Raymond Dalgleish

14PUBLICATIONS
65CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsOphthalmology and optometry not elsewhere classifiedOptometryOncology and carcinogenesis not elsewhere classified
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Publications (14)

|Jun 17, 2026
The WHO Classification of Genetic Tumour Syndromes: Considerations for Genetics.

|May 22, 2026
Re: "A novel splice-altering frameshift variant in the COL1A1 gene underlies osteogenesis imperfecta type I: molecular characterization of a four-generation Chinese pedigree and literature review".

|Jul 19, 2024
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification.

Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga

|Jun 10, 2024
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery.

Daniel Danis, Michael J Bamshad, Yasemin Bridges

|May 16, 2022
Dissecting the phenotypic variability of osteogenesis imperfecta.

Nadia Garibaldi, Roberta Besio, Raymond Dalgleish

|Oct 07, 2021
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions.

Elspeth A Bruford, Cristina R Antonescu, Andrew J Carroll

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Frequent Collaborators

5 joint publications

Peter J Freeman

3 joint publications

Alexander J Lazar

3 joint publications

Elspeth A Bruford

3 joint publications

John F Wagstaff