Parastoo Momeni

Frontotemporal dementia and its subtypes: a genome-wide association study

Raffaele Ferrari, Dena G. Hernandez, Michael A. Nalls et al. · The Lancet Neurology · 2014 · 394 citations · Full text

Alzheimer's Disease, Dementia, Frontotemporal Dementia +3

Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I

Parastoo Momeni, Gernot Glöckner, Olaf Schmidt et al. · Nature Genetics · 2000 · 372 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

H.‐J. Lüdecke, Jörg Schaper, Peter Meinecke et al. · The American Journal of Human Genetics · 2001 · 234 citations · Full text

Genetic Disorder, Genetics, Genetic Epidemiology +4

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

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

M. Masellis, Parastoo Momeni, Wendy S. Meschino et al. · Brain · 2006 · 198 citations