Articles with public access mandates - Michael Snyder - National Institute for Health Research, 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: 4
BRAIN COMMUNICATIONS AIN COMMUNICATIONS
S Boddy, M Islam, T Moll, JKD Burrows, A McGown, A Bhargava, ...
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
Genetic effects on gene expression across human tissues
GTEx Consortium Lead analysts: Aguet François 1 Brown Andrew A. 2 3 4 Castel ...
Nature 550 (7675), 204-213, 2017
Design and implementation of the international genetics and translational research in transplantation network
BJ Keating, J Van Setten, PA Jacobson, MV Holmes, SS Verma, ...
Transplantation 99 (11), 2401-2412, 2015
Available based on mandate: 15
Deep learning modeling of rare noncoding genetic variants in human motor neurons defines CCDC146 as a therapeutic target for ALS
S Zhang, T Moll, J Rubin-Sigler, S Tu, S Li, E Yuan, M Liu, A Butt, ...
medRxiv, 2024
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis
C Harvey, M Weinreich, JAK Lee, AC Shaw, L Ferraiuolo, H Mortiboys, ...
Heliyon 10 (3), 2024
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
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
Exerkines in health, resilience and disease
LS Chow, RE Gerszten, JM Taylor, BK Pedersen, H Van Praag, S Trappe, ...
Nature Reviews Endocrinology 18 (5), 273-289, 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
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
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
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
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
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
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
EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis
S Martin-Almedina, I Martinez-Corral, R Holdhus, A Vicente, E Fotiou, ...
The Journal of clinical investigation 126 (8), 3080-3088, 2016
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis
E Fotiou, S Martin-Almedina, MA Simpson, S Lin, K Gordon, G Brice, ...
Nature communications 6 (1), 8085, 2015
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