D. Goossens

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

Kristel Sleegers, Nathalie Brouwers, Ilse Gijselinck et al. · Brain · 2006 · 404 citations · Full text

Genomic App Duplication, Cerebral Amyloid Angiopathy, Genetics +19

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1

Arvid Suls, Peter Dedeken, Karolien Goffin et al. · Brain · 2008 · 340 citations · Full text

Neurological Disorder, Glucose Uptake, Social Sciences +16

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis et al. · Nature Genetics · 2005 · 259 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Molecular Neuroscience +8

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

Yurii S. Aulchenko, Ilse A Hoppenbrouwers, Sreeram V. Ramagopalan et al. · Nature Genetics · 2008 · 193 citations

Disease Susceptibility, Genetic Disorder, Genetics +7

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

Yukihide Momozawa, Myriam Mni, Kayo Nakamura et al. · Nature Genetics · 2010 · 186 citations · Full text

Inflammation, Immunology, Pathology +6