Helen E. Baxendale

Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

Sri V. V. Deevi, Eleanor F. Dewhurst, Lorena E. Lorenzo, 2017, Circulation.

Clinical and laboratory correlates of lung disease and cancer in adults with idiopathic hypogammaglobulinaemia

B. Grimbacher, P. Arkwright, H. Baxendale, 2016, Clinical and experimental immunology.

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

Henning Gall, Fengyuan Hu, Kevin Rue-Albrecht, 2018, American journal of human genetics.

Familial Hepatopulmonary Syndrome in Common Variable Immunodeficiency

W. Griffiths, S. Holmes, Alison M. Condliffe, 2015, Journal of Clinical Immunology.

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

Crina Samarghitean, Vera Matser, Scott Hackett, 2018, The Journal of allergy and clinical immunology.

Protection against Streptococcus pneumoniae lung infection after nasopharyngeal colonization requires both humoral and cellular immune responses

R. Wilson, R. José, H. Baxendale, 2014, Mucosal Immunology.

1 Whole genome sequencing of a sporadic primary immunodeficiency cohort 2

Sri V. V. Deevi, Nicholas S. Gleadall, K. Stirrups, 2020 .

1 Whole genome sequencing of a sporadic primary immunodeficiency cohort 2

Lynch, Gilmour, Sri V. V. Deevi, 2020 .