Articles with public access mandates - Blair H Smith - National Institute for Health Research, UKLearn more
NoteFor this mandate, articles should be available from specific locations.
OverallMRCWellcomeNIHCSOBBSRCNIHREuropean CommissionBHFESRCCancer Research UKDFGNHMRCAcademy of FinlandNWOVersus Arthritis, UKSwedish Research CouncilZonMwBMBFAHAVAUK Research & InnovationSNSFARCCIHRHelmholtzDHFDFFDiabetes UKDoris Duke Charitable FoundationGovernment of SpainGovernment of ItalyLeducq Foundation, USAFWOINSERMKnut and Alice Wallenberg FoundationDMTJDRFHealth Data Research, UKMacArthurNSFCDCTIAction on Hearing Loss, UKNSFFWFFRQSGenome CanadaSSHRCA*StarEPSRCDOEGatesDoDUSEDUSDAIDRCNSERCDNRFDSFTekesFORTEMarianne and Marcus Wallenberg FoundationBank of Sweden Tercentenary FoundationNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKFondazione CariploRCNNMRCAIRC Foundation for Cancer Research in ItalyNational Research Foundation, SingaporeRoyal Society UKMedical Research Future Fund, AustraliaHealth and Care Research Wales
Not available based on mandate: 11
Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease
MR Johnson, K Shkura, SR Langley, A Delahaye-Duriez, P Srivastava, ...
Nature neuroscience 19 (2), 223-232, 2016
Systematic review and meta-analysis of genetic risk factors for neuropathic pain
A Veluchamy, HL Hebert, W Meng, CNA Palmer, BH Smith
Pain 159 (5), 825-848, 2018
Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions
R Nilufer, B Karina, C Paraskevi, D Rebecca, G Genevieve, G Ayush, ...
BioRxiv, 406967, 2018
New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries
N Shrine, AL Guyatt, AM Erzurumluoglu, VE Jackson, BD Hobbs, ...
BioRxiv, 343293, 2018
Multi-ancestry genome-wide association study improves resolution of genes, pathways and pleiotropy for lung function and chronic obstructive pulmonary disease
N Shrine, AG Izquierdo, J Chen, R Packer, RJ Hall, AL Guyatt, C Batini, ...
medrxiv, 2022.05. 11.22274314, 2022
SMIM1 absence is associated with reduced energy expenditure and excess weight
L Stefanucci, C Moslemi, AR Tomé, S Virtue, G Bidault, NS Gleadall, ...
Med, 2024
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
SM Willems, NHJ Ng, J Fernandez, RS Fine, E Wheeler, J Wessel, ...
Wellcome Open Research 8 (483), 483, 2023
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
BH Smith, C Palmer, X Zhu, CD Brown
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
P Surendran, EV Feofanova, N Lahrouchi, I Ntalla, S Karthikeyan, J Cook, ...
Nature genetics 53 (5), 762-762, 2021
Assessing the impact of SIGN 136 on opioid prescribing rates in Scotland: An interrupted time series analysis
HL Hébert, DR Morales, N Torrance, BH Smith, LA Colvin
medRxiv, 2021.02. 19.21251770, 2021
SNPs associated with HHIP expression have differential effects on lung function in males and females
KA Fawcett, M Obeidat, CA Melbourne, N Shrine, AL Guyatt, C John, ...
bioRxiv, 594457, 2019
Available based on mandate: 42
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
JJ Lee, R Wedow, A Okbay, E Kong, O Maghzian, M Zacher, ...
Nature genetics 50 (8), 1112-1121, 2018
Physical activity and exercise for chronic pain in adults: an overview of Cochrane Reviews
LJ Geneen, RA Moore, C Clarke, D Martin, LA Colvin, BH Smith
Cochrane database of systematic reviews, 2017
Genome-wide association study identifies 74 loci associated with educational attainment
A Okbay, JP Beauchamp, MA Fontana, JJ Lee, TH Pers, CA Rietveld, ...
Nature 533 (7604), 539-542, 2016
Timing, rates and spectra of human germline mutation
R Rahbari, A Wuster, SJ Lindsay, RJ Hardwick, LB Alexandrov, S Al Turki, ...
Nature genetics 48 (2), 126-133, 2016
The IASP classification of chronic pain for ICD-11: chronic neuropathic pain
J Scholz, NB Finnerup, N Attal, Q Aziz, R Baron, MI Bennett, R Benoliel, ...
Pain 160 (1), 53-59, 2019
Large-scale discovery of novel genetic causes of developmental disorders
Nature 519 (7542), 223-228, 2015
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
R Karlsson Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, ...
Nature genetics 51 (2), 245-257, 2019
Exome-wide association study of plasma lipids in> 300,000 individuals
DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ...
Nature genetics 49 (12), 1758-1766, 2017
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
A Mahajan, J Wessel, SM Willems, W Zhao, NR Robertson, AY Chu, ...
Nature genetics 50 (4), 559-571, 2018
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