Ese Mudanohwo

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

Laurie Robak, Iris E. Jansen, Jeroen van Rooij et al. · Brain · 2017 · 451 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

Alexandria Beilina, Iakov N. Rudenko, Alice Kaganovich et al. · Proceedings of the National Academy of Sciences · 2014 · 367 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management

Victoria Nesbitt, Robert D. S. Pitceathly, Douglass M. Turnbull et al. · Journal of Neurology Neurosurgery & Psychiatry · 2013 · 229 citations

Life Sciences, Genetics, Molecular Genetics +17

<i>C9orf72</i> expansions are the most common genetic cause of Huntington disease phenocopies

Davina J. Hensman Moss, Mark Poulter, Jon Beck et al. · Neurology · 2013 · 203 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Huntington's disease phenocopies are clinically and genetically heterogeneous

Edward J. Wild, Ese Mudanohwo, Mary G. Sweeney et al. · Movement Disorders · 2008 · 116 citations · Full text

Life Sciences, Genetics, Neurology +14