Andrew R. Webster

City Road
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 369 publications

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.

Journal: Investigative ophthalmology & visual science

Published: August 10, 2026

XXYLT1 and Mendelian Retinal Dystrophy.

XXYLT1 and Mendelian Retinal Dystrophy.

Journal: JAMA ophthalmology

Published: July 30, 2026

Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.

Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.

Journal: Research square

Published: July 17, 2026

The AP5B1 p.(Leu785Pro) variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

The AP5B1 p.(Leu785Pro) variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

Journal: HGG advances

Published: June 23, 2026

The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

Journal: HGG advances

Published: June 23, 2026

Small bowel perforation secondary to swallowed denture impaction at an NSAID-induced ileal diaphragm.

Small bowel perforation secondary to swallowed denture impaction at an NSAID-induced ileal diaphragm.

Journal: Journal of surgical case reports

Published: June 12, 2026

A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discovery.

A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discovery.

Journal: medRxiv : the preprint server for health sciences

Published: May 25, 2026

MERTK-associated retinal dystrophy: clinical course and imaging.

MERTK-associated retinal dystrophy: clinical course and imaging.

Journal: Ophthalmic genetics

Published: May 04, 2026

A Novel Motion-Management Workflow Using Abdominal Compression and Exhale Breath-Hold for Patients With Hepatobiliary Malignancies: A Feasibility Evaluation.

A Novel Motion-Management Workflow Using Abdominal Compression and Exhale Breath-Hold for Patients With Hepatobiliary Malignancies: A Feasibility Evaluation.

Journal: Clinical oncology (Royal College of Radiologists (Great Britain))

Published: April 28, 2026

Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genes.

Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genes.

Journal: Eye (London, England)

Published: April 21, 2026

Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental Disorder.

Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental Disorder.

Journal: Investigative ophthalmology & visual science

Published: March 11, 2026

Biallelic germline variants in the hematologic malignancy predisposition gene DDX41 cause retinal dystrophy through dysregulation of retinal homeostasis.

Biallelic germline variants in the hematologic malignancy predisposition gene DDX41 cause retinal dystrophy through dysregulation of retinal homeostasis.

Journal: medRxiv : the preprint server for health sciences

Published: February 06, 2026

Showing 1-12 of 369

Last Updated: 09/26/2026