Items where authors include "Smith, KGC"

Article

Lawless, D, Allen, HL, Thaventhiran, JED et al. (7 more authors) (2023) Prevalence of CFTR variants in PID patients with bronchiectasis - an important modifying co-factor. Journal of Allergy and Clinical Immunology, 152 (1). pp. 257-265. ISSN 0091-6749

Fulford, TS, Grumont, R, Wirasinha, RC et al. (12 more authors) (2021) c-Rel employs multiple mechanisms to promote the thymic development and peripheral function of regulatory T cells in mice. European Journal of Immunology, 51 (8). pp. 2006-2026. ISSN 0014-2980

Thaventhiran, JED, Lango Allen, H, Burren, OS et al. (57 more authors) (2020) Whole-genome sequencing of a sporadic primary immunodeficiency cohort. Nature, 583. pp. 90-95. ISSN 0028-0836

Thaventhiran, JED, Lango Allen, H, Burren, OS et al. (56 more authors) (2020) Whole-genome sequencing of a sporadic primary immunodeficiency cohort. Nature, 583. pp. 90-95. ISSN 0028-0836

Turro, E, Astle, WJ, Megy, K et al. (60 more authors) (2020) Whole-genome sequencing of patients with rare diseases in a national health system. Nature, 583. pp. 96-102. ISSN 0028-0836

Wei, W, Tuna, S, Keogh, MJ et al. (426 more authors) (2019) Germline selection shapes human mitochondrial DNA diversity. Science, 364 (6442). 749-+. ISSN 0036-8075

Tuijnenburg, P, Lango Allen, H, Burns, SO et al. (28 more authors) (2018) Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans. Journal of Allergy and Clinical Immunology, 142 (4). pp. 1285-1296. ISSN 0091-6749

Whitworth, J, Smith, PS, Martin, J-E et al. (330 more authors) (2018) Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes. The American Journal of Human Genetics, 103 (1). pp. 3-18. ISSN 0002-9297

Lawless, D, Geier, CB, Farmer, JR et al. (43 more authors) (2018) Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency. Journal of Allergy and Clinical Immunology, 141 (6). pp. 2303-2306. ISSN 0091-6749

Ortiz-Fernández, L, Carmona, FD, López-Mejías, R et al. (14 more authors) (2018) Cross-phenotype analysis of Immunochip data identifies KDM4C as a relevant locus for the development of systemic vasculitis. Annals of the Rheumatic Diseases, 77 (4). pp. 589-595. ISSN 0003-4967