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Identification of recurrent mutations in Cushing’s disease

The overall goal of the Identification of recurrent mutations in Cushing’s disease project is to study the impact of whole-exome sequencing (WES) on the clinical care of cancer patients and oncology provider practices. The aims of Project are to implement and establish the feasibility of WES in patients with USP8 wild-type corticotroph adenomas; to develop a framework for understanding of the molecular mechanism of the pathogenesis of corticotroph adenoma.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001004136 Illumina HiSeq 2500 44
Publications Citations
Identification of recurrent USP48 and BRAF mutations in Cushing's disease.
Nat Commun 9: 2018 3171
61