Andrew R.J. Curtis

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease

Andrew R.J. Curtis, Constanze Fey, Christopher M. Morris et al. · Nature Genetics · 2001 · 539 citations

Neurodegenerative Diseases, Molecular Neuroscience, Genetic Disorder +11

Neuroferritinopathy: A Window on the Role of Iron in Neurodegeneration

Douglas E. Crompton, Patrick F. Chinnery, Constanze Fey et al. · Blood Cells Molecules and Diseases · 2002 · 75 citations

Neurodegenerative Diseases, Neurological Disorder, Neuroprotection +5

Preliminary observation of elevated levels of nanocrystalline iron oxide in the basal ganglia of neuroferritinopathy patients

Dimitri Hautot, Quentin A. Pankhurst, Christopher M. Morris et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2006 · 70 citations · Full text

Nanomedicine, Neuroferritinopathy Patients, Neurobiology Of Disease +12

Narrowing the Critical Region within 11q24–qter for Hypoplastic Left Heart and Identification of a Candidate Gene, JAM3, Expressed during Cardiogenesis

Helen M. Phillips, Glenn L. Renforth, C. Mirella Spalluto et al. · Genomics · 2002 · 50 citations

Cardiomyopathy, Systems Biology, Cardiac Reprogramming +10

Adult‐onset generalized dystonia due to a mutation in the neuroferritinopathy gene

Pablo Mir, Mark J. Edwards, Andrew R.J. Curtis et al. · Movement Disorders · 2004 · 32 citations