Thomas Nixon

Homozygous Type IX collagen variants (<i>COL9A1</i>, <i>COL9A2</i>, and <i>COL9A3</i>) causing recessive Stickler syndrome—Expanding the phenotype

Thomas Nixon, Philip Alexander, Allan J. Richards et al. · American Journal of Medical Genetics Part A · 2019 · 43 citations

Mendelian Disorder, Autoimmune Disease, Family Members +15

Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasia

Thomas Nixon, Allan J. Richards, Laura K. Towns et al. · European Journal of Human Genetics · 2018 · 35 citations · Full text

Stickler syndrome – lessons from a national cohort

Martin P. Snead, Allan J. Richards, Annie McNinch et al. · Eye · 2021 · 27 citations · Full text

Inherited and de novo biallelic pathogenic variants in <i>COL11A1</i> result in type 2 Stickler syndrome with severe hearing loss

Thomas Nixon, Allan J. Richards, Adrian Lomas et al. · Molecular Genetics & Genomic Medicine · 2020 · 15 citations · Full text

Feasibility of simple machine learning approaches to support detection of non-glaucomatous visual fields in future automated glaucoma clinics

Peter Thomas, Thomas Chan, Thomas Nixon et al. · Eye · 2019 · 13 citations · Full text

Engineering, Machine Learning, Machine Learning Tool +16