Whole-Genome sequencing and genetic variant analysis of a quarter Horse mare

Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses

(2011) R. R. Bellone et al.   Briefings in Functional Genomics

Accurate and comprehensive sequencing of personal genomes

(2011) S. S. Ajay et al.   GENOME RESEARCH

High-Resolution Analysis of Parent-of-Origin Allelic Expression in the Mouse Brain

(2010) C. Gregg et al.   SCIENCE

Whole-Genome SNP Association in the Horse: Identification of a Deletion in Myosin Va Responsible for Lavender Foal Syndrome

(2010) Samantha A. Brooks et al.   PLoS Genetics

Evaluation of allele frequencies of inherited disease genes in subgroups of American Quarter Horses

(2009) Robert C. Tryon et al.   JAVMA-JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION

A Genome Scan for Positive Selection in Thoroughbred Horses

(2009) Jingjing Gu et al.   PLoS One

Genome Sequence, Comparative Analysis, and Population Genetics of the Domestic Horse

(2009) C. M. Wade et al.   SCIENCE

Carpometacarpal Osteoarthritis in Thirty-Three Horses

(2009) LUCA PANIZZI et al.   VETERINARY SURGERY

Maize Inbreds Exhibit High Levels of Copy Number Variation (CNV) and Presence/Absence Variation (PAV) in Genome Content

(2009) Nathan M. Springer et al.   PLoS Genetics

Partial deletion of theLAMA3gene is responsible for hereditary junctional epidermolysis bullosa in the American Saddlebred Horse

(2008) K. T. Graves et al.   ANIMAL GENETICS

The horse pseudoautosomal region (PAR): characterization and comparison with the human, chimp and mouse PARs

(2008) T Raudsepp et al.   CYTOGENETIC AND GENOME RESEARCH

Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis

(2008) Molly E. McCue et al.   GENOMICS

A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse

(2008) Gerli Rosengren Pielberg et al.   NATURE GENETICS

Equine diseases caused by known genetic mutations

(2008) Carrie J. Finno et al.   VETERINARY JOURNAL

Missense Mutation in Exon 2 of SLC36A1 Responsible for Champagne Dilution in Horses

(2008) Deborah Cook et al.   PLoS Genetics