Noa Greenberg-Kushnir

3PUBLICATIONS
15CO-AUTHORS
NeonatologyGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (3)

|Oct 14, 2024
Long-term hematopoietic dysfunction in patients with large-scale mitochondrial DNA deletion syndromes.

Noa Greenberg-Kushnir, Liron D Grossmann, Assaf Arie Barg

|Dec 16, 2019
A Large Cohort of RAG1/2-Deficient SCID Patients-Clinical, Immunological, and Prognostic Analysis.

Noa Greenberg-Kushnir, Yu Nee Lee, Amos J Simon

|Jul 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.

Amos J Simon, Atar Lev, Yong Zhang

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