Alex D. Shaw

Newtown, NSW, Australia

Last Updated: 09/26/2026

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Found 13 publications

Evaluation of Urine Nephrin:Creatine Ratio Longitudinally in Pregnancy for the Detection of Preeclampsia and Kidney Damage in Women With Pre-Existing Diabetes.

Evaluation of Urine Nephrin:Creatine Ratio Longitudinally in Pregnancy for the Detection of Preeclampsia and Kidney Damage in Women With Pre-Existing Diabetes.

Journal: The journal of obstetrics and gynaecology research

Published: October 09, 2025

A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.

A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.

Journal: Journal of psychiatry & neuroscience : JPN

Published: March 17, 2021

De Novo Gene Variants and Familial Bipolar Disorder.

De Novo Gene Variants and Familial Bipolar Disorder.

Journal: JAMA network open

Published: May 09, 2020

CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.

CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.

Journal: Brain : a journal of neurology

Published: August 01, 2019

Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes

Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes

Journal: Journal of psychiatry & neuroscience : JPN

Published: May 17, 2019

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.

Journal: PLoS genetics

Published: July 01, 2018

An examination of multiple classes of rare variants in extended families with bipolar disorder.

An examination of multiple classes of rare variants in extended families with bipolar disorder.

Journal: Translational psychiatry

Published: January 22, 2018

Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls.

Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls.

Journal: Translational psychiatry

Published: September 14, 2017

Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts.

Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts.

Journal: Journal of the American Academy of Child and Adolescent Psychiatry

Published: May 08, 2017

Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

Journal: Brain : a journal of neurology

Published: May 09, 2015

Neuregulin 1 expression and electrophysiological abnormalities in the Neuregulin 1 transmembrane domain heterozygous mutant mouse.

Neuregulin 1 expression and electrophysiological abnormalities in the Neuregulin 1 transmembrane domain heterozygous mutant mouse.

Journal: PloS one

Published: February 16, 2014

Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder.

Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder.

Journal: PloS one

Published: July 29, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026