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

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

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2001 2017

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: Research - peer-reviewArticle

complement
neurons
toxicity
mutation
genes

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: Research - peer-reviewArticle

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: Research - peer-reviewLetter

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: Research - peer-reviewArticle

Induced Pluripotent Stem Cells
Alleles
Gene Editing
Clustered Regularly Interspaced Short Palindromic Repeats
Point Mutation

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

Churpek, J. E. , Pyrtel, K. , Kanchi, K. L. , Shao, J. , Koboldt, D. , Miller, C. A. , Shen, D. , Fulton, R. , O'Laughlin, M. , Fronick, C. , Pusic, I. , Uy, G. L. , Braunstein, E. M. , Levis, M. , Ross, J. , Elliott, K. , Heath, S. , Jiang, A. , Westervelt, P. , DiPersio, J. F. & 7 others Link, D. C., Walter, M. J., Welch, J., Wilson, R., Ley, T. J., Godley, L. A. & Graubert, T. A. Nov 26 2015 In : Blood. 126, 22, p. 2484-2490 7 p.

Research output: Research - peer-reviewArticle

Myelodysplastic Syndromes
Germ Cells
Familial Acute Myeloid Leukemia with Mutated Cebpa
Genes
Acute Myeloid Leukemia