Author

Belinda R. Gray

Royal Prince Alfred HospitalORCID 0000-0002-9966-0329Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:GWAS / association mapping· 1 Assay:protein structure· 1

Frequent Co-Authors

ANJALI TIKU OWENSiD· 2 shared James S. WareiD· 2 shared Jodie InglesiD· 2 shared Victoria Nicole ParikhiD· 2 shared Adam S. HelmsiD· 1 shared Aditya SinghiD· 1 shared Alessia Argiro· 1 shared Alexandre PereiraiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenomics

ANJALI TIKU OWENSORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

GenomicsbioRxivPreprintOct 7, 2025

Spatial genomics of the cardiac sarcomere

Christian Cadisch, Victoria Nicole Parikh, Megan E. Grove…·Euan Angus Ashley

The paper integrates genomic and structural data to identify variant intolerance regions in cardiac sarcomere genes and links them to disease mechanisms in hypertrophic cardiomyopathy.

DOI 10.1101/2025.10.07.680947

humanDNA methylation

Genetic & Genomic MedicineCirculation Genomic and Precision MedicinePeer-reviewedApr 21, 2025

Clinical Validity of Autosomal Dominant ALPK3 Loss-of-function Variants as a Cause of Hypertrophic Cardiomyopathy

Sophie Hespe, Emma S. Singer, Chloe M. Reuter…·Jodie Ingles

The paper evaluates the clinical validity of heterozygous ALPK3 loss-of-function variants as a cause of hypertrophic cardiomyopathy, finding strong gene-disease association with reduced penetrance.

3 citations

humanstatistical model