Top Stories
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As division chief and chief genomics officer at CUIMC, Dr. Posey is poised to advance Columbia's momentum in genomic medicine.
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Father-daughter team Drs. Natasha and Rudolph Leibel work in parallel at the forefront of science and medicine to improve the treatment of patients with diabetes and obesity.
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Columbia researchers are working to determine the prevalence of autoimmune diabetes with a monogenic cause and the factors that can identify those most likely to have it.
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Dr. Josh Milner studies rare causes of common diseases such as atopic dermatitis. He uses a step by step diagnostic approach to determine if there is an underlying genetic cause.
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Latest News
- March 9, 2021
Dr. Adolfo Ferrando and his lab members focus primarily on deciphering the mechanisms that lead to chemotherapy resistance and relapse in acute lymphoblastic leukemia.
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- February 26, 2021
When Dr. Wendy Chung identified the Olson children's rare disease, “It was like someone turned on the flashlight, and at least now we have a vision of how to move forward," says their mother Colleen.
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- February 25, 2021
Priyanka Ahimaz and other genetic counselors educate patients about genetic disorders and help them navigate the complexities of having a genetic diagnosis.
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- October 5, 2020
Monica Bhatia, MD, director of Columbia’s Pediatric Stem Cell Transplant Program, is participating in a trial evaluating gene editing as a curative treatment for patients with sickle cell disease.
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- October 20, 2018
Columbia’s pediatric critical care team is offering genetic sequencing to children admitted to the ICU. The goal: to arrive at more accurate diagnoses of complicated disorders.
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