Articles with public access mandates - Blair H Smith - European CommissionLearn more
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
Available based on mandate: 50
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
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
Neuropathic pain: an updated grading system for research and clinical practice
NB Finnerup, S Haroutounian, P Kamerman, R Baron, DLH Bennett, ...
Pain 157 (8), 1599-1606, 2016
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
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
A Okbay, Y Wu, N Wang, H Jayashankar, M Bennett, SM Nehzati, ...
Nature genetics 54 (4), 437-449, 2022
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
J Wessel, AY Chu, SM Willems, S Wang, H Yaghootkar, JA Brody, ...
Nature communications 6 (1), 5897, 2015
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
AE Justice, TW Winkler, MF Feitosa, M Graff, VA Fisher, K Young, L Barata, ...
Nature communications 8 (1), 14977, 2017
Genome-wide association for major depression through age at onset stratification: major depressive disorder working group of the psychiatric genomics consortium
RA Power, KE Tansey, HN Buttenschøn, S Cohen-Woods, T Bigdeli, ...
Biological psychiatry 81 (4), 325-335, 2017
Effect of smoking on blood pressure and resting heart rate: a Mendelian randomization meta-analysis in the CARTA consortium
A Linneberg, RK Jacobsen, T Skaaby, AE Taylor, ME Fluharty, ...
Circulation: Cardiovascular Genetics 8 (6), 832-841, 2015
Directional dominance on stature and cognition in diverse human populations
PK Joshi, T Esko, H Mattsson, N Eklund, I Gandin, T Nutile, AU Jackson, ...
Nature 523 (7561), 459-462, 2015
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
MT Landi, DT Bishop, S MacGregor, MJ Machiela, AJ Stratigos, P Ghiorzo, ...
Nature genetics 52 (5), 494-504, 2020
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
P Suri, MR Palmer, YA Tsepilov, MB Freidin, CG Boer, MS Yau, DS Evans, ...
PLoS genetics 14 (9), e1007601, 2018
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 52 (12), 1314-1332, 2020
Risk factors for neuropathic pain in diabetes mellitus
HL Hébert, A Veluchamy, N Torrance, BH Smith
Pain 158 (4), 560-568, 2017
Multiancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions
PS De Vries, MR Brown, AR Bentley, YJ Sung, TW Winkler, I Ntalla, ...
American journal of epidemiology 188 (6), 1033-1054, 2019
Cohort profile: genetics of diabetes audit and research in Tayside Scotland (GoDARTS)
HL Hebert, B Shepherd, K Milburn, A Veluchamy, W Meng, F Carr, ...
International journal of epidemiology 47 (2), 380-381j, 2018
The genetics of neuropathic pain from model organisms to clinical application
M Calvo, AJ Davies, HL Hebert, GA Weir, EJ Chesler, NB Finnerup, ...
Neuron 104 (4), 637-653, 2019
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
N Rahmioglu, S Mortlock, M Ghiasi, PL Møller, L Stefansdottir, ...
Nature genetics 55 (3), 423-436, 2023
Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations
O Van Hecke, PR Kamerman, N Attal, R Baron, G Bjornsdottir, ...
Pain 156 (11), 2337-2353, 2015
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