Dean G. Phelan

Flemington Road
Parkville, VIC 3052, Australia

Last Updated: 09/26/2026

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Found 31 publications

Variant interpretation training for the genomics era: Learning outcomes to inform professional competencies and education.

Variant interpretation training for the genomics era: Learning outcomes to inform professional competencies and education.

Journal: American journal of human genetics

Published: November 17, 2025

AC electrical transport detection of magnetic properties of small, granular, and heterogeneous samples.

AC electrical transport detection of magnetic properties of small, granular, and heterogeneous samples.

Journal: The Review of scientific instruments

Published: November 25, 2024

Integrated multi-omics for rapid rare disease diagnosis on a national scale.

Integrated multi-omics for rapid rare disease diagnosis on a national scale.

Journal: Nature medicine

Published: December 15, 2022

Ethylmalonic encephalopathy masquerading as meningococcemia.

Ethylmalonic encephalopathy masquerading as meningococcemia.

Journal: Cold Spring Harbor molecular case studies

Published: January 14, 2022

Synthesis and characterization of bulk Nd1-x Sr x NiO2 and Nd1-x Sr x NiO3.

Synthesis and characterization of bulk Nd1-x Sr x NiO2 and Nd1-x Sr x NiO3.

Journal: Physical review materials

Published: June 18, 2021

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.

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

Published: March 24, 2021

Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.

Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.

Journal: European journal of human genetics : EJHG

Published: November 10, 2020

The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.

The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.

Journal: Journal of the neurological sciences

Published: September 01, 2020

Intertwined density waves in a metallic nickelate.

Intertwined density waves in a metallic nickelate.

Journal: Nature communications

Published: July 24, 2020

Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System.

Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System.

Journal: JAMA

Published: June 24, 2020

Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review.

Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review.

Journal: Molecular genetics & genomic medicine

Published: April 30, 2020

A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients.

A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients.

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

Published: April 23, 2020

Showing 1-12 of 31

Last Updated: 09/26/2026