Two years ago, the very first NR2F1 Family and Scientific Conference was held in Orlando, Florida. Last month, the second Conference took place in Orlando on April 3 – 5....
Posted by | April 15, 2024
Dr. Magdalena Laugsch, genetic researcher Dr. Magdalena Laugsch, of the Heidelberg Institute for Human Genetics, is a researcher in the field of genetics. She obtained her Ph.D. degree at the Institute...
Posted by | February 12, 2024
With 2024 having come to an end, we want to take a moment to look back on all that we achieved. The NR2F1 Foundation has accomplished a great deal, especially...
Posted by | October 30, 2023
First research strategy meeting In January this year we held our first ever Strategic Planning session and developed our 5-year strategy (check it out here on our website). On October...
Posted by | September 20, 2023
We have some exciting news! The NR2F1 Foundation will be hosting a research development meeting next month at the University of Denver in Colorado. Scheduled to run all day Saturday,...
Posted by | July 11, 2023
June 10th, 2023, was a beautiful sunny day in Philadelphia, PA, as hundreds of cyclists rode to raise money for rare disease research. Riders had a choice of what distance...
Posted by | March 16, 2023
In collaboration with a multi-disciplinary CVI team led by Dr. Veeral Shah, a pediatric neuro-ophthalmologist, the NR2F1 Foundation helped make history with the launch of the first day of the...
Posted by | January 6, 2023
The NR2F1 Foundation had a tremendous year of achievements in 2022, so as the year has come to a close, we look back and reflect on all that has happened during...
Posted by | December 7, 2022
One of the primary objectives of the NR2F1 Foundation has been the expansion of our global research network for BBSOAS research. We will provide initial funds for a project called...
Posted by | August 23, 2022
Edith In March of 2020, 12 months-old Edith received the diagnosis of having BBSOAS, also known as Bosch-Boonstra-Schaaf Optic Atrophy Syndrome. It is one of the rarest neurological disorders in...
