Articles with public access mandates - Michael Snyder - Genome CanadaLearn 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 UKDoris Duke Charitable FoundationLeducq Foundation, USASusan G. KomenNASAFWODNRFOTKAFormasDHFGovernment 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
Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing
G Robertson, M Hirst, M Bainbridge, M Bilenky, Y Zhao, T Zeng, ...
Nature methods 4 (8), 651-657, 2007
Available based on mandate: 5
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Mapping pathways and phenotypes by systematic gene overexpression
R Sopko, D Huang, N Preston, G Chua, B Papp, K Kafadar, M Snyder, ...
Molecular cell 21 (3), 319-330, 2006
Genome-wide relationship between histone H3 lysine 4 mono-and tri-methylation and transcription factor binding
AG Robertson, M Bilenky, A Tam, Y Zhao, T Zeng, N Thiessen, T Cezard, ...
Genome research 18 (12), 1906-1917, 2008
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway
GM Enns, V Shashi, M Bainbridge, MJ Gambello, FR Zahir, T Bast, ...
Genetics in Medicine 16 (10), 751-758, 2014
Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients
L Bryant, D Li, SG Cox, D Marchione, EF Joiner, K Wilson, K Janssen, ...
Science advances 6 (49), eabc9207, 2020
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