Alison M. Meynert

Crewe Road
Edinburgh, SCT, United Kingdom

Last Updated: 09/26/2026

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Found 45 publications

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Journal: European journal of human genetics : EJHG

Published: December 22, 2025

Uncovering the molecular signature of feline diffuse iris melanoma through transcriptomic analysis of disease severity.

Uncovering the molecular signature of feline diffuse iris melanoma through transcriptomic analysis of disease severity.

Journal: Scientific reports

Published: March 14, 2025

Somatic BRCA1/2 mutations are associated with a similar survival advantage to their germline counterparts in tubo-ovarian high grade serous carcinoma.

Somatic BRCA1/2 mutations are associated with a similar survival advantage to their germline counterparts in tubo-ovarian high grade serous carcinoma.

Journal: European journal of cancer (Oxford, England : 1990)

Published: December 10, 2024

Divergent trajectories to structural diversity impact patient survival in high grade serous ovarian cancer.

Divergent trajectories to structural diversity impact patient survival in high grade serous ovarian cancer.

Journal: Nature communications

Published: October 03, 2024

Oronasal mucosal melanoma is defined by two transcriptional subtypes in humans and dogs with implications for diagnosis and therapy.

Oronasal mucosal melanoma is defined by two transcriptional subtypes in humans and dogs with implications for diagnosis and therapy.

Journal: The Journal of pathology

Published: July 30, 2024

Whole Genome Sequencing of "Mutation-Negative" Individuals With Cornelia de Lange Syndrome.

Whole Genome Sequencing of "Mutation-Negative" Individuals With Cornelia de Lange Syndrome.

Journal: Human mutation

Published: May 25, 2024

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.

Journal: Science (New York, N.Y.)

Published: April 25, 2024

Whole genome sequencing enhances molecular diagnosis of primary ciliary dyskinesia.

Whole genome sequencing enhances molecular diagnosis of primary ciliary dyskinesia.

Journal: Pediatric pulmonology

Published: March 22, 2024

Genetic variation at 11q23.1 confers colorectal cancer risk by dysregulation of colonic tuft cell transcriptional activator POU2AF2.

Genetic variation at 11q23.1 confers colorectal cancer risk by dysregulation of colonic tuft cell transcriptional activator POU2AF2.

Journal: Gut

Published: February 14, 2024

Mutational scanning reveals oncogenic CTNNB1 mutations have diverse effects on signaling.

Mutational scanning reveals oncogenic CTNNB1 mutations have diverse effects on signaling.

Journal: Nature genetics

Published: August 16, 2023

Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome.

Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome.

Journal: Journal of medical genetics

Published: April 10, 2023

Rapid evolution of colistin resistance in a bioreactor model of infection of Klebsiella pneumoniae.

Rapid evolution of colistin resistance in a bioreactor model of infection of Klebsiella pneumoniae.

Journal: Communications biology

Published: March 16, 2023

Showing 1-12 of 45

Last Updated: 09/26/2026