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Showing results for "early life"

Invasive aspergillosis in adult patients in Australia and New Zealand: 2017–2020

New and emerging risks for invasive aspergillosis (IA) bring the need for contemporary analyses of the epidemiology and outcomes of IA, in order to improve clinical practice.

European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation

Atopic dermatitis is a common inflammatory skin condition and prior genome-wide association studies have identified 71 associated loci. In the current study we conducted the largest AD GWAS to date combining previously reported cohorts with additional available data.

Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms

To investigate the genetic architecture of internalizing symptoms in childhood and adolescence.

A genome-wide association study of total child psychiatric problems scores

Substantial genetic correlations have been reported across psychiatric disorders and numerous cross-disorder genetic variants have been detected. To identify the genetic variants underlying general psychopathology in childhood, we performed a genome-wide association study using a total psychiatric problem score.

Project Officer, The ORIGINS Project

The Opportunity The ORIGINS Project is a longitudinal pregnancy cohort, following 10,000 families over a decade, to improve child and adult outcomes

Research Assistant: ORIGINS

Work as a Research Assistant with ORIGINS

Project Coordinator, Ear Health (Telehealth Project)

The Opportunity: The Ear Health Team are currently developing an innovative ear and hearing health and telehealth program for children in WA and

Research Assistant, Ear Health Team

The Opportunity: The Ear Health Team are currently working on developing innovative ear and hearing health and telehealth programs for children in WA

Parental origin of mutations

We hypothesised that MECP2 mutations occur predominantly on the male derived X chromosome.