Dr Paul Brennan
| “I’m quite proud of how we’ve handled it”: health professionals’ experiences of returning additional findings from the 100,000 genomes project | 2024 |
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Dr Max Robinson
Dr Paul Brennan
| Development and external validation of a head and neck cancer risk prediction model | 2024 |
|
Dr Paul Brennan
| Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome | 2024 |
|
Dr Paul Brennan
| Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice | 2024 |
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Dr Paul Brennan
| The impact of inversions across 33,924 families with rare disease from a national genome sequencing project | 2024 |
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Dr Paul Brennan
| Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UK | 2022 |
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Professor Grainne Gorman
Professor Rita Horvath
Dr Richard Quinton
Dr Andrew Schaefer
Dr Patrick Yu Wai Man
et al. | 100,000 genomes pilot on rare-disease diagnosis in health care — Preliminary report | 2021 |
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