Fingerprint Fingerprint is based on mining the text of the persons scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 3 Similar Profiles
DiGeorge Syndrome Medicine & Life Sciences
Mesoderm Medicine & Life Sciences
Induced Pluripotent Stem Cells Medicine & Life Sciences
Glycosylphosphatidylinositols Medicine & Life Sciences
Genes Medicine & Life Sciences
Cochlea Medicine & Life Sciences
Inner Ear Medicine & Life Sciences
Ear Medicine & Life Sciences

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Research Output 2001 2018

A case report on 2 unique presentations of upper extremity deep vein thrombosis

Yunce, M., Sharma, A., Braunstein, E., Streiff, M. B. & Lum, Y. W. Mar 1 2018 In : Medicine (United States). 97, 11, e9944

Research output: Contribution to journalArticle

Upper Extremity Deep Vein Thrombosis
Upper Extremity
Thoracic Outlet Syndrome
Surgical Decompression
Subclavian Vein

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

Yuan, X., Li, Z., Baines, A. C., Gavriilaki, E., Ye, Z., Wen, Z., Braunstein, E. M., Biesecker, L. G., Cheng, L., Dong, X. & Brodsky, R. A. Apr 1 2017 In : PLoS ONE. 12, 4, e0174074

Research output: Contribution to journalArticle

Glycosylphosphatidylinositols
Neurons
Toxicity
complement
neurodevelopment

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

Braunstein, E. M., Li, R., Sobreira, N., Marosy, B., Hetrick, K., Doheny, K., Gocke, C. D., Valle, D., Brodsky, R. A. & Cheng, L. Jul 15 2016 (Accepted/In press) In : Leukemia.

Research output: Contribution to journalArticle

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

Li, R., Sobreira, N., Witmer, P. D., Pratz, K. W. & Braunstein, E. M. May 31 2016 In : Haematologica. 101, 6, p. e228-e231

Research output: Contribution to journalLetter

Germ-Line Mutation
Acute Myeloid Leukemia

Efficient and allele-specific genome editing of disease loci in human iPSCs

Smith, C., Abalde-Atristain, L., He, C., Brodsky, B. R., Braunstein, E. M., Chaudhari, P., Jang, Y. Y., Cheng, L. & Ye, Z. Mar 5 2015 In : Molecular Therapy. 23, 3, p. 570-577 8 p.

Research output: Contribution to journalArticle

Induced Pluripotent Stem Cells
Clustered Regularly Interspaced Short Palindromic Repeats
Alleles
Point Mutation
Guide RNA