Articles with public access mandates - Michael Snyder - Wellcome TrustLearn 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: 3
Prediction of susceptibility to first-line tuberculosis drugs by DNA sequencing
CRyPTIC Consortium and the 100,000 Genomes Project
New England Journal of Medicine 379 (15), 1403-1415, 2018
Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity
S Zhang, J Cooper-Knock, AK Weimer, C Harvey, TH Julian, C Wang, J Li, ...
medRxiv, 2021.06. 15.21258703, 2021
BRAIN COMMUNICATIONS AIN COMMUNICATIONS
S Boddy, M Islam, T Moll, JKD Burrows, A McGown, A Bhargava, ...
Available based on mandate: 26
The GTEx Consortium atlas of genetic regulatory effects across human tissues
GTEx Consortium
Science 369 (6509), 1318-1330, 2020
A comparative encyclopedia of DNA elements in the mouse genome
F Yue, Y Cheng, A Breschi, J Vierstra, W Wu, T Ryba, R Sandstrom, Z Ma, ...
Nature 515 (7527), 355-364, 2014
Dynamic landscape and regulation of RNA editing in mammals
MH Tan, Q Li, R Shanmugam, R Piskol, J Kohler, AN Young, KI Liu, ...
Nature 550 (7675), 249-254, 2017
A high-stringency blueprint of the human proteome
S Adhikari, EC Nice, EW Deutsch, L Lane, GS Omenn, SR Pennington, ...
Nature communications 11 (1), 5301, 2020
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci
V Tragante, MR Barnes, SK Ganesh, MB Lanktree, W Guo, ...
The American Journal of Human Genetics 94 (3), 349-360, 2014
Co-expression networks reveal the tissue-specific regulation of transcription and splicing
A Saha, Y Kim, ADH Gewirtz, B Jo, C Gao, IC McDowell, BE Engelhardt, ...
Genome research 27 (11), 1843-1858, 2017
Multiomics modeling of the immunome, transcriptome, microbiome, proteome and metabolome adaptations during human pregnancy
MS Ghaemi, DB DiGiulio, K Contrepois, B Callahan, TTM Ngo, ...
Bioinformatics 35 (1), 95-103, 2019
Physical exercise is a risk factor for amyotrophic lateral sclerosis: Convergent evidence from Mendelian randomisation, transcriptomics and risk genotypes
TH Julian, N Glascow, ADF Barry, T Moll, C Harvey, YC Klimentidis, ...
EBioMedicine 68, 2021
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
The gut microbiome: a key player in the complexity of amyotrophic lateral sclerosis (ALS)
SL Boddy, I Giovannelli, M Sassani, J Cooper-Knock, MP Snyder, E Segal, ...
BMC medicine 19, 1-14, 2021
Biallelic mutations in ATP5F1D, which encodes a subunit of ATP synthase, cause a metabolic disorder
M Oláhová, WH Yoon, K Thompson, S Jangam, L Fernandez, ...
The American Journal of Human Genetics 102 (3), 494-504, 2018
Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis
F Yang, J Wang, BL Pierce, LS Chen, F Aguet, KG Ardlie, BB Cummings, ...
Genome research 27 (11), 1859-1871, 2017
Engineering genetic predisposition in human neuroepithelial stem cells recapitulates medulloblastoma tumorigenesis
M Huang, J Tailor, Q Zhen, AH Gillmor, ML Miller, H Weishaupt, J Chen, ...
Cell stem cell 25 (3), 433-446. e7, 2019
A review of Mendelian randomization in amyotrophic lateral sclerosis
TH Julian, S Boddy, M Islam, J Kurz, KJ Whittaker, T Moll, C Harvey, ...
Brain 145 (3), 832-842, 2022
De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease
S Takahashi, G Andreoletti, R Chen, Y Munehira, A Batra, NA Afzal, ...
Genome medicine 9, 1-11, 2017
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
WISP3 mutation associated with pseudorheumatoid dysplasia
MR Sailani, J Chappell, I Jingga, A Narasimha, A Zia, JL Lynch, ...
Molecular Case Studies 4 (1), a001990, 2018
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