Author

Megan E. Wadon

Cardiff UniversityORCID 0000-0002-7694-6228Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Anita ThapariD· 1 shared Elliott ReesiD· 1 shared George KiroviD· 1 shared Grace Hosking· 1 shared Joanna MartiniD· 1 shared K. LangleyiD· 1 shared Michael C. O’DonovaniD· 1 shared Michael John OweniD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

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9 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anita ThaparORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineTranslational PsychiatryPeer-reviewedMay 12, 2020

A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder

Joanna Martin, Grace Hosking, Megan E. Wadon…·Anita Thapar

This study identifies de novo copy number variants in children with ADHD, finding a higher mutation rate compared to controls and associations with known neurodevelopmental disorder loci.

23 citations

humanwhole-genome sequencing

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