, 2024Peer-reviewedGenetic & Genomic Medicine