Alex D. Shaw

University of Exeter — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index398citations21works0.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(7), Genomics and Rare Diseases(6), Autism Spectrum Disorder Research(4), Genetic Associations and Epidemiology(4), Bipolar Disorder and Treatment(3)

Publications21 total

EXPLORING THE NEUROBIOLOGICAL AND PSYCHOLOGICAL MECHANISMS OF KETAMINE IN PROBLEMATIC GAMBLING: A MECHANISTIC STUDY
The International Journal of Neuropsychopharmacology·2025Open Access
A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of <i>ANK3</i> and additional rare alleles at 10q11-q21
Journal of Psychiatry and Neuroscience·2021· 9 citedOpen Access
De Novo Gene Variants and Familial Bipolar Disorder
JAMA Network Open·2020· 16 citedOpen Access
CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis
Brain·2020· 83 citedOpen Access
Truncating variant burden in high-functioning autism and pleiotropic effects of <i>LRP1</i> across psychiatric phenotypes
Journal of Psychiatry and Neuroscience·2019· 30 citedOpen Access
COMBINED WHOLE EXOME SEQUENCING AND LINKAGE ANALYSIS REVEALS LINKAGE TO 10Q11-10Q21 LOCUS WHICH IS NOT EXPLAINED BY GWAS-ASSOCIATED SNP OR RARE VARIANTS IN ANK3
European Neuropsychopharmacology·2019
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
PLoS Genetics·2018· 45 citedOpen Access
Truncating Variant Burden in High Functioning Autism and Pleiotropic Effects of <i>LRP1</i> Across Psychiatric Phenotypes
2018Open Access
Comprehensive cross-disorder analyses of <i>CNTNAP2</i> suggest it is unlikely to be a primary risk gene for psychiatric disorders
2018· 5 citedOpen Access
An examination of multiple classes of rare variants in extended families with bipolar disorder
Translational Psychiatry·2018· 40 citedOpen Access
Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls
Translational Psychiatry·2018· 13 citedOpen Access
Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts
2017
Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts
Journal of the American Academy of Child & Adolescent Psychiatry·2017· 43 citedOpen Access
ADDRESSING RARE VARIANT CONTRIBUTIONS TO THE GENETIC ARCHITECTURE OF BIPOLAR DISORDER, UTILIZING EXTENDED FAMILIES WITH HIGHLY PENETRANT FORMS OF ILLNESS
UWA Profiles and Research Repository (University of Western Australia)·2017
Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12–16 October 2014
Psychiatric Genetics·2015Open Access
Neuregulin 1 Expression and Electrophysiological Abnormalities in the Neuregulin 1 Transmembrane Domain Heterozygous Mutant Mouse
PLoS ONE·2015· 22 citedOpen Access
Is<i>CHCHD10</i>Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?: Figure 1
Brain·2015· 19 citedOpen Access
Characterisation of Genetic Variation in ST8SIA2 and Its Interaction Region in NCAM1 in Patients with Bipolar Disorder
PLoS ONE·2014· 32 citedOpen Access
Calfacilitin is a calcium channel modulator essential for initiation of neural plate development
Nature Communications·2013· 41 citedOpen Access
S04-01 Calfacilitin: A new player in neural induction
Mechanisms of Development·2009
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Frequent Co-authors

Janice M. Fullerton(14), Peter R. Schofield(11), Claudio Toma(11), Philip B. Mitchell(10), Anna Heath(7), Kerrie D. Pierce(5), Carol Dobson‐Stone(2), Marianne Hallupp(2), William S. Brooks(2), Olivier Piguet(2), Glenda M. Halliday(2), John B. Kwok(2), Holly C. Wilcox(2), Anne L. Glowinski(2), Kelly S. Benke(2), Masoud Kamali(2), Leslie A. Hulvershorn(2), Emma K. Stapp(2), Howard J. Edenberg(2), Gloria Roberts(2)