Items where authors include "Anwar, R"
Article
Wu, B, Rice, L, Shrimpton, J et al. (9 more authors) (2021) Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A) cause a primary immunodeficiency disorder. eLife, 10. e72559. ISSN 2050-084X
Stockdale, C, Rice, L, Carter, C et al. (7 more authors) (2021) Novel Case of Tripeptidyl Peptidase 2 Deficiency Associated with Mild Clinical Phenotype. Journal of Clinical Immunology, 41 (5). pp. 1123-1127. ISSN 0271-9142
Stremenova Spegarova, J, Lawless, D orcid.org/0000-0001-8496-3725, Mohamad, SMB et al. (24 more authors) (2020) Germline TET2 loss of function causes childhood immunodeficiency and lymphoma. Blood, 136 (9). pp. 1055-1066. ISSN 0006-4971
Lawless, D orcid.org/0000-0001-8496-3725, Lango Allen, H, Thaventhiran, J et al. (6 more authors) (2019) Predicting the Occurrence of Variants in RAG1 and RAG2. Journal of Clinical Immunology, 39 (7). pp. 688-701. ISSN 0271-9142
Rice, L, Stockdale, C, Berry, I et al. (10 more authors) (2019) A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype. Journal of Clinical Immunology, 39 (3). pp. 249-256. ISSN 0271-9142
Lawless, D, Pathak, S, Scambler, TE et al. (3 more authors) (2018) A Case of Adult-Onset Still’s Disease Caused by a Novel Splicing Mutation in TNFAIP3 Successfully Treated With Tocilizumab. frontiers in Immunology, 9. ARTN 1527. ISSN 1664-3224
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
Lawless, D orcid.org/0000-0001-8496-3725, Mistry, A, Wood, PM et al. (7 more authors) (2017) Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy. Journal of Clinical Immunology, 37 (7). pp. 617-622. ISSN 0271-9142
Touqan, N, Diggle, CP, Verghese, ET et al. (7 more authors) (2013) An observational study on the expression levels of MDM2 and MDMX proteins, and associated effects on P53 in a series of human liposarcomas. BMC Clinical Pathology, 13 (1). 32. pp. 1-9. ISSN 1472-6890
Carr, IM orcid.org/0000-0001-9544-1068, Diggle, CP, Khan, K et al. (8 more authors) (2012) Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype. PLoS One, 7 (8). ARTN e43466. ISSN 1552-4973