Hilary C. Martin

Cambridge, ENG CB101SA, United Kingdom

Last Updated: 09/26/2026

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Found 79 publications

An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.

An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2026

Increased signaling of the Neanderthal growth hormone receptor.

Increased signaling of the Neanderthal growth hormone receptor.

Journal: Current biology : CB

Published: January 08, 2026

Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants.

Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants.

Journal: medRxiv : the preprint server for health sciences

Published: December 08, 2025

A spatial transcriptomic atlas of autism-associated genes identifies convergence in the developing human thalamus.

A spatial transcriptomic atlas of autism-associated genes identifies convergence in the developing human thalamus.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Genetic and sociodemographic factors associated with trajectories of physical and mental health multimorbidity in a South Asian cohort in the UK: A multistate modelling analysis.

Genetic and sociodemographic factors associated with trajectories of physical and mental health multimorbidity in a South Asian cohort in the UK: A multistate modelling analysis.

Journal: PLoS medicine

Published: November 11, 2025

Combining polygenic risk scores to understand genetic liability to physical-mental health multimorbidity in UK Biobank.

Combining polygenic risk scores to understand genetic liability to physical-mental health multimorbidity in UK Biobank.

Journal: Human molecular genetics

Published: October 09, 2025

Landscape of parental postzygotic mutations across >11,000 rare disease trios.

Landscape of parental postzygotic mutations across >11,000 rare disease trios.

Journal: American journal of human genetics

Published: September 16, 2025

Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseases.

Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseases.

Journal: American journal of human genetics

Published: September 15, 2025

Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders.

Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders.

Journal: Genome medicine

Published: July 09, 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

Common and rare genetic variant associations with cognitive performance across development in British birth cohorts.

Common and rare genetic variant associations with cognitive performance across development in British birth cohorts.

Journal: Nature human behaviour

Published: January 04, 2025

Exome sequencing of UK birth cohorts.

Exome sequencing of UK birth cohorts.

Journal: Wellcome open research

Published: November 26, 2024

Showing 1-12 of 79

Last Updated: 09/26/2026