Author

Sophie L Chick

Cardiff UniversityORCID 0009-0004-6941-7338Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Detelina GrozevaiD· 1 shared Elliott ReesiD· 1 shared James WaltersiD· 1 shared Julie H. WilliamsiD· 1 shared Michael C. O’DonovaniD· 1 shared Michael John OweniD· 1 shared Peter HolmansiD· 1 shared Rebecca SimsiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Detelina GrozevaORCID

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1 paper

Recent·Most cited

Analysis of exome sequencing data implicates rare coding variants in STAG1 and ZNF136 in schizophrenia

Sophie L Chick, Peter Holmans, Detelina Grozeva, Rebecca Sims, Julie H. Williams, Michael John Owen, Michael C. O’Donovan, James Walters, Elliott Rees

This study identifies rare coding variants in STAG1 and ZNF136 associated with schizophrenia using exome sequencing data from 28,898 cases and 103,041 controls.

medRxiv · Oct 14, 2024 · PreprintGenetic & Genomic Medicine