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Biorxiv : the Preprint Server for Biology|March 13, 2023
Genome-scale requirements for dynein-based trafficking revealed by a high-content arrayed CRISPR screenChun Hao Wong, Steven W Wingett, Chen Qian, et al.
The Journal of Cell Biology|March 6, 2024
Genome-scale requirements for dynein-based transport revealed by a high-content arrayed CRISPR screenChun Hao Wong, Steven W Wingett, Chen Qian, et al.
Neurobiology of Aging|September 8, 2015
The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patientsChun Hao Wong, Simon Topp, Athina Soragia Gkazi, et al.
Neurobiology of Aging|July 17, 2021
A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decayMarc Gotkine, Martina de Majo, Chun Hao Wong, et al.
Neurobiology of Aging|December 16, 2014
Novel mutations support a role for Profilin 1 in the pathogenesis of ALSBradley N Smith, Caroline Vance, Emma L Scotter, et al.
Neurobiology of Aging|August 3, 2016
C9ORF72 and UBQLN2 mutations are causes of amyotrophic lateral sclerosis in New Zealand: a genetic and pathologic study using banked human brain tissueEmma L Scotter, Leon Smyth, J Ames W T Bailey, et al.
Neuron|April 11, 2017
Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor DevelopmentSwapna Thomas-Jinu, Patricia M Gordon, Triona Fielding, et al.
Neurobiology of Aging|July 24, 2018
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase functionMartina de Majo, Simon D Topp, Bradley N Smith, et al.
Science Translational Medicine|May 5, 2017
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosisBradley N Smith, Simon D Topp, Claudia Fallini, et al.
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