Anna Heath

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

J. Fullerton, P. Mitchell, P. Schofield, 2018, bioRxiv.

An examination of multiple classes of rare variants in extended families with bipolar disorder

Janice M. Fullerton, J. Fullerton, P. Mitchell, 2018, Translational Psychiatry.

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

Janice M. Fullerton, J. Fullerton, P. Mitchell, 2018, bioRxiv.

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

Janice M. Fullerton, J. Fullerton, P. Mitchell, 2014, PloS one.

Assessing oxidative pathway genes as risk factors for bipolar disorder.

J. Fullerton, P. Mitchell, P. Schofield, 2010, Bipolar disorders.

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

Janice M. Fullerton, J. Fullerton, P. Mitchell, 2021, Journal of psychiatry & neuroscience : JPN.

Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls

Janice M. Fullerton, T. Whitford, J. Fullerton, 2018, Translational Psychiatry.

Prevalence of Choroidal Abnormalities and Lisch Nodules in Children Meeting Clinical and Molecular Diagnosis of Neurofibromatosis Type 1

E. Héon, P. Parkin, A. Vincent, 2022, Translational vision science & technology.

Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy

J. Fullerton, B. Kamien, J. Harraway, 2014, American journal of medical genetics. Part A.