Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia

Lydia Forestier-Zhang, Laura Watts, Alison Turner, +7

Orphanet Journal of Rare Diseases

The RUDY study platform – a novel approach to patient driven research in rare musculoskeletal diseases

M K Javaid, Lydia Forestier-Zhang, Laura Watts, +15

Orphanet Journal of Rare Diseases

<i>ERAP1</i> association with ankylosing spondylitis is attributable to common genotypes rather than rare haplotype combinations

Amity R. Roberts, Louise Appleton, Adrián Cortés, +4

Proceedings of the National Academy of Sciences

The RUDY study: using digital technologies to enable a research partnership

Harriet Teare, Joanna Hogg, Jane Kaye, +6

European Journal of Human Genetics

Improving patient outcomes in fibrous dysplasia/McCune-Albright syndrome: an international multidisciplinary workshop to inform an international partnership

Alison M. Boyce, Alison Turner, Laura Watts, +12

Archives of Osteoporosis

International PartnershipUterine FibroidsOphthalmologyFibrous Dysplasia/mccune-albright SyndromeInternational Multidisciplinary Workshop +2

Neuropathic-like Pain in Fibrous Dysplasia/McCune-Albright Syndrome

Tiahna Spencer, Laura Watts, Anushka Soni, +4

The Journal of Clinical Endocrinology & Metabolism

Chiari malformation, syringomyelia and bulbar palsy in X linked hypophosphataemia

Laura Watts, P Wordsworth

BMJ Case Reports

Thumb HypoplasiaRare DiseasesGenetic TestingSpinal Cord InjuryChiari Malformation +10

Serial Alu sequence transposition interrupting a human B creatine kinase pseudogene

S. Tony, J Ifegwu, Laura Watts, +3

Genomics

Systems BiologyNatural SciencesMolecular BiologyMolecular GeneticsGene Expression +2

Patient experiences of participation in a medical student teaching workshop

Laura Watts, Tess McPherson, Joanna Robson, +2

Medical Teacher

Rare musculoskeletal diseases in adults: a research priority setting partnership with the James Lind Alliance

Gerda Mickute, Kristina Staley, Heather Delaney, +15

Orphanet Journal of Rare Diseases