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Claire Homan

University of South Australia

Australia

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Research Interests

Biostatistics

20%

Virology

10%

Medical Science

40%

Hematology

20%

Genomic

20%

Hemophilia

20%

Graft-versus-host Disease

10%

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Articles5

Somatic mutational landscape of hereditary hematopoietic malignancies caused by germ line RUNX1, GATA2, and DDX41 variants.

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Year:

2023

Clonal hematopoiesis in patients with <i>ANKRD26</i> or <i>ETV6</i> germline mutations

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Year:

2022

The RUNX1 Database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

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Year:

2021

Disrupted Excitatory Synaptic Contacts and Altered Neuronal Network Activity Underpins the Neurological Phenotype in PCDH19-Clustering Epilepsy (PCDH19-CE).

Article Link

Year:

2021

RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML

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Year:

2020

Collaborators7

Andreas Schreiber

Affiliate Senior Lecturer

University of Adelaide

AUSTRALIA

Belinda Phipson

Lab head

Walter and Eliza Hall Institute of Medical Research

AUSTRALIA

Kai Yu

National Human Genome Research Institute

UNITED STATES

Anna Brown

Adjunct Associate Professor

University of South Australia

AUSTRALIA

Christopher Hahn

University of South Australia

AUSTRALIA

Michael W. Drazer

University of Chicago Medicine

UNITED STATES

David Lawrence

University of South Australia

AUSTRALIA

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