Award

NIHR203312

Funder: Isaac Newton Trust

Funded outputs count: 15

Funder award ID: NIHR203312

OpenAlex ID: G5298934099

Risk factors for persistent Staphylococcus aureus nasal carriage in the community

2026 · Ewan Harrison, Stephen Kaptoge, et al. · Research Square

Rapid Whole Genome Sequencing Enhances Pediatric Cancer Diagnosis

2026 · Aditi Vedi, Jamie Trotman, et al. · Nature Communications

Mapping human visual contrast sensitivity and vision loss across the visual field with model-based fMRI

2026 · Hugo T. Chow-Wing-Bom, Matteo Lisi, et al. · eLife

Author response: Mapping human visual contrast sensitivity and vision loss across the visual field with model-based fMRI

2026 · Hugo T Chow-Wing-Bom, Matteo Lisi, et al. · eLife

Reviewer #3 (Public review): Mapping human visual contrast sensitivity and vision loss across the visual field with model-based fMRI

2026 · eLife

Reviewer #2 (Public review): Mapping human visual contrast sensitivity and vision loss across the visual field with model-based fMRI

2026 · eLife

Reviewer #1 (Public review): Mapping human visual contrast sensitivity and vision loss across the visual field with model-based fMRI

2026 · eLife

eLife Assessment: Mapping human visual contrast sensitivity and vision loss across the visual field with model-based fMRI

2026 · Xilin Zhang · eLife

Diagnosis Through Whole Genome Sequencing and Care Utilization in Children With Severe Illness

2026 · Joao M. L. Dias, Ravi P. More, et al. · JAMA Network Open

Consensus Recommendations for the Clinical Management of Wolfram syndrome Using a Delphi Method

2026 · Josephine Elliott, Saumel Ahmadi, et al. · medRxiv · 2

ADHD and intelligence polygenic scores associations with developmental dimensions in children with attention, learning and memory difficulties

2026 · Andrea M. Santangelo, Olena Ohlei, et al. · European Child & Adolescent Psychiatry

Human 3D epithelioids enable continuous long-term clonal evolution studies across multiple epithelial tissues

2026 · Ines S Ferreira, Alberto Pradilla-Dieste, et al. · bioRxiv (Cold Spring Harbor Laboratory)

Recessive variants in mitochondrial complex I nuclear subunits are an underrated cause of optic atrophy

2025 · Claudio Fiorini, Neringa Jurkute, et al. · Brain · 2

CRISPRa-Mediated Increase of OPA1 Expression in Dominant Optic Atrophy

2025 · Giada Becchi, Michael Whitehead, et al. · International Journal of Molecular Sciences · 2

Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial

2024 · Patrick Yu-Wai-Man, Valerio Carelli, et al. · Cell Reports Medicine · 55