Author

Cheng Yee Nixon

Observed name: Cheng-Yee Nixon

Institution: Neuroscience Research Australia

Observed institutions: UNSW Sydney, Canterbury Health Laboratories, Prince of Wales Hospital, Canterbury District Health Board, NSW Health Pathology, Neuroscience Research Australia

OpenAlex ID: A5071113340

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay

2018 · Keren Machol, Justine Rousseau, et al. · The American Journal of Human Genetics · 87

The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy

2020 · Lisa G. Riley, Joëlle Rudinger‐Thirion, et al. · Human Mutation · 36

CDH1 Mutation Distribution and Type Suggests Genetic Differences between the Etiology of Orofacial Clefting and Gastric Cancer

2020 · Arthavan Selvanathan, Cheng Yee Nixon, et al. · Genes · 16

Clinically Responsive Genomic Analysis Pipelines

2021 · Samantha Leigh Sundercombe, Marina Berbic, et al. · Journal of Molecular Diagnostics · 12

Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly

2023 · Margaux Serey-Gaut, Marisol Cortes, et al. · The American Journal of Human Genetics · 7

Works count: 5

Citation count: 158

H-index: 5

I10-index: 4