Author

K. Langley

Cardiff UniversityORCID 0000-0002-2033-2657Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Genetics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 4 Approach:statistical model· 4 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:fine-mapping· 1 Research Focus:polygenic risk· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Anita ThapariD· 4 shared Joanna MartiniD· 4 shared Michael C. O’DonovaniD· 3 shared Anders Dupont BørglumiD· 2 shared Barbara FrankeiD· 2 shared Benjamin M. NealeiD· 2 shared Bru CormandiD· 2 shared Ditte DemontisiD· 2 shared

Activity by Year

2017-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 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

4 shared papersGenetic & Genomic Medicine

Anita ThaparORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 22, 2022

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

Sheng Wang, Belinda Lei Wang, Vanessa Drury…·Arthur Jeremy Willsey

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky

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

𝕏 PostBluesky

GeneticsNature GeneticsPeer-reviewedNov 23, 2018

✦ In-depth digest

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

Ditte Demontis, Raymond Kenney Walters, Joanna Martin…·Benjamin M. Neale

Genome-wide association meta-analysis of 20,183 ADHD cases and 35,191 controls finds 12 significant loci; signal concentrates in conserved regions, constrained genes, and CNS regulatory elements.

2,202 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsBiological PsychiatryPeer-reviewedDec 2, 2017

A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

Joanna Martin, Raymond Kenney Walters, Ditte Demontis…·Gerd Lehmkuhl

This study investigates genetic mechanisms underlying sex bias in ADHD prevalence using genome-wide data and finds no mean polygenic burden difference across sexes but increased risk in female siblings and comorbid conditions.

199 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky