Part of the Genetic Phenomena Commons

Works in Genetic Phenomena

2019

Association of CamK2A genetic variants with transition time from occasional to regular heroin use in a sample of heroin-dependent individuals, Antonia Eirich, Teresa Biermann, Christian P Müller, Johannes Kornhuber, Beben Benyamin, Gary K. Hulse, Dieter B. Wildenauer, Sibylle G. Schwab
Research outputs 2014 to 2021

DNA methylation of the clusterin promoter: Associations with Alzheimer’s Disease risk and related phenotypes, Madeline Peretti
Theses: Doctorates and Masters

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2018

A polygenic risk score derived from episodic memory weighted genetic variants is associated with cognitive decline in preclinical Alzheimer’s disease, Tenielle Porter, Samantha C. Burnham, Greg Savage, Yen Ying Lim, Paul Maruff, Lidija Milicic, Madeline Peretti, David Ames, Colin L. Masters, Ralph N. Martins, Stephanie Rainey-Smith, Christopher C. Rowe, Olivier Salvado, Kevin Taddei, David Groth, Guiseppe Verdile, Victor L. Villemagne, Simon M. Laws
Research outputs 2014 to 2021

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Type 2 diabetes mellitus: Integrative analysis of multiomics data for biomarker discovery, Siqi Ge, Youxin Wang, Song Manshu, Xingang Li, Xinwei Yu, Hao Wang, Jing Wang, Qiang Zeng, Wei Wang
Research outputs 2014 to 2021

2012

Genetic Outcomes of Consanguineous Marriages, Alan Bittles, Michael Black
Research outputs 2012

2009

Metabolomic investigation of a new rat model of autosomal recessive polycystic kidney disease, Hayley White
Theses : Honours

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2000

Molecular investigations in the role of the GALK1 Gene in Galactokinase Deficiency, Michael L. Hunter
Theses : Honours

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A linkage study of autism using multipoint sib-pair analysis, Tamara Rogers
Theses: Doctorates and Masters

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1999

Molecular studies of splice sites in the Canine Dystrophin Gene, Hayley Durling
Theses : Honours

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1993

Detection of point mutations in the dystrophin gene, John Pedretti
Theses : Honours

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