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NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.

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Schwerd T. et al, (2018), Mucosal Immunol, 11, 562 - 574

Manifesto for a healthy and health-creating society.

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Crisp N. et al, (2016), Lancet, 388, e24 - e27

Resolving TYK2 locus genotype-to-phenotype differences in autoimmunity.

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Dendrou CA. et al, (2016), Sci Transl Med, 8

10 years of the UK's National Institute for Health Research.

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Bell J., (2016), Lancet (London, England), 387, 1978 - 1979

On the Recognition of Global Excellence in Medical Research.

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Naylor CD. and Bell JI., (2015), JAMA, 314, 1125 - 1126

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.

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Taylor JC. et al, (2015), Nat Genet, 47, 717 - 726

A new social contract for medical innovation.

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Horne R. et al, (2015), Lancet, 385, 1153 - 1154

Erythrocytosis associated with a novel missense mutation in the BPGM gene.

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Petousi N. et al, (2014), Haematologica, 99, e201 - e204

Stratified medicines: towards better treatment for disease.

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Bell J., (2014), Lancet (London, England), 383 Suppl 1, S3 - S5

A clinical conundrum: the detrimental effect of TNF antagonists in multiple sclerosis.

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Dendrou CA. et al, (2013), Pharmacogenomics, 14, 1397 - 1404

Big data tip the scale

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Dendrou CA. et al, (2013), Nature Medicine, 19, 138 - 139

Genomewide association studies and common disease--realizing clinical utility.

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Fugger L. et al, (2012), N Engl J Med, 367, 2370 - 2371

TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis.

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Gregory AP. et al, (2012), Nature, 488, 508 - 511

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