Skip to main content
Premium Trial:

Request an Annual Quote

People in the News: Richard Klausner, Dietrich Stephan

Premium

Richard Klausner has been named senior vice president and chief medical officer at Illumina.

Klausner joins Illumina from the Column Group, a venture capital firm. He previously served as executive director for global health at the Bill and Melinda Gates Foundation and as director of the US National Cancer Institute from 1995 to 2001.

Klausner holds an MD from Duke Medical School.


Dietrich Stephan has been named chair of the department of human genetics at the University of Pittsburgh Graduate School of Public Health and will also serve as the associate director of the Institute for Personalized Medicine, a collaborative initiative between the University of Pittsburgh Schools of the Health Sciences and UPMC.

Stephan was most recently founder, president, and CEO of Silicon Valley Biosystems. He also co-founded personal genetics firm Navigenics. Prior to that, Stephan held a number of roles at the Translational Genomics Research Institute, including director of neurogenomics. He was also head of the NIH Neuroscience Microarray Consortium for seven years.

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.