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JCI Insight|March 23, 2018
Germline mutations in the alternative pathway of complement predispose to HELLP syndromeArthur J Vaught, Evan M Braunstein, Jagar Jasem, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|March 1, 1993
Prospective study of magnetic resonance imaging and SPECT bone scans in renal allograft recipients: evidence for a self-limited subclinical abnormality of the hipA R Siddiqui, K K Kopecky, H N Wellman, et al.Blood|December 9, 2019
Complement activity and complement regulatory gene mutations are associated with thrombosis in APS and CAPSShruti Chaturvedi, Evan M Braunstein, Xuan Yuan, et al.American Journal of Hematology|August 30, 2021
Major adverse cardiovascular events in survivors of immune-mediated thrombotic thrombocytopenic purpuraMax A Brodsky, Senthil Sukumar, Sruthi Selvakumar, et al.Blood|August 22, 2019
Reduced ADAMTS13 activity during TTP remission is associated with stroke in TTP survivorsHarshvardhan Upreti, Jamil Kasmani, Kathryn Dane, et al.The Journal of Biological Chemistry|January 1, 2004
Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entryAkos Zsembery, James A Fortenberry, Lihua Liang, et al.Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Genetic and Epigenetic Dysregulation of CR1 is Associated with Catastrophic Antiphospholipid Syndrome (CAPS)Nikhil Ranjan, Michael Cole, Gloria F Gerber, et al.Cancers|July 2, 2021
Germline ERBB2/HER2 Coding Variants Are Associated with Increased Risk of Myeloproliferative NeoplasmsEvan M Braunstein, Hang Chen, Felicia Juarez, et al.Annals of the Rheumatic Diseases|August 21, 2025
Genetic and epigenetic dysregulation of CR1 is associated with catastrophic antiphospholipid syndromeNikhil Ranjan, Michael A Cole, Gloria F Gerber, et al.Leukemia|December 21, 2022
Recurrent germline variant in ATM associated with familial myeloproliferative neoplasmsEvan M Braunstein, Eddie Imada, Sergiu Pasca, et al.Pageof 17