Brendan Kelley

Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis

Nicola J. Rutherford, Yong‐Jie Zhang, Matt Baker et al. · PLoS Genetics · 2008 · 458 citations · Full text

Neurodegenerative Diseases, Ubiquitin Inclusions, Amyotrophic Lateral Sclerosis +13

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative

Rosa Rademakers, Matt Baker, Jennifer Gass et al. · The Lancet Neurology · 2007 · 216 citations

Mendelian Disorder, Genetic Disorder, Genetics +10

Prominent phenotypic variability associated with mutations in Progranulin

Brendan Kelley, Wael Haidar, Bradley F. Boeve et al. · Neurobiology of Aging · 2007 · 181 citations · Full text

Biology, Mendelian Disorder, Genetic Disorder +6

Vascular risk factors and cognitive impairment in a stroke-free cohort

Fred Unverzagt, Leslie A. McClure, Virginia G. Wadley et al. · Neurology · 2011 · 145 citations · Full text

Young-Onset Dementia

Brendan Kelley, Bradley F. Boeve, Keith A. Josephs · Archives of Neurology · 2008 · 122 citations