George Mcgillivray

Melbourne, VIC, Australia

Last Updated: 09/26/2026

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Found 72 publications

Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.

Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.

Journal: The Journal of clinical investigation

Published: September 11, 2025

Atypical presentations of fetal polycystic kidney disease demonstrates the utility of a genomic autopsy for accurate post-mortem diagnoses.

Atypical presentations of fetal polycystic kidney disease demonstrates the utility of a genomic autopsy for accurate post-mortem diagnoses.

Journal: Human genomics

Published: September 10, 2025

Australian patients' experiences of undergoing whole exome sequencing for fetal structural anomalies prior to receiving results.

Australian patients' experiences of undergoing whole exome sequencing for fetal structural anomalies prior to receiving results.

Journal: Journal of genetic counseling

Published: May 01, 2025

Utility of genome-wide methylation array in the diagnosis of NLRP7-associated gestational trophoblastic disease.

Utility of genome-wide methylation array in the diagnosis of NLRP7-associated gestational trophoblastic disease.

Journal: Pathology

Published: March 31, 2025

Childhood outcomes of fetal genomic copy-number variants: The prenatal microarray cohort study.

Childhood outcomes of fetal genomic copy-number variants: The prenatal microarray cohort study.

Journal: Genetics in medicine open

Published: January 24, 2025

Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformation.

Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformation.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: January 16, 2025

The PreGen Research Program: Implementing Prenatal Genomic Testing in Australia-A Commentary.

The PreGen Research Program: Implementing Prenatal Genomic Testing in Australia-A Commentary.

Journal: The Australian & New Zealand journal of obstetrics & gynaecology

Published: October 23, 2024

Outcomes of children diagnosed antenatally with sex chromosome aneuploidies.

Outcomes of children diagnosed antenatally with sex chromosome aneuploidies.

Journal: Journal of paediatrics and child health

Published: September 12, 2023

Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless.

Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless.

Journal: Orphanet journal of rare diseases

Published: August 09, 2023

Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt.

Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt.

Journal: American journal of human genetics

Published: August 06, 2023

Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.

Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.

Journal: Nature medicine

Published: July 10, 2023

Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort.

Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort.

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

Published: June 30, 2023

Showing 1-12 of 72

Last Updated: 09/26/2026