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Search results (14)

« Back to Publications

Decoding Treatment Choice: Genetic and Phenotypic Analyses of Long-term Antidepressant Acceptability

Walker A. et al, (2025)

Polypharmacy in psychiatry: Evidence-based medicine or a Sisyphean solution?

Halstead S. et al, (2025), Aust N Z J Psychiatry, 59, 661 - 664

Brain cell-type shifts in Alzheimer's disease, autism, and schizophrenia interrogated using methylomics and genetics.

Yap CX. et al, (2024), Sci Adv, 10

Connecting clinical and genetic heterogeneity in ADHD.

Yap CX. and Gratten J., (2024), Nat Genet, 56, 195 - 196

Interactions between the lipidome and genetic and environmental factors in autism.

Yap CX. et al, (2023), Nat Med, 29, 936 - 949

Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD.

Gandal MJ. et al, (2022), Nature, 611, 532 - 539

Autism-related dietary preferences mediate autism-gut microbiome associations.

Yap CX. et al, (2021), Cell, 184, 5916 - 5931.e17

Phenotypic and genetic factors associated with differential consent to record linkage for prescription history in the Australian Genetics of Depression Study

Gomez L. et al, (2021)

Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.

Yap CX. et al, (2021), Mol Autism, 12

Dissection of genetic variation and evidence for pleiotropy in male pattern baldness.

Yap CX. et al, (2018), Nat Commun, 9

Author Correction: Misestimation of heritability and prediction accuracy of male-pattern baldness.

Yap CX. et al, (2018), Nat Commun, 9

Trans-eQTLs identified in whole blood have limited influence on complex disease biology.

Yap CX. et al, (2018), Eur J Hum Genet, 26, 1361 - 1368

Misestimation of heritability and prediction accuracy of male-pattern baldness.

Yap CX. et al, (2018), Nat Commun, 9

Signatures of negative selection in the genetic architecture of human complex traits.

Zeng J. et al, (2018), Nat Genet, 50, 746 - 753