Joanna M. Howson

Old Road Campus, Roosevelt Drive
Oxford, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 85 publications

Empowering digital health management with on-device large language models for glucose prediction: a model development and validation study.

Empowering digital health management with on-device large language models for glucose prediction: a model development and validation study.

Journal: EBioMedicine
Published: November 18, 2025

Deciphering tissue-specific protein regulation for insights into cardiometabolic disease.

Deciphering tissue-specific protein regulation for insights into cardiometabolic disease.

Journal: Molecular metabolism
Published: October 24, 2025

Genetic architecture of sleep in a genome wide association study of device measured sleep traits.

Genetic architecture of sleep in a genome wide association study of device measured sleep traits.

Journal: Nature communications
Published: September 22, 2025

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Journal: Nature genetics
Published: June 08, 2025

Lipoprotein(a) concentrations and secondary outcomes following first-time acute coronary syndrome: The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS).

Lipoprotein(a) concentrations and secondary outcomes following first-time acute coronary syndrome: The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS).

Journal: Atherosclerosis
Published: March 18, 2025

Dissecting metabolic dysfunction- and alcohol-associated liver disease (MetALD) using proteomic and metabolomic profiles.

Dissecting metabolic dysfunction- and alcohol-associated liver disease (MetALD) using proteomic and metabolomic profiles.

Journal: Journal of hepatology
Published: October 23, 2024

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.

Journal: medRxiv : the preprint server for health sciences
Published: April 22, 2024

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.

Journal: Nature
Published: April 07, 2024

Interpretable machine learning leverages proteomics to improve cardiovascular disease risk prediction and biomarker identification.

Interpretable machine learning leverages proteomics to improve cardiovascular disease risk prediction and biomarker identification.

Journal: Communications medicine
Published: March 28, 2024

Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets.

Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets.

Journal: medRxiv : the preprint server for health sciences
Published: December 11, 2023

Plasma Proteomics to Identify Drug Targets for Ischemic Heart Disease.

Plasma Proteomics to Identify Drug Targets for Ischemic Heart Disease.

Journal: Journal of the American College of Cardiology
Published: May 19, 2023

Prognostic modelling of clinical outcomes after first-time acute coronary syndrome in New Zealand.

Prognostic modelling of clinical outcomes after first-time acute coronary syndrome in New Zealand.

Journal: Heart (British Cardiac Society)
Published: October 13, 2022
Showing 1-12 of 85

Last Updated: 09/26/2026