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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.

Journal article

Paul MS. et al, (2024), American journal of human genetics, 111

Machine learning-enabled maternal risk assessment for women with pre-eclampsia (the PIERS-ML model): a modelling study.

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Montgomery-Csobán T. et al, (2024), The Lancet. Digital health, 6, e238 - e250

Redefining clinical practice through spatial profiling: a revolution in tissue analysis.

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Mulholland EJ. and Leedham SJ., (2024), Annals of the Royal College of Surgeons of England, 106, 305 - 312

Structure and function of Semaphorin-5A glycosaminoglycan interactions

Journal article

Nagy GN. et al, (2024), Nature Communications, 15

Central tolerance shapes the neutralizing B cell repertoire against a persisting virus in its natural host.

Journal article

Florova M. et al, (2024), Proc Natl Acad Sci U S A, 121

De novo variants in DENND5B cause a neurodevelopmental disorder.

Journal article

Scala M. et al, (2024), Am J Hum Genet, 111, 529 - 543

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