| The CBM-opathies—a rapidly expanding spectrum of human inborn errors of immunity caused by mutations in the CARD11-BCL10-MALT1 complex HY Lu, BM Bauman, S Arjunaraja, B Dorjbal, JD Milner, AL Snow, ... Frontiers in immunology 9, 2078, 2018 | 117 | 2018 |
| Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease M Sharma, D Leung, M Momenilandi, LCW Jones, L Pacillo, AE James, ... Journal of Experimental Medicine 220 (5), e20221755, 2023 | 78 | 2023 |
| Size-dependent anti-inflammatory activity of a peptide-gold nanoparticle hybrid in vitro and in a mouse model of acute lung injury W Gao, Y Wang, Y Xiong, L Sun, L Wang, K Wang, HY Lu, A Bao, ... Acta biomaterialia 85, 203-217, 2019 | 66 | 2019 |
| Germline CBM-opathies: from immunodeficiency to atopy HY Lu, CM Biggs, G Blanchard-Rohner, SY Fung, M Sharma, SE Turvey Journal of Allergy and Clinical Immunology 143 (5), 1661-1673, 2019 | 63 | 2019 |
| Inborn errors of immunity manifesting as atopic disorders M Vaseghi-Shanjani, KL Smith, RJ Sara, BP Modi, A Branch, M Sharma, ... Journal of Allergy and Clinical Immunology 148 (5), 1130-1139, 2021 | 42 | 2021 |
| A Germline Mutation in the C2 Domain of PLCγ2 Associated with Gain-of-Function Expands the Phenotype for PLCG2-Related Diseases T Novice, A Kariminia, KL Del Bel, H Lu, M Sharma, CJ Lim, J Read, ... Journal of Clinical Immunology 40, 267-276, 2020 | 39 | 2020 |
| Limitations of Qdot labelling compared to directly-conjugated probes for single particle tracking of B cell receptor mobility L Abraham, HY Lu, RC Falcão, J Scurll, T Jou, B Irwin, R Tafteh, MR Gold, ... Scientific reports 7 (1), 11379, 2017 | 38 | 2017 |
| Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiency HY Lu, M Sharma, AA Sharma, A Lacson, A Szpurko, J Luider, ... Journal of Allergy and Clinical Immunology 148 (6), 1559-1574. e13, 2021 | 25 | 2021 |
| Real-time 3D stabilization of a super-resolution microscope using an electrically tunable lens R Tafteh, L Abraham, D Seo, HY Lu, MR Gold, KC Chou Optics Express 24 (20), 22959-22970, 2016 | 18 | 2016 |
| Human MALT1 deficiency and predisposition to infections HY Lu, SE Turvey Current Opinion in Immunology 72, 1-12, 2021 | 17 | 2021 |
| A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency IRF4 International Consortium, O Fornes, A Jia, HS Kuehn, Q Min, ... Science immunology 8 (79), eade7953, 2023 | 14 | 2023 |
| Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancy M Sharma, MP Fu, HY Lu, AA Sharma, BP Modi, C Michalski, S Lin, ... Blood, The Journal of the American Society of Hematology 140 (17), 1858-1874, 2022 | 13 | 2022 |
| Integrating knowledge of protein sequence with protein function for the prediction and validation of new MALT1 substrates PA Bell, S Scheuermann, F Renner, CL Pan, HY Lu, SE Turvey, ... Computational and Structural Biotechnology Journal 20, 4717-4732, 2022 | 13 | 2022 |
| Combination therapy with proteasome inhibitors and TLR agonists enhances tumour cell death and IL-1β production AC Tang, SM Rahavi, SY Fung, HY Lu, H Yang, CJ Lim, GS Reid, ... Cell Death & Disease 9 (2), 162, 2018 | 13 | 2018 |
| A novel germline heterozygous BCL11B variant causing severe atopic disease and immune dysregulation HY Lu, R Sertori, AV Contreras, M Hamer, M Messing, K Del Bel, ... Frontiers in Immunology, 4895, 2021 | 12 | 2021 |
| The importance of functional validation after next‐generation sequencing: evaluation of a novel CARD11 variant. HY Lu, M Sharma, CM Biggs, YH Huang, KE Shopsowitz, P Frosk, ... Pediatric Allergy & Immunology 29 (6), 2018 | 11 | 2018 |
| Fetal hemoglobin regulation in beta-thalassemia HY Lu, SH Orkin, VG Sankaran Hematology/Oncology Clinics of North America 37 (2), 301-312, 2023 | 10 | 2023 |
| MALT1-dependent cleavage of HOIL1 modulates canonical NF-kB signaling and inflammatory responsiveness SY Fung, HY Lu, M Sharma, AA Sharma, A Saferali, A JIa, L Abraham, ... Frontiers in Immunology 12, 4255, 2021 | 10* | 2021 |
| Clinical IRAK4 deficiency caused by homozygosity for the novel IRAK4 (c. 1049delG, p. Gly350Glufs* 15) variant A Jia, E James, HY Lu, M Sharma, BP Modi, CM Biggs, KJ Hildebrand, ... Molecular Case Studies 6 (3), a005298, 2020 | 10 | 2020 |
| Monogenic immune disorders and severe atopic disease CM Biggs, HY Lu, SE Turvey Nature Genetics 49 (8), 1162-1163, 2017 | 9 | 2017 |
Stuart TurveyCanada Research Chair in Pediatric Precison Health, University of British Columbia確認したメール アドレス: cw.bc.ca