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

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

David C. GlahnORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Genetic & Genomic MedicineHuman Genetics and Genomics AdvancesPeer-reviewedAug 12, 2024

Copy number variants differ in frequency across genetic ancestry groups

Laura M. Schultz, Alexys Knighton, Guillaume Huguet…·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.

5 citations

humanwhole-genome sequencing

𝕏 PostBluesky