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People in the News: Olivier Danos, Frank Witney, John Radak

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Biogen Idec has hired Olivier Danos as senior VP of gene therapy. Danos will report to Douglas Williams, executive VP of R&D at Biogen Idec. At Biogen Idec, he will be in charge of the gene therapy research group, which develops new technologies for gene transfer and genome engineering.

Before joining the firm, Danos was senior VP of molecular medicine, synthetic biology, and gene regulation at Kadmon Pharmaceuticals; directed the Gene Therapy Consortium at the University of London; and led a gene therapy research effort at the Necker Hospital, Enfants Malades in Paris.


Exagen Diagnostics has appointed Frank Witney and John Radak as independent directors, effective September 18. Witney is president and CEO of Affymetrix and Radak is CFO of the biotech product development firm ArborGen Inc.

Simultaneously, Exagen also announced that Samuel Riccitelli and Michael Walsh will no longer serve on its board. That brings the company's board of directors to seven members, six of which are independent directors.

The Scan

Positive Framing of Genetic Studies Can Spark Mistrust Among Underrepresented Groups

Researchers in Human Genetics and Genomics Advances report that how researchers describe genomic studies may alienate potential participants.

Small Study of Gene Editing to Treat Sickle Cell Disease

In a Novartis-sponsored study in the New England Journal of Medicine, researchers found that a CRISPR-Cas9-based treatment targeting promoters of genes encoding fetal hemoglobin could reduce disease symptoms.

Gut Microbiome Changes Appear in Infants Before They Develop Eczema, Study Finds

Researchers report in mSystems that infants experienced an enrichment in Clostridium sensu stricto 1 and Finegoldia and a depletion of Bacteroides before developing eczema.

Acute Myeloid Leukemia Treatment Specificity Enhanced With Stem Cell Editing

A study in Nature suggests epitope editing in donor stem cells prior to bone marrow transplants can stave off toxicity when targeting acute myeloid leukemia with immunotherapy.