Lachlan A. Jolly

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

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

Lam Son Nguyen, Lachlan A. Jolly, Cheryl Shoubridge et al. · Molecular Psychiatry · 2011 · 123 citations · Full text

Immunogenetics, Immunology, Transcriptome Profiling +8

A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24

Mark Corbett, Melanie Bahlo, Lachlan A. Jolly et al. · The American Journal of Human Genetics · 2010 · 118 citations · Full text

Neurological Disorder, Intellectual Disability Syndrome, Genetics +8

Viperin is an important host restriction factor in control of Zika virus infection

Kylie H. Van der Hoek, Nicholas S. Eyre, Byron Shue et al. · Scientific Reports · 2017 · 111 citations · Full text