| Year |
Citation |
Score |
| 2020 |
Chaturvedi S, Braunstein EM, Brodsky RA. Antiphospholipid syndrome: complement activation, complement gene mutations and therapeutic implications. Journal of Thrombosis and Haemostasis : Jth. PMID 32881236 DOI: 10.1111/Jth.15082 |
0.381 |
|
| 2020 |
Vaught AJ, Braunstein E, Chaturvedi S, Blakemore K, Brodsky RA. 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. PMID 32338085 DOI: 10.1080/14767058.2020.1755650 |
0.323 |
|
| 2019 |
Chaturvedi S, Braunstein EM, Yuan X, Yu J, Alexander A, Chen H, Gavriilaki E, Alluri RK, Streiff MB, Petri M, Crowther MA, McCrae KR, Brodsky RA. Complement activity and complement regulatory gene mutations are associated with thrombosis in APS and CAPS. Blood. PMID 31812994 DOI: 10.1182/Blood.2019003863 |
0.309 |
|
| 2019 |
Karantanos T, Chaturvedi S, Gocke CD, Williams DM, Moliterno AR, Braunstein EM. ATM Germline Variant Increases the Risk of MPN Progression Blood. 134: 835-835. DOI: 10.1182/Blood-2019-125362 |
0.318 |
|
| 2018 |
Vaught AJ, Braunstein EM, Jasem J, Yuan X, Makhlin I, Eloundou S, Baines AC, Merrill SA, Chaturvedi S, Blakemore K, Sperati CJ, Brodsky RA. Germline mutations in the alternative pathway of complement predispose to HELLP syndrome. Jci Insight. 3. PMID 29563339 DOI: 10.1172/Jci.Insight.99128 |
0.374 |
|
| 2017 |
Yuan X, Li Z, Baines AC, Gavriilaki E, Ye Z, Wen Z, Braunstein EM, Biesecker LG, Cheng L, Dong X, Brodsky RA. 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. PMID 28441409 DOI: 10.1371/Journal.Pone.0174074 |
0.436 |
|
| 2016 |
Li R, Sobreira N, Witmer D, Pratz KW, Braunstein EM. Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemia. Haematologica. PMID 26944477 DOI: 10.3324/Haematol.2015.139790 |
0.343 |
|
| 2015 |
Churpek JE, Pyrtel K, Kanchi KL, Shao J, Koboldt D, Miller CA, Shen D, Fulton R, O'Laughlin M, Fronick C, Pusic I, Uy GL, Braunstein EM, Levis M, Ross J, et al. Genomic analysis of germline and somatic variants in familial myelodysplasia/acute myeloid leukemia. Blood. PMID 26492932 DOI: 10.1182/Blood-2015-04-641100 |
0.323 |
|
| 2015 |
Smith C, Abalde-Atristain L, He C, Brodsky BR, Braunstein EM, Chaudhari P, Jang YY, Cheng L, Ye Z. 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. PMID 25418680 DOI: 10.1038/Mt.2014.226 |
0.324 |
|
| 2015 |
Braunstein EM, Li R, Sobreira N, Gocke C, Brodsky RA, Valle D, Cheng L. A Germline Mutation in ERBB3 Predisposes to Inherited Erythroid Myelodysplasia/Erythroleukemia Blood. 126: 4105-4105. DOI: 10.1182/Blood.V126.23.4105.4105 |
0.349 |
|
| 2014 |
Braunstein EM, Moliterno AR. Back to biology: new insights on inheritance in myeloproliferative disorders. Current Hematologic Malignancy Reports. 9: 311-8. PMID 25195195 DOI: 10.1007/S11899-014-0232-3 |
0.324 |
|
| 2013 |
Yuan X, Braunstein EM, Ye Z, Liu CF, Chen G, Zou J, Cheng L, Brodsky RA. Generation of glycosylphosphatidylinositol anchor protein-deficient blood cells from human induced pluripotent stem cells. Stem Cells Translational Medicine. 2: 819-29. PMID 24113066 DOI: 10.5966/Sctm.2013-0069 |
0.396 |
|
| 2009 |
Braunstein EM, Monks DC, Aggarwal VS, Arnold JS, Morrow BE. Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis. Bmc Developmental Biology. 9: 31. PMID 19476657 DOI: 10.1186/1471-213X-9-31 |
0.614 |
|
| 2009 |
Monks DC, Braunstein EM, Morrow BE. Tbx1 regulates mesenchymal–epithelial signaling necessary for inner ear development Developmental Biology. 331: 477-478. DOI: 10.1016/J.Ydbio.2009.05.342 |
0.628 |
|
| 2008 |
Braunstein EM, Crenshaw EB, Morrow BE, Adams JC. Cooperative function of Tbx1 and Brn4 in the periotic mesenchyme is necessary for cochlea formation. Journal of the Association For Research in Otolaryngology : Jaro. 9: 33-43. PMID 18231833 DOI: 10.1007/S10162-008-0110-6 |
0.698 |
|
| 2006 |
Arnold JS, Braunstein EM, Ohyama T, Groves AK, Adams JC, Brown MC, Morrow BE. Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients. Human Molecular Genetics. 15: 1629-39. PMID 16600992 DOI: 10.1093/Hmg/Ddl084 |
0.73 |
|
| 2006 |
Arnold JS, Werling U, Braunstein EM, Liao J, Nowotschin S, Edelmann W, Hebert JM, Morrow BE. Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations. Development (Cambridge, England). 133: 977-87. PMID 16452092 DOI: 10.1242/Dev.02264 |
0.723 |
|
| 2005 |
McBride SM, Choi CH, Wang Y, Liebelt D, Braunstein E, Ferreiro D, Sehgal A, Siwicki KK, Dockendorff TC, Nguyen HT, McDonald TV, Jongens TA. Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome. Neuron. 45: 753-64. PMID 15748850 DOI: 10.1016/J.Neuron.2005.01.038 |
0.323 |
|
| 2002 |
Madison BB, Dunbar L, Qiao XT, Braunstein K, Braunstein E, Gumucio DL. cis elements of the villin gene control expression in restricted domains of the vertical (crypt) and horizontal (duodenum, cecum) axes of the intestine Journal of Biological Chemistry. 277: 33275-33283. PMID 12065599 DOI: 10.1074/Jbc.M204935200 |
0.371 |
|
| 2002 |
Braunstein EM, Qiao XT, Madison B, Pinson K, Dunbar L, Gumucio DL. Villin: A marker for development of the epithelial pyloric border Developmental Dynamics. 224: 90-102. PMID 11984877 DOI: 10.1002/Dvdy.10091 |
0.326 |
|
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