Evan M. Braunstein, Ph.D.
Affiliations: | 2008 | Yeshiva University, New York, NY, United States |
Area:
GeneticsGoogle:
"Evan Braunstein"Mean distance: 23748
Parents
Sign in to add mentor| Bernice Morrow | grad student | 2008 | Yeshiva University | |
| (Investigation of the role of Tbx1, an essential T -box gene, in the mesoderm during embryogenesis.) | ||||
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Publications
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| Chaturvedi S, Braunstein EM, Brodsky RA. (2020) Antiphospholipid syndrome: complement activation, complement gene mutations and therapeutic implications. Journal of Thrombosis and Haemostasis : Jth |
| Vaught AJ, Braunstein E, Chaturvedi S, et al. (2020) A review of the alternative pathway of complement and its relation to HELLP syndrome: is it time to consider HELLP syndrome a disease of the alternative pathway. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 1-9 |
| Chaturvedi S, Braunstein EM, Yuan X, et al. (2019) Complement activity and complement regulatory gene mutations are associated with thrombosis in APS and CAPS. Blood |
| Karantanos T, Chaturvedi S, Gocke CD, et al. (2019) ATM Germline Variant Increases the Risk of MPN Progression Blood. 134: 835-835 |
| Vaught AJ, Braunstein EM, Jasem J, et al. (2018) Germline mutations in the alternative pathway of complement predispose to HELLP syndrome. Jci Insight. 3 |
| Yuan X, Li Z, Baines AC, et al. (2017) A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model. Plos One. 12: e0174074 |
| Li R, Sobreira N, Witmer D, et al. (2016) Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemia. Haematologica |
| Churpek JE, Pyrtel K, Kanchi KL, et al. (2015) Genomic analysis of germline and somatic variants in familial myelodysplasia/acute myeloid leukemia. Blood |
| Smith C, Abalde-Atristain L, He C, et al. (2015) Efficient and allele-specific genome editing of disease loci in human iPSCs. Molecular Therapy : the Journal of the American Society of Gene Therapy. 23: 570-7 |
| Braunstein EM, Li R, Sobreira N, et al. (2015) A Germline Mutation in ERBB3 Predisposes to Inherited Erythroid Myelodysplasia/Erythroleukemia Blood. 126: 4105-4105 |