Laurence A. Bindoff

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

Correlation between Genetic and Geographic Structure in Europe

Óscar Lao, Timothy T. Lu, Michael Nothnagel et al. · Current Biology · 2008 · 514 citations · Full text

Molecular Ecology, Human Variation, Medicine +8

Multi-system neurological disease is common in patients with OPA1 mutations

Patrick Yu‐Wai‐Man, Philip G. Griffiths, Gráinne S. Gorman et al. · Brain · 2010 · 437 citations · Full text

FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study

Anu Suomalainen, Jenni M. Elo, Kirsi H. Pietiläinen et al. · The Lancet Neurology · 2011 · 414 citations · Full text

Diagnostic Study, Fibrosis, Mitochondrial Function +3

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.

Neil Howell, Laurence A. Bindoff, D A McCullough et al. · PubMed · 1991 · 399 citations