Reuben M. Buckley

This study uses a genotype-first approach to identify new mutations related to craniofacial morphology and stature in dogs, highlighting the role of allelic heterogeneity in breed trait selection.

The paper evaluates low-pass whole genome sequencing and imputation in dogs, optimizing variant filtering to reduce imputation error and provides guidelines for GWAS using imputed genotypes.

The paper presents an improved long-read assembly of the dog reference genome, significantly enhancing contiguity and gene annotation.

This paper presents a domestic cat whole exome sequencing resource, demonstrating its effectiveness in identifying known and novel disease-associated variants across various breeds.

The paper presents a new domestic cat genome assembly using long-read sequencing, identifies novel variants associated with cancer and dwarfism, and highlights the utility of feline genomics for biomedical research.

The paper identifies variants in the Hairless gene associated with hypotrichia and roaning in lykoi cats by comparing whole genome sequencing data from a lykoi cat to a non-lykoi dataset.

The paper identifies a 7 bp deletion in GDF7 causing a heritable forebrain commissural malformation in cats, validated through genomic analysis and pedigree studies.

This study identifies a novel gene region associated with feline disproportionate dwarfism, suggesting a potential model for human undiagnosed dwarfism cases.