The aims of the public symposium are to provide an update on progress of the initiative, to hear from the childhood cancer community on recent
The webinar will include an update on the program from NIH staff, and presentations featuring findings from Kids First investigators and other data users from
Join the Children’s Brain Tumor Network(CBTN)’s operations center team as they address questions and technical issues related accessing CBTN data and conducting research within the Gabriella Miller Kids First Data Resource
On Friday, February 25, just ahead of the international observance of Rare Disease Day, you’re invited to join the NIH Common Fund-supported Gabriella Miller Kids
By CAC2 Individual Member Joe Baber Because of my grandson, Conor, a neuroblastoma survivor, I have met so many people in our childhood cancer community
[vc_row][vc_column][vc_column_text] This month, Dr. Gregory Reaman was named by the Childhood Cancer Data Initiative (CCDI) as the new Scientific Director. In this role, Dr. Reaman
The National Cancer Institute’s new Molecular Characterization Initiative (MCI) fosters data sharing in childhood cancer research. The program is expanding comprehensive molecular characterization of tumors
[vc_row][vc_column][vc_column_text] The Childhood Cancer Data Catalog is a searchable database of National Cancer Institute and other pediatric cancer resources and is part of NCI’s Childhood Cancer
The National Cancer Institute’s new Molecular Characterization Initiative (MCI) fosters data sharing in childhood cancer research. The program currently offers comprehensive molecular characterization of tumors
[vc_row][vc_column][vc_column_text][/vc_column_text][vc_single_image image=”12167″ img_size=”medium” alignment=”center”][vc_empty_space][vc_column_text]In our December CAC2 All-Member webinar, Mariah Forster Olson (Neuroblastoma Children’s Cancer Society) represented the CAC2 Survivorship Interest Group and hosted Nickhill Bhakta, MD, MPH. Dr.
