Janel O. Johnson
National Institutes of Health(US)National Institute on Aging(US)
Publications by Year
Research Areas
Amyotrophic Lateral Sclerosis Research, Neurogenetic and Muscular Disorders Research, Neurological diseases and metabolism, Genetic Neurodegenerative Diseases, Parkinson's Disease Mechanisms and Treatments
Most-Cited Works
- → A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD(2011)4,423 cited
- → Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS(2010)1,222 cited
- → Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study(2012)1,213 cited
- → Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis(2014)441 cited
- → A Genome-Wide Association Study of Myasthenia Gravis(2015)218 cited
- → Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis(2014)151 cited
- → Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease(2012)138 cited
- → Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis(2012)102 cited
- → Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation inC19orf12(2013)92 cited
- → Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis(2021)78 cited