P. Roby

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

Steve D. M. Brown, Ian C. Gray, Zuzanna Tymowska-Lalanne, 2000, Nature Genetics.

Towards a mutant map of the mouse – new models of neurological, behavioural, deafness, bone, renal and blood disorders

Claire E. Thornton, S. Rastan, E. Fisher, 2004, Genetica.

Autosomal dominant (Beukes) premature degenerative osteoarthropathy of the hip joint maps to an 11-cM region on chromosome 4q35.

S. Eyre, Jane Worthington, P. Beighton, 1999, American journal of human genetics.

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.

S. Rastan, K. Steel, P. Mburu, 2001, Human molecular genetics.

Identification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate gene.

S. Eyre, K. Wolstencroft, P. Beighton, 2005, Journal of medical genetics.

Identification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate gene

S. Eyre, K. Wolstencroft, P. Beighton, 2002, Journal of medical genetics.

Linkage of a marker in intron D of the estrogen synthase locus to rheumatoid arthritis.

A. Silman, S. Eyre, S. John, 1999, Arthritis and rheumatism.

Identification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate gene.

S. Eyre, K. Wolstencroft, P. Beighton, 2005, Journal of medical genetics.