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Mathew Wallis

11PUBLICATIONS

216CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Disease surveillanceNeurogeneticsMedical infection agents (incl. prions)Cancer genetics

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Publications (11)

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|Aug 12, 2025

Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Renee Johnson, Robert A Fletcher, Stacey Peters

|Nov 26, 2024

Assessing the unmet needs of genomic testing in Australia: a geospatial exploration.

Sarah Casauria, Felicity Collins, Susan M White

|Oct 29, 2024

Measuring the impact of rare diseases in Tasmania, Australia.

Philippa Scanlon, Garry Ridler, Genevieve Say

|Jul 26, 2024

Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.

Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree

|Jun 11, 2024

Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study.

Amali C Mallawaarachchi, Lindsay Fowles, Louise Wardrop

|Jun 11, 2024

A deep intronic variant in MME causes autosomal recessive Charcot-Marie-Tooth neuropathy through aberrant splicing.

Bianca R Grosz, Jevin M Parmar, Melina Ellis

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Frequent Collaborators

2 joint publications

Annabel K Sangree

2 joint publications

Zdeněk Sedláček

2 joint publications

Lucie Dupuis

2 joint publications

Rajesh Angireddy

2 joint publications

Katie Clarkson

2 joint publications

Emily E Lubin

2 joint publications

Irene Valenzuela

2 joint publications

Roberto Mendoza-Londono

2 joint publications

Dana E Layo-Carris

2 joint publications

Nicholas Pachter

Frequent Collaborators

2 joint publications

Annabel K Sangree

2 joint publications

Zdeněk Sedláček

2 joint publications

Lucie Dupuis

2 joint publications

Rajesh Angireddy

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