Kathryn P Burdon

University of Tasmania

Australia

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Articles (10)

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2022

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2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Collaborators (20)

Emmanuelle Souzeau

Flinders University

AUSTRALIA

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Mark Chia

AUSTRALIA

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Richard Mills

Flinders University

AUSTRALIA

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Adnan Tufail

University College London

UNITED KINGDOM

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Terri Young

Professor

University of Wisconsin-Madison

UNITED STATES

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Juho Wedenoja

University of Helsinki

FINLAND

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Joshua Schmidt

Flinders University

AUSTRALIA

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Joseph Marsh

University of Edinburgh

UNITED KINGDOM

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Paul Baird

Professorial Fellow

University of Melbourne

AUSTRALIA

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Stuart MacGregor

Professor

QIMR Berghofer Medical Research Institute

AUSTRALIA

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Xin Lin

University of Melbourne

AUSTRALIA

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Kaylene Young

University of Tasmania

AUSTRALIA

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David Garway-Heath

University College London

UNITED KINGDOM

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Jamie Craig

Flinders University

AUSTRALIA

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Joan Bailey-Wilson

Co-Branch Chief

National Human Genome Research Institute

UNITED STATES

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Tom MacGillivray

University of Edinburgh

UNITED KINGDOM

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Seyhan Yazar

University of Western Australia

AUSTRALIA

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Kenji Yamashiro

Professor and Chairman

Kochi Medical School, Kochi University

JAPAN

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John D. Hulleman

University of Texas Southwestern Medical Center

UNITED STATES

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Virginie Verhoeven

Erasmus University Rotterdam

NETHERLANDS

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Kathryn P Burdon

Research Interests

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Articles (10)

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Evaluating gap junction variants for a role in pediatric cataract: an overview of the genetic landscape and clinical classification of variants in the <i>GJA3</i> and <i>GJA8</i> genes

Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort

The Association of Alcohol Consumption with Glaucoma and Related Traits: Findings from the UK Biobank.

Specifications of the ACMG/AMP variant curation guidelines for myocilin

Novel plasma and brain proteins that are implicated in multiple sclerosis

Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging

Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123 (American Journal of Ophthalmology (2022) 233 (111–123), (S0002939421003366), (10.1016/j.ajo.2021.06.014))

Gene Set Enrichment Analsyes Identiify Pathways Involved in Genetic Risk for Diabetic Retinopathy: GSEA Identify Pathways Involved in Genetic Risk for DR

Generation and characterisation of four multiple sclerosis iPSC lines from a single family

Collaborators (20)

Emmanuelle Souzeau

Mark Chia

Richard Mills

Adnan Tufail

Terri Young

Juho Wedenoja

Joshua Schmidt

Joseph Marsh

Paul Baird

Stuart MacGregor

Xin Lin

Kaylene Young

David Garway-Heath

Jamie Craig

Joan Bailey-Wilson

Tom MacGillivray

Seyhan Yazar

Kenji Yamashiro

John D. Hulleman

Virginie Verhoeven

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