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Dr Adam Jackson is an Academic Clinical Fellow at the Manchester Centre for Genomic Medicine, part of Manchester University NHS Foundation Trust and The University of Manchester. He holds the qualifications MBChB, MSc, PhD and MRCP. His research focuses on identifying genetic causes of severe epilepsy and neurodevelopmental disorders, including leading studies on biallelic variants in the RNU2-2 gene published in Nature Genetics in 2026. He serves as an early career researcher in the NIHR Manchester BRC’s Rare Conditions Theme and has contributed to discoveries improving diagnoses for patients with rare genetic conditions.
