[HTML][HTML] Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

…, GW Montgomery, J He, D Fan, J Fowdar… - Genome medicine, 2019 - Springer
Background DNA methylation changes with age. Chronological age predictors built from DNA
methylation are termed ‘epigenetic clocks’. The deviation of predicted age from the actual …

[HTML][HTML] Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson's disease

CL Vallerga, F Zhang, J Fowdar, AF McRae, T Qi… - Nature …, 2020 - nature.com
An improved understanding of etiological mechanisms in Parkinson’s disease (PD) is urgently
needed because the number of affected individuals is projected to increase rapidly as …

Association of schizophrenia risk with disordered niacin metabolism in an Indian genome-wide association study

…, H Smith, C Filippich, K Patel, J Fowdar… - JAMA …, 2019 - jamanetwork.com
Importance Genome-wide association studies (GWASs) in European populations have
identified more than 100 schizophrenia-associated loci. A schizophrenia GWAS in a unique …

[HTML][HTML] Investigation of homocysteine-pathway-related variants in essential hypertension

JY Fowdar, MV Lason, AL Szvetko, RA Lea… - International journal of …, 2012 - hindawi.com
Hyperhomocysteinemia (hHcy) has been associated with an increased risk of cardiovascular
disease and stroke. Essential hypertension (EH), a polygenic condition, has also been …

Pipeline to gene discovery-Analysing familial Parkinsonism in the Queensland Parkinson's Project

SR Bentley, S Bortnick, I Guella, JY Fowdar… - Parkinsonism & related …, 2018 - Elsevier
Introduction Family based study designs provide an informative resource to identify disease-causing
mutations. The Queensland Parkinson's Project (QPP) has been involved in …

No association between MTHFR A1298C and MTRR A66G polymorphisms, and MS in an Australian cohort

AL Szvetko, J Fowdar, J Nelson, N Colson… - Journal of the …, 2007 - Elsevier
Multiple sclerosis (MS) is a complex neurological disease that affects the central nervous
system (CNS) resulting in debilitating neuropathology. Pathogenesis is primarily defined by …

A genome-wide association study of essential hypertension in an Australian population using a DNA pooling approach

JY Fowdar, R Grealy, Y Lu, LR Griffiths - Molecular genetics and genomics, 2017 - Springer
Despite the success of genome-wide association studies (GWAS) in detecting genetic loci
involved in complex traits, few susceptibility genes have been detected for essential …

Improved prediction of chronological age from DNA methylation limits it as a biomarker of ageing

…, AK Henders, GW Montgomery, J He, D Fan, J Fowdar… - bioRxiv, 2018 - biorxiv.org
DNA methylation is associated with age. The deviation of age predicted from DNA
methylation from actual age has been proposed as a biomarker for ageing. However, a better …

[HTML][HTML] Hunting for familial Parkinson's disease mutations in the post genome era

…, HE Sherman, HM Neuendorf, AM Sykes, JY Fowdar… - Genes, 2021 - mdpi.com
Parkinson’s disease (PD) is typically sporadic; however, multi-incident families provide a
powerful platform to discover novel genetic forms of disease. Their identification supports …

Investigation of the role of the GABRG2 gene variant in migraine

T Chen, M Murrell, J Fowdar, B Roy, R Grealy… - Journal of the …, 2012 - Elsevier
Migraine is the most common neurological disorder worldwide affecting about 12% of the
worldwide population. This disorder has been classed into two main types of migraine—with …