Heath A - Search Results

1

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

Fullerton JM, Klauser P, Lenroot RK, Shaw AD, Overs B, Heath A, Cairns MJ, Atkins J, Scott R; Australian Schizophrenia Research Bank; Schofield PR, Weickert CS, Pantelis C, Fornito A, Whitford TJ, Weickert TW, Zalesky A. Fullerton JM, et al. Among authors: heath a. Transl Psychiatry. 2018 Jan 22;8(1):21. doi: 10.1038/s41398-017-0052-z. Transl Psychiatry. 2018. PMID: 29353880 Free PMC article.

2

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

Toma C, Shaw AD, Allcock RJN, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. Toma C, et al. Among authors: heath a. Transl Psychiatry. 2018 Mar 13;8(1):65. doi: 10.1038/s41398-018-0113-y. Transl Psychiatry. 2018. PMID: 29531218 Free PMC article.

3

Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder.

Shaw AD, Tiwari Y, Kaplan W, Heath A, Mitchell PB, Schofield PR, Fullerton JM. Shaw AD, et al. Among authors: heath a. PLoS One. 2014 Mar 20;9(3):e92556. doi: 10.1371/journal.pone.0092556. eCollection 2014. PLoS One. 2014. PMID: 24651862 Free PMC article.

4

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

Toma C, Pierce KD, Shaw AD, Heath A, Mitchell PB, Schofield PR, Fullerton JM. Toma C, et al. Among authors: heath a. PLoS Genet. 2018 Dec 26;14(12):e1007535. doi: 10.1371/journal.pgen.1007535. eCollection 2018 Dec. PLoS Genet. 2018. PMID: 30586385 Free PMC article.

5

Assessing oxidative pathway genes as risk factors for bipolar disorder.

Fullerton JM, Tiwari Y, Agahi G, Heath A, Berk M, Mitchell PB, Schofield PR. Fullerton JM, et al. Among authors: heath a. Bipolar Disord. 2010 Aug;12(5):550-6. doi: 10.1111/j.1399-5618.2010.00834.x. Bipolar Disord. 2010. PMID: 20712757

6

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

Kamien B, Harraway J, Lundie B, Smallhorne L, Gibbs V, Heath A, Fullerton JM. Kamien B, et al. Among authors: heath a. Am J Med Genet A. 2014 Mar;164A(3):782-8. doi: 10.1002/ajmg.a.36345. Epub 2013 Dec 19. Am J Med Genet A. 2014. PMID: 24357335

7

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

Toma C, Shaw AD, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. Toma C, et al. Among authors: heath a. J Psychiatry Neurosci. 2021 Mar 17;46(2):E247-E257. doi: 10.1503/jpn.200083. J Psychiatry Neurosci. 2021. PMID: 33729739 Free PMC article.

8

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

Kamien B, Harraway J, Lundie B, Smallhorne L, Gibbs V, Heath A, Fullerton JM. Kamien B, et al. Among authors: heath a. Am J Med Genet A. 2015 Jun;167(6):1424. doi: 10.1002/ajmg.a.36846. Epub 2015 Apr 2. Am J Med Genet A. 2015. PMID: 25846131 No abstract available.

9

Investigation of circadian disruption in bipolar disorder.

Fullerton J, Heath A, Mitchell P, Schofield P. Fullerton J, et al. Among authors: heath a. Acta Neuropsychiatr. 2006 Dec;18(6):251. doi: 10.1017/S0924270800030283. Acta Neuropsychiatr. 2006. PMID: 27397185 No abstract available.

10

Developments in the Design, Conduct, and Reporting of Child Health Trials.

Baba A, Aregbesola A, Caldwell PHY, Elliott SA, Elsman EBM, Fernandes RM, Hartling L, Heath A, Kelly LE, Preston J, Sammy A, Webbe J, Williams K, Woolfall K, Klassen TP, Offringa M. Baba A, et al. Among authors: heath a. Pediatrics. 2024 Jun 4:e2024065799. doi: 10.1542/peds.2024-065799. Online ahead of print. Pediatrics. 2024. PMID: 38832441

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