Molecular Medicine and Chronic Diseases Research Center (CIMUS)
Singular centre
Monash University
Melbourne, AustraliaPublications in collaboration with researchers from Monash University (22)
2024
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A genome-wide association meta-analysis of all-cause and vascular dementia
Alzheimer's and Dementia, Vol. 20, Núm. 9, pp. 5973-5995
2023
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A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
Breast cancer research : BCR, Vol. 25, Núm. 1, pp. 93
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A second update on mapping the human genetic architecture of COVID-19
Nature
2022
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Efficacy of empagliflozin in heart failure with preserved versus mid-range ejection fraction: a pre-specified analysis of EMPEROR-Preserved
Nature Medicine, Vol. 28, Núm. 12, pp. 2512-2520
2021
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Breast cancer risk genes - Association analysis in more than 113,000 women
New England Journal of Medicine, Vol. 384, Núm. 5, pp. 428-439
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Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk
Journal of the National Cancer Institute, Vol. 113, Núm. 3, pp. 329-337
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Empagliflozin in heart failure with a preserved ejection fraction
New England Journal of Medicine, Vol. 385, Núm. 16, pp. 1451-1461
2020
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Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (Nature Communications, (2020), 11, 1, (4748), 10.1038/s41467-020-18151-y)
Nature Communications
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Baseline characteristics of patients with heart failure with preserved ejection fraction in the EMPEROR-Preserved trial
European Journal of Heart Failure, Vol. 22, Núm. 12, pp. 2383-2392
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Pan-cancer analysis of whole genomes
Nature, Vol. 578, Núm. 7793, pp. 82-93
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Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
Nature Communications, Vol. 11, Núm. 1
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Sex differences in oncogenic mutational processes
Nature Communications, Vol. 11, Núm. 1
2019
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Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1)
Nature Communications
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Genome-wide association study of germline variants and breast cancer-specific mortality
British Journal of Cancer, Vol. 120, Núm. 6, pp. 647-657
2018
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Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants
Nature Communications, Vol. 9, Núm. 1
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Germline variation at 8q24 and prostate cancer risk in men of European ancestry
Nature Communications, Vol. 9, Núm. 1
2016
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Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond
PLoS Pathogens, Vol. 12, Núm. 7
2015
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Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk
Human Molecular Genetics, Vol. 24, Núm. 5, pp. 1478-1492
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Ghrelin
Molecular Metabolism, Vol. 4, Núm. 6, pp. 437-460
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Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1
Scientific Reports, Vol. 5