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Alex D. Shaw

Neuroscience Research Australia

16

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324

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A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.

2021 Journal of Psychiatry & Neuroscience
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CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.

2020 Brain
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De Novo Gene Variants and Familial Bipolar Disorder.

2020
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Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes

2019 Journal of Psychiatry & Neuroscience
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Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders

2018 PLOS Genetics
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ADDRESSING RARE VARIANT CONTRIBUTIONS TO THE GENETIC ARCHITECTURE OF BIPOLAR DISORDER, UTILIZING EXTENDED FAMILIES WITH HIGHLY PENETRANT FORMS OF ILLNESS

2017 European Neuropsychopharmacology
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Neuregulin 1 expression and electrophysiological abnormalities in the Neuregulin 1 transmembrane domain heterozygous mutant mouse

2015 PLOS ONE
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Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014 [Conference Material]

2015
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Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

2015 Brain
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Characterisation of Genetic Variation in ST8SIA2 and Its Interaction Region in NCAM1 in Patients with Bipolar Disorder

2014 PLOS ONE
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Citations (21)