Author

Ingrid King

Murdoch Children's Research InstituteORCID 0000-0002-3970-9186Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Assay:proteomics· 1

Frequent Co-Authors

Adam T. PiersiD· 2 shared Alexandra ButtersiD· 2 shared Amy BakeriD· 2 shared Carlos C. Smith-DíaziD· 2 shared Cas SimonsiD· 2 shared Daniel G. MacArthuriD· 2 shared David A. ElliottiD· 2 shared Ebony RichardsoniD· 2 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Adam T. PiersORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

SECISBP2 Deficiency Causes a Lethal Perinatal Cardiomyopathy

Carlos C. Smith-Díaz, Natasha Henden, Natalie P. Stewart, Samantha J. Bryen, Mark Evan Graham, Claire Margaret Lawley, Alexandra Butters, Adam T. Piers, Amy Baker, David A. Elliott, Ebony Richardson, Edward Formaini, Enzo R. Porrello, Helen Doyle, Igor E. Konstantinov, , Jodie Ingles

This study identifies a homozygous SECISBP2 variant causing lethal perinatal cardiomyopathy through loss of selenoprotein function, including GPX4, and suggests a ferroptosis mechanism.

medRxiv · Jul 24, 2026 · PreprintGenetic & Genomic Medicine

Proteomics Uncovers Cryptic JPH2 Loss in Paediatric Dilated Cardiomyopathy

Carlos C. Smith-Díaz, Valerii Iaprintsev, Hannah Huckstep, Ivan Macciocca, Adam T. Piers, Natasha Henden, Samantha J. Bryen, Natalie P. Stewart, Alexandra Butters, Amy Baker, Laura Catto, Leah F. Kemp, Ingrid King, Lina H.H. Le, David A. Elliott, , Jodie Ingles

This study uses proteomics to identify a cryptic JPH2 loss-of-function in a paediatric DCM patient, revealing a novel mechanism of recessive disease.

medRxiv · Jun 17, 2026 · PreprintGenetic & Genomic Medicine