Back to Biology: New Insights on Inheritance in Myeloproliferative Disorders

od Braunstein, Evan M., Moliterno, Alison R.
Wydane w Curr Hematol Malig Rep (2014)

Antiphospholipid syndrome: Complement activation, complement gene mutations, and therapeutic implications

od Chaturvedi, Shruti, Braunstein, Evan M., Brodsky, Robert A.
Wydane w J Thromb Haemost (2021)

Cooperative Function of Tbx1 and Brn4 in the Periotic Mesenchyme is Necessary for Cochlea Formation

od Braunstein, Evan M., Crenshaw III, E. Bryan, Morrow, Bernice E., Adams, Joe C.
Wydane 2008

Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis

od Braunstein, Evan M, Monks, Dennis C, Aggarwal, Vimla S, Arnold, Jelena S, Morrow, Bernice E
Wydane 2009

Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemia

od Li, Ruijuan, Sobreira, Nara, Witmer, P. Dane, Pratz, Keith W., Braunstein, Evan M.
Wydane w Haematologica (2016)

Direct activation of the alternative complement pathway by SARS-CoV-2 spike proteins is blocked by factor D inhibition

od Yu, Jia, Yuan, Xuan, Chen, Hang, Chaturvedi, Shruti, Braunstein, Evan M., Brodsky, Robert A.
Wydane w Blood (2020)

Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients

od Arnold, Jelena S., Braunstein, Evan M., Ohyama, Takahiro, Groves, Andrew K., Adams, Joe C., Brown, M. Christian, Morrow, Bernice E.
Wydane 2006

Generation of Glycosylphosphatidylinositol Anchor Protein-Deficient Blood Cells From Human Induced Pluripotent Stem Cells

od Yuan, Xuan, Braunstein, Evan M., Ye, Zhaohui, Liu, Cyndi F., Chen, Guibin, Zou, Jizhong, Cheng, Linzhao, Brodsky, Robert A.
Wydane 2013

COVID-19 vaccines induce severe hemolysis in paroxysmal nocturnal hemoglobinuria

od Gerber, Gloria F., Yuan, Xuan, Yu, Jia, Cher, Benjamin A. Y., Braunstein, Evan M., Chaturvedi, Shruti, Brodsky, Robert A.
Wydane w Blood (2021)

A prospective quality improvement initiative in adult hemophagocytic lymphohistiocytosis to improve testing and a framework to facilitate trigger identification and mitigate hemorr...

od Merrill, Samuel A., Naik, Rakhi, Streiff, Michael B., Shanbhag, Satish, Lanzkron, Sophie, Braunstein, Evan M., Moliterno, Alison M., Brodsky, Robert A.
Wydane w Medicine (Baltimore) (2018)

Efficient and Allele-Specific Genome Editing of Disease Loci in Human iPSCs

od Smith, Cory, Abalde-Atristain, Leire, He, Chaoxia, Brodsky, Brett R, Braunstein, Evan M, Chaudhari, Pooja, Jang, Yoon-Young, Cheng, Linzhao, Ye, Zhaohui
Wydane w Mol Ther (2015)

A germline ERBB3 variant is a candidate for predisposition to erythroid MDS/erythroleukemia

od Braunstein, Evan M., Li, Ruijuan, Sobreira, Nara, Marosy, Beth, Hetrick, Kurt, Doheny, Kim, Gocke, Christopher D., Valle, David, Brodsky, Robert A., Cheng, Linzhao
Wydane w Leukemia (2016)

Sex determines the presentation and outcomes in MPN and is related to sex-specific differences in the mutational burden

od Karantanos, Theodoros, Chaturvedi, Shruti, Braunstein, Evan M., Spivak, Jerry, Resar, Linda, Karanika, Styliani, Williams, Donna M., Rogers, Ophelia, Gocke, Christopher D., Moliterno, Alison R.
Wydane w Blood Adv (2020)

Outcomes of a clinician-directed protocol for discontinuation of complement inhibition therapy in atypical hemolytic uremic syndrome

od Chaturvedi, Shruti, Dhaliwal, Noor, Hussain, Sarah, Dane, Kathryn, Upreti, Harshvardhan, Braunstein, Evan M., Yuan, Xuan, Sperati, C. John, Moliterno, Alison R., Brodsky, Robert A.
Wydane w Blood Adv (2021)

A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model

od Yuan, Xuan, Li, Zhe, Baines, Andrea C., Gavriilaki, Eleni, Ye, Zhaohui, Wen, Zhexing, Braunstein, Evan M., Biesecker, Leslie G., Cheng, Linzhao, Dong, Xinzhong, Brodsky, Robert A.
Wydane w PLoS One (2017)

Germline mutations in the alternative pathway of complement predispose to HELLP syndrome

od Vaught, Arthur J., Braunstein, Evan M., Jasem, Jagar, Yuan, Xuan, Makhlin, Igor, Eloundou, Solange, Baines, Andrea C., Merrill, Samuel A., Chaturvedi, Shruti, Blakemore, Karin, Sperati, C. John, Brodsky, Robert A.
Wydane w JCI Insight (2018)

Reduced ADAMTS13 activity during TTP remission is associated with stroke in TTP survivors

od Upreti, Harshvardhan, Kasmani, Jamil, Dane, Kathryn, Braunstein, Evan M., Streiff, Michael B., Shanbhag, Satish, Moliterno, Alison R., Sperati, C. John, Gottesman, Rebecca F., Brodsky, Robert A., Kickler, Thomas S., Chaturvedi, Shruti
Wydane w Blood (2019)

Complement activity and complement regulatory gene mutations are associated with thrombosis in APS and CAPS

od Chaturvedi, Shruti, Braunstein, Evan M., Yuan, Xuan, Yu, Jia, Alexander, Alice, Chen, Hang, Gavriilaki, Eleni, Alluri, Ravi, Streiff, Michael B., Petri, Michelle, Crowther, Mark A., McCrae, Keith R., Brodsky, Robert A.
Wydane w Blood (2020)

Germline ERBB2/HER2 Coding Variants Are Associated with Increased Risk of Myeloproliferative Neoplasms

od Braunstein, Evan M., Chen, Hang, Juarez, Felicia, Yang, Fanghan, Tao, Lindsay, Makhlin, Igor, Williams, Donna M., Chaturvedi, Shruti, Pallavajjala, Aparna, Karantanos, Theodoros, Martin, Renan, Wohler, Elizabeth, Sobreira, Nara, Gocke, Christopher D., Moliterno, Alison R.
Wydane w Cancers (Basel) (2021)

Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia

od Churpek, Jane E., Pyrtel, Khateriaa, Kanchi, Krishna-Latha, Shao, Jin, Koboldt, Daniel, Miller, Christopher A., Shen, Dong, Fulton, Robert, O’Laughlin, Michelle, Fronick, Catrina, Pusic, Iskra, Uy, Geoffrey L., Braunstein, Evan M., Levis, Mark, Ross, Julie, Elliott, Kevin, Heath, Sharon, Jiang, Allan, Westervelt, Peter, DiPersio, John F., Link, Daniel C., Walter, Matthew J., Welch, John, Wilson, Richard, Ley, Timothy J., Godley, Lucy A., Graubert, Timothy A.
Wydane w Blood (2015)