| Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus AE Wandstrat, C Nguyen, N Limaye, AY Chan, S Subramanian, XH Tian, ... Immunity 21 (6), 769-780, 2004 | 322 | 2004 |
| Discovery of stimulation-responsive immune enhancers with CRISPR activation DR Simeonov, BG Gowen, M Boontanrart, TL Roth, JD Gagnon, ... Nature 549 (7670), 111-115, 2017 | 277 | 2017 |
| Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders A Stray-Pedersen, HS Sorte, P Samarakoon, T Gambin, IK Chinn, ... | 277 | 2017 |
| Primary immunodeficiency diseases: genomic approaches delineate heterogeneous Mendelian disorders A Stray-Pedersen, HS Sorte, P Samarakoon, T Gambin, IK Chinn, ... Journal of Allergy and Clinical Immunology 139 (1), 232-245, 2017 | 277 | 2017 |
| Distinct interferon signatures and cytokine patterns define additional systemic autoinflammatory diseases AA de Jesus, Y Hou, S Brooks, L Malle, A Biancotto, Y Huang, KR Calvo, ... The Journal of clinical investigation 130 (4), 1669-1682, 2020 | 169 | 2020 |
| Combined Immunodeficiency Due to MALT1 Mutations, Treated by Hematopoietic Cell Transplantation D Punwani, H Wang, AY Chan, MJ Cowan, J Mallott, U Sunderam, ... Journal of clinical immunology 35 (2), 135-146, 2015 | 108 | 2015 |
| Early vs. delayed diagnosis of severe combined immunodeficiency: a family perspective survey A Chan, C Scalchunes, M Boyle, JM Puck Clinical immunology 138 (1), 3-8, 2011 | 102 | 2011 |
| A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70Novel ZAP70-associated human autoimmune syndrome AY Chan, D Punwani, TA Kadlecek, MJ Cowan, JL Olson, EF Mathes, ... The Journal of experimental medicine 213 (2), 155-165, 2016 | 95 | 2016 |
| Analysis of pulmonary features and treatment approaches in the COPA syndrome JL Tsui, OA Estrada, Z Deng, KM Wang, CS Law, BM Elicker, KD Jones, ... ERJ open research 4 (2), 2018 | 86 | 2018 |
| Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: a working group report of the Primary Immunodeficiency Diseases Committee of … IK Chinn, AY Chan, K Chen, J Chou, MJ Dorsey, J Hajjar, AM Jongco III, ... Journal of Allergy and Clinical Immunology 145 (1), 46-69, 2020 | 74 | 2020 |
| Hematopoietic cell transplantation in patients with primary immune regulatory disorders (PIRD): a primary immune deficiency treatment consortium (PIDTC) survey AY Chan, JW Leiding, X Liu, BR Logan, LM Burroughs, EJ Allenspach, ... Frontiers in immunology 11, 239, 2020 | 64 | 2020 |
| Primary immune regulatory disorders: a growing universe of immune dysregulation AY Chan, TR Torgerson Current Opinion in Allergy and Clinical Immunology 20 (6), 582-590, 2020 | 62 | 2020 |
| B cell–intrinsic CD84 and Ly108 maintain germinal center B cell tolerance EB Wong, C Soni, AY Chan, PP Domeier, T Abraham, N Limaye, TN Khan, ... The Journal of Immunology 194 (9), 4130-4143, 2015 | 50 | 2015 |
| Identification of novel, clinically correlated autoantigens in the monogenic autoimmune syndrome APS1 by proteome-wide PhIP-Seq SE Vazquez, EMN Ferré, DW Scheel, S Sunshine, B Miao, ... Elife 9, e55053, 2020 | 48 | 2020 |
| Central tolerance to self revealed by the autoimmune regulator A Chan, MS Anderson Annals of the New York Academy of Sciences 1356 (1), 80, 2015 | 48 | 2015 |
| Monogenic early-onset lymphoproliferation and autoimmunity: natural history of STAT3 gain-of-function syndrome JW Leiding, TP Vogel, VGJ Santarlas, R Mhaskar, MR Smith, A Carisey, ... Journal of Allergy and Clinical Immunology 151 (4), 1081-1095, 2023 | 45 | 2023 |
| The role of SAP and the SLAM family in autoimmunity AY Chan, JM Westcott, JM Mooney, EK Wakeland, JD Schatzle Current opinion in immunology 18 (6), 656-664, 2006 | 44 | 2006 |
| A human mutation in STAT3 promotes type 1 diabetes through a defect in CD8+ T cell tolerance JT Warshauer, JA Belk, AY Chan, J Wang, AR Gupta, Q Shi, N Skartsis, ... Journal of Experimental Medicine 218 (8), e20210759, 2021 | 35 | 2021 |
| Exome Sequencing Reveals Mutations in AIRE as a Cause of Isolated Hypoparathyroidism D Li, EA Streeten, A Chan, W Lwin, L Tian, R Pellegrino da Silva, CE Kim, ... The Journal of Clinical Endocrinology & Metabolism 102 (5), 1726-1733, 2017 | 31 | 2017 |
| Elastase 3B mutation links to familial pancreatitis with diabetes and pancreatic adenocarcinoma PC Moore, JT Cortez, CE Chamberlain, D Alba, AC Berger, Z Quandt, ... The Journal of clinical investigation 129 (11), 4676-4681, 2019 | 30 | 2019 |
