Christopher Mark Watson

37PUBLICATIONS
120CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)AutoimmunityEpigenetics (incl. genome methylation and epigenomics)Craniofacial biologyVision science
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Publications (37)

|Jul 20, 2026
Diagnostic discovery of structural variants causing foveal hypoplasia using SVRare and long-read nanopore sequencing.

|Jul 01, 2026
Identification of DNA sequence variants in the Vasculo-Behcet disease patient using whole exome sequencing: a pilot study from Pakistan.

|Jun 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders.

|Apr 11, 2026
ACP4 Variants in Hypoplastic Amelogenesis Imperfecta.

Lu Liu, Cheuk Wang Au, Ummey Hany

|Apr 03, 2026
Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library.

Jenny Lord, Alistair T Pagnamenta, Letizia Vestito

|Feb 23, 2026
Exploratory whole-exome sequencing identifies candidate DNA variants in Ocular Behcet disease: a pilot study from a Pakistani cohort.

Ayesha Waqas, Azra Yasmin, Christopher Mark Watson

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Frequent Collaborators

9 joint publications

James A Poulter

8 joint publications

Chris F Inglehearn

6 joint publications

Ummey Hany

4 joint publications

Manir Ali