Author

Peter Gibbs

The University of MelbourneORCID 0000-0003-1423-4484Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-exome sequencing· 3 Research Focus:differential expression· 1 Research Focus:polygenic risk· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Finlay MacraeiD· 3 shared Ingrid WinshipiD· 3 shared Anne M. MurrayiD· 2 shared Bryony A. ThompsoniD· 2 shared Daniel D. BuchananiD· 2 shared Jane M. TilleriD· 2 shared John J. McNeiliD· 2 shared Moeen RiaziD· 2 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Finlay MacraeORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of Molecular DiagnosticsPeer-reviewedNov 14, 2022

Evaluating multiple next-generation sequencing derived tumor features to accurately predict DNA mismatch repair status

Romy Walker, Peter Georgeson, Khalid Mahmood…·Daniel D. Buchanan

The paper evaluates multiple next-generation sequencing features to predict DNA mismatch repair status in tumors, finding that combining features improves accuracy across different cancer types.

13 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineCancersPeer-reviewedJul 14, 2021

Genomic risk prediction for breast cancer in older women

Paul A Lacaze, Andrew Bakshi, Moeen Riaz…·John J. McNeil

This study evaluates a polygenic risk score for breast cancer in women aged 70 and older, finding it improves risk prediction beyond conventional factors.

8 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintOct 22, 2019

Resilience to dominant genetic disease in the healthy elderly

Paul A Lacaze, Robert Sebra, Moeen Riaz…·Eric Schadt

The paper screens healthy elderly individuals to identify those resilient to genetic diseases despite high genetic risk, finding 141 individuals without associated disease despite pathogenic variants.

DOI 10.1101/19006932

humanwhole-exome sequencing

𝕏 PostBluesky