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Meredith Wilson

5PUBLICATIONS

39CO-AUTHORS

Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Implementation science and evaluationGene mappingAcoustics and noise control (excl. architectural acoustics)

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Publications (5)

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|Jun 08, 2023

Integrated multi-omics for rapid rare disease diagnosis on a national scale.

Sebastian Lunke, Sophie E Bouffler, Chirag V Patel

|Aug 15, 2022

Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis.

Lisa J Ewans, Andre E Minoche, Deborah Schofield

|Jan 29, 2021

Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level.

Stephanie Best, Helen Brown, Sebastian Lunke

|Jul 18, 2020

Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission").

Edwin P Kirk, Royston Ong, Kirsten Boggs

|May 16, 2020

A Case Series of X-Linked Deafness-2 with Sensorineural Hearing Loss, Stapes Fixation, and Perilymphatic Gusher: MR Imaging and Clinical Features of Hypothalamic Malformations.

J-A Prat Matifoll, M Wilson, R Goetti

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Frequent Collaborators

2 joint publications

Edwin P Kirk

2 joint publications

Zornitza Stark

2 joint publications

Gemma R Brett

2 joint publications

Sulekha Rajagopalan

1 joint publications

J-A Prat Matifoll

1 joint publications

R Goetti

1 joint publications

C Birman

1 joint publications

John Christodoulou

1 joint publications

E Peadon

1 joint publications

A Prats-Uribe

Frequent Collaborators

2 joint publications

Edwin P Kirk

2 joint publications

Zornitza Stark

2 joint publications

Gemma R Brett

2 joint publications

Sulekha Rajagopalan

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