Items where authors include "Cookson, MR"
Article
Johnson, JO, Chia, R, Miller, DE et al. (295 more authors) (2021) Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis. JAMA Neurology, 78 (10). pp. 1236-1248. ISSN 2168-6149
Klionsky, DJ, Abdel-Aziz, AK, Abdelfatah, S et al. (2926 more authors) (2021) Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition). Autophagy, 17 (1). pp. 1-382. ISSN 1554-8627
Janel, JO, Chia, R, Kumaran, R et al. (50 more authors) (2019) Mutations in the sphingolipid pathway gene SPTLC1 are a cause of amyotrophic lateral sclerosis. SSRN. (Submitted)
Jansen, IE, Ye, H, Heetveld, S et al. (71 more authors) (2017) Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome Biology, 18 (1). ISSN 1474-7596