Heidi G. Sutherland

60 Musk Ave
Kelvin Grove, QLD 4059, Australia

Last Updated: 09/26/2026

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Found 80 publications

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Journal: Clinical genetics

Published: May 08, 2026

Whole-exome sequencing identifies matrisomal gene associations in monogenic cerebral small vessel disease.

Whole-exome sequencing identifies matrisomal gene associations in monogenic cerebral small vessel disease.

Journal: Journal of neurology

Published: April 09, 2026

Identification of Copy Number Variations in Familial Hemiplegic Migraine Genes in Suspected Hemiplegic Migraine Patients.

Identification of Copy Number Variations in Familial Hemiplegic Migraine Genes in Suspected Hemiplegic Migraine Patients.

Journal: Biomedicines

Published: March 24, 2026

Machine learning-based prediction of Familial Hemiplegic Migraine risk from genetic variants.

Machine learning-based prediction of Familial Hemiplegic Migraine risk from genetic variants.

Journal: Computers in biology and medicine

Published: February 16, 2026

Identification of case-specific copy number variants reveals novel genetic insights into familial hemiplegic migraine pathogenesis.

Identification of case-specific copy number variants reveals novel genetic insights into familial hemiplegic migraine pathogenesis.

Journal: Genomics

Published: December 21, 2025

An ACOT4 Multi-Nucleotide Variant Is Associated with Cardiovascular Risk in Norfolk Island and UK Biobank Cohorts.

An ACOT4 Multi-Nucleotide Variant Is Associated with Cardiovascular Risk in Norfolk Island and UK Biobank Cohorts.

Journal: Genes

Published: December 12, 2025

The Use of Population Isolates to Identify Metabolic Syndrome's Genetic Aetiology.

The Use of Population Isolates to Identify Metabolic Syndrome's Genetic Aetiology.

Journal: Molecular genetics & genomic medicine

Published: October 28, 2025

The Spectrum of NOTCH3 Variants in an Australian CADASIL Cohort.

The Spectrum of NOTCH3 Variants in an Australian CADASIL Cohort.

Journal: Genes

Published: September 30, 2025

Therapeutic Potentials of the Seaweed-Derived Compounds for Alzheimer's Disease.

Therapeutic Potentials of the Seaweed-Derived Compounds for Alzheimer's Disease.

Journal: Molecules (Basel, Switzerland)

Published: September 23, 2025

Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder.

Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder.

Journal: Genes

Published: June 17, 2025

New composite phenotypes enhance chronic kidney disease classification and genetic associations.

New composite phenotypes enhance chronic kidney disease classification and genetic associations.

Journal: PLoS genetics

Published: December 02, 2024

Sirtuin Proteins and Memory: A Promising Target in Alzheimer's Disease Therapy?

Sirtuin Proteins and Memory: A Promising Target in Alzheimer's Disease Therapy?

Journal: Nutrients

Published: November 03, 2024

Showing 1-12 of 80

Last Updated: 09/26/2026