Alex Morris

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

John Mitchell, Praveen Paul, Han-Jou Chen et al. · Proceedings of the National Academy of Sciences · 2010 · 243 citations · Full text

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Mendelian Disorder +15

The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder

Bradley Smith, Stephen Newhouse, Aleksey Shatunov et al. · European Journal of Human Genetics · 2012 · 229 citations · Full text

Amyotrophic Lateral Sclerosis, Genetic Disorder, Genetics +8

Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis

Han-Jou Chen, Georgia Anagnostou, Andrea Chai et al. · Journal of Biological Chemistry · 2010 · 174 citations · Full text

A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene

Tin Aung, Louise Ocaka, Neil D. Ebenezer et al. · Human Genetics · 2001 · 139 citations

Opa1 Gene, Ocular Disease, Ophthalmology +7

Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)☆

Samantha Johnson, Stephanie Halford, Alex Morris et al. · Genomics · 2003 · 105 citations

Developmental Biology, Genetic Disorder, Medicine +9