Lucinda Murray

Newcastle, NSW 2298, Australia

Last Updated: 09/26/2026

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Found 8 publications

The Healthcare and Societal Costs of Familial Intellectual Disability.

The Healthcare and Societal Costs of Familial Intellectual Disability.

Journal: International journal of environmental research and public health

Published: November 24, 2023

SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder.

SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder.

Journal: Nature communications

Published: January 25, 2023

RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features.

RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features.

Journal: American journal of human genetics

Published: May 22, 2020

Pre-genetics clinic resource evaluation for adults with intellectual disability: The pre-genetics clinic aid.

Pre-genetics clinic resource evaluation for adults with intellectual disability: The pre-genetics clinic aid.

Journal: Journal of genetic counseling

Published: November 30, 2019

Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity.

Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity.

Journal: Human mutation

Published: October 25, 2019

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.

Journal: Molecular psychiatry

Published: November 23, 2017

Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies.

Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies.

Journal: American journal of human genetics

Published: November 13, 2017

A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations.

A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations.

Journal: American journal of human genetics

Published: August 20, 2017

Showing 1-8 of 8

Last Updated: 09/26/2026