Claire C. Homan

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

Anna Brown, Peer Arts, Catherine Carmichael et al. · Blood Advances · 2020 · 150 citations · Full text

Allelic Variant, Developmental Biology, Somatic Mutations +15

Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth

Claire C. Homan, Raman Kumar, Lam Son Nguyen et al. · The American Journal of Human Genetics · 2014 · 144 citations · Full text

Neurodegenerative Diseases, Developmental Biology, Molecular Neuroscience +10

The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth

Lachlan A. Jolly, Claire C. Homan, R. Jacob et al. · Human Molecular Genetics · 2013 · 127 citations · Full text

Genetics, Social Sciences, Psychiatric Genetics +17

Zinc and Zinc Transporters in Macrophages and Their Roles in Efferocytosis in COPD

Rhys Hamon, Claire C. Homan, Hai B. Tran et al. · PLoS ONE · 2014 · 89 citations · Full text

Asthma, Zinc Transporters, Inflammatory Lung Disease +20

GATA2 deficiency syndrome: A decade of discovery

Claire C. Homan, Parvathy Venugopal, Peer Arts et al. · Human Mutation · 2021 · 66 citations · Full text