Lisa Willcocks

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Keren Carss, Gavin Arno, Marie Erwood et al. · The American Journal of Human Genetics · 2016 · 484 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A CD8+ T cell transcription signature predicts prognosis in autoimmune disease

Eoin McKinney, Paul Lyons, Edward J Carr et al. · Nature Medicine · 2010 · 378 citations · Full text

Life Sciences, Cell Biology, Immunology +14

Whole-genome sequencing of a sporadic primary immunodeficiency cohort

James Thaventhiran, Hana Lango Allen, Oliver S. Burren et al. · Nature · 2020 · 242 citations · Full text

Life Sciences, Immunology, Molecular Genetics +13

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Paul Tuijnenburg, Hana Lango Allen, Siobhan O. Burns et al. · Journal of Allergy and Clinical Immunology · 2018 · 235 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Copy number of <i>FCGR3B,</i> which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake

Lisa Willcocks, Paul Lyons, Menna R. Clatworthy et al. · The Journal of Experimental Medicine · 2008 · 229 citations · Full text

Life Sciences, Genetics, Immunology +16