Bryan Mclaughlin

Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 8 publications

Autosomal dominant primary hyperparathyroidism in the Keeshond dog breed is strongly associated with a missense variant in sirtuin-6.

Autosomal dominant primary hyperparathyroidism in the Keeshond dog breed is strongly associated with a missense variant in sirtuin-6.

Journal: Animal genetics

Published: June 26, 2025

A novel hereditary encephalopathy in four related Labrador Retrievers associated with a missense variant in the ALDH5A1 gene.

A novel hereditary encephalopathy in four related Labrador Retrievers associated with a missense variant in the ALDH5A1 gene.

Journal: Journal of veterinary internal medicine

Published: June 23, 2025

A TTPA deletion is associated with retinopathy with vitamin E deficiency in the English Cocker Spaniel dog.

A TTPA deletion is associated with retinopathy with vitamin E deficiency in the English Cocker Spaniel dog.

Journal: G3 (Bethesda, Md.)

Published: October 08, 2024

Exonic Short Interspersed Nuclear Element Insertion in FAM161A Is Associated with Autosomal Recessive Progressive Retinal Atrophy in the English Shepherd.

Exonic Short Interspersed Nuclear Element Insertion in FAM161A Is Associated with Autosomal Recessive Progressive Retinal Atrophy in the English Shepherd.

Journal: Genes

Published: June 19, 2024

Multiocular defect in the Old English Sheepdog: A canine form of Stickler syndrome type II associated with a missense variant in the collagen-type gene COL11A1.

Multiocular defect in the Old English Sheepdog: A canine form of Stickler syndrome type II associated with a missense variant in the collagen-type gene COL11A1.

Journal: PloS one

Published: July 04, 2023

An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs.

An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs.

Journal: PloS one

Published: March 02, 2017

A novel locus on canine chromosome 13 is associated with cataract in the Australian Shepherd breed of domestic dog.

A novel locus on canine chromosome 13 is associated with cataract in the Australian Shepherd breed of domestic dog.

Journal: Mammalian genome : official journal of the International Mammalian Genome Society

Published: December 03, 2014

ADAMTS17 mutation associated with primary lens luxation is widespread among breeds.

ADAMTS17 mutation associated with primary lens luxation is widespread among breeds.

Journal: Veterinary ophthalmology

Published: November 05, 2011

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Last Updated: 09/26/2026