| Notch initiates the endothelial-to-mesenchymal transition in the atrioventricular canal through autocrine activation of soluble guanylyl cyclase ACY Chang, YX Fu, VC Garside, K Niessen, L Chang, M Fuller, A Setiadi, ... Developmental cell 21 (2), 288-300, 2011 | 186 | 2011 |
| Differential regulation of transforming growth factor β signaling pathways by Notch in human endothelial cells YX Fu, A Chang, L Chang, K Niessen, S Eapen, A Setiadi, A Karsan Journal of Biological Chemistry 284 (29), 19452-19462, 2009 | 130 | 2009 |
| Malignancy-associated haemophagocytic lymphohistiocytosis A Setiadi, A Zoref-Lorenz, CY Lee, MB Jordan, LYC Chen The Lancet Haematology 9 (3), e217-e227, 2022 | 72 | 2022 |
| A longitudinal single-cell atlas of treatment response in pediatric AML S Lambo, DL Trinh, RE Ries, D Jin, A Setiadi, M Ng, VG Leblanc, ... Cancer Cell 41 (12), 2117-2135. e12, 2023 | 25 | 2023 |
| Clinical and laboratory features associated with myeloperoxidase expression in pediatric B‐lymphoblastic leukemia E McGinnis, D Yang, N Au, D Morrison, KM Chipperfield, AF Setiadi, L Liu, ... Cytometry Part B: Clinical Cytometry 100 (4), 446-453, 2021 | 16 | 2021 |
| 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 |
| The significance of peripheral blood minimal residual disease to predict early disease response in patients with B‐cell acute lymphoblastic leukemia A Setiadi, D Owen, A Tsang, R Milner, S Vercauteren International journal of laboratory hematology 38 (5), 527-534, 2016 | 12 | 2016 |
| Machine learning optimized multiparameter radar plots for B‐cell acute lymphoblastic leukemia minimal residual disease analysis KE Shopsowitz, L Liu, A Setiadi, M Al‐Bakri, S Vercauteren Cytometry Part B: Clinical Cytometry 102 (5), 342-352, 2022 | 10 | 2022 |
| COVID-19, haemophagocytic lymphohistiocytosis, and infection-induced cytokine storm syndromes C Spaner, M Goubran, A Setiadi, LYC Chen The Lancet. Infectious Diseases 22 (7), 937, 2022 | 9 | 2022 |
| CD138-negative plasma cell myeloma: a diagnostic challenge and a unique entity AF Setiadi, Y Sheikine BMJ Case Reports CP 12 (11), e232233, 2019 | 7 | 2019 |
| CRP and sCD25 help distinguish between adult‐onset Still's disease and HLH M Beckett, C Spaner, M Goubran, J Wade, JA Avina‐Zubieta, A Setiadi, ... European Journal of Haematology 113 (5), 576-583, 2024 | 2 | 2024 |
| Circulating rhabdoid tumor cells in the peripheral blood of a neonate M Al‐Bakri, J Terry, K Chipperfield, D Morrison, A Setiadi American Journal of Hematology 97 (12), 1664-1665, 2022 | 2 | 2022 |
| A sinister case of pseudothrombocytosis MN Loyzer, A Setiadi British Journal of Haematology 205 (2), 403-403, 2024 | 1 | 2024 |
| Expanding the molecular and phenotypic spectrum of CTLA‐4 insufficiency. S Duke, J Maiarana, P Yousefi, E Burks, S Gerrie, A Setiadi, A Amid, ... Pediatric Allergy & Immunology 35 (2), 2024 | 1 | 2024 |
| A germline heterozygous dominant negative IKZF2 variant causing syndromic primary immune regulatory disorder and ICHAD HY Lu, M Vaseghi-Shanjani, AJ Lam, M Sharma, A Mohajeri, J Gillies, ... medRxiv, 2023.09. 09.23295301, 2023 | 1 | 2023 |
| Human germline biallelic complete NFAT1 deficiency causes the triad of progressive joint contractures, osteochondromas, and susceptibility to B cell malignancy M Sharma, MP Fu, HY Lu, AA Sharma, BP Modi, C Michalski, S Lin, ... medRxiv, 2022.01. 30.22269378, 2022 | 1 | 2022 |
| The role of C-reactive protein and ferritin in the diagnosis of HLH, adult-onset still’s disease, and COVID-19 cytokine storm M Goubran, C Spaner, S Stukas, A Zoref-Lorenz, K Shojania, M Beckett, ... Scientific Reports 14 (1), 31306, 2024 | | 2024 |
| 212 Human ASXL1 Deficiency Causes Epigenetic Dysfunction, Combined Immunodeficiency and EBV–Associated Hodgkin Lymphoma M Fu, M Sharma, P Yousefi, S Merrill, R Tan, B Modi, KL Del Bel, R Deyell, ... Clinical Immunology 262, 110154, 2024 | | 2024 |
| Monolobated megakaryocytes in Diamond–Blackfan anemia with RPL5 mutation at disease presentation mimicking myelodysplastic syndrome A Setiadi, C Singh, A Li, N Au, A Amid Pediatric Blood & Cancer 71 (2), e30771, 2024 | | 2024 |
| Human ASXL1 Deficiency Causes Epigenetic Dysfunction, Combined Immunodeficiency and EBV–Associated Hodgkin Lymphoma MP Fu, M Sharma, SM Merrill, P Yousefi, R Tan, BP Modi, KD Bel, ... medRxiv, 2023.12. 20.23300096, 2023 | | 2023 |