John D. Dean

Ernest Jones Drive
Macleod, VIC 3085, Australia

Last Updated: 09/26/2026

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Found 75 publications

Renin-Angiotensin System inhibitors (RASi) are not nephrotoxic - they protect the kidneys and the heart.

Renin-Angiotensin System inhibitors (RASi) are not nephrotoxic - they protect the kidneys and the heart.

Journal: Clinical medicine (London, England)

Published: December 30, 2025

Renin-angiotensin system inhibitors (RASi) are not nephrotoxic - they protect the kidneys and the heart.

Renin-angiotensin system inhibitors (RASi) are not nephrotoxic - they protect the kidneys and the heart.

Journal: Clinical medicine (London, England)

Published: December 30, 2025

Diaphragmatic Hernia in a Newborn With COL1A1-Associated Classical Ehlers-Danlos Syndrome.

Diaphragmatic Hernia in a Newborn With COL1A1-Associated Classical Ehlers-Danlos Syndrome.

Journal: Case reports in genetics

Published: August 01, 2025

Utility of genome sequencing and group-enrichment to support splice variant interpretation in Marfan syndrome.

Utility of genome sequencing and group-enrichment to support splice variant interpretation in Marfan syndrome.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 27, 2025

Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results.

Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results.

Journal: American journal of human genetics

Published: November 01, 2024

Future Hospital Commission - 10 years on. What's changed, what's new and what's next?

Future Hospital Commission - 10 years on. What's changed, what's new and what's next?

Journal: Future healthcare journal

Published: August 02, 2024

PACS2, PACS1, and VACTERL: A Clinical Overlap.

PACS2, PACS1, and VACTERL: A Clinical Overlap.

Journal: Molecular syndromology

Published: February 29, 2024

PSMC5 insufficiency and P320R mutation impair proteasome function.

PSMC5 insufficiency and P320R mutation impair proteasome function.

Journal: Human molecular genetics

Published: February 21, 2024

Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders.

Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders.

Journal: Genetics in medicine open

Published: November 14, 2023

A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorder.

A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorder.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 10, 2023

New and follow-up outpatient appointments are out of date concepts.

New and follow-up outpatient appointments are out of date concepts.

Journal: BMJ (Clinical research ed.)

Published: September 18, 2023

VIKING II, a worldwide observational cohort of volunteers with northern isles ancestry.

VIKING II, a worldwide observational cohort of volunteers with northern isles ancestry.

Journal: International journal of population data science

Published: September 06, 2023

Showing 1-12 of 75

Last Updated: 09/26/2026