P. Dai

Recommendations for next generation sequencing data reanalysis of unsolved cases with suspected Mendelian disorders: A systematic review and meta-analysis.

T. Phan, J. Mcgaughran, L. Ewans, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Everolimus-Induced Remission of Classic Kaposi’s Sarcoma Secondary to Cryptic Splicing Mediated CTLA4 Haploinsufficiency

S. Tangye, B. Gloss, T. Phan, 2020, Journal of Clinical Immunology.

Paraneoplastic pemphigus: Diagnostic mimics, confounders and management challenges in a series of five long‐term survivors from a single centre

Ming-Wei Lin, M. Taylor, M. Schifter, 2022, Skin health and disease.

Validation of phospholipase A2 receptor direct immunofluorescence staining in the diagnosis of primary membranous glomerulonephritis.

K. Byth, Ming-Wei Lin, D. Brown, 2020, Pathology.

Hyper-IgM and acquired C1q complement deficiency in a patient with de novo ATM mutation

Ming-Wei Lin, T. Ohnesorg, L. Burnett, 2023, Oxford medical case reports.

Autoinflammation Masquerading as Autoimmunity in an Adult with Heterozygous p.E250K PSTPIP1 Mutation

L. March, T. Phan, M. Danta, 2019, Journal of Clinical Immunology.