Simon Hammans

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

Christopher J. Klein, Maria Victoria Botuyan, Yanhong Wu et al. · Nature Genetics · 2011 · 395 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations

Ichizo Nishino, Antonella Spinazzola, Alexandros Papadimitriou et al. · Annals of Neurology · 2000 · 343 citations

Life Sciences, Genetics, Neurology +17

Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

Beverley Anderson, Paul R. Kasher, Joséphine Mayer et al. · Nature Genetics · 2012 · 291 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.

M A McShane, Simon Hammans, M G Sweeney et al. · PubMed · 1991 · 255 citations

Life Sciences, Neurology, Neuroscience +14

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

Simon Hammans, M G Sweeney, Martin Brockington et al. · The Lancet · 1991 · 182 citations

Life Sciences, Genetics, Molecular Genetics +16