David A. Parry

Edinburgh, SCT, United Kingdom

Last Updated: 09/26/2026

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Found 105 publications

Impact of Market Access Delays on Time to Patient Access: Multi-Country Comparative Analysis Assessing the First Commercial Launch Indications for Five Oncology Medicines Across Europe and Canada.

Impact of Market Access Delays on Time to Patient Access: Multi-Country Comparative Analysis Assessing the First Commercial Launch Indications for Five Oncology Medicines Across Europe and Canada.

Journal: Journal of market access & health policy

Published: January 09, 2026

A progeria syndrome links DNA hypermethylation to age-related pathology.

A progeria syndrome links DNA hypermethylation to age-related pathology.

Journal: Nature genetics

Published: April 07, 2025

Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures.

Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures.

Journal: American journal of human genetics

Published: February 11, 2025

The challenges of using ultrasound to measure the trachea: a brief report.

The challenges of using ultrasound to measure the trachea: a brief report.

Journal: Critical care (London, England)

Published: February 07, 2025

Could resistance training prevent or improve work-related musculoskeletal disorders among surgeons?

Could resistance training prevent or improve work-related musculoskeletal disorders among surgeons?

Journal: Annals of the Royal College of Surgeons of England

Published: October 22, 2024

CDK4 loss-of-function mutations cause microcephaly and short stature.

CDK4 loss-of-function mutations cause microcephaly and short stature.

Journal: Genes & development

Published: September 20, 2024

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom.

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom.

Journal: Ophthalmology science

Published: August 02, 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

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.

Journal: American journal of human genetics

Published: May 03, 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

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom.

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom.

Journal: medRxiv : the preprint server for health sciences

Published: April 08, 2024

Genetic Findings in Short Turkish Children Born to Consanguineous Parents.

Genetic Findings in Short Turkish Children Born to Consanguineous Parents.

Journal: Hormone research in paediatrics

Published: February 13, 2024

Showing 1-12 of 105

Last Updated: 09/26/2026