Articles with public access mandates - Michael Snyder - Motor Neurone Disease Association, UKLearn more
NoteFor this mandate, articles should be available from specific locations.
OverallNIHNSFHHMIAHAWellcomeSNSFEuropean CommissionMTADOENIHRVACIHRDFGMRCGatesNSERCNSFCGovernment of SpainDoDNKFIKnut and Alice Wallenberg FoundationSwedish Research CouncilDamon Runyon Cancer Research FoundationCZIState of CalifoniaNHMRCMotor Neurone Disease Association, UKGenome CanadaDFFBBSRCBHFCancer Research UKFWODoris Duke Charitable FoundationLeducq Foundation, USASusan G. KomenNASADNRFOTKAFormasDHFGovernment of ItalyVillum FoundationINSERMBMBFCPRITGBMFFRQSCASEMBLAcademy of FinlandNWOAcademy of Medical Sciences, UKZonMwANRKWFTUBITAKRWJFUSDAFWFARCHSFDBTTelethonESRCNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKWHOFondazione CariploKNAWNMRCUK Research & InnovationCGIARV Foundation, USALung Cancer Research Foundation, USABrain Tumour Charity, UKCarlsberg Foundation DKHFSP
Not available based on mandate: 1
BRAIN COMMUNICATIONS AIN COMMUNICATIONS
S Boddy, M Islam, T Moll, JKD Burrows, A McGown, A Bhargava, ...
Available based on mandate: 6
Low expression of EXOSC2 protects against clinical COVID-19 and impedes SARS-CoV-2 replication
T Moll, V Odon, C Harvey, MO Collins, A Peden, J Franklin, E Graves, ...
Life Science Alliance 6 (1), 2023
Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity
S Zhang, J Cooper-Knock, AK Weimer, M Shi, L Kozhaya, D Unutmaz, ...
Cell systems 13 (8), 598-614. e6, 2022
Mitochondrial function determines severity but not risk of amyotrophic lateral sclerosis
C Harvey, M Weinreich, S Zhang, PJ Hop, RAJ Zwamborn, K van Eijk, ...
BioRxiv, 2022.05. 31.494229, 2022
Unbiased metabolome screen leads to personalized medicine strategy for amyotrophic lateral sclerosis
S Boddy, M Islam, T Moll, J Kurz, D Burrows, A McGown, A Bhargava, ...
Brain Communications 4 (2), fcac069, 2022
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
S Zhang, J Cooper-Knock, AK Weimer, M Shi, T Moll, JNG Marshall, ...
Neuron 110 (6), 992-1008. e11, 2022
Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene
J Cooper-Knock, S Zhang, KP Kenna, T Moll, JP Franklin, S Allen, ...
Cell Reports 33 (9), 2020
Publication and funding information is determined automatically by a computer program