Louise M. Burmeister

Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 13 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

Correction: Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog.

Correction: Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog.

Journal: PloS one

Published: July 28, 2022

A Missense Variant in the Bardet-Biedl Syndrome 2 Gene (BBS2) Leads to a Novel Syndromic Retinal Degeneration in the Shetland Sheepdog.

A Missense Variant in the Bardet-Biedl Syndrome 2 Gene (BBS2) Leads to a Novel Syndromic Retinal Degeneration in the Shetland Sheepdog.

Journal: Genes

Published: October 01, 2021

Deafness in Australian Cattle Dogs associated to QTL on chromosome 20 in genome-wide association study analyses.

Deafness in Australian Cattle Dogs associated to QTL on chromosome 20 in genome-wide association study analyses.

Journal: Animal genetics

Published: June 25, 2021

Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog.

Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog.

Journal: PloS one

Published: September 21, 2020

Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel RETREG1 variant.

Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel RETREG1 variant.

Journal: Journal of veterinary internal medicine

Published: April 24, 2020

A genome-wide association study of deafness in three canine breeds.

A genome-wide association study of deafness in three canine breeds.

Journal: PloS one

Published: December 11, 2019

A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs.

A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs.

Journal: BMC genetics

Published: December 09, 2019

A novel TYRP1 variant is associated with liver and tan coat colour in Lancashire Heelers.

A novel TYRP1 variant is associated with liver and tan coat colour in Lancashire Heelers.

Journal: Animal genetics

Published: June 19, 2019

Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration.

Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration.

Journal: Genes

Published: April 15, 2019

Clinical, histopathological and genetic characterisation of oculoskeletal dysplasia in the Northern Inuit Dog.

Clinical, histopathological and genetic characterisation of oculoskeletal dysplasia in the Northern Inuit Dog.

Journal: PloS one

Published: March 28, 2019

A variant in OLFML3 is associated with pectinate ligament abnormality and primary closed-angle glaucoma in Border Collies from the United Kingdom.

A variant in OLFML3 is associated with pectinate ligament abnormality and primary closed-angle glaucoma in Border Collies from the United Kingdom.

Journal: Veterinary ophthalmology

Published: December 10, 2018

Showing 1-12 of 13

Last Updated: 09/26/2026