Thomas R W Nixon (Thomas Nixon)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 5

Top Topics

Dna Methylation

Circulating Tumor

Top Venues

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

European journal of human genetics : EJHG

Eye (London, England)

This page only lists publications with an associated author ORCID identifier.

Publications

Thomas R W Nixon, Rebecca L Davie, Martin P Snead
Posterior vitreous detachment and retinal tear - a prospective study of community referrals. Eye (London, England) (2023)
Thomas R W Nixon, Allan J Richards, Howard Martin, Phillip Alexander, Martin P Snead
Autosomal Recessive Stickler Syndrome. Genes 13 (7) (2022)
Thomas R W Nixon, Allan J Richards, Adrian Lomas, Stephen Abbs, Pradeep Vasudevan, Annie McNinch, Phillip Alexander, Martin P Snead
Inherited and de novo biallelic pathogenic variants in COL11A1 result in type 2 Stickler syndrome with severe hearing loss. Molecular genetics & genomic medicine 8 (9) (2020)
Thomas R W Nixon, Philip Alexander, Allan Richards, Annie McNinch, Philip W P Bearcroft, Jan Cobben, Martin P Snead
Homozygous Type IX collagen variants (COL9A1, COL9A2, and COL9A3) causing recessive Stickler syndrome-Expanding the phenotype. American journal of medical genetics. Part A 179 (8) (2019)
Thomas R W Nixon, Allan Richards, Laura K Towns, Gavin Fuller, Stephen Abbs, Philip Alexander, Annie McNinch, Richard N Sandford, Martin P Snead
Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasia. European journal of human genetics : EJHG 27 (3) (2018)