Diana W Bianchi

Early life and education

Bianchi grew up in New York City. She graduated from Hunter College High School.

Bianchi earned a B.A. magna cum laude from University of Pennsylvania and an M.D. from Stanford University School of Medicine. While at Stanford she performed her doctoral research with Leonard Herzenberg, Ph.D., studying the use of flow cytometry to develop a noninvasive cytogenetic prenatal diagnostic test for Down syndrome. One of Herzenberg’s children had Down syndrome, so the project had both scientific and personal significance for her mentor. She completed her postdoctoral work at Boston Children’s Hospital and Harvard Medical School.

Career

Bianchi joined the faculty at Harvard University in 1986, concurrently assuming a position as an attending neonatologist and geneticist at Boston Children’s Hospital. In 1993, Bianchi left to take a position at Tufts University School of Medicine, receiving an endowed chair in 2002.

In 2007, Bianchi became Editor-in-Chief of Prenatal Diagnosis, the official journal of the International Society for Prenatal Diagnosis. In 2010, she founded the Mother Infant Research Institute (MIRI) at Tufts Medical Center, assuming the position of Executive Director. Bianchi is one of four authors of the book Fetology: Diagnosis and Management of the Fetal Patient, which won the Association of American Publishers award for the best textbook in clinical medicine in 2000.

Bianchi has worked for many years on developing methods to isolate intact fetal cells from maternal blood as a noninvasive way to obtain fetal material for genetic diagnosis. While the work proved challenging due to the relative rarity of the fetal cells in the mother’s blood, the research led to an unexpected finding. Bianchi discovered that intact fetal cells remain in the mother's blood and organs for decades following pregnancy, with the possibility of migrating to the site of an injury in the mother, dividing and changing into the cells needed to fix the problem. This has led to a field of study known as fetal cell microchimerism.

Bianchi also has worked extensively on noninvasive prenatal testing (NIPT) using DNA sequencing of fetal and placental DNA fragments in the blood of pregnant women. This technology has been used in clinical prenatal care since 2011. In addition, Bianchi has pioneered the study of the amniotic fluid fetal transcriptome to develop new approaches to prenatal treatment of genetic conditions. She is a former member of the Clinical Advisory Board of Verinata Health, an Illumina company.

In 2014, Bianchi was the lead author on a study published in the New England Journal of Medicine that examined cell free fetal DNA test performance in a general obstetrical population. This study showed that cell free DNA testing had lower false positive rates and higher positive predictive values than maternal serum biochemistry analyses with or without ultrasound measurements of the back of the fetal neck. Bianchi has also studied the underlying biological reasons for false positive results following NIPT. She has shown that maternal malignancies can cause genome-wide imbalance that presents as a false positive result of fetal aneuploidy. Currently, Bianchi is working with a mouse model to develop a prenatal treatment that could be given to a pregnant woman carrying a fetus with Down syndrome. The goal of the work is to improve brain development in the womb and neurocognition after birth.

Bianchi was appointed as NICHD Director on August 25, 2016. In this role, she oversees research on pediatric health and development, maternal health, medical rehabilitation, population dynamics, reproductive health, and intellectual and developmental disabilities.

Significant papers

Awards

Leadership positions in professional societies

Patents issued